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Taussig Cancer Institute
2008Outcomes
9500 Euclid Avenue, Cleveland, OH, 44195
© The Cleveland Clinic Foundation 2009
Cleveland Clinic is a nonprofit multispecialty academic medical center. Founded in 1921, it is dedicated to providing quality specialized care and includes an outpatient clinic, a hospital with more than 1,000 staffed beds, an education institute and a research institute.
Please visit us on the Web at clevelandclinic.org.
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Taussig Cancer Institute 85
Resources for Physicians
Cleveland Clinic Secure Online Services
Cleveland Clinic uses state-of-the-art digital information systems to offer secure online services such as online medical second opinions, medical record access, patient treatment progress for referring physicians (see below), and imaging interpretations by our subspecialty trained radiologists. For more information, please visit eclevelandclinic.org.
MyChart This secure online tool connects patients to their own health information from the privacy of their home any time, day or night. Some features include renewing prescriptions, reviewing test results and viewing medications, all online. For the convenience of physicians and patients across the country, MyChart now offers a secure connection to GoogleTM Health. Google Health users can securely share personal health information with Cleveland Clinic, and record and share the details of their Cleveland Clinic treatment with the physicians and healthcare providers of their choice. To establish a MyChart account, visit clevelandclinic.org/mychart.
DrConnect Whether you are referring from near or far, DrConnect streamlines communication from Cleveland Clinic physicians to your office. This complimentary online tool offers secure access to your patient’s treatment progress at Cleveland Clinic. With one-click convenience, you can track your patient’s care using the secure DrConnect website. To establish a DrConnect account, visit clevelandclinic.org/drconnect or email [email protected].
MyConsult Online Medical Second Opinion This secure online service provides specialist consultations from our Cleveland Clinic experts and remote medical second opinions for more than 1,000 life-threatening and life-altering diagnoses. MyConsult is particularly valuable for people who wish to avoid the time and expense of travel. For more information, visit clevelandclinic.org/myconsult, email [email protected] or call 800.223.2273, ext 43223.
Critical Care Transport: Anywhere in the world
Cleveland Clinic’s critical care transport team serves critically ill and highly complex patients across the globe. The transport fleet comprises mobile ICU vehicles, helicopters and fixed-wing aircraft. The transport teams are staffed by physicians, critical care nurse practitioners, critical care nurses, paramedics and ancillary staff, and are customized to meet the needs of the patient. Critical care transport is available for children and adults. To arrange a transfer for STEMI (ST elevated myocardial infarction), acute stroke, ICH (intracerebral hemorrhage), SAH (subarachnoid hemorrhage) or aortic syndromes, call 877.279.CODE (2633). For all other transfers, call 216.444.8302 or 800.553.5056.
CME Opportunities: Live and Online
Cleveland Clinic’s Center for Continuing Education’s website, clevelandclinicmeded.com, offers hundreds of convenient, complimentary learning opportunities, from webcasts and podcasts to a host of medical publications including the Disease Management Project Online Medical Textbook, with more than 150 chapters. The site also offers a schedule of live CME courses, including international summits that focus on key areas of translational research. Many live CME courses are hosted in Cleveland, an economical option for business travel. Physicians can manage their CME credits by using the myCME Web Portal. Available 24/7, the site offers CME opportunities to medical professionals across the globe.
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1
To promote quality improvement, Cleveland Clinic has created a series of Outcomes books similar to this one for many of its institutes. Designed for a physician audience, the Outcomes books contain a summary of our surgical and medical trends and approaches, data on patient volume and outcomes, and a review of new technologies and innovations.
Although we are unable to report all outcomes for all treatments provided at Cleveland Clinic — omission of outcomes for a particular treatment does not mean we necessarily do not offer that treatment — our goal is to increase
unavailable, we often report process measures associated with improved outcomes. When process measures are unavailable, we may report volume measures; a volume/outcome relationship has been demonstrated for many treatments, particularly those involving surgical techniques.
In addition to our internal efforts to measure clinical quality, Cleveland Clinic supports transparent public reporting of healthcare quality data and participates in the following public reporting initiatives:
(www.qualitycheck.org)
(www.hospitalcompare.hhs.gov)
Our commitment to providing accurate, timely information about patient care will also help patients and referring physicians make informed healthcare decisions.
quality/outcomes.
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Outcomes 20082
Dear Colleague,
On behalf of Cleveland Clinic, I am pleased to present our 2008 Outcomes books. The primary purpose of our annual Outcomes book initiative is to promote quality improvement at Cleveland Clinic, thereby optimizing the care we provide to our
accountability, transparency and results.
requiring hospitals to report more and more quality and patient safety data. We view our Outcomes books as voluntary supplements to the required public reporting and an opportunity to share selected innovations with colleagues across the country.
Designed for the physician reader, each book in the annual series focuses on care provided by one of our patient-centered
content informative.
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Taussig Cancer Institute 3
what’s inside
Institute Overview 06
Quality and Outcomes Measures
Solid Tumor Oncology 12
Colorectal Cancer 20
Upper Aerodigestive Tract 28
Esophageal 28
Contact Information 82
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Outcomes 20084
Chairman’s Letter
I am pleased to present our 2008 Outcomes, an abridged review of the Taussig Cancer Institute’s results, trends and research. The Taussig Cancer Institute continues its mission of providing innovative, high quality care through our commitment to meticulous clinical practice, augmented by a portfolio of clinical, translational and basic research, as well as undergraduate and graduate education.
As you will see in the pages that follow, we have had a busy year, with more than 600 publications (only a selection of which are listed in this book), more than 260,000 patient visits, and the acquisition of many new peer-reviewed grants, contracts, and discoveries, as well as increasing the involvement of our patients inclinical trials.
We have participated actively in many quality assurance initiatives, and have developed several business tools to
Hospital Review’s
2008, we created a new regional structure that combines our cancer initiatives across the Cleveland Clinic health
trials to open at regional sites, allowing patients to access novel therapy closer to home, and recruitment hasbeen brisk.
Our already robust translational research efforts were enhanced this year with the creation of a new Department
researchers continue to advance cancer diagnosis, prognosis and therapeutics.
prostate during radiation therapy for optimal treatment with minimal side effects.
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Taussig Cancer Institute
more patients an opportunity to mobilize stem cells for transplantation.
provide another forum for community physician education in oncology, as do our regular grand rounds sessions that are broadcast to many sites. In this edition of our Outcomesbook, we provide data on our clinical outcomes and
interesting and useful in your own practice and look forward to continued collaboration with you.
Chairman and Director, Taussig Cancer Institute
5
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Institute Overview
51Total number of
grants awarded
in 2008
Outcomes 20086
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Taussig Cancer Institute
150 +Number of national
presentations made by
Taussig Cancer Institute
staff in 2008
150 +Number of courses
taught or directed by
Taussig Cancer Institute
staff in 2008
Cleveland Clinic’s Taussig Cancer Institute provides outstanding multidisciplinary
patients individualized treatment plans based on the best standard of care and access to new and emerging treatment options. The institute is organized to include the departments of:
In addition to these departments, the institute includes the
Taussig Cancer Institute was rated number one in Ohio by U.S. News & World Reportdepartments, which are focused on multidisciplinary care, groundbreaking research, and technological advancements. We are proud to offer the same care and variety of research opportunities at many of our Cleveland Clinic regional locations as we do at Cleveland Clinic main campus. In addition, we are focused on community outreach
chemocare.com
7
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Outcomes 2008
Institute Overview
Taussig Cancer Institute
Total outpatient chairs 60
80%
patients enrolled
in investigator-
initiated trials
out of all patients
participating in
research trials
8
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Hematology and Medical Oncology
Disease Group/Treatment Outpatient Visits/Consults Inpatient Visits/Consults Patients
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10
Institute Overview
Radiation Oncology
Outcomes 2008
Radiation Oncology Special Procedures
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Regional Oncology – Hematology Oncology
Regional Oncology – Radiation Oncology
Taussig Cancer Institute 11
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Outcomes 2008
Solid Tumor Oncology | Respiratory
The multidisciplinary physician teams at the Taussig Cancer Institute are comprised of medical and radiation oncologists, surgical oncologists, and translational research physician scientists. These teams develop individual treatment plans for patients diagnosed with cancer including
productive and innovative translational research program.
