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卡铂、紫杉醇和吉西他滨联合氨磷汀用于晚期非小细胞肺癌的新型三联化疗方案:一项II期研究。

New triplet chemotherapy combination with carboplatin, paclitaxel and gemcitabine plus amifostine support in advanced non small cell lung cancer: a phase II study.

作者信息

Illiano A, Barletta E, De Marino V, Battiloro C, Barzelloni M, Scognamiglio F, Rossi N, Zampa G, De Bellis M, Gridelli C

机构信息

VI Divisione di Pneumologia, Ospedale Monaldi, Napoli, Italy.

出版信息

Anticancer Res. 2000 Sep-Oct;20(5C):3999-4003.

Abstract

New triplet chemotherapy combinations are under investigation in advanced non small cell lung cancer (NSCLC). Carboplatin, plus paclitaxel, plus gemcitabine is among the most active and promising regimens. The use of more aggressive chemotherapy in order to improve results can increase toxicity. Amifostine (WR-2721) reduces toxicity of radiotherapy and chemotherapy and protects selectively a number of normal, but not neoplastic, tissue. Based on this background, we performed a phase II study on carboplatin, plus paclitaxel, plus gemcitabine with amifostine support in advanced NSCLC. Patients received chemotherapy at the following dosage: carboplatin AUC 5, i.v., at day 1; paclitaxel 175 mg/m2, i.v. by 3-hour infusion, at day 1; gemcitabine 1000 mg/m2, i.v. by 3-hour infusion, at days 1 and 8; every 3 weeks for a maximum of 6 cycles. Amifostine was administered at the dose of 740 mg/m2, i.v., at day 1 of each cycle. Seventeen patients entered the study. They were prevalently male, median age was 62 years, PS (ECOG) was 0 in 10 cases (58.8%), 1 in 6 (35.3%) and 2 in 1 (5.9%). Histology was epidermoid in 8 cases (47%) and adenocarcinoma in 9 (53%). We observed 8 (47.5%) objective responses with 2 (11.7%) complete responses. Median time to progression and median survival were 24 and 36 weeks, respectively. Treatment was well tolerated. The main toxicity was as follows: grade 3 neutropenia, grade 2 thrombocytopenia and grade 3 anemia in one (5.8%) case; grade 2 peripheral neurologic toxicity in 3 (17.6%) patients; grade 2 cardiac toxicity (atrial fibrillation) in one case; and grade 3 respiratory toxicity (dispnoea) in one patient. These data indicate that this combination has promising activity and tolerability. A randomized trial comparing carboplatin plus paclitaxel, plus gemcitabine versus carboplatin, plus paclitaxel, plus gemcitabine, plus amifostine in advanced NSCLC is warranted.

摘要

新型三联化疗方案正在晚期非小细胞肺癌(NSCLC)中进行研究。卡铂、紫杉醇加吉西他滨是最具活性和前景的方案之一。为了提高疗效而使用更积极的化疗会增加毒性。氨磷汀(WR - 2721)可降低放疗和化疗的毒性,并选择性地保护一些正常组织而非肿瘤组织。基于此背景,我们对晚期NSCLC患者进行了一项关于卡铂、紫杉醇加吉西他滨联合氨磷汀支持治疗的II期研究。患者接受如下剂量的化疗:卡铂AUC 5,静脉注射,第1天;紫杉醇175 mg/m²,静脉滴注3小时,第1天;吉西他滨1000 mg/m²,静脉滴注3小时,第1天和第8天;每3周进行一次,最多6个周期。氨磷汀在每个周期的第1天以740 mg/m²的剂量静脉注射。17名患者进入研究。他们大多为男性,中位年龄为62岁,体力状况(ECOG)评分为0的有10例(58.8%),评分为1的有6例(35.3%),评分为2的有1例(5.9%)。组织学类型为鳞状细胞癌的有8例(47%),腺癌的有9例(53%)。我们观察到8例(47.5%)客观缓解,其中2例(11.7%)完全缓解。中位疾病进展时间和中位生存期分别为24周和36周。治疗耐受性良好。主要毒性如下:1例(5.8%)出现3级中性粒细胞减少、2级血小板减少和3级贫血;3例(17.6%)患者出现2级周围神经毒性;1例出现2级心脏毒性(心房颤动);1例患者出现3级呼吸毒性(呼吸困难)。这些数据表明该联合方案具有良好的活性和耐受性。有必要进行一项随机试验,比较晚期NSCLC患者使用卡铂加紫杉醇加吉西他滨与卡铂加紫杉醇加吉西他滨加氨磷汀的疗效。

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