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交替使用氨柔比星联合顺铂化疗和伊立替康联合顺铂每周方案治疗广泛期小细胞肺癌。

Alternating chemotherapy with amrubicin plus cisplatin and weekly administration of irinotecan plus cisplatin for extensive-stage small cell lung cancer.

机构信息

Department of Clinical Oncology, Tokyo Medical University Hospital, 6-7-1, Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.

出版信息

Anticancer Res. 2013 Mar;33(3):1117-23.

Abstract

BACKGROUND

A phase II study was conducted in order to determine the tumor efficacy and tolerance of alternating chemotherapy for extensive-stage small cell lung cancer (ED-SCLC).

PATIENTS AND METHODS

Twenty patients with previously-untreated ED-SCLC were enrolled in the study. At least four courses of chemotherapy consisting of alternation of two drug combinations were given: alternating cycles of amrubicin and cisplatin with weekly administration of irinotecan and cisplatin at 3- or 4-week intervals.

RESULTS

The overall response rate was 85.0% (17/20). The median duration of overall survival and progression-free survival were 359 days and 227 days, respectively. Hematological toxicity was the main adverse event. Grade 3 or 4 neutropenia, thrombocytopenia and anemia were observed in 20 (100%), 4 (20%) and 6 (30%) patients, respectively. With regard to non-hematological adverse events, grade 3 or 4 anorexia, diarrhea, febrile neutropenia and infection were observed in 5 (25%), 2 (10%), 2 (10%) and 2 (10%) patients, respectively. No treatment-related death occurred during either regimen.

CONCLUSION

The novel alternating non-cross-resistant chemotherapy was probably active against ED-SCLC and had acceptable toxicities. Further evaluation of this treatment for ED-SCLC in randomized phase III trials is warranted.

摘要

背景

为了确定广泛期小细胞肺癌(ED-SCLC)交替化疗的肿瘤疗效和耐受性,进行了一项 II 期研究。

患者和方法

本研究纳入了 20 例未经治疗的 ED-SCLC 患者。至少给予四周期化疗,包括两种药物组合的交替周期:阿霉素和顺铂交替周期与每周给予伊立替康和顺铂,间隔 3 或 4 周。

结果

总体缓解率为 85.0%(17/20)。总生存和无进展生存的中位时间分别为 359 天和 227 天。血液学毒性是主要的不良事件。3 或 4 级中性粒细胞减少、血小板减少和贫血分别见于 20 例(100%)、4 例(20%)和 6 例(30%)患者。关于非血液学不良事件,3 或 4 级厌食、腹泻、发热性中性粒细胞减少和感染分别见于 5 例(25%)、2 例(10%)、2 例(10%)和 2 例(10%)患者。两种方案均未发生与治疗相关的死亡。

结论

新型非交叉耐药交替化疗可能对 ED-SCLC 有效,且毒性可接受。需要在随机 III 期试验中进一步评估这种 ED-SCLC 治疗方法。

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