Respiratory
service developed in collaboration with surgical, radiation and medical oncologists. The Thoracic
12
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100
80
60
40
20
00-3 4-6 7-9 10-12 13-15 16-18 19-21 22-24 25-27 28-30 >30
Number of Patients
Days to Appointment
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
CCRef
Appointments beyond seven days at patient’s request
appointment or on the date that accommodates their scheduling preferences. The survival
J Clin Oncol
CC = Cleveland Clinic
National Cancer Institute; 2008. http://seer.cancer.gov/faststats/selections.php?series=cancer.
patients with lung
cancer are seen within
a week of their request
for an appointment.
Lung CancerDays from New Patient Appointment Request to Appointment forPatients with Lung Cancer (N = 275)2008
Five-Year Survival for Patients with Lung Cancer (N = 2,673)
13
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14
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
Stage I CC (N = 644)Stage I RefStage II CC (N = 134)Stage II RefStage III CC (N = 864)Stage III Ref
Percent Survival
The Taussig Cancer
Institute Department
accrued the most
patients in lung
cancer trials in the
collaborative trials from
Solid Tumor Oncology | Respiratory
Outcomes 2008
CC = Cleveland Clinic
software (www.seer.cancer.gov/seerstatwww.seer.cancer.gov)
Five-Year Survival of Patients with Lung Cancer by Stage at Diagnosis (N = 1,642)
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15
Non-Small-Cell Lung Cancer
CC = Cleveland ClinicAJCC Cancer
Staging Manual
CC = Cleveland ClinicAJCC Cancer
Staging Manual
Taussig Cancer Institute
The Department of
Radiation Oncology
accrued the most
patients in lung
cancer trials for the
Radiation Therapy
Oncology Group (RTOG)
collaborative trials
from 2005 to 2008.
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 640)Stage III RefStage IV CC (N = 289)Stage IV Ref
Overall Survival of Patients with Stage II Non-Small-Cell Lung Cancer Treated with Radiation (N = 93)
Overall Survival of Patients with Stage III and IV Non-Small-Cell Lung Cancer Treated with Radiation (N = 929)
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage II CCStage II Ref
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Outcomes 2008
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 71)Stage III RefStage IV CC (N = 41)Stage IV Ref
Solid Tumor Oncology | Respiratory
Small-Cell Lung CancerOverall Survival of Patients with Stage III and IV Small-Cell Lung Cancer Treated with Radiation (N = 112)
16
CC = Cleveland ClinicAJCC Cancer
Staging Manual
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Solid Tumor Oncology | Genitourinary
The Taussig Cancer Institute’s Genitourinary (GU) Oncology Program is one of the largest and most comprehensive programs in the United States and is dedicated to exceptional clinical care including chemotherapy, radiotherapy and clinical research for patients with early through advanced disease. The primary mission is to provide clinical care and conduct clinical research for patients with GU neoplasms: testicular, bladder, prostate, kidney, and adrenal cancers. The GU Medical Oncology Program and Radiation Department enrolled 114 patients in clinical trials in 2008.
The department offers innovative state-of-the-art care for patients with prostate cancer. Image guidance for external beam radiation therapy delivery, enhanced cancer outcomes and reduced treatment-related morbidity. Cleveland Clinic’s prostate brachytherapy program is one of the largest in the country. The program also has been subjected to rigorous quality control reviews and continues its growth in both the number of patients served and the innovative approaches to treatment to reduce post-treatment toxicity. Cleveland Clinic’s prostate cancer program also is active in clinical research and was one of only six institutions to participate in a prospective study to assess quality of life after treatment for prostate cancer (Sanda MG, et al. Quality of life and satisfaction with outcome among prostate-cancer survivors. N Engl J Med. 2008;358(12):1250-61). Forty-two percent of all patients treated with brachytherapy in the trial were treated at Cleveland Clinic.
The GU Medical Oncology Program and Radiation Department enrolled 114 patients in clinical trials in 2008.
17
Outcomes 2008
Solid Tumor Oncology | Genitourinary
Treatment Type Five-Year Biochemical Relapse-Free Survival, %
Percent Biochemical Relapse-Free Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5 6 7 8 9 1310 11 12
RT (N = 497) RP (N = 1,135)PI (N = 737)
Prostate Cancer
Percent Biochemical Relapse-Free Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5 6 7 8 9 1310 11 12
RT (N = 496)RP (N = 2,124)PI (N = 1,348)
Biochemical Relapse-Free Survival for Patients with Low Risk Prostate Cancer by Treatment Type (N = 3,968)
Biochemical Relapse-Free Survival for Patients with Intermediate Risk Prostate Cancer by Treatment Type (N = 2,369)
Treatment Type Five-Year Biochemical Relapse-Free Survival, %
18
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Taussig Cancer Institute
Treatment Type Five-Year Biochemical Relapse-Free Survival, %
Percent Biochemical Relapse-Free Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5 6 7 8 9 1310 11 12
RT (N = 777) RP (N = 654)PI (N = 231)
Biochemical Relapse-Free Survival for Patients with High Risk Prostate Cancer by Treatment Type (N = 1,662)
In 2008,for the second year in
Oncology Department
performed more
than prostate
brachytherapy
procedures.
19
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Outcomes 2008
Solid Tumor Oncology | Gastrointestinal
treatment for patients with these and other rare gastrointestinal cancers such as neuroendocrine tumors and anal cancers.
of clinical trials sponsored by the National Cancer Institute, along with cooperative group trials, industry-sponsored trials,
genetic counseling to patients when warranted.
Colorectal Cancer
At the Taussig Cancer Institute, we strive to ensure patients are seen by an oncologist as soon as possible or on the date that
Ann Ocol. 2008
80
60
40
20
00-3 4-6 7-9 10-12 13-15 16-18 19-21 22-24 25-27 28-30 >30
Number of Patients
Days to Appointment
Days from New Patient Appointment Request to Appointment for Patients with Colon Cancer (N = 320)2008
20
Appointments beyond seven days at patient’s request
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CC = Cleveland Clinicwww.seer.cancer.gov/seerstat)
www.seer.cancer.gov
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 697)Stage III RefStage IV CC (N = 377)Stage IV Ref
CC = Cleveland Clinic
http://seer.cancer.gov/faststats/selections.php?series=cancer
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
CCRef
Five-Year Survival for Patients with Colon Cancer (N = 2,502)
5-Year Survival of Patients with Stage III and IV Colon Cancer by Stage at Diagnosis (N = 1,074)
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Outcomes 2008
Solid Tumor Oncology | Gastrointestinal
Surgical Expertise — Colorectal Liver Metastases
chemotherapy alone is near zero. But in a large, long-term follow-up study
Ann Surg
chorioembryonic antigen value before surgery were predictors of increasedsurvival in this study.
22
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oncologists and plastic surgeons collaborate with each patient to develop an individualized treatment plan consistent with national and international guidelines. Weekly conferences of surgeons, medical oncologists, radiation oncologists, nurses, genetic counselors, radiologists and pathologists review
and radiation are treated at the Taussig Cancer Institute.
Breast Cancer
New patients requesting an appointment at the Taussig Cancer Institute are seen within a week or on the date they prefer. Diagnosis and treatment of breast cancer at an early stage clearly improves treatment outcomes. Time-to-treatment is also a factor that may impact outcomes and has been investigated with respect
surgery (J Clin Oncol. Breast Cancer Res and Treat.
4,845Number of
patients with
breast cancer
seen in 2008
120
80
100
60
40
20
00-3 4-6 7-9 10-12 13-15 16-18 19-21 22-24 25-27 28-30 >30
Number of Patients
Days to Appointment
Days from New Patient Appointment Request to Appointment for Patients with Breast Cancer (N = 374)2008
Solid Tumor Oncology | Gynecological
Appointments beyond seven days at patient’s request
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24
Solid Tumor Oncology | Gynecological
American Joint Committee on Cancer (AJCC) Stage I-IV breast cancer CC = Cleveland Clinic Ref = Reference group as reported in: Surveillance Epidemiology and End Results (SEER): NCI’s Surveillance Research Program. Bethesda, MD: National Cancer Institute; 2008. http://seer.cancer.gov/faststats/selections.php?series=cancer. Linked to Data Type- Seer Survival; Statistic Type – Relative Survival Rates by Survival Time; Year Range – 1988-2004; Race/Ethnicity – All Races; Sex – Female; Age Range – All Ages; Cancer Site – Breast, Female. Accessed March 18, 2009.
