Hensley Martee L, Blessing John A, Degeest Koen, Abulafia Ovadia, Rose Peter G, Homesley Howard D
Memorial Sloan-Kettering Cancer Center, Department of Medical Oncology, 1275 York Avenue, New York, NY 10021, USA.
Gynecol Oncol. 2008 Jun;109(3):323-8. doi: 10.1016/j.ygyno.2008.02.024. Epub 2008 Apr 18.
Doxorubicin-based treatment is standard therapy for metastatic uterine leiomyosarcoma. There is no standard second-line therapy. We determined activity of fixed-dose rate gemcitabine plus docetaxel as second-line treatment for metastatic uterine leiomyosarcoma.
Eligible women with unresectable uterine leiomyosarcoma progressing after prior cytotoxic therapy were treated with gemcitabine 900 mg/m(2) days one and eight over 90 min, plus docetaxel 100 mg/m(2) on day 8 of a 21-day cycle with granulocyte growth factor. Patients with prior pelvic radiation received lower doses. Response Evaluation Criteria in Solid Tumors (RECIST) response was assessed by computed tomography (CT).
Forty-eight of 51 women were evaluable for response (one wrong histology, two never treated). Prior therapy was doxorubicin-based in 90%, and ifosfamide-based in 6%. The overall objective response rate is 27%, with complete response in 6.3% (3/48), and partial response in 20.8% (10/48). An additional 50% (24/48) had stable disease (median duration 5.4 months). The median number of cycles per patient was 5.5 (range 1-22); 73% of patients remained progression-free at 12 weeks and 52% at 24 weeks. The predominant toxicity was uncomplicated myelosuppression: thrombocytopenia grade 3 (29%), grade 4 (10.4%); neutropenia grade 3 (12.5%), grade 4 (8.3%) anemia grade 3 (20.8%), grade 4 (4.2%). While pulmonary toxicity was reported, no patient had drug-related pneumonitis/hypoxia-type toxicity. Median progression-free survival (PFS) was 5.6+ months (range 0.7-27+ months). The median duration of objective response was 9+ months (range 3.9-24.5+ months).
Fixed-dose rate gemcitabine plus docetaxel is active second-line therapy for uterine leiomyosarcoma.
以阿霉素为基础的治疗是转移性子宫平滑肌肉瘤的标准疗法。目前尚无标准的二线治疗方案。我们确定了固定剂量率的吉西他滨联合多西他赛作为转移性子宫平滑肌肉瘤二线治疗的活性。
符合条件的女性患者,在先前的细胞毒性治疗后出现不可切除的子宫平滑肌肉瘤进展,在21天周期的第1天和第8天接受90分钟静脉滴注吉西他滨900mg/m²,同时在第8天接受多西他赛100mg/m²,并给予粒细胞生长因子。先前接受过盆腔放疗的患者剂量较低。通过计算机断层扫描(CT)评估实体瘤疗效评价标准(RECIST)反应。
51名女性中有48名可评估反应(1名组织学诊断错误,2名未接受治疗)。90%的患者先前接受过以阿霉素为基础的治疗,6%的患者接受过以异环磷酰胺为基础的治疗。总体客观缓解率为27%,完全缓解率为6.3%(3/48),部分缓解率为20.8%(10/48)。另外50%(24/48)的患者病情稳定(中位持续时间5.4个月)。每位患者的中位周期数为5.5(范围1 - 22);73%的患者在12周时无进展,52%的患者在24周时无进展。主要毒性为无并发症的骨髓抑制:3级血小板减少(29%),4级(10.4%);3级中性粒细胞减少(12.5%),4级(8.3%);3级贫血(20.8%),4级(4.2%)。虽然有肺部毒性的报告,但没有患者出现与药物相关的肺炎/缺氧型毒性。中位无进展生存期(PFS)为5.6 +个月(范围0.7 - 27 +个月)。客观缓解的中位持续时间为9 +个月(范围3.9 - 24.5 +个月)。
固定剂量率的吉西他滨联合多西他赛是子宫平滑肌肉瘤有效的二线治疗方案。