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米托蒽醌、甲氨蝶呤、长春新碱及卡铂一线联合化疗方案(MIMOC)治疗晚期乳腺癌

First-line combination chemotherapy with mitoxantrone, methotrexate, vincristine and carboplatin (MIMOC) in advanced breast cancer.

作者信息

Bafaloukos D, Samonis G, Klinaki A, Daliani D, Karvounis N, Bacoyiannis C, Karabelis A, Milonakis N, Kosmidis P

机构信息

2nd Department of Medical Oncology, Metaxa's Cancer Institute of Piraeus, Greece.

出版信息

Eur J Cancer. 1993;29A(6):851-3. doi: 10.1016/s0959-8049(05)80422-8.

Abstract

51 patients with stage IIIB and IV breast cancer entered a prospective phase II study of combination chemotherapy that consisted of mitoxantrone (8 mg/m2) day 1, methotrexate (25 mg/m2) day 1, vincristine (1 mg/m2) day 2 and carboplatin (250 mg/m2) day 2 (MIMOC) given in a 3-weekly schedule. None had received prior chemotherapy for metastatic disease, although 16 patients were given adjuvant chemotherapy. Objective response to treatment was seen in 29 of 48 patients analysed for response (60%) with 8 complete responses (CR). 7 out of 8 patients with stage IIIB disease responded, 2 of them completely. Responses were seen in all sites but the best results were achieved in lung metastases with 50% CR. The median duration of response was 8 months and the median time to disease progression was 12 months. The main toxicity was nausea and vomiting which was severe in 20% of the patients. Other toxicities were mild. MIMOC was administered on an out-patient basis and appears to be effective as first-line treatment in advanced breast cancer.

摘要

51例IIIB期和IV期乳腺癌患者进入一项前瞻性II期联合化疗研究,化疗方案为每3周一次,第1天给予米托蒽醌(8mg/m²)、甲氨蝶呤(25mg/m²),第2天给予长春新碱(1mg/m²)和卡铂(250mg/m²)(MIMOC方案)。尽管16例患者接受过辅助化疗,但均未接受过针对转移性疾病的一线化疗。在48例接受疗效分析的患者中,29例(60%)出现客观缓解,其中8例完全缓解(CR)。8例IIIB期疾病患者中有7例缓解,其中2例完全缓解。所有转移部位均出现缓解,但肺转移的缓解效果最佳,完全缓解率为50%。中位缓解持续时间为8个月,疾病进展的中位时间为12个月。主要毒性反应为恶心和呕吐,20%的患者症状严重。其他毒性反应较轻。MIMOC方案为门诊给药,似乎可作为晚期乳腺癌的一线有效治疗方案。

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