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
CCRef
Five-Year Survival for Female Patients with Breast Cancer (N = 3,815) 1996 – 2004
Outcomes 2008
25
American Joint Committee on Cancer (AJCC) cancer staging CC = Cleveland Clinic Ref = Software: Surveillance Research Program, National Cancer Institute SEER*Stat software (www.seer.cancer.gov/seerstat) version 6.4.4. Data: Surveillance, Epidemiology, and End Results (SEER) Program (www.seer.cancer.gov) SEER*Stat Database: Incidence - SEER 17 Regs, Nov 2007 Sub (1973-2005 varying) - Linked To County Attributes - Total U.S., 1969-2005 Counties, National Cancer Institute, DCCPS, Surveillance Research Program, Cancer Statistics Branch, released March 2008, based on the November 2007 submission.
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
Stage I CC (N = 1,831)Stage I RefStage II CC (N = 1,532)Stage II RefStage III CC (N = 311)Stage III RefStage IV CC (N = 144)Stage IV Ref
Five-Year Survival of Patients with Breast Cancer by Stage at Diagnosis (N = 3,818) 1996 – 2003
Taussig Cancer Institute
Outcomes 200826
Solid Tumor Oncology | Gynecological
CC = Cleveland Clinic
al. AJCC Cancer Staging Manua
CC = Cleveland Clinic
AJCC Cancer Staging Manual
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
Stage 0 CC (N = 221)Stage 0 RefStage I or II CC (N = 1,518)Stage I or II Ref
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 232)Stage III RefStage IV CC (N = 135)Stage IV Ref
Overall Survival of Patients with Stage 0, I and II Breast Cancer Treated with Radiation (N = 1,739)
Overall Survival of Patients with Stage III and IV Breast Cancer Treated with Radiation (N = 367)
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Cervical Cancer
treatment for patients with cervical cancer.
CC = Cleveland Clinic
Int J Gynaecol Obstet
CC = Cleveland Clinic
Int J Gynaecol Obstet
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage I CC (N = 113)Stage I RefStage II CC (N = 61)Stage II Ref
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 94)Stage III RefStage IV CC (N = 30)Stage IV Ref
Overall Survival of Patients with Stage I and II Cervical Cancer Treated with Radiation (N = 174)
Overall Survival of Patients with Stage III and IV Cervical Cancer Treated with Radiation (N = 124)
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Outcomes 200828
Solid Tumor Oncology | Upper Aerodigestive Tract
The treatment of patients with cancers of the upper aerodigestive tract is based on a multidisciplinary approach involving patient assessment by surgical, medical and radiation oncologists. Individualized treatment plans for patients with these malignancies are developed through the collaborative efforts of all specialists. The treatment strategy is tailored for each patient according to the patient’s disease site, cancer stage, general health and the anticipated side effects of treatment.
chemotherapy to increase local regional control, cure rates and improve quality of life. Clinical research is primarily driven by in-house protocols.
Esophageal Cancer
CC = Cleveland Clinic
http://seer.cancer.gov/faststats/selections.php?series=cancer
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
CCRef
Five-Year Survival for Patients with Esophageal Cancer (N = 441)
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Taussig Cancer Institute
CC = Cleveland Clinicsoftware
(www.seer.cancer.gov/seerstatwww.seer.cancer.gov)
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4 5
Localized CC (N = 111)Localized RefRegional CC (N = 143)Regional RefDistant CC (N = 106)Distant Ref
Five-Year Survival of Patients with Esophageal Cancer by Stage at Diagnosis (N = 360)
29
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Outcomes 200830
Solid Tumor Oncology | Upper Aerodigestive Tract
N Engl J Med
Percent Survival
Years Since Treatment
0
6
8
4
2
10
0 1 2 3 4 5 6 7 8 9 10
Stage IIA (N = 86)Stage IIB (N = 38)Stage III (N = 161)Stage IVA (N = 61)Stage IVB (N = 34)
Overall Survival of Patients with Stage II, III and IV Esophageal Cancer Treated with Radiation (N = 380)
Percent Survival at Five Years by Stage
IIA IIB III IVA IVB
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Hypopharynx Cancer
CC = Cleveland ClinicAJCC Cancer
Staging Manual
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 15)Stage III RefStage IV CC (N = 43)Stage IV Ref
Overall Survival of Patients with Stage III and IV Hypopharynx Cancer Treated with Radiation (N = 58)
31
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Outcomes 200832
Solid Tumor Oncology | Upper Aerodigestive Tract
CC = Cleveland Clinic
ID, et al. AJCC Cancer Staging Manual
Laryngeal Cancer
CC = Cleveland Clinic
ID, et al. AJCC Cancer Staging Manual
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage I CC (N = 76)Stage I RefStage II CC (N = 58)Stage II Ref
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 52)Stage III RefStage IV CC (N = 101)Stage IV Ref
Overall Survival of Patients with Stage I and II Laryngeal Cancer Treated with Radiation (N = 134)
Overall Survival of Patients with Stage III and IV Laryngeal Cancer Treated with Radiation (N = 153)
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Taussig Cancer Institute
CC = Cleveland Clinic Ref = Reference group as reported in: Greene FL, Page DL, Fleming ID, et al. AJCC Cancer Staging Manual. 6th ed. New York, NY: Springer Science & Business Media; 2002.
Nasopharyngeal Cancer
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 17)Stage III RefStage IV CC (N = 26)Stage IV Ref
Overall Survival of Patients with Stage III and IV Nasopharyngeal Cancer Treated with Radiation (N = 43) 1996 – 2008
33
Outcomes 200834
Solid Tumor Oncology | Upper Aerodigestive Tract
Oral Cancer
CC = Cleveland Clinic
ID, et al. AJCC Cancer Staging Manual
CC = Cleveland Clinic
ID, et al. AJCC Cancer Staging Manual
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage II CCStage II Ref
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 48)Stage III RefStage IV CC (N = 128)Stage IV Ref
Overall Survival of Patients with Stage II Oral Cancer Treated with Radiation (N = 24)
Overall Survival of Patients with Stage III and IV Oral Cancer Treated with Radiation (N = 176)
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Oropharyngeal Cancer
CC = Cleveland Clinic
ID, et al. AJCC Cancer Staging Manual
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage II CCStage II Ref
Percent Survival
Years Since Treatment
0
60
80
40
20
100
0 1 2 3 4 5
Stage III CC (N = 78)Stage III RefStage IV CC (N = 251)Stage IV Ref
Overall Survival of Patients with Stage II Oropharyngeal Cancer Treated with Radiation (N = 23)
Overall Survival of Patients with Stage III and IV Oropharyngeal Cancer Treated with Radiation (N = 329)
CC = Cleveland Clinic
ID, et al. AJCC Cancer Staging Manual
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Outcomes 2008
Solid Tumor Oncology | Palliative Medicine
including prevalence and treatment. This program includes an acute inpatient palliative medicine unit, inpatient consultation
As reported by patients discharged in 2008 from palliative medicine service.
35% No35% No
65% Yes65% Yes
100%100%
Discussed at Admission/Transfer
26% No26% No
74% Yes74% Yes
100%100%
Discussed at Discharge
Advanced Directives Discussed with Patient (N = 891)2008
36
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As reported by patients discharged in 2008 from palliative medicine service.
As reported by patients discharged in 2008 from palliative medicine service.
896Number of
patients admitted
to the palliative
medicine service
in 2008
700
600
500
400
300
100
200
0
Number of Patients
Pain Present atDischarge
Present at admission (N = 603)Developed during hospital stay (N = 23)Present at discharge (N = 436)
4% Worse4% Worse
15% Same15% Same
81% Better81% Better
100%100%
Pain Reported at Admission, Developed During Stay and at Discharge (N = 626)2008
Pain Status at Discharge (N = 626)2008
37
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38
Solid Tumor Oncology | Palliative Medicine
As reported by patients discharged in 2008 from palliative medicine service.
