Feasibility and Response of Concurrent Weekly Docetaxel with Radical Radiotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma

Objective: (1) To study the feasibility, adverse effects and response of concurrent weekly Docetaxel with radical radiotherapy in inoperable locally advanced head and neck squamous cell carcinoma. (2) To assess the compliance and tolerance of weekly Docetaxel with radiotherapy. Material and Met...

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Main Authors: Jomon Raphael C, Rajesh I, Rajesh B, Selvamani B, Subhashini John
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2015-03-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/5614/10819_CE(Ra1)_F(GH)_PF1(PAK)_PFA(AK)_PF2(PAG).pdf
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author Jomon Raphael C
Rajesh I
Rajesh B
Selvamani B
Subhashini John
author_facet Jomon Raphael C
Rajesh I
Rajesh B
Selvamani B
Subhashini John
author_sort Jomon Raphael C
collection DOAJ
description Objective: (1) To study the feasibility, adverse effects and response of concurrent weekly Docetaxel with radical radiotherapy in inoperable locally advanced head and neck squamous cell carcinoma. (2) To assess the compliance and tolerance of weekly Docetaxel with radiotherapy. Material and Methods: Twenty one patients with stage III and IV head and neck squamous cell carcinoma satisfying inclusion criteria were selected and treated with conventional external radiotherapy of 70Gy in 35 fractions with weekly concurrent Docetaxel (15mg/ sqm), administered one hour before radiotherapy. Assessment of toxicities and evaluationof response was carried out. Results: Majority of patients had stage IV diseaseand 17/21 (81%) received the planned radiotherapydose of 70Gy and ≥4 cycles of weekly chemotherapy. Duration of treatment ranged from 7.1to 11.2 weeks. The toxicities noted were Grade III mucositis in 57% and grade III skin reaction in 23%, grade III dysphagia in 38% and grade II weight loss in 23% of patients. Systemic toxicities associated with chemotherapy were minimal and there was no dose limiting toxicities. The overall locoregional response at first follow up was 85%, with complete response of 70% and partial response of 15%. Conclusion: Concurrent Docetaxel is a feasible and suitable alternate to Cisplatin and 5-Fluorouracil chemotherapy with good patient compliance. The late toxicities and survival need to be followed up.
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spelling doaj.art-82e6d2d87de749c887ea4643ada7328a2022-12-22T01:14:53ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2015-03-0193XC01XC0410.7860/JCDR/2015/10819.5614Feasibility and Response of Concurrent Weekly Docetaxel with Radical Radiotherapy in Locally Advanced Head and Neck Squamous Cell CarcinomaJomon Raphael C0Rajesh I1Rajesh B2Selvamani B3Subhashini John4Associate Professor, Department of Radiotherapy, Amala Instittute of Medical Sciences, Thrissur, Kerala, India.Associate Professor, Department of Radiotherapy Unit II, Christian Medical College, Vellore, Tamilnadu, India.Associate Professor, Department of Radiotherapy Unit II, Christian Medical College, Vellore, Tamilnadu, India.Professor, Department of Radiotherapy Unit II, Christian Medical College, Vellore, Tamilnadu, India.Professor, Department of Radiotherapy Unit II, Christian Medical College, Vellore, Tamilnadu, India.Objective: (1) To study the feasibility, adverse effects and response of concurrent weekly Docetaxel with radical radiotherapy in inoperable locally advanced head and neck squamous cell carcinoma. (2) To assess the compliance and tolerance of weekly Docetaxel with radiotherapy. Material and Methods: Twenty one patients with stage III and IV head and neck squamous cell carcinoma satisfying inclusion criteria were selected and treated with conventional external radiotherapy of 70Gy in 35 fractions with weekly concurrent Docetaxel (15mg/ sqm), administered one hour before radiotherapy. Assessment of toxicities and evaluationof response was carried out. Results: Majority of patients had stage IV diseaseand 17/21 (81%) received the planned radiotherapydose of 70Gy and ≥4 cycles of weekly chemotherapy. Duration of treatment ranged from 7.1to 11.2 weeks. The toxicities noted were Grade III mucositis in 57% and grade III skin reaction in 23%, grade III dysphagia in 38% and grade II weight loss in 23% of patients. Systemic toxicities associated with chemotherapy were minimal and there was no dose limiting toxicities. The overall locoregional response at first follow up was 85%, with complete response of 70% and partial response of 15%. Conclusion: Concurrent Docetaxel is a feasible and suitable alternate to Cisplatin and 5-Fluorouracil chemotherapy with good patient compliance. The late toxicities and survival need to be followed up.https://jcdr.net/articles/PDF/5614/10819_CE(Ra1)_F(GH)_PF1(PAK)_PFA(AK)_PF2(PAG).pdfchemoirradiationcisplatinhead and neck cancer
spellingShingle Jomon Raphael C
Rajesh I
Rajesh B
Selvamani B
Subhashini John
Feasibility and Response of Concurrent Weekly Docetaxel with Radical Radiotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma
Journal of Clinical and Diagnostic Research
chemoirradiation
cisplatin
head and neck cancer
title Feasibility and Response of Concurrent Weekly Docetaxel with Radical Radiotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma
title_full Feasibility and Response of Concurrent Weekly Docetaxel with Radical Radiotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma
title_fullStr Feasibility and Response of Concurrent Weekly Docetaxel with Radical Radiotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma
title_full_unstemmed Feasibility and Response of Concurrent Weekly Docetaxel with Radical Radiotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma
title_short Feasibility and Response of Concurrent Weekly Docetaxel with Radical Radiotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma
title_sort feasibility and response of concurrent weekly docetaxel with radical radiotherapy in locally advanced head and neck squamous cell carcinoma
topic chemoirradiation
cisplatin
head and neck cancer
url https://jcdr.net/articles/PDF/5614/10819_CE(Ra1)_F(GH)_PF1(PAK)_PFA(AK)_PF2(PAG).pdf
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