Pectasides Dimitrios, Pectasides Eirini, Papaxoinis George, Xiros Nikolaos, Sykiotis Constantinos, Papachristodoulou Antonios, Tountas Nikolaos, Panayiotides John, Economopoulos Theofanis
2nd Department of Internal Medicine, Propaedeutic, Oncology Section, University of Athens, Attikon University Hospital, Haidari, Athens, Greece.
Gynecol Oncol. 2008 Sep;110(3):299-303. doi: 10.1016/j.ygyno.2008.05.017. Epub 2008 Jul 7.
The purpose of this study was to evaluate the activity and toxicity of carboplatin, paclitaxel and pegylated liposomal doxorubicin combination in advanced or recurrent of the uterine carcinosarcoma.
Twenty-nine eligible patients with measurable disease were treated with carboplatin [area under the curve (AUC) 5], paclitaxel 175 mg/m(2) and pegylated liposomal doxorubicin 25 mg/m(2) every 3 weeks for 6-8 cycles.
There were 10 complete responses (CRs) (34%) and 8 partial responses (PRs) (28%) for an overall response rate (RR) of 62% (95% confidence interval [CI], 43-81%). The median progression-free survival (PFS) was 8.2 months (95% CI, 4.1-12.2 months) and the median overall survival (OS) was 16.4 months (95% CI, 14.7-18.0 months). There was no statistically significant difference between histology and response to therapy. Patients with PS of 0 or 1 had a higher RR than those with worst PS. Toxicity was generally mild except for myelotoxicity. Neutropenia grade 3/4 was recorded in 52% of patients and 10% experienced febrile neutropenia. Anemia grade 3 or 4 developed in 27% of patients and thrombocytopenia grade 3 or 4 in 31% of patients. Three patients (10%) developed grade 3 sensory neuropathy and only 2 patients (8%) grade 3 palmar-plantar erythrodysesthesias. No treatment-related deaths were recorded in our series.
The combination of carboplatin, paclitaxel and pegylated liposomal doxorubicin appears to have activity in advanced, persistent or recurrent endometrial carcinosarcoma with an acceptable toxicity profile.
本研究旨在评估卡铂、紫杉醇和聚乙二醇化脂质体阿霉素联合用药治疗晚期或复发性子宫癌肉瘤的活性和毒性。
29例符合条件的可测量疾病患者接受卡铂[曲线下面积(AUC)5]、紫杉醇175mg/m²和聚乙二醇化脂质体阿霉素25mg/m²治疗,每3周1次,共6 - 8个周期。
有10例完全缓解(CR)(34%)和8例部分缓解(PR)(28%),总缓解率(RR)为62%(95%置信区间[CI],43 - 81%)。中位无进展生存期(PFS)为8.2个月(95%CI,4.1 - 12.2个月),中位总生存期(OS)为16.4个月(95%CI,14.7 - 18.0个月)。组织学与治疗反应之间无统计学显著差异。PS为0或1的患者RR高于PS较差的患者。除骨髓毒性外,毒性一般较轻。52%的患者出现3/4级中性粒细胞减少,10%的患者出现发热性中性粒细胞减少。27%的患者出现3或4级贫血,31%的患者出现3或4级血小板减少。3例患者(10%)出现3级感觉神经病变,仅2例患者(8%)出现3级手足红斑感觉异常。本系列中未记录到与治疗相关的死亡。
卡铂、紫杉醇和聚乙二醇化脂质体阿霉素联合用药似乎对晚期、持续性或复发性子宫内膜癌肉瘤有活性,且毒性可接受。