As reported by patients discharged in 2008 from palliative medicine service.
400
300
100
200
0
Number of Patients
Dyspnea Present atDischarge
Present at admission (N = 272)Developed during hospital stay (N = 32)Present at discharge (N = 173)
15% Worse15% Worse
17% Same17% Same
68% Better68% Better
100%100%
Shortness of Breath (SOB) / Dyspnea at Admission, Developed During Stay andat Discharge (N = 304)2008
Shortness of Breath (SOB) / Dyspnea Status at Discharge (N = 304)2008
Outcomes 2008
65306_CCFBCH_Text_ACG 38 6/23/09 1:12:54 PM
39
As reported by patients discharged in 2008 from palliative medicine service.
As reported by patients discharged in 2008 from palliative medicine service.
400
300
100
200
0
Number of Patients
Nausea Present atDischarge
Present at admission (N = 271)Developed during hospital stay (N = 22)Present at discharge (N = 118)
8% Worse8% Worse11% Same11% Same
81% Better81% Better100%100%
Nausea at Admission, Developed During Stay and at Discharge (N = 293)2008
Nausea Status at Discharge (N = 293) 2008
Taussig Cancer Institute
65306_CCFBCH_Text_ACG 39 6/23/09 1:12:57 PM
Outcomes 2008
Solid Tumor Oncology | Palliative Medicine
As reported by patients discharged in 2008 from palliative medicine service.
As reported by patients discharged in 2008 from palliative medicine service.
300
100
200
0
Number of Patients
Constipation Present atDischarge
Present at admission (N = 173)Developed during hospital stay (N = 44)Present at discharge (N = 92)
21% Worse21% Worse
14% Same14% Same
65% Better65% Better
100%100%
Constipation at Admission, Developed During Stay and at Discharge (N = 217)2008
Constipation Status at Discharge (N = 217)2008
40
65306_CCFBCH_Text_ACG 40 6/23/09 1:13:00 PM
Taussig Cancer Institute
As reported by patients discharged in 2008 from palliative medicine service.
As reported by patients discharged in 2008 from palliative medicine service.
300
100
200
0
Number of Patients
Pain Present atDischarge
Present at admission (N = 161)Developed during hospital stay (N = 53)Present at discharge (N = 165)
30% Worse30% Worse
26% Same26% Same
44% Better44% Better
100%100%
Delirium at Admission, Developed During Stay and at Discharge (N = 214)2008
Delirium Status at Discharge (N = 214)2008
41
65306_CCFBCH_Text_ACG 41 6/23/09 1:13:09 PM
Outcomes 2008
Hematologic Oncology and Blood Disorders | Bone Marrow Transplant
The Taussig Cancer Institute offers patients with cancers of the blood, bone marrow,
may include chemotherapy and bone marrow transplantation. There are several specialized programs within the Taussig Cancer Institute that ensure each patient is provided optimal care.
reduced intensity, related and unrelated transplants using cell sources including bone marrow, peripheral stem cell, and umbilical cord blood for patients with leukemias, lymphomas, and other hematological malignancies and bone marrow failure states.
to providing the best clinical care and novel treatment options emerging from the
Cleveland Clinic’s Taussig Cancer Institute.
42
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Taussig Cancer Institute
Bone Marrow Transplant
peripheral stem cell and umbilical cord transplants are performed for patients with leukemias, lymphomas and other hematological malignancies and bone marrow
many ways we ensure our patients achieve successful outcomes.
100
80
02006 2007 2008
101N = 108 8948 64 62
60
40
20
Percent Survival
AllogeneicAutologous
30-Day Survival Rate in Autologous and Allogeneic Transplants (Including Mini-allo and Cord Treatment)
43
65306_CCFBCH_Text_ACG 43 6/23/09 1:13:17 PM
44
100
80
02006 2007 2008
101N = 108 8948 64 62
60
40
20
Percent Survival
AllogeneicAutologous
120
02005 2006 2007
N = 192 101 0 108 5
100
60
80
40
20
Number
Non-Relapse MortalityAutologous Transplants
100-Day Survival Rate in Autologous and Allogeneic Transplants
Non-Relapse Mortality One Year After Autologous Transplant
Outcomes 2008
Hematologic Oncology and Blood Disorders | Bone Marrow Transplant
65306_CCFBCH_Text_ACG 44 6/23/09 1:13:26 PM
45
20
02006 2007 2008
101N = 108 8948 64 62
15
10
5
Days
AllogeneicAutologous
40
02006 2007 2008
101N = 108 8948 64 62
30
20
10
Days
AllogeneicAutologous
Average Number of Days to Engraftment for Autologous and Allogeneic Transplants
Average Length of Stay for Autologous and Allogeneic Transplants
Taussig Cancer Institute
65306_CCFBCH_Text_ACG 45 6/23/09 1:13:34 PM
46
Acute Myeloid Leukemia (AML) and Acute Lymphoblastic Leukemia (ALL)
Log rank P = 0.2 Hazard ratio = 1.08 (P = 0.63)
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 2 4 6 8
Weekend, median = 0.71 years (N = 82)Weekday, median = 0.75 years (N = 253)
Overall Survival for Patients with Acute Myeloid Leukemia by Weekday and Weekend Admission (N = 335) 1994 – 2008
Outcomes 2008
Taussig Cancer Institute’s Acute Leukemia Program is a worldwide leader in the treatment of acute myeloid and lymphoblastic leukemia. Each year, about 120 new patients with a diagnosis of acute leukemia are seen at Cleveland Clinic, making this one of the largest acute leukemia programs in the world. Patient care is provided on a dedicated inpatient unit by a multidisciplinary team of physicians, nurses, physician assistants, social workers and case managers, all specializing in leukemia. In addition, patients benefit from the team’s close collaboration with the Bone Marrow Transplant Program. This specialized care results in minimal delays to the initiation of chemotherapy; negates the effect of weekend vs. weekday admission; and results in treatment-related mortality rates that are much lower, and survival rates that are much higher, than national averages. Clinical research programs optimize personalized inpatient and outpatient approaches to treating acute leukemias that are age- and disease-specific.
Hematologic Oncology and Blood Disorders | Acute Myeloid Leukemia
47
Time to Triple Lumen Catheter and Induction Therapy for Patients with Acute Myeloid Leukemia by Patient Age 1994 – 2008
Characteristic < 60 yr ≥ 60 yr P-value (N = 189) (N = 216)
Time to triple lumen catheter, mean days 2.97 2.96 0.99
Time to induction, mean days 2.1 2.7 0.02
Mortality of Patients with Acute Myeloid Leukemia by Patient Age 1994 – 2008
Mortality < 60 yr, % ≥ 60 yr, % (N = 189) (N = 216)
In-hospital 6.9 16.2
30-day 5.8 14.7
Within 15 days of chemotherapy 1.1 4.9
Taussig Cancer Institute
Outcomes 2008
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 2 4 6 8
Age ≥ 60, median survival = 0.53 years (N = 188)Age < 60, median survival = 1.3 years (N = 148)
Percent Disease-free Survival
Years Since Complete Remission
0
60
80
40
20
100
0 2 4 6
Age ≥ 60, median survival = 0.58 years (N = 73)Age < 60, median survival = 0.84 years (N = 52)
Overall Survival for Patients with Acute Myeloid Leukemia by Patient Age (N = 336)
Disease-free Survival for Patients with Acute Myeloid Leukemia by Patient Age(N = 125)
48
Hematologic Oncology and Blood Disorders | Acute Myeloid Leukemia
65306_CCFBCH_Text_ACG 48 6/23/09 1:13:43 PM
Taussig Cancer Institute 49
This research was originally published in Bloodet al. Time from diagnosis to treatment initiation predicts survival in younger, but not older, acute myeloid leukemia patients. Blood
results and the aggregate results.
