xavier badoux, william wierda, susan o'brien, stefan faderl, steven kornblau,
DESCRIPTION
A Phase II Study of Lenalidomide as Initial Treatment of Elderly Patients with Chronic Lymphocytic Leukemia. Xavier Badoux, William Wierda, Susan O'Brien, Stefan Faderl, Steven Kornblau, Kimberly Yerrow, Zeev Estrov, Hagop Kantarjian, Michael Keating and Alessandra Ferrajoli. - PowerPoint PPT PresentationTRANSCRIPT
A Phase II Study of Lenalidomide as Initial
Treatment of Elderly Patients with Chronic Lymphocytic
Leukemia
Xavier Badoux, William Wierda, Susan O'Brien, Stefan Faderl, Steven Kornblau,
Kimberly Yerrow, Zeev Estrov, Hagop Kantarjian,
Michael Keating and Alessandra Ferrajoli
DisclosuresXavier Badoux, MB BS
Research Support/P.I. No disclosures Employee No disclosures Consultant No disclosures Major Stockholder No disclosures Speakers’ Bureau No disclosures Scientific Advisory Board No disclosuresPresentation includes discussion of off-label use of lenalidomide in CLL.
Lenalidomide in Elderly CLL: Introduction
• Median age at diagnosis of CLL: 72 years • Elderly patients with CLL
– Under-represented in clinical trials– Increased toxicity with chemoimmunotherapy
• Lenalidomide – Immunomodulatory drug– Oral administration – Active in relapsed CLL
SEER Cancer Statistics Review, NCI (2009); Eichhorst B, Leuk & Lymph (2009); Chanan-Khan A et al. JCO (2006); Ferrajoli A et al. Blood (2008).
Lenalidomide in Elderly CLL: Study Design
• Phase II, 60 patients • Untreated and symptomatic (NCI-WG)• Age ≥ 65 yrs• Creatinine <2 mg/dL, bilirubin<2 mg/dL• Performance status 0-2• Response assessed at end of Cycle 3,
then every 6 cycles (2008 NCI-WG)
ClinicalTrials.gov (ID# NCT00535873)
Lenalidomide in Elderly CLL: Treatment Schedule
• Lenalidomide – 5 mg orally daily x 2 cycles (56 days)– Increase by 5 mg/cycle (28 days) to
maximum 25 mg daily– Treatment continued until progression
• Allopurinol 300 mg d1-14 • No mandated antibiotic, anti-viral, DVT or tumor flare prophylaxis
• Efficacy: 1. Progression-free survival 2. Clinical Responses (2008 NCI-WG)
• Toxicity:Grade 3-4 non-hematological
• Correlative Studies:Lymphocyte subsets analysis: blood and
marrowSerum immunoglobulin levels
Lenalidomide in Elderly CLL: Study Endpoints
Lenalidomide in Elderly CLL: Patient Pre-treatment Characteristics
Characteristic N (%); median [range]Age, years 71 [66-85]Rai stage, III or IV 18 (30)Lymphocytes, x 109/L 76 [2.5 – 227]2-microglobulin, mg/L 4.3 [2.0 – 10.2]IGHV, unmutated 33/55* (60)11q deletion 14 (23)17p deletion 6 (10)Marrow CD38, ≥30% 30/59** (51)Not evaluable: *IgVH: n=5, **CD38: n=1
Lenalidomide in Elderly CLL: Response (2008 NCI-WG Criteria)
N = 60 NCI Responsen patients %
CR* 6 10 CRi* 3 5 Nodular PR 3 5 PR 25 42ORR 37 62*4 patients with flow cytometry negative CR
Analysis time 3 cycles 9 cycles 15 cycles 21 cycles
ITT/No on Rx. 60/54 60/43 59/38 53/30
NCI Response n (%) n (%) n (%) n (%)
CR/CRi* - 1 (2) 5 (8) 7 (13)
Nodular PR - 6 (10) 4 (7) 5 (9) PR 24 (40) 27 (45) 27 (46) 18 (34)
ORR 24 (40) 34 (57) 36 (61) 30 (57)
Lenalidomide in Elderly CLL: Responses at Assessment Times
Patient characteristicNCI-WG Response (%)
n CR/CRi/nPR OR
Age, years65 - 74 43 26 72≥ 75 17 6 35*
Rai stage0 – II 42 21 64III or IV 18 17 56
β2-M, mg/L< 4 26 27 69≥ 4 34 15 56
IGHV genesMutated 22 5* 50Unmutated 33 30 73
FISH hierarchy
Deletion 13q 15 33 73Negative 12 8 50Trisomy 12 13 15 92Deletion 11q 14 29 57Deletion 17p 6 0 0*
Lenalidomide in Elderly CLL: Responses by Pre-treatment Characteristics
*p<0.05
Lenalidomide in Elderly CLL: Overall and Progression-free Survival
Median follow-up 23 months:
OS = 90%
PFS = 60%
Lenalidomide in Elderly CLL: Normalization of PB Lymphocytes (n=38)
*p<0.001
Lenalidomide in Elderly CLL: Reconstitution of BM Lymphocytes (n=38)
*p<0.001,**p<0.01
(%)
Lenalidomide in Elderly CLL: Improvement in Serum Igs (n=37)
8 / 16 (50%) patients with IgG<600mg/dl → normalized serum IgG
* p<0.001
Cycles of therapy Cycles of therapy
Hematological toxicity*Toxicity as % of cycles
Grade 3 Grade 4Neutropenia 26 12Thrombocytopenia 13 <1Anemia 0 0
Lenalidomide in Elderly CLL: Hematological Toxicity
*NCI-working group criteria
Infections (N=60)Grade ≥ 3
n episodes n (%) patientsSepsis 1 1 (2)Pneumonia/Bronchitis 3 2 (3)Upper Respiratory 0 0 (0)Urinary 0 0 (0)Other infections 1 1 (2)Fever, neutropenic 3 3 (5)Fever, non-neutropenic 3 2 (3)
Lenalidomide in Elderly CLL: Infections
Toxicity (N=60)Grade 1 - 2 Grade ≥3
n of patients %n of
patients%
Fatigue 53 88 2 3Constipation 30 50 1 2Diarrhea 30 50 0 0Tumor flare 30 50 0 0Rash 28 47 0 0Nausea 21 35 0 0Dyspnea 20 33 1 2Pruritus 20 33 1 2Neuropathy: sensory 9 15
0 0
Neuropathy: motor 4 7 0 0
Lenalidomide in Elderly CLL: Other Toxicities
• Lenalidomide as frontline therapy in elderly CLL– Estimated 2-year OS 90%; 2-year PFS 60% – ORR 62 %; CR/CRi 15% – Quality of response improves with time
• Myelosuppression most common toxicity• No severe tumor flare or tumor lysis syndrome• ↑ serum Ig levels• Normalization of lymphocyte populations
Lenalidomide in Elderly CLL: Conclusions
Thank you
Lenalidomide dose NNCI-WG Response (%)
CR/CRi/nPR OR
Mean DoseCycles 1 - 6
< 5mg 26 4 35
≥ 5mg 34 32* 82**
Lenalidomide in Elderly CLL: Clinical Responses by Dose Intensity
*p<0.01, **p<0.001
Lenalidomide in Elderly CLL: Best Clinical Response: 2008 NCI-WG