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甲氨蝶呤、VM - 26(替尼泊苷)、丙卡巴肼和地塞米松治疗难治性淋巴瘤:癌症与白血病B组研究7902

Treatment of refractory lymphoma with methotrexate, VM-26 (teniposide), procarbazine, and dexamethasone: Cancer and Leukemia Group B study 7902.

作者信息

Lachant N A, Anderson J, Ginsberg S J, Cooper M R, Hurd D D, Bloomfield C D, Gottlieb A J

机构信息

Division of Hematology/Oncology, S.U.N.Y. Health Sciences Center, Syracuse.

出版信息

Med Pediatr Oncol. 1988;16(6):375-7. doi: 10.1002/mpo.2950160604.

Abstract

Seventy-eight individuals previously treated with chemotherapy for non-Hodgkin's lymphoma were enrolled in a phase II pilot study employing methotrexate 100 mg/M2 iv (day 1), calcium leucovorin 10 mg/M2 iv and/or po q6h (days 2-4), VM-26 (teniposide) 100 mg/M2 iv (days 2 and 9), procarbazine 100 mg/M2 po (days 2-15), and dexamethasone 15 mg/M2po (days 2-8) (MV26PD). Thirty percent of the 78 patients treated had a response to therapy (8% complete, 22% partial). Twenty-four percent of patients with diffuse histiocytic (large cell) lymphoma had a response (12% complete, 12% partial). The estimated failure-free survival was 41% at 3 months and the median survival (death from any cause) was 4.5 months for the entire cohort. Two individuals, including one individual with diffuse histiocytic lymphoma, remain in a complete response for over 900 days. Significant hematologic toxicity and infectious complications were seen in this heavily pretreated group of patients. MV26PD represents an active combination of agents for the treatment of non-Hodgkin's lymphoma. The optimal dosing for MV26PD remains to be determined.

摘要

78名先前接受过非霍奇金淋巴瘤化疗的患者参加了一项II期试验性研究,该研究采用以下治疗方案:静脉注射甲氨蝶呤100 mg/M²(第1天),静脉注射和/或口服亚叶酸钙10 mg/M²,每6小时一次(第2 - 4天),静脉注射威猛(替尼泊苷)100 mg/M²(第2天和第9天),口服丙卡巴肼100 mg/M²(第2 - 15天),口服地塞米松15 mg/M²(第2 - 8天)(MV26PD方案)。接受治疗的78例患者中有30%对治疗有反应(8%完全缓解,22%部分缓解)。弥漫性组织细胞(大细胞)淋巴瘤患者中有24%有反应(12%完全缓解,12%部分缓解)。整个队列的3个月无失败生存率估计为41%,中位生存期(任何原因导致的死亡)为4.5个月。两名患者,包括一名弥漫性组织细胞淋巴瘤患者,持续完全缓解超过900天。在这群接受过大量预处理的患者中观察到了显著的血液学毒性和感染并发症。MV26PD方案是治疗非霍奇金淋巴瘤的一种有效的联合用药方案。MV26PD方案的最佳剂量仍有待确定。

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