Chauhan Ashok, Singh Harmeet, Sharma Tejpal, Manocha K K
Department of Radiotherapy, Pt. B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak-124001, India.
Afr Health Sci. 2008 Sep;8(3):149-55.
Management of advanced head and neck carcinoma is a challenging proposition. Presently concomitant chemo-irradiation has become the standard of care in such patients. Many chemotherapeutic drugs have shown radio-sensitising effects when used concomitantly along with radiation. The present study was carried out with the objective of assessing the feasibility and efficacy of low dose gemcitabine as radiosensitizer when used during radical radiotherapeutic management of patients with locally advanced head and neck carcinomas.
From November 2000 to March 2003, eighty histopathologically proven cases of squamous cell head and neck carcinoma were included in this trial, 40 patients were randomly assigned to receive radiotherapy alone and 40 patients to receive gemcitabine along with radiotherapy.
All patients were assessable for toxicity and response. Severe mucositis (WHO level 5 reactions were observed in 67% patients in the CT/RT group vs 16% patients in the RT only group. No severe hematological toxicity was seen. The rates of complete and partial responses were 42.5% & 57.5% respectively for RT only and 62.5% &37.5%, respectively for CT/RT group. There was no significant difference in the response rates at the end of treatment but disease free survival at three years was better in the CT/RT group (63.3% vs 20%). Nine of the 17 patients with complete response in the radiation only group developed relapse while no relapses were seen in CT/RT group.
In the present study the combination of gemcitabine and radiotherapy has not shown any statistical difference in locoregional control but survival advantage was seen as compared to radiotherapy alone. At the same time more mucosal and skin toxicity was encountered when Gemcitabine is given concurrently with radiation.
晚期头颈癌的治疗是一项具有挑战性的任务。目前,同步放化疗已成为这类患者的标准治疗方法。许多化疗药物与放疗同时使用时已显示出放射增敏作用。本研究旨在评估低剂量吉西他滨作为放射增敏剂在局部晚期头颈癌患者根治性放疗管理期间使用的可行性和疗效。
从2000年11月至2003年3月,本试验纳入了80例经组织病理学证实的头颈鳞状细胞癌病例,40例患者随机分配接受单纯放疗,40例患者接受吉西他滨联合放疗。
所有患者均可评估毒性和反应。严重黏膜炎(WHO 5级反应)在同步放化疗组的67%患者中观察到,而单纯放疗组为16%患者。未观察到严重血液学毒性。单纯放疗组的完全缓解率和部分缓解率分别为42.5%和57.5%,同步放化疗组分别为62.5%和37.5%。治疗结束时反应率无显著差异,但同步放化疗组三年无病生存率更好(63.3%对20%)。单纯放疗组17例完全缓解患者中有9例复发,而同步放化疗组未见复发。
在本研究中,吉西他滨与放疗联合在局部区域控制方面未显示出任何统计学差异,但与单纯放疗相比有生存优势。同时,吉西他滨与放疗同时使用时会出现更多的黏膜和皮肤毒性。