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环磷酰胺、阿霉素和派普化疗素联合治疗转移性乳腺癌

Combination chemotherapy of metastatic breast carcinoma with cyclophosphamide, adriamycin, and peptichemio.

作者信息

Legha S S, Ajani J A, Blumenschein G R, Hortobagyi G N, Buzdar A U

出版信息

Cancer. 1984 May 1;53(9):1836-40. doi: 10.1002/1097-0142(19840501)53:9<1836::aid-cncr2820530906>3.0.co;2-p.

Abstract

Thirty patients with metastatic carcinoma of the breast were treated with a combination of cyclophosphamide, Adriamycin (doxorubicin), and peptichemio (CAP) as an induction regimen, and maintenance regimen consisting of thiotepa, methotrexate, and 5-fluorouracil (TMF). Twenty-four patients were evaluable. Thirteen patients achieved an objective response for a response rate of 54.0% (complete remission plus partial remission). Median duration of response was 9.5 months (0-32+). The CAP regimen had severe myelotoxicity that led to dose reductions in 67% of patients. Furthermore, 50% of the patients required delay (greater than 28-day interval) in chemotherapy courses because of myelosuppression, and peptichemio had to be discontinued in seven patients. The CAP chemotherapy as an induction regimen for metastatic breast carcinoma resulted in underutilization of Adriamycin, and proved to be inferior to other Adriamycin-containing regimens. Although peptichemio used as a single agent had significant activity against breast cancer, it was not suitable for prolonged use in conjunction with other myelosuppressive agents. However, it may have a role in second-line therapy of metastatic breast cancer in conjunction with nonmyelosuppressive agents. The authors were unable to test the efficacy of non-cross-resistant maintenance therapy with TMF in this trial.

摘要

30例转移性乳腺癌患者接受了环磷酰胺、阿霉素(多柔比星)和匹服平(CAP)联合方案作为诱导治疗方案,以及由噻替派、甲氨蝶呤和5-氟尿嘧啶组成的维持治疗方案(TMF)。24例患者可进行评估。13例患者获得客观缓解,缓解率为54.0%(完全缓解加部分缓解)。中位缓解持续时间为9.5个月(0至32 +个月)。CAP方案有严重的骨髓毒性,导致67%的患者减少剂量。此外,50%的患者因骨髓抑制需要延迟(间隔大于28天)化疗疗程,7例患者不得不停用匹服平。CAP化疗作为转移性乳腺癌的诱导治疗方案导致阿霉素未得到充分利用,且被证明劣于其他含阿霉素的方案。虽然匹服平作为单一药物对乳腺癌有显著活性,但它不适合与其他骨髓抑制药物长期联合使用。然而,它可能在与非骨髓抑制药物联合用于转移性乳腺癌的二线治疗中发挥作用。在本试验中,作者未能测试TMF非交叉耐药维持治疗的疗效。

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