This research was originally published in Bloodbut not older, acute myeloid leukemia patients. Blood
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 2 2 3 4
More than 5 days from diagnosis to treatment
P = 0.009
Less than or equal to 5 days from diagnosis to treatment
Percent Survival
Years Since Diagnosis
0
60
80
40
20
100
0 1 2 3 4
More than five days from diagnosis to treatment
P = 0.81
Less than or equal to five days from diagnosis to treatment
Survival by Interval from Diagnosis to Treatment for Patients Less Than 60 Years Old with Acute Myeloid Leukemia(N = 653)
Survival by Interval from Diagnosis to Treatment for Patients 60 or More Years Old with Acute Myeloid Leukemia(N = 664)
65306_CCFBCH_Text_ACG 49 6/23/09 1:13:46 PM
Outcomes 200850
and their families, investigation of lymphoma pathobiology, and development of innovative treatments. Individualized patient care is achieved through weekly multidisciplinary clinicopathologic conferences to ensure accurate diagnosis and determine the best treatment plan for the patient.
Percent Survival
Years Since Transplant
0
60
80
40
20
100
0 1 2 3 4
Diffuse Large B Cell Lymphoma (N = 82)Hodgkin Disease (N = 61)Follicular Lymphoma (N = 45)
Overall Survival for Patients with Lymphoma Receiving Autologous Bone Marrow Transplants (N = 188)
Hematologic Oncology and Blood Disorders | Lymphoma
65306_CCFBCH_Text_ACG 50 6/23/09 1:13:51 PM
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65306_CCFBCH_Text_ACG 51 6/23/09 1:14:02 PM
Outcomes 200852
Cleveland Clinic has placed a renewed emphasis on improving the patient
that patients seek more than solely a successful clinical outcome, the mission
the well-being of our patients, families and employees in a way that elevates Cleveland Clinic’s reputation as one of the world’s best hospitals.
institutes to research and implement innovative patient- and family-based programs that support this mission.
Outpatient – Taussig Cancer Institute
100
80
0
60
40
20
Percent
Excellent Very Good Good Fair Poor
Source: Quality Data Management, a national hospital survey vendor
2008 (N = 2,912)2007 (N = 2,824)
Overall Rating of Outpatient Care and Services
Patient Experience
65306_CCFBCH_Text_ACG 52 6/23/09 1:14:03 PM
Taussig Cancer Institute 53
Recommend Outpatient Provider
100
80
0
60
40
20
Percent
Excellent Very Good Good Fair Poor
Source: Quality Data Management, a national hospital survey vendor
2008 (N = 2,912)2007 (N = 2,824)
Rating of Outpatient Provider
100
80
0
60
40
20
Percent
ExtremelyLikely
Source: Quality Data Management, a national hospital survey vendor
Very Likely SomewhatLikely
SomewhatUnlikely
VeryUnlikely
2008 (N = 2,912)2007 (N = 2,824)
65306_CCFBCH_Text_ACG 53 6/23/09 1:14:05 PM
Outcomes 200854
100
80
0
6064% 64%
77%
40
20
Percent
Rate Hospital Would Recommend
% respondentschoosing 9 or 10
% respondents choosing'definitely yes'
Source: Quality Data Management and Press Ganey, national hospital survey vendors
For comparison purposes, 2007 and Q1 2008 HCAHPS scores have been adjusted toaccount for a survey mode administration change as recommended by CMS.
2008 total survey respondents = 4212007 total survey respondents = 341
76%
HCAHPS Overall Assessment
Inpatient – Taussig Cancer Institute
reporting are available at www.hospitalcompare.hhs.gov.
Patient Experience
65306_CCFBCH_Text_ACG 54 6/23/09 1:14:07 PM
Taussig Cancer Institute 55
100
80
0
60
40
20
Percent
DischargeInformation
DoctorCommunication
NurseCommunication
PainManagement
RoomClean
CommunicationNew Medications
Responsivenessto Needs
Quiet atNight
Respondents choosing 'always' or 'yes'
Source: Quality Data Management and Press Ganey, national hospital survey vendors
For comparison purposes, 2007 and Q1 2008 HCAHPS scores have been adjusted to account for a survey mode administration changeas recommended by CMS.
2008 total survey respondents = 4212007 total survey respondents = 341
HCAHPS Domains of Care
65306_CCFBCH_Text_ACG 55 6/23/09 1:14:08 PM
Surgical OverviewPatient Experience
New patients requesting an appointment are seen within a week or on the date they request.
5656 Outcomes 2008
65306_CCFBCH_Text_ACG 56 6/23/09 1:14:20 PM
Taussig Cancer Institute
New patients requesting an appointment at the Taussig Cancer Institute are seen within a
scheduling preferences.
Patient Access
5,000
4,000
3,000
2,000
1,000
00-3 4-6 7-9 10-12 13-15 16-18 19-21 22-24 25-27 28-30 >30
Number of Patients
Days to Appointment
57
Appointments beyond seven days at patient’s request
65306_CCFBCH_Text_ACG 57 6/23/09 1:14:24 PM
Innovations
58 Outcomes 2008
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Taussig Cancer Institute 59
Patient Care Initiatives
Patient Navigation
decades, disparities in cancer treatment and outcomes
a potentially powerful intervention for addressing these disparities.
patients in overcoming barriers and guide the patient through
additional patient navigation programs and may serve as the basis for other potential interventions designed to eliminate disparities in cancer treatment.
understand what is available and to build relationships with community centers;
community outreach endeavors;
developing relationships between Cleveland Clinic
long term;
inpatient navigation role;
Cleveland Clinic.
enrollment began on Nov. 20, 2008. The sample of patients
new patients who require chemotherapy following surgery;
that requires additional testing. During this time, we are developing processes with pathology and radiology to identify
to ensure patients receive timely diagnosis and treatment.
The navigators are working closely with the social workers,
made to the social workers to address psychosocial issues outside the navigator’s scope of practice, such as housing, substance abuse, mental health issues and prosthetics.
The navigators have encountered various barriers to care. They are working to resolve barriers to care including transportation, access to healthcare, lack of insurance and
transportation and lack of insurance. We have developed processes to address the various barriers using resources within the community and organization. We created a resource manual to serve as a quick reference, providing information on services available locally and nationally.
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Outcomes 2008
Innovations
Research Across Cleveland Clinic Health System
continues to lead the way in innovative trials availableto patients. In 2008, Taussig continued its robust research
research trials.
The new regional structure, effective in 2008, created a combined Cancer Center across Cleveland Clinic health
rising enrollment numbers because of the increased access to trials across Cleveland Clinic health system as well as a dedicated manager working as a liaison between Cleveland Clinic’s main campus and regional locations. This produced focus on choosing the most appropriate trials to open at the regional locations allowing patients to access novel therapy
disease sites.
The regional research program also is supported by the
Taussig Cancer Institute’s partnership called, “The Clinical
Taussig continues to lead the way in advances in care for patients with cancer and now provides that care closerto home.
60
700 +Number of patients
enrolled in research
trials in 2008
65306_CCFBCH_Text_ACG 60 6/23/09 1:14:37 PM
Taussig Cancer Institute
Translational Hematology and Oncology Research
translational researchers have taken in advancing cancer diagnosis, prognosis and therapeutics. As a result of improved understanding of the human genome and its
within the malignant cell that present more targets for which
SNP-A: Beyond Metaphase Cytogenetics
led to the application of whole genome scanning using high density DNA arrays as a diagnostic karyotyping test that
nucleotide polymorphisms array-based karyotyping greatly increases the diagnostic yield of traditional cytogenetics leading to detection of previously cryptic cytogenetic defects.
currently being introduced as a routine cytogenetic test.
novel, previously unappreciated type of chromosomal lesion in cancer called uniparental disomy or copy-neutral loss of heterozygosity. The importance of this type of lesion is in its relative prevalence and the fact that recurrent areas of uniparental disomy point towards the presence of mutations in genes contained in the affected areas. These studies show an association between homozygous mutations and somatic uniparental disomy, point toward a new paradigm in cytogenetics and pave the way to discovery of novel pathogenetic mutations in cancer. These studies resulted in multiple published manuscripts in Blood, British Journal of Hematology, Leukemia and Journal of Clinical Oncology.
61
65306_CCFBCH_Text_ACG 61 6/23/09 1:14:58 PM
Outcomes 2008
Innovations
62
Principles of SNP-A Karyotyping
Left:
Right:
probes, blue line represents average copy number) as well as allele copy number determination (green lines represent heterozygous cells).
decrease in the density of heterozygous cells.
