Phase II study of gefitinib for the treatment of recurrent and metastatic nasopharyngeal carcinoma.

Head & Neck Pub Date : 2008-07-01 DOI:10.1002/hed.20792
Daniel T T Chua, William I Wei, Maria P Wong, Jonathan S T Sham, John Nicholls, Gordon K H Au
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引用次数: 105

Abstract

Background: This single-center, phase II study assessed the safety/tolerability and initial efficacy of gefitinib in patients with nasopharyngeal carcinoma (NPC) pretreated with platinum-based chemotherapy.

Methods: Patients with recurrent and metastatic NPC who had treatment failure with at least 2 lines of chemotherapy including platinum were given gefitinib at a fixed dose of 250 mg daily. Treatment was continued until the patient experienced unacceptable side effects or disease progression.

Results: Nineteen patients were enrolled, having had treatment failure with a median of 2 chemotherapy regimens. Treatment was well tolerated, and only grades 1 to 2 adverse events were observed. None of the patients achieved partial or complete response. Median time-to-progression was 4 months, and median overall survival was 16 months.

Conclusion: Gefitinib was well tolerated, but the response rate was poor in this heavily pretreated study population, and its use in NPC is not recommended outside the context of clinical trial.

吉非替尼治疗复发和转移性鼻咽癌的II期研究。
背景:这项单中心II期研究评估了吉非替尼在接受铂基化疗的鼻咽癌(NPC)患者中的安全性/耐受性和初始疗效。方法:复发和转移性鼻咽癌患者,治疗失败,至少2线化疗包括铂给予吉非替尼固定剂量250mg /天。治疗持续进行,直到患者出现不可接受的副作用或疾病进展。结果:19例患者入组,治疗失败,中位数为2个化疗方案。治疗耐受性良好,仅观察到1至2级不良事件。没有患者达到部分或完全缓解。中位进展时间为4个月,中位总生存期为16个月。结论:吉非替尼耐受性良好,但在大量预处理的研究人群中反应率较低,在临床试验背景外不推荐用于鼻咽癌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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