radiotherapy and chemotherapy in ent
TRANSCRIPT
RADIOTHERAPY AND
CHEMOTHERAPY
IN ENTDr Manpreet Singh Nanda
Associate Professor ENTMMMC&H Solan
RADIOTHERAPY IN ENT Treatment of lesion with ionizing
radiation Modes of RT External beam/ Teletherapy 90% MC Use photon (X Rays, gamma rays) and
electron beams FROM DISTANCE Skin sparing, better precision,
diminished bone absorption
Brachytherapy Uses radio active material in close contact
with lesion Types Moulds – applied to the surface of the lesion Interstitial implants – applied into tissues –
tumours of tongue and lips Intercavity implants – placed in cavity next
to the lesions – maxillary antrum, nasopharynx
As needles (radium 226, cobalt 60) or as seeds or grains ( I – 125)
Unsealed radionuclide therapy IV/oral radionuclide isotopes Spares normal tissue Eg- radioactive iodine for follicular thyroid ca Conformal radiotherapy Conforms to the size and shape of tumour Delivers max to target areas, min to
surrounding tissues and sharply cuts off critical areas
Intensity modulated RT- spares normal tissue – nasopharynx, larynx, PNS
Cyberknife stereotactic RT
RADIATION UNITS Energy deposited in unit of material Rad – radiation absorbed dose – 100
ergs deposited/gram of material Gy – gray – SI unit – 1 joule deposited/kg
of material 1 Gy = 100 rads 1 Cgy = 1 rad
TYPES Curative RT Early cancers/ small lesions To preserve function of organ Alone Benign lesions – angifibroma Dose 60-70 Gy, depend on the extent of
the lesion
Palliative RT Indications Advanced lesions where total control of
disease is not expected Distant metatasis Poor nutritional status Systemic diseases affecting heart, lung,
kidney Role To control pain, bleeding, obstruction to
airway or food passage
Adjuvant RT/Combination RT As adjuvant to surgery or CT, before or after Role To achieve better control of disease To eradicate microscopic extension of
tumour To increase survival rate in advanced lesions Types Pre op RT Post op RT Intra op RT
Pre operative RT Advantages Reduces tumour bulk and make it operable Eliminates occult metastasis in regional ln Prevent distant metastasis Blocks lymphatics, reduces chances of
dissemination of tumour during surgery Response better as oxygenation of tumour
not hampered Note – the interval between RT and
surgery < 6 weeks
Dose – 45-50 Gy Disadvantages Central part of large tumour responds
poorly to RT Reduced vitality of tissue leading to
increased chances of post op complications like delayed wound healing, flap necrosis, fistula formation and carotid blowout
Post operative RT Indications – stage III, IV Positive margins, invasion of bone or
cartilage, extracapsular invasion of ln, multiple neck nodes size > 3 cm
Within 6 weeks of surgery, dose 55-65 Gy Advantages More effective as bulk has already been
removed Lesser post op complications Can be done for residual tumours
Disadvantages Poor response to RT due to affected blood
supply Tumour cells are squeezed into blood supply
and lymphatics at the time of surgery leading to increased chances of distant metastasis
Intra operative RT At time of surgery Single large dose given to exposed tumour
bed Critical areas not included in field of RT
Fractionation schedules Normal fractionation 2Gy/ day – fraction dose 30 fractions 5 days/ week for a period of 6 weeks Total dose 60 Gy Hyperfractionation – increased number of
fractions, less dose Hypofractionation – less number of
fractions, higher dose Accelerated fractionation – shorten the
overall time
Split course fractionation RT is given in two halves with a gap of 2
weeks in between To allow acute reactions to settle Factors affecting response to RT Tumour size – small tumours better
response Tumour type – lymphoid tissue,
anaplastic – more responsive Adeno ca – radioresistant
Complications of RT Depend on site/ dose/ fractions Early Radiation sickness – loss of appetite, nausea Mucositis – stomatitis, glossitis, ulcers in oral
cavity and oropharynx, persist for 8- 12 weeks post RT
Skin reactions – erythema Pharyngeal and laryngeal oedema leading to
dysphagia and stridor Fungal infection – candidiasis Dysfunction of salivary and lacrimal glands
