Serkies K, Jassem J, Dziadziuszko R
Department of Oncology and Radiotherapy, Medical University of Gdańsk, 7 Debinki Street, 80-211 Gdańsk, Poland.
Int J Gynecol Cancer. 2006 May-Jun;16(3):1152-6. doi: 10.1111/j.1525-1438.2006.00548.x.
The efficacy and toxicity of mitomycin C (MMC), ifosfamide, and cisplatin in cervical cancer were evaluated. Between January 1997 and August 2003, 46 patients with locally recurrent, persistent, or disseminated cervical cancer were treated with MMC 6 mg/m(2), ifosfamide 3 g/m(2), and cisplatin 50 mg/m(2) (MIC regimen) repeated every 3 weeks (maximum six cycles). In eight patients (17%), the tumor involved the pelvis alone, in 11 (24%) the pelvis and extrapelvic sites, and 27 (59%) had only distant lesions. A total of 213 MIC cycles were administered (median six cycles per patient). Of the 44 evaluable patients, the overall response rate was 34% (9% complete and 25% partial responses). Median progression-free interval was 6 months (95% confidence interval [CI], 4-7 months), and overall survival was 10 months (95% CI, 6-14 months). Objective response was obtained in two patients (11%) with pelvic relapse within previously irradiated area and in 13 (50%) of those with extrapelvic lesions (P= 0.01). Leukopenia was seen in 59% of patients (grade 3 in 9%). Nonhematologic side effects were mild and relatively infrequent. In conclusion, MIC regimen provides satisfactory efficacy with acceptable toxicity in advanced cervical cancer patients. Better response is seen in lesions outside of the previously irradiated area.
评估了丝裂霉素C(MMC)、异环磷酰胺和顺铂在宫颈癌中的疗效及毒性。1997年1月至2003年8月期间,46例局部复发、持续性或播散性宫颈癌患者接受MMC 6 mg/m²、异环磷酰胺3 g/m²和顺铂50 mg/m²(MIC方案)治疗,每3周重复一次(最多六个周期)。8例患者(17%)肿瘤仅累及盆腔,11例(24%)累及盆腔及盆腔外部位,27例(59%)仅有远处病变。共进行了213个MIC周期(每位患者中位数为六个周期)。在44例可评估患者中,总缓解率为34%(9%完全缓解,25%部分缓解)。无进展生存期的中位数为6个月(95%置信区间[CI],4 - 7个月),总生存期为10个月(95% CI,6 - 14个月)。在先前放疗区域内盆腔复发的2例患者(11%)以及盆腔外病变的13例患者(50%)中获得了客观缓解(P = 0.01)。59%的患者出现白细胞减少(3级的占9%)。非血液学副作用轻微且相对少见。总之,MIC方案在晚期宫颈癌患者中提供了令人满意的疗效且毒性可接受。在先前放疗区域外的病变中观察到更好的缓解。