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局限期小细胞肺癌同步放化疗:西南肿瘤协作组研究

Concurrent chemotherapy/radiotherapy for limited small-cell lung carcinoma: a Southwest Oncology Group Study.

作者信息

McCracken J D, Janaki L M, Crowley J J, Taylor S A, Giri P G, Weiss G B, Gordon W, Baker L H, Mansouri A, Kuebler J P

机构信息

Brooke Army Medical Center, Ft Sam Houston, TX.

出版信息

J Clin Oncol. 1990 May;8(5):892-8. doi: 10.1200/JCO.1990.8.5.892.

DOI:10.1200/JCO.1990.8.5.892
PMID:2159055
Abstract

The Southwest Oncology Group (SWOG) has conducted a phase II study to explore the efficacy and toxicity of initial, concurrent use of radiation therapy with cisplatin, etoposide (VP-16), and vincristine in limited-stage small-cell carcinoma of the lung. Two courses of cisplatin, VP-16, and vincristine chemotherapy were given with concurrent radiotherapy (XRT) to the primary tumor to a total dose of 4,500 cGy. Elective brain XRT was given to all patients concurrent with a third course of cisplatin/VP-16 therapy. Consolidation chemotherapy consisting of vincristine, methotrexate, and VP-16 alternating with Adriamycin (doxorubicin; Adria Laboratories, Columbus, OH) and cyclophosphamide, was given for 12 weeks following the initial induction chemotherapy/XRT program. Patients with a complete response had all therapy discontinued. Among 154 eligible patients treated, the complete response rate was 56%, with a partial response rate of 27%. The median survival is 17.5 months with an estimated 30% survival rate at 4 years from initiation of treatment. Combined modality toxicities were acceptable with the predominant toxicity being moderate to severe leukopenia and mild radiation esophagitis. The results of this treatment program appear superior to any previously reported by our group and compare favorably to those in the literature at large.

摘要

西南肿瘤协作组(SWOG)开展了一项II期研究,以探索在局限期小细胞肺癌中初始同时使用放疗与顺铂、依托泊苷(VP - 16)和长春新碱的疗效及毒性。给予两个疗程的顺铂、VP - 16和长春新碱化疗,并同时对原发肿瘤进行放疗(XRT),总剂量达4500 cGy。对所有患者在进行第三个疗程顺铂/VP - 16治疗的同时给予选择性脑XRT。在初始诱导化疗/XRT方案之后,给予由长春新碱、甲氨蝶呤和VP - 16与阿霉素(多柔比星;阿德里亚实验室,俄亥俄州哥伦布市)和环磷酰胺交替组成的巩固化疗,为期12周。完全缓解的患者停止所有治疗。在154例符合条件接受治疗的患者中,完全缓解率为56%,部分缓解率为27%。中位生存期为17.5个月,从治疗开始起4年的估计生存率为30%。联合治疗的毒性是可接受的,主要毒性为中度至重度白细胞减少和轻度放射性食管炎。该治疗方案的结果似乎优于我们组之前报告的任何结果,并且与总体文献中的结果相比也更有利。

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