Abbreviations:
This research was originally published in Blood Blood.
End-labeling
Whole genome view
CN
CN
AABBAB
65306_CCFBCH_Text_ACG 62 6/23/09 1:15:03 PM
Taussig Cancer Institute
Comparison of Current Technologies to Identify Clonal Chromosomal Lesions
clones, and ability to screen for new lesions is compared using four karyotyping techniques (top to bottom row): metaphase cytogenetics;
63
Output of Method Resolution Sensitivity UPD Dividing Cells Distinction of Screening forMethod Detection Needed Individual clones New Lesions
MetaphaseCytogenetics
FISH
SNP Arrays
CGH Arrays
Deletion 20q Trisomy 8
65306_CCFBCH_Text_ACG 63 6/23/09 1:15:06 PM
Outcomes 2008
Innovations
64
The Role of TET2 Mutations in Myelodysplastic Syndromes
Through application of whole genome scanning,
recurrent microdeletions and copy neutral loss of
inactivating mutations of this gene. TET2 appears to be a
stem cells. We have discovered that TET2 mutations are present in a large number of patients with chronic myelomonocytic leukemia in blasts crisis, myelodysplastic syndromes and myeloproliferative/myelodysplastic syndromes. This discovery has broad diagnostic implications and opens new research avenues into the pathogenesis of leukemias that result from this mutation.
evolution in several myeloid malignancies including some forms of acute myelogenous leukemia, chronic myelomonocytic leukemia and myelodysplastic syndrome.
the Cbl gene family establishing a new class of mutations in genes responsible for degradation of activated tyrosine
point towards pathogenic mechanisms and also convey very poor prognosis, they have diagnostic and therapeutic
CancerResearchsubmitted to The New England Journal of Medicine.
65306_CCFBCH_Text_ACG 64 6/23/09 1:15:24 PM
Taussig Cancer Institute
Overcoming Melanoma Resistance by Identifying andInhibiting Novel Targets
correction of causes of aberrant signaling and/or gene product
to overcome resistance to melanoma. The preliminary data generated has provided the basis for a new grant proposal
been evaluated as part of multi-institutional trials to improve currently available therapies. One of these, a monoclonal
Uveal Melanoma Micrometastasis
Department of Ophthalmic Oncology at Cleveland Clinic Cole Eye Institute, current studies in the laboratory of Dr. Triozzi have focused on uveal melanoma, the most common intra-ocular malignancy in adults. Even with advances in the diagnosis and local treatment, there has not been
disease still occuring frequently and often resulting in death. Angiogenesis is a critical step in the formation and progression of metastasis. The abnormal blood vessels that develop in metastatic tumors not only promote growth but also are a barrier to the delivery of therapeutic agents. The
in the understanding of the molecular mechanisms of tumor angiogenesis to the treatment of patients with uveal melanoma.
65
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Outcomes 200866
Innovations
DNMT1 Depletion Is Targeted Therapy Against Cancer
cancer cells and encourage the growth of healthy cells. Current treatments kill both cancer cells and healthy cells, which lead to numerous side effects. They found that the mechanisms that cause cancer cells to divide and grow uncontrollably are often
the growth of the cancer cells. The alternative approach has not yet been tried in humans, but the team hopes to start clinical trials soon.
65306_CCFBCH_Text_ACG 66 6/23/09 1:15:51 PM
Taussig Cancer Institute 67
Development of Novel Chemotherapeutic Agents
continue to focus on the synthesis of a chemotherapeutic compound, nitrosylcobalamin (NO-Cbl) that consists of nitric
up by the cell, but inside lysosomes, the drug releases nitric
from institutional funds, an oral formulation of the drug
spontaneously occurring tumors have been treated with the
Preclinical Testing of Novel Therapeutic Agents
in various mouse cancer models. To date, this new
and has shown activity against several different human
Radiation Oncology
Hyperthermia Therapy for Surface and Recurrent Tumors
hyperthermia therapy, providing an important treatment option for patients with surface and recurrent tumors.
therapy, hyperthermia therapy allows radiation oncologists to increase the delivery of radiation to the tumor while minimizing damage to healthy tissues.
within a few centimeters of the surface of the body, such
recurrent disease, a second course of standard radiation therapy may not be possible because of the increased risk of damage to healthy tissues. By effectively increasing the radiation dose to the tumor without increasing unwanted side effects, hyperthermia therapy is an important treatment
delivered though a probe for prostate, head and neck, and
65306_CCFBCH_Text_ACG 67 6/23/09 1:16:08 PM
68
Innovations
Calypso™ 4D Localization System for Prostate Cancer
prostate during radiation therapy treatment for optimal targeting of radiation and minimizing side effects, such as impotence, incontinence and rectal bleeding.
During an outpatient procedure similar to a biopsy, three rice-grain-sized electromagnetic transponders are implanted in the prostate. The transponders communicate with Calypso using safe radiofrequency waves so that Calypso monitors
during treatment. Calypso allows radiation oncologists to precisely monitor radiation therapy and to make quick decisions about patient care.
at Taussig Cancer Institute participated in the initial clinical
Electronic Treatment Charts
treatment chart records in 2008—one of the few radiation oncology departments that have advanced to a completely paperless system. Electronic treatment chart records include information about radiation therapy such as electronic
radiation dose history, patient schedules, patient charges and dosimetric computer planning documents. The move to paperless treatment chart records allows physicians, physicists and therapists to simultaneously update patient treatment information from any location in the department or by radiation oncologists through secured remote access. Electronic treatment chart records help radiation oncology
providing faster treatment delivery to patients.
Outcomes 2008
65306_CCFBCH_Text_ACG 68 6/23/09 1:16:29 PM
Taussig Cancer Institute 69
Bone Marrow Transplant
Bicyclam Derivative for Hematopoietic Stem Cell Mobilization
investigator for an international study of a novel small-molecule bicyclam derivative for
cells for bone marrow transplantation. Based on
be able to undergo bone marrow transplantation
Surgery
Robotic Liver Resection
Cleveland Clinic surgeons have started a laparoscopic robotic-assisted liver resection program at the
accurate dissection. With the ultimate goal to do anatomic
laparoscopic robotic liver resection in the last quarter of 2008 for malignant liver tumors, including hepatocellular cancer, colorectal metastasis and sarcoma metastasis. Because the incisions are smaller, patients are discharged from the hospital in one to three days, returning home sooner. As of the fourth quarter 2008, there have been no complications using robotic-assisted liver resection. The laparoscopic robotic-assisted liver resection program at
65306_CCFBCH_Text_ACG 69 6/23/09 1:16:42 PM
Outcomes 2008
Selected Publications
The Taussig Cancer Institute staff authored more than
go to www.clevelandclinic.org/quality/outcomes.
600 PublicationsAdelstein DJ, Rodriguez CP. Current and emerging standards of concomitant chemoradiotherapy. Semin Oncol. 2008
Adelstein DJin head and neck cancer. J Clin Oncol
Advani ASSobecks R, Sekeres M, Copelan EKalaycio M. Time to post-remission therapy is an independent prognostic factor in adults with acute lymphoblastic leukemia. Leuk Lymphoma. 2008
Advani AS, Rodriguez CBaz R, Kalaycio M, Sobecks R, Sekeres M, Tripp B,
progression-free and overall survival in patients with newly Leuk Res
Cheriyath V Reu FJ, Borden EC.
