Schippert Cordula, Warm Mathias, Blohmer Jens-Uwe, du Bois Andreas, Lück Hans-Joachim
Klinik für Frauenheilkunde und Geburtshilfe, Medizinische Hochschule Hannover, Germany.
Onkologie. 2012;35(9):500-4. doi: 10.1159/000341839. Epub 2012 Aug 13.
Patients with metastatic breast cancer (MBC) with disease progression after anthracycline-and/or taxane-containing therapy need an effective drug regimen with low toxicity. Mitomycin C (MMC) and vinorelbine (VNR) are suitable candidates for combination therapy in the second-/third-line treatment of MBC. This study evaluates the safety and efficacy of an MMC/VNR combination chemotherapy in pretreated patients with MBC.
In a phase II trial, patients with anthracycline-and/or taxane-pretreated MBC were treated with MMC 8 mg/m(2) (day 1) and VNR 25 mg/m(2) (days 1 and 8) every 4 weeks for up to 6 cycles or until disease progression.
In 51 eligible patients, 13 (26%) partial remissions (PRs), 20 (39%) stable diseases (SDs) and 18 (35%) progressive diseases (PDs) were observed. The median progression-free survival (PFS) was 5.0 months. The main grade 3/4 toxicities were neutrocytopenia (41%), granulocytopenia (37%), and thrombocytopenia (4%). Other hematological and non-hematological toxicities were mostly mild.
The combination of MMC and VNR is an effective and relatively well-tolerated regimen for anthracycline- and/or taxane-pretreated patients with MBC and is suitable for outpatient therapy.
接受含蒽环类药物和/或紫杉烷类药物治疗后疾病进展的转移性乳腺癌(MBC)患者需要一种低毒性的有效药物方案。丝裂霉素C(MMC)和长春瑞滨(VNR)是MBC二线/三线治疗联合疗法的合适候选药物。本研究评估了MMC/VNR联合化疗在经预处理的MBC患者中的安全性和疗效。
在一项II期试验中,对接受过蒽环类药物和/或紫杉烷类药物预处理的MBC患者,每4周给予MMC 8 mg/m²(第1天)和VNR 25 mg/m²(第1天和第8天)治疗,最多6个周期或直至疾病进展。
在51例符合条件的患者中,观察到13例(26%)部分缓解(PR)、20例(39%)疾病稳定(SD)和18例(35%)疾病进展(PD)。中位无进展生存期(PFS)为5.0个月。主要的3/4级毒性反应为中性粒细胞减少(41%)、粒细胞减少(37%)和血小板减少(4%)。其他血液学和非血液学毒性大多较轻。
MMC和VNR联合方案对接受过蒽环类药物和/或紫杉烷类药物预处理的MBC患者是一种有效且耐受性相对良好的方案,适用于门诊治疗。