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含米托蒽醌的联合化疗用于非霍奇金淋巴瘤患者

[Mitoxantrone-containing combination chemotherapy in patients with non-Hodgkin's lymphoma].

作者信息

Kimura I, Ohnoshi T, Masaoka T, Sampi K, Namba K

出版信息

Gan To Kagaku Ryoho. 1986 Oct;13(10):3034-9.

PMID:3532959
Abstract

Thirty-one patients with advanced non-Hodgkin's lymphoma were entered in a trial of a four-drug combination of mitoxantrone, cyclophosphamide, vincristine, and prednisolone (MCOP). This trial was intended to test the efficacy of substituting mitoxantrone for adriamycin in the CHOP combination, and to evaluate tumor response in patients who had received anthracycline antibiotic therapy. Of 31 patients, 25 were fully evaluated for tumor response and toxicity. There were 7 responses (4 complete, 3 partial) among 9 patients who had received radiation alone or chemotherapy not containing anthracycline antibiotics, whereas there were 7 responses (3 complete, 4 partial) in 16 patients who had been given anthracycline-containing chemotherapy. Median duration of response was 11+ weeks (range; 5 to 43+ weeks). The major toxicity was myelosuppression, although patients tolerated this well. This study suggested that mitoxantrone is not fully cross-resistant with anthracycline antibiotics and that MCOP is an effective regimen in patients with previously treated non-Hodgkin's lymphoma. However, when salvage chemotherapy for CHOP-failure is intended, cyclophosphamide and vincristine in MCOP should be further substituted by other agents such as etoposide and cis-platinum.

摘要

31例晚期非霍奇金淋巴瘤患者参加了米托蒽醌、环磷酰胺、长春新碱和泼尼松龙(MCOP)四药联合方案的试验。该试验旨在测试在CHOP方案中用米托蒽醌替代阿霉素的疗效,并评估接受过蒽环类抗生素治疗的患者的肿瘤反应。31例患者中,25例对肿瘤反应和毒性进行了全面评估。在仅接受过放疗或未接受含蒽环类抗生素化疗的9例患者中,有7例有反应(4例完全缓解,3例部分缓解);而在接受过含蒽环类化疗的16例患者中,有7例有反应(3例完全缓解,4例部分缓解)。反应的中位持续时间为11 +周(范围:5至43 +周)。主要毒性是骨髓抑制,不过患者对此耐受性良好。该研究表明米托蒽醌与蒽环类抗生素并非完全交叉耐药,且MCOP方案对既往接受过治疗的非霍奇金淋巴瘤患者是一种有效的治疗方案。然而,当打算对CHOP方案治疗失败进行挽救化疗时,MCOP方案中的环磷酰胺和长春新碱应进一步用依托泊苷和顺铂等其他药物替代。

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