Oncogene
Borden ECimatinib mesylate at two dose levels in patients with unresectable or metastatic gastrointestinal stromal tumors
J Clin Oncol
Borden ECperspective. Nat Rev Drug Discov
70
65306_CCFBCH_Text_ACG 70 6/23/09 1:16:47 PM
Taussig Cancer Institute
Maciejewski JP
inhibitor eculizumab for the treatment of patients with Blood
Bukowski RM. Optimizing utilization of targeted therapies in genitourinary cancers. Clin Genitourin Cancer. 2008
Bukowski RM. What role do combinations of interferon and
renal cell carcinoma? Clin Genitourin Cancer. 2008
Bukowski RM J Oncol Pract
Bukowski RMrenal cell carcinoma. Curr Oncol Rep
Bukowski RMnovel drug development? Clin Genitourin Cancer. 2008
Chao ST, Barnett GH, Vogelbaum MA, Angelov L, Weil RJ,Neyman G Suh JHradiosurgery effectively treats recurrences from whole-brain radiation therapy. Cancer
Lichtin A, Pohlman B,Macklis R. Bilateral panocular involvement with mantle-cell lymphoma. J Clin Oncol
Ciezki JP
doubling time]. J Urol
71
65306_CCFBCH_Text_ACG 71 6/23/09 1:16:50 PM
Outcomes 200872
Selected Publications
Cohen PA
dendritic cells. Blood
Bukowski R, Rini B, Finke JH, Tannenbaum C.
cell carcinoma, synergize to induce T-cell apoptosis. Cancer Res
Davis Msurvival prediction in the terminally ill: Commentary.J Palliat Med
Davis M. Opioids and fatal drug poisoning. J Pain Palliat Care Pharmacother
Davis MPthe ground are we? Support Care Cancer. 2008
Davis MP. Cancer constipation: are opioids really the culprit? Support Care Cancer
Davis MP. Oral nabilone capsules in the treatment of chemotherapy-induced nausea and vomiting and pain. Expert Opin Investig Drugs
Raghavan D. Circulating tumor cells predict
resistant prostate cancer. Clin Cancer Res. 2008
Dean RM
graft-versus-host disease. J Clin Oncol. 2008 Dec
Dreicer R
Cancer
Dreicer Rprogress: what’s wrong with this picture? Cancer. 2008
Dreicer R. Chemotherapy for the palliation of advanced prostate cancer. J Support Oncol
Dreicer Rpatients with metastatic prostate cancer. Urol Oncol. 2008
O’Keefe CLSekeres MA
Maciejewski JP
uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies. Cancer Res
Estfan B, Walsh D. The cough from hell: diazepam for intractable cough in a patient with renal cell carcinoma.J Pain Symptom Manage
Finke JH, Rini BGarcia J, Dreicer R,
Bukowski Rand decreases T-regulatory cells in renal cell carcinoma patients. Clin Cancer Res
Raghavan D
prostate cancer trial. J Clin Oncol
65306_CCFBCH_Text_ACG 72 6/23/09 1:16:51 PM
Taussig Cancer Institute 73
Garcia JAinhibition as a therapeutic strategy in the management of urologic malignancies. Mol Cancer Ther. 2008
Garcia JA, Klein EA, Magi-Galluzzi C Triozzi P,Dreicer Rsargramostim and thalidomide in patients with locally advanced prostate carcinoma. Clin Cancer Res. 2008
Cockrell E, Silverstein RLinteractions with endothelial cell-derived microparticles and contributes to thrombosis in mice. J Clin Invest. 2008
O’Keefe CL, Sekeres MAMaciejewski JP. Chromosomal lesions and uniparental
Blood
Raghavan DSweetenham JW
Oncology. J Clin Oncol
Hansel DE, Rini BIrenal cancer: new genes and diagnostic and therapeutic opportunities. Expert Rev Anticancer Ther. 2008
Borden EC,
and clinical outcome in the North American Intergroup
J Clin Oncol
Juliano JJ Suh JHoncocytoma: A case report. Urol Oncol. 2008
Kalaycio M, Advani A, Pohlman B, Sekeres M, Tripp B,Sobecks R. Timed sequential induction
chemotherapy and risk-adapted postremission therapy foracute myelogenous leukemia. Am J Hematol. 2008
Kalaycio Mtreatment for patients with chronic lymphocytic leukemia. Clinical Leukemia
Adelstein DJBorden ECmalignant mesothelioma of the pleura: A phase II study of
Lung Cancer.
Lee DRini B
T cells in a dose-dependent fashion. Blood. 2008 Aug
Klein EA Raghavan D, Dreicer R.
prostatectomy. J Clin Oncol
65306_CCFBCH_Text_ACG 73 6/23/09 1:16:52 PM
Outcomes 200874
Selected Publications
Lagman R, Walsh D LeGrand SB, Davis MP.A day in the life: a case series of acute care palliative medicine--the Cleveland model. Am J Hosp Palliat Care.
Bukowski RPelley R
capecitabine in patients with advanced colorectal cancer. Clin Cancer Res
Bolwell BJ Copelan E
of prior imatinib mesylate on the outcome of hematopoietic cell transplantation for chronic myeloid leukemia. Blood
LeGrand SB
practice. Ann Intern Med
Pohlman B, Sweetenham J
lymphomas. N Engl J Med
Lichtin AECleve Clin J Med
Maciejewski JPcytogenetic tool in hematologic malignancies. Blood. 2008
Macklis RM
American Journal of Hematology/Oncology
Bolwell BJ, Bredeson CN, Copelan EA
Blood. 2008
Spiro TP,Daw HA. The utility of
lymphoma. Am J Clin Oncol
Pohlman B
large B-cell lymphoma treated with anthracycline-based J Clin Oncol.
Pennell NA
in patients with advanced thyroid cancer. Thyroid. 2008
65306_CCFBCH_Text_ACG 74 6/23/09 1:16:52 PM
Taussig Cancer Institute
Raghavan D, Klein EAreinventing the wheel...but this time it is round. J Clin Oncol.
Raghavan Ddata. Cleve Clin J Med
Rini BI, Bukowski RM. Targeted therapy for metastatic renal cell carcinoma: a home run or a work in progress? Oncology(Williston Park)
Rini BIMekhail T, Garcia J, Dreicer R,
Bukowski RMwith metastatic renal cell carcinoma. Cancer
Rini BIfor molecularly-targeted therapy in renal cell carcinoma. Urol Oncol
Rini BI
compared with interferon alfa monotherapy in patients with J Clin
Oncol
Rini BI Bukowski RM,
Antitumor activity and biomarker analysis of sunitinib in patients with bevacizumab-refractory metastatic renal cell carcinoma. J Clin Oncol
Rini BI CurrOpin Oncol
Rini BIpatient? Oncology (Williston Park)
Rini BIcarcinoma. Community Oncology
Rini BI. Is sorafenib plus interferon alpha 2b safe and effective in patients with renal cell carcinoma? Nat Clin Pract Urol
Rini BIrenal cell carcinoma. Nat Clin Pract Oncol. 2008
Rini BI. Quantifying hypertension in patients with cancer treated with sorafenib. Lancet Oncol
Rini BIof rapamycin. Clin Cancer Res
Rini BIcarcinoma. Clin Adv Hematol Oncol
Lichtin AE. Use of epoetin and darbepoetin in patients
guideline update. Blood
Lichtin AE. Use of epoetin and darbepoetin in patients
guideline update. J Clin Oncol
Rodriguez CP, Adelstein DJ Saxton JP,Lorenz RR
preservation after multiagent concurrent chemoradiotherapy. Head Neck
75
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Outcomes 200876
Selected Publications
Rodriguez CP, Baz R Kalaycio ME,Advani A, Sobecks R, Sekeres MA. Impact of socioeconomic status and distance from treatment center on survival in patients receiving remission induction therapy for newly diagnosed acute myeloid leukemia. Leuk Res. 2008
Mahadevan A, Klein ECiezki J
Quality of life and satisfaction with outcome amongprostate-cancer survivors. N Engl J Med
Saunthararajah Y
effectiveness of decitabine in severe sickle cell disease. Br J Haematol
Maciejewski JP. Dasatinib, a small-molecule protein tyrosine kinase inhibitor, inhibits T-cell activation and proliferation. Blood
Dreicer R
patients with progressive prostate cancer and castrate levels
J Clin Oncol. 2008
Sekeres MAoutcomes in patients with myelodysplastic syndromes with
Clinical Leukemia. 2008
Sekeres MA, Maciejewski JP
cytopenias and response to lenalidomide in patients with lower-risk myelodysplastic syndromes. J Clin Oncol. 2008
Sekeres MAMaciejewski JP
physician surveys. J Natl Cancer Inst. 2008 Nov
Sekeres MA. Treatment of older adults with acute myeloid leukemia: state of the art and current perspectives. Haematologica
Sobecks RMKalaycio M, Andresen S, Pohlman B,
Dean R, Sweetenham J, Macklis RCopelan E, Maciejewski JP, Bolwell BJ
on achievement of T-cell complete donor chimerism in related donor nonmyeloablative allogeneic hematopoietic stem cell transplantation. Bone Marrow Transplant. 2008
Sobecks RM, Dean RMacklis R, Andresen S, Kalaycio M, Pohlman B
Sweetenham J, Copelan E, Bolwell BJ
allogeneic hematopoietic stem cell transplantation. Bone Marrow Transplant
Sweetenham JWHematol Oncol Clin North Am
Sweetenham JW
for radiation therapy. Leuk Lymphoma
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Raghavan D
surgeon volume predict bleeding with open radical retropubic prostatectomy. BJU Int
Tendulkar RD
brachytherapy for recurrent airway obstruction from hyperplastic granulation tissue. Int J Radiat Oncol Biol Phys.
