You need JavaScript to view this

Randomized phase III trial of postoperative radiochemotherapy {+-} amifostine in head and neck cancer. Is there evidence for radioprotection?

Abstract

Purpose: Experimental and clincial data suggest a reduction of radiation-induced acute toxicity by amifostine (A). We investigated this issue in a randomized trial comparing radiochemotherapy (RT + CT) versus radiochemotherapy plus amifostine (RC + CT + A) in patients with head and neck cancer. Patients and Methods: 56 patients with oro-/hypopharynx or larynx cancer (T1-2 N1-2 G3, T3-4 N0-2 G1-3) were randomized to received RC + CT alone or RC + CT + A. Patients were irradiated up to 60 Gy (R0) or 70 Gy (R1/2) and received chemotherapy (70 mg/m{sup 2} carboplatin, day 1-5 week 1 and 5 of radiotherapy). 250 mg amifostine were applied daily before each radiotherapy session. Acute toxicity was evaluated according to the common toxicity criteria (CTC). As for acute xerostomia, patients with laryngeal cancer were excluded from evaluation. Results: 50 patients were evaluable (25 patients in the RC + CT, 25 patients in the RC + CT + A group). Clinical characteristics were well balanced in both treatment groups. Amifostine provided reduction in acute xerostomia and mucositis but had no obvious influence on Karnofsky performance status, body weight, cutaneous side effects, and alopecia. The differences between both groups were statistically significant for acute xerostomia  More>>
Authors:
Vacha, P; Fehlauer, F; Mahlmann, B; Marx, M; Richter, E; [1]  Hinke, A; [2]  Sommer, K; [3]  Feyerabend, T [4] 
  1. Dept. of Radiation Oncology and Nuclear Medicine, Univ. of Luebeck (Germany)
  2. WiSP Research Inst., Langenfeld (Germany)
  3. Dept. of Head and Neck Surgery, Univ. of Luebeck (Germany)
  4. Practice for Radiation Therapy Bonn-Rhein-Sieg, Bonn (Germany)
Publication Date:
Jun 01, 2003
Product Type:
Journal Article
Resource Relation:
Journal Name: Strahlentherapie und Onkologie; Journal Volume: 179; Journal Issue: 6; Other Information: PBD: Jun 2003
Subject:
63 RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS; 62 RADIOLOGY AND NUCLEAR MEDICINE; NEOPLASMS; CARCINOMAS; SURGERY; EFFICIENCY; PATIENTS; RADIATION DOSES; CHEMOTHERAPY; COMBINED THERAPY; HEAD; NECK; PHARYNX; LARYNX; SIDE EFFECTS; EARLY RADIATION EFFECTS; CLASSIFICATION
OSTI ID:
20389909
Country of Origin:
Germany
Language:
English
Other Identifying Numbers:
Journal ID: ISSN 0179-7158; STONE4; TRN: DE03FB731
Submitting Site:
DEN
Size:
page(s) 385-390
Announcement Date:
Nov 14, 2003

Citation Formats

Vacha, P, Fehlauer, F, Mahlmann, B, Marx, M, Richter, E, Hinke, A, Sommer, K, and Feyerabend, T. Randomized phase III trial of postoperative radiochemotherapy {+-} amifostine in head and neck cancer. Is there evidence for radioprotection?. Germany: N. p., 2003. Web.
Vacha, P, Fehlauer, F, Mahlmann, B, Marx, M, Richter, E, Hinke, A, Sommer, K, & Feyerabend, T. Randomized phase III trial of postoperative radiochemotherapy {+-} amifostine in head and neck cancer. Is there evidence for radioprotection?. Germany.
Vacha, P, Fehlauer, F, Mahlmann, B, Marx, M, Richter, E, Hinke, A, Sommer, K, and Feyerabend, T. 2003. "Randomized phase III trial of postoperative radiochemotherapy {+-} amifostine in head and neck cancer. Is there evidence for radioprotection?" Germany.
@misc{etde_20389909,
title = {Randomized phase III trial of postoperative radiochemotherapy {+-} amifostine in head and neck cancer. Is there evidence for radioprotection?}
author = {Vacha, P, Fehlauer, F, Mahlmann, B, Marx, M, Richter, E, Hinke, A, Sommer, K, and Feyerabend, T}
abstractNote = {Purpose: Experimental and clincial data suggest a reduction of radiation-induced acute toxicity by amifostine (A). We investigated this issue in a randomized trial comparing radiochemotherapy (RT + CT) versus radiochemotherapy plus amifostine (RC + CT + A) in patients with head and neck cancer. Patients and Methods: 56 patients with oro-/hypopharynx or larynx cancer (T1-2 N1-2 G3, T3-4 N0-2 G1-3) were randomized to received RC + CT alone or RC + CT + A. Patients were irradiated up to 60 Gy (R0) or 70 Gy (R1/2) and received chemotherapy (70 mg/m{sup 2} carboplatin, day 1-5 week 1 and 5 of radiotherapy). 250 mg amifostine were applied daily before each radiotherapy session. Acute toxicity was evaluated according to the common toxicity criteria (CTC). As for acute xerostomia, patients with laryngeal cancer were excluded from evaluation. Results: 50 patients were evaluable (25 patients in the RC + CT, 25 patients in the RC + CT + A group). Clinical characteristics were well balanced in both treatment groups. Amifostine provided reduction in acute xerostomia and mucositis but had no obvious influence on Karnofsky performance status, body weight, cutaneous side effects, and alopecia. The differences between both groups were statistically significant for acute xerostomia and nonsignificant, but with a trend for mucositis. Conclusions: According to our results, there is a radioprotective effect on salivary glands and a potential effect on oral mucosa by amifostine in postoperative radiotherapy combined with carboplatin. To improve the radio- and chemoprotective effects of amifostine in clinical practice, the application of a higher dose (> 250 mg) seems to be necessary. (orig.)}
journal = []
issue = {6}
volume = {179}
journal type = {AC}
place = {Germany}
year = {2003}
month = {Jun}
}