首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Neoadjuvant chemotherapy/gefitinib followed by concurrent chemotherapy/radiation therapy/gefitinib for patients with locally advanced squamous carcinoma of the head and neck.
【24h】

Neoadjuvant chemotherapy/gefitinib followed by concurrent chemotherapy/radiation therapy/gefitinib for patients with locally advanced squamous carcinoma of the head and neck.

机译:新辅助化疗/吉非替尼,然后同时化疗/放疗/吉非替尼用于局部晚期头颈部鳞癌患者。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND:: The authors evaluated the feasibility, toxicity, and efficacy of gefitinib added to first-line combined-modality therapy for patients with locally advanced squamous carcinoma of the head and neck. METHODS:: Patients with biopsy-proven locally advanced squamous carcinoma of the head and neck who had low expected cure rates with local treatment modalities alone were eligible for this treatment. All patients received a 6-week induction course of docetaxel, carboplatin, infusional 5-fluorouracil, and gefitinib (250 mg daily). Gefitinib was continued while patients received concurrent weekly docetaxel and radiation therapy. After the completion of radiation therapy, gefitinib was continued until patients developed disease progression or for a maximum of 24 months. RESULTS:: Sixty-two patients (53% with stage IV disease) received protocol treatment, and 50 patients (81%) were able to complete the regimen. The addition of gefitinib increased the incidence of grade 3/4 mucositis (27%) and diarrhea(16%) during induction therapy but did not appear to add substantially to toxicity during concurrent chemoradiation. The estimated 3-year progression-free and overall survival rates for the entire group were 41% and 54%, respectively. CONCLUSIONS:: The addition of gefitinib was associated with a moderate increase in toxicity with this combined modality regimen, particularly during induction therapy. Although this regimen was efficacious, the survival results overlap with results reported with chemoradiation alone. The role of epidermal growth factor receptor inhibitors in first-line, combined-modality therapy for patients with head and neck cancer remains undefined. Cancer 2009. (c) 2009 American Cancer Society.
机译:背景:作者评估了吉非替尼联合一线联合方式治疗局部晚期头颈部鳞癌患者的可行性,毒性和疗效。方法:经活检证实的局部晚期头颈部鳞状细胞癌,仅采用局部治疗方式的预期治愈率低的患者,才有资格接受该治疗。所有患者均接受多西他赛,卡铂,5-氟尿嘧啶输注和吉非替尼(每天250 mg)的6周诱导疗程。患者同时接受每周多西他赛和放疗同时接受吉非替尼治疗。放疗结束后,继续进行吉非替尼治疗,直至患者疾病进展或最长持续24个月。结果:62名患者(IV期疾病为53%)接受了方案治疗,而50名患者(81%)能够完成该方案。吉非替尼的添加在诱导治疗期间增加了3/4级粘膜炎(27%)和腹泻(16%)的发生率,但似乎并未显着增加同时放化疗期间的毒性。估计整个组的3年无进展生存率和总生存率分别为41%和54%。结论:吉非替尼的加入与这种联合治疗方案的毒性中度增加有关,特别是在诱导治疗期间。尽管该方案有效,但其存活结果与仅化学放疗报告的结果重叠。表皮生长因子受体抑制剂在头颈癌患者的一线联合治疗中的作用尚不清楚。癌症2009。(c)2009美国癌症协会。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号