Triozzi PL, Aldrich W, Dombos C. Differential effects of imatinib mesylate against uveal melanoma in vitro and in vivo. Melanoma Res
Triozzi PL, Eng Cmelanoma. Cancer Treat Rev
Videtic GMabdominal wall: complete response with radiotherapy alone. Technol Cancer Res Treat
Videtic GMM
Energy Agency (IAEA) consultants’ meeting on elective nodal irradiation in lung cancer: non-small-cell lung cancer
Int J Radiat Oncol Biol Phys. 2008 Oct
Videtic GMM, Rice TW Suh JH, Saxton JP,Adelstein DJ, Mekhail TM. Utility of positron emission tomography compared with mediastinoscopy for delineating involved lymph nodes in stage III lung cancer: insights for radiotherapy planning from a surgical cohort. Int J Radiat Oncol Biol Phys
Wilkinson DA
Br J Radiol
Wu Y
immortalized endometrial stromal cells. Fertil Steril. 2008
Wu Yproliferation of endometriotic cells in vitro. Gynecol Obstet Invest
Cohen PA
CancerRes
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Outcomes 20087878
Staff Listing
Chairman and Director
Deputy Director
Director of Scott Hamilton “CARES” Center
Department of Hematologic Oncology and Blood Disorder
ChairmanDirector, Bone Marrow Transplant Program
Department of Radiation Oncology
Chairman
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Department of Regional Oncology
Chairman
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Outcomes 20088080
Staff Listing
Department of Solid Tumor Oncology
Chairman
Section of Palliative Medicine
Chairman
Department of Translational Hematology andOncology Research
Chairman
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Taussig Cancer Institute
Center for Clinical Research
Director
Taussig Cancer Institute.
Taussig Cancer Institute
clevelandclinic.org/staff.
8181
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Contact Information
General Patient Referral
Taussig Cancer Institute Appointments/Referrals
Bone Marrow Transplant Program Appointments/Referrals
This internationally recognized program offers autologous, allogeneic, reduced intensity, related and unrelated transplants. Cell sources include bone marrow, peripheral stem cell and umbilical cord blood transplants for treating patients with leukemias, lymphomas, and other hematological malignancies and bone marrow failure states.
Bone Marrow Failure Clinic Appointments/Referrals
hemoglobinuria, large granular lymphocytic leukemia and other immune-mediated hematologic diseases.
Radiation Oncology Appointments/Referrals
Cancer Answer Line
second opinion
Helen Meyers McLoraine Patient Resource Center
teaching and educational video viewing
related events
On the Web at clevelandclinic.org/cancer
Additional Contact Information
General Information
Hospital Patient Information
Patient Appointments
Medical Concierge
Complimentary assistance for out-of-state patients and families
Global Patient Services/International Center
Complimentary assistance for international patients and families
clevelandclinic.org/gps
Cleveland Clinic in Florida
For address corrections or changes, please call
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Taussig Cancer Institute 8383
Institute Locations
Cleveland Clinic (Main Campus)
Taussig Cancer Institute
Beachwood Family Health and Surgery Center
Fairview Hospital
Hillcrest Hospital
Independence Cancer Center
Lorain Family Health and Surgery Center
Strongsville Family Health and Surgery Center
Westlake Family Health Center
Willoughby Hills Family Health Center
Wooster Family Health Center
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Outcomes 20088484
Cleveland Clinic Overview
bundling all clinical specialties into integrated practice units called institutes. An institute combines all the
under a single roof. Each institute has a single leadership and focuses the energies of multiple professionals onto the
point-of-care service, institutes will improve the patient
outpatient clinic, specialty institutes and supporting labs
Cleveland Clinic Abu Dhabi (United Arab Emirates), a multispecialty care hospital and clinic, is scheduled to
associates and postdoctoral fellows are involved in laboratory-based, translational and clinical research. Total
federal agencies, non-federal societies and associations, endowment funds and other sources. In an effort to bring research from bench to bedside, Cleveland Clinic
at any given time.
offers all students full tuition scholarships. The program will
Cleveland Clinic is consistently ranked among the top hospitals in America by U.S.News & World Report, and our
clevelandclinic.org.
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Resources for Physicians
Cleveland Clinic Secure Online Services
Cleveland Clinic uses state-of-the-art digital information systems to offer secure online services such as online medical second opinions, medical record access, patient treatment progress for referring physicians (see below), and imaging interpretations by our subspecialty trained radiologists. For more information, please visit eclevelandclinic.org.
MyChart This secure online tool connects patients to their own health information from the privacy of their home any time, day or night. Some features include renewing prescriptions, reviewing test results and viewing medications, all online. For the convenience of physicians and patients across the country, MyChart now offers a secure connection to GoogleTM Health. Google Health users can securely share personal health information with Cleveland Clinic, and record and share the details of their Cleveland Clinic treatment with the physicians and healthcare providers of their choice. To establish a MyChart account, visit clevelandclinic.org/mychart.
DrConnect Whether you are referring from near or far, DrConnect streamlines communication from Cleveland Clinic physicians to your office. This complimentary online tool offers secure access to your patient’s treatment progress at Cleveland Clinic. With one-click convenience, you can track your patient’s care using the secure DrConnect website. To establish a DrConnect account, visit clevelandclinic.org/drconnect or email [email protected].
MyConsult Online Medical Second Opinion This secure online service provides specialist consultations from our Cleveland Clinic experts and remote medical second opinions for more than 1,000 life-threatening and life-altering diagnoses. MyConsult is particularly valuable for people who wish to avoid the time and expense of travel. For more information, visit clevelandclinic.org/myconsult, email [email protected] or call 800.223.2273, ext 43223.
Critical Care Transport: Anywhere in the world
Cleveland Clinic’s critical care transport team serves critically ill and highly complex patients across the globe. The transport fleet comprises mobile ICU vehicles, helicopters and fixed-wing aircraft. The transport teams are staffed by physicians, critical care nurse practitioners, critical care nurses, paramedics and ancillary staff, and are customized to meet the needs of the patient. Critical care transport is available for children and adults. To arrange a transfer for STEMI (ST elevated myocardial infarction), acute stroke, ICH (intracerebral hemorrhage), SAH (subarachnoid hemorrhage) or aortic syndromes, call 877.279.CODE (2633). For all other transfers, call 216.444.8302 or 800.553.5056.
CME Opportunities: Live and Online
Cleveland Clinic’s Center for Continuing Education’s website, clevelandclinicmeded.com, offers hundreds of convenient, complimentary learning opportunities, from webcasts and podcasts to a host of medical publications including the Disease Management Project Online Medical Textbook, with more than 150 chapters. The site also offers a schedule of live CME courses, including international summits that focus on key areas of translational research. Many live CME courses are hosted in Cleveland, an economical option for business travel. Physicians can manage their CME credits by using the myCME Web Portal. Available 24/7, the site offers CME opportunities to medical professionals across the globe.
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Taussig Cancer Institute
2008Outcomes
9500 Euclid Avenue, Cleveland, OH, 44195
© The Cleveland Clinic Foundation 2009
Cleveland Clinic is a nonprofit multispecialty academic medical center. Founded in 1921, it is dedicated to providing quality specialized care and includes an outpatient clinic, a hospital with more than 1,000 staffed beds, an education institute and a research institute.
Please visit us on the Web at clevelandclinic.org.
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