卡培他滨联合卡铂治疗晚期非小细胞肺癌的Ii期临床试验

Bhuvana Sagar, Fadi Estaphan, D. W. Spell, F. Klementich, Dennie V. Jones
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引用次数: 1

摘要

卡铂是许多非小细胞肺癌(NSCLC)治疗方案的支柱。5-氟尿嘧啶(5-FU)在NSCLC中具有适度活性,并与铂类似物协同作用。该试验评估了卡培他滨(一种口服5FU前药)与卡铂在不可切除的非小细胞肺癌患者中的活性和毒性。入选标准包括未治疗的可测量的IIIB/IV期NSCLC, ECOG表现状态< 2,器官功能充足。第1天给予卡铂,AUC=5,第1-14天给予卡培他滨4000mg,每28天给予一次。每隔一个周期进行肿瘤评估。15例患者(中位年龄= 64;中位表现状态= 0)入组并接受46个疗程的方案治疗;13例可评价缓解,5例部分缓解(38.5%)。5例因毒性退出;四个可能与学习治疗有关。中位生存期为8个月。卡培他滨和卡铂在非小细胞肺癌中有活性。由于目前的治疗方案毒性太大,因此不需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Pilot Phase Ii Study Of Capecitabine With Carboplatin In Patients With Advanced Nonsmall Cell Lung Cancer
Carboplatin forms the backbone of many regimens for nonsmall cell lung cancer (NSCLC). 5-fluorouracil (5-FU) is modestly active in NSCLC and is synergistic with platinum analogs. This trial evaluated the activity and toxicity of capecitabine, an oral 5FU prodrug, with carboplatin in patients with unresectable NSCLC. Eligibility criteria included untreated measurable stage IIIB/IV NSCLC, ECOG performance status < 2, and adequate organ function. Carboplatin, AUC=5, was administered on day one, with capecitabine, 4000 mg days 1-14, every 28 days. Tumor assessments were obtained every other cycle. Fifteen patients (median age = 64; median performance status = 0) were enrolled and received 46 cycles of protocol therapy; 13 were evaluable for response, with 5 partial responses (38.5%). Five withdrew due to toxicity; four possibly related to study therapy. Median survival was 8 months. Capecitabine and carboplatin are active in NSCLC. Further investigation is not warranted, as this current regimen is too toxic.
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