Late Non healing ulcer Atrophy of skin and mucosa, SMF Bone marrow depression Dental decay Recurrent infections Osteo and chondroradionecrosis (mandible >
maxilla) Malignancy – papilly thyroid ca, orbital
osteosarcoma Middle ear effusion, SNHL, vestibular symptoms Retinopathy and cataract Hypothyroidism and pituitary defect
Patient care during RT Nutrition Diet rich in proteins, vitamins, iron and
minerals NG feed, blood transfusion Avoid alcohol, tobacco, spicy food Teeth care Dental evaluation and extraction if
needed 2-3 weeks before RT to prevent osteoradionecrosis
Skin care Keep skin dry – avoid wetting or shaving Avoid exposure to sunlight Wear soft clothes Use antibiotic steroid ointment Oral care Avoid irritating mouth washes Milk of magnesia used to prevent erosion
of teeth and protect inflammatory area Xylocaine viscus to relieve pain and
discomfort
Care against infection Topical application of nystatin and
clotrimazole ointment over oral cavity and oropharynx
Protective against candida infection
CHEMOTHERAPY IN ENT Use of chemical compounds in treatment of
neoplastic diseases so as to destroy the offending ca cells without affecting the normal cells
Classification Alkylating agents – cyclophasphamide,
cisplatin (dose – 50-100 mg/m2 IV over 3 weeks), carboplatin (dose – 360 mg/m2 IV over 4 weeks)
Antimetabolites – methotrexate, 5 FU, bleomycin, mitomycin
Vinca alkaloids – vincristine, vinblastin
Taxanes – paclitaxel, docetaxel Radio active isotopes – radio active
iodine Hormones – androgen, oestrogen,
progesterone Indications To make RT more effective for primary
tumour Combined with RT for organ preservation Lesser extensive surgery To control metastatic disease
Types Palliative CT In advanced lesions or recurrence with
aim to relieve symptoms Cisplatin + 5 FU, cisplatin + mtx,
carboplatin + 5 FU, cisplatin + bleomycin, cisplatin + bleomycin + mtx
Combined modality treatment Before, during or after RT/surgery
Induction/ anterior/ NAC Before surgery or RT To reduce tumour burden, downstaging of
tumour Organ preservation – preservation of
functions of organs like swallowing, speech Increase survival rate Decrease distant metastasis Improve quality of life Response rate 60-90% after 3 cycles Complete response 20-30%, cisplatin, 5 FU,
carboplatin
Chemoradiation/ concomittant CT RT/ concurrent CT RT
Simultaneous Unresectable tumours To improve regional and local control of
disease Increases toxicity Survival rates not increased Cisplatin, 5 FU, bleomycin, mitomycin
Adjuvant or posterior RT After surgery or RT To cure micrometastasis and distant
metastasis Surgery not delayed No blurring of tumour margins Intra arterial CT In advanced salivary glands and PNS
tumours PNS – superficial temporal artery
Single agent CT 33% response Complete response 5 % Combination CT Using 2 or more drugs Not much improved survival rate though
much improved response rate Cisplatin + 5 FU – oral cavity, oropharynx,
nasopharynx, hypopharynx, larynx ca 3 cycles
Pre CT work up History and clinical exam – exclude renal,
cardiac, pulmonary disease CBC – Hb, TLC, DLC, platelets Urine exam..... RFT, LFT – cisplatin/mtx Radiology – X Ray chest, CT, MRI, USG
abdomen PFT - bleomycin ECG - adriamycin Audiometry - cisplatin
Response Complete response – no evidence of
tumour for 4 weeks Partial response – 50% tumour regression Minor response - < 50% tumour regression Stable disease – no tumour regression Progressive disease – 25% increase in
tumour growth Factors affecting response – TNM
staging, site, nodal extension, nutrition, h/o previous surgery, CT, RT
Toxicity Stomatitis, alopecia of skin Nausea, vomiting Diarrhoea Bone marrow depression, myelosuppression Nephrotoxic – mtx, cisplatin Ototoxic – cisplatin Neurotoxic – vincristine, vinblastin Cardiotoxic – adriamycin (doxorubicin) Bladder haemorrhage – cyclophosphamide Pulmonary fibrosis - bleomycin
Chemoprevention Administration of drugs which inhibit
carcinogenesis or reverse a premalignant condition
Indications – premalignant lesions, family history, high risk cases
Agents Retinoids – synthetic and natural analogues
of vitamin A Carotenoids – beta carotene, yellow skin Vitamin E Calcium, selenium, N acetyl cysteine