Pyriform sinus tumours principles of management

28
PYRIFORM SINUS TUMOURS PRINCIPLES OF MANAGEMENT DR.ROOHIA

Transcript of Pyriform sinus tumours principles of management

PYRIFORM SINUS TUMOURS PRINCIPLES OF MANAGEMENT

DR.ROOHIA

The goals of treatment for this patient population are:

(1) cure with preservation of function (2) palliation with minimal morbidity

Factors Affecting Choice of Treatment

Age:pts above the age of 75yrs hv poor prognosis due to their general poor condition surviaval rate is about 10% comparable to others.

Associated Medical Conditions should be included when considering treatment options

Eligibility criteria for investigational nonsurgical chemoradiation protocols include

adequate performance status as well as reasonable hematologic, hepatic, renal

and cardiovascular function

Past Medical/Surgical History previous exposure to platinum

compounds makes significant responses less likely.

Repeat external irradiation or brachytherapy are poor options for patients who have received prior radiotherapy to the head and neck

TNM Staging, Quality of life

Ca Pyriform sinusT1/T2

Good exposure on MLscopy

Endoscopic CO2 laser resection; neck dissection if N+

Poor exposure on ML scopy

RT/CT+RT to the primary & neck

T3

Mobile cords; superficial infiltration

Good exosure on MLscopy

Endoscopic CO2 laser resection

1.If resection margins

unsatisfactory –postop RT

2.If N+ Neck

dissection+post op RT

If resection margins satisfactory ,N0

-withhold RT, treat with 2 cycles of adj

CT &follow up regularly

Poor exposur on Mlscopy

Lateralised lesion

1.CT followed by a. RT in good resonders b.NTPL+RT in poor

res2.NTPL+RT

Cord fixity; deep infiltration

Non-lateralised

1.sequential/concurrent chemo radiation

2.Total LP+RT

NTPL/TOTAL LP with Neck dissection+post op RT

T4;N0/N+

Radiotherapy

Radiotherapy as a single treatment modality for early (T1-T2) pyriform sinus carcinoma(curative RT)

 The rates of local control decrease in bulky T2 lesions, in those larger than 2.5 cm,

and in those extending to the apex of the pyriform

sinus. Better results in terms of local control are observed in patients with favorable T2 lesions characterized

by exophytic tumor, good airway, normal cord mobility, and uninvolved apex. 

Conventionally fractionated radiotherapy employing total doses of 60-70 Gy in 30-35 fractions,(2Gy/fraction) over 6-7 weeks

Accelerated fraction RT: same dose given over shorter period

HyPer fraction RT: traditional dose broken into smaller fractions over same time

Prevents repopulation of tumour Decrese duration of treatment and hos stay

In too advanced disease,distant metastasis,poor condition for sugery palliative RT .

Dose depends on extent &tolerance of tissues.

If RT alone- can be delivered with external beam or brachytherapy or both

Combined RT with surgery or CT Preop RT: poorly oxygenated cells are

much less susceptible to irradiation than oxygenated cells

Indications for post-oP radiotherapy

POST OP RT: Identification of tumour extent more accurate Technical performance easier in tissue planes

have not been altered by fibrosi,fusions,increased vascularity due to RT.

Results are poor if delayed beyond 6 wks Minimum tumour dose 50-60Gy daily fractions

2Gy to whole operative bed with boost 63Gy to sites of increased risk.

DFS- 2yrs -74% Over all survival 5yrs -31%(RTOG)

RT to nodes : >3cm nodes oor response to RT 53-83% response rste seen in nodal involvement N0,N1- cotrol with RT N2,N3- needs CT/RT if clinically radiologically

incomplete resonse then surgery. If neck dissetion lanned after 4-6wks of RT then

dose can be reduced frm 70 to 50Gy. Involvement of low level nodes –needs reduction

in dose to avoid damage to brachial plexus

Advances in RT: Ct based high precision RT IMRT IGRT Advantage increased QOL Eg: decreased dose to arotid gland –

saliva flow preserved-xerostomia reduced

Common acute & late toxicities of radiation

CHEMOTHERAPY

Goals of organ preservation: Maintainance of oral alimentation Protection of laryngeal airway Intelligible laryngeal speech

Chemotherapy

Role of chemotherapy is mainly as combination or for palliation

Neoadjuvant chemotherapy followed by RT(The Veteran’s Affairs study)

CT given before surgery/RT.more efficient drug delivery can occur.

A)CT responders well respond to RT B)CT response downstage disease may allow RT

effective C)CT may reduce incidence of distance metastasis

when local disease well controlled Laryngeal preservation 62% Overall survival35%

Concurrent chemo-RT(RTOG)(T3/T4) RT &CT used simultaneously in uresectable

disease. 3arm study 1)neoadjuvant CT(cisplatin+5FU) followed by

RT. 2)RT with concurrent CT(cisplatin100mg/m2 on

1,22,43 days) 3)RT alone Excluded T4 those cartilage eroded,inavde

tongue

ResultsatA)2 yr intact larynx in 88% RT+concurrent CT 75% neoadjuvant CT followed RT 70% RT aloneB)Locoregional control 78%,61%,56% C)Distant metastasis suressed inCT based regeme….

Over all survival rate is sameD)High-grade toxic effects greater with CT Based

regemeE)Mucosal toxicity concurrent RT+cisplatin higher

Adjuvant CT: CT after surgery or RT goal of this secondary treatment is palliation &rarely has longterm benefits.

Induction CT+ concurrent chemoRT: Addition of taxane tomcisplatin ,5FU

under study to imrove survival outcomes.

Commonly used CT agents in pyriform sinus tumours

Cis platinum: Inorganic metal comound binds to DNA causes

inter or intra strands cross linking Dose:80-120mg/m2 every 3-4wkly with mannitol

diuresis. 5FU: Competes with enzyme thymidylate

synthetase,inhibiting tymidine formation decrese in DNA synthesis.

Dose:10-15mg/kg/wk 400-500mg/m2 daily for 5days IV as loading dose

followed by 400-500mg/m2 wkly IV.OR

Side effects of chemotherapy

TAXANES:paclitaxel-135-250mg/m2 3-24hrs every 3wks

docetaxel-60-100mg/m2 bolus every 3wks

These act on G2 phase cause arrest of cell cycle

Toxocity:neutropenia,infection

Novel CT agents which acts on EGFR: Monoclonal antibodies-

cetuximab4oomg/m2 initially followed by 250mg/m2 per wk

Small molecular tyrosine kinase inhibitors -erlotinib -gefitinib 80-90% of H&N cancers over expresses

EGFR…

SURGICAL MANAGEMENT

THANK YOU