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细胞减灭术和腹腔热灌注化疗作为晚期上皮性卵巢癌的初始治疗:多机构 II 期试验。

Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy as upfront therapy for advanced epithelial ovarian cancer: multi-institutional phase-II trial.

机构信息

Peritoneal Surface Malignancy Program, Department of Surgery, National Cancer Institute, via Venezian 1, 20133 Milan, Italy.

出版信息

Gynecol Oncol. 2011 Aug;122(2):215-20. doi: 10.1016/j.ygyno.2011.05.004. Epub 2011 Jun 12.

Abstract

OBJECTIVE

The primary end-point of this multi-institutional phase-II trial was to assess results in terms of overall survival after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) in treatment-naive epithelial ovarian cancer (EOC) with advanced peritoneal involvement. Secondary end-points were treatment morbi-mortality and outcome effects of time to subsequent adjuvant systemic chemotherapy (TTC).

METHODS

Twenty-six women with stage III-IV EOC were prospectively enrolled in 4 Italian centers to undergo CRS and closed-abdomen HIPEC with cisplatin and doxorubicin. Then they received systemic chemotherapy with carboplatin (AUC 6) and paclitaxel (175 mg/m(2)) for 6 cycles.

RESULTS

Macroscopically complete cytoreduction was achieved in 15 patients; only minimal residual disease (≤2.5 mm) remained in 11. Major complications occurred in four patients and postoperative death in one. After a median follow-up of 25 months, 5-year overall survival was 60.7% and 5-year progression-free survival 15.2% (median 30 months). Excluding operative death, all the patients underwent systemic chemotherapy at a median of 46 days from combined treatment (range: 29-75). The median number of cycles per patient was 6 (range: 1-8). The time to chemotherapy did not affect the OS or PFS.

CONCLUSIONS

In selected patients with advanced stage EOC, upfront CRS and HIPEC provided promising results in terms of outcome. Morbidity was comparable to aggressive cytoreduction without HIPEC. Postoperative recovery delayed the initiation of adjuvant systemic chemotherapy but not sufficiently to impact negatively on survival. These data warrant further evaluation in a randomized clinical trial.

摘要

目的

本多中心二期临床试验的主要终点是评估新辅助细胞减灭术(CRS)和腹腔内热灌注化疗(HIPEC)联合治疗伴有广泛腹膜侵犯的上皮性卵巢癌(EOC)患者的总生存(OS)。次要终点是治疗相关死亡率和后续辅助全身化疗(TTC)时间的结果影响。

方法

26 名 III 期-IV 期 EOC 患者前瞻性纳入 4 个意大利中心,行 CRS 和闭合腹腔 HIPEC 治疗,药物为顺铂和多柔比星。然后,患者接受卡铂(AUC 6)和紫杉醇(175mg/m2)全身化疗 6 个周期。

结果

15 例患者达到宏观完全缓解;11 例患者仅有微小残留病灶(≤2.5mm)。4 例患者发生主要并发症,1 例术后死亡。中位随访 25 个月后,5 年 OS 为 60.7%,5 年无进展生存率为 15.2%(中位 30 个月)。排除手术死亡后,所有患者在联合治疗后中位 46 天(范围 29-75)接受全身化疗。中位每位患者化疗周期数为 6 个(范围 1-8)。化疗时间不影响 OS 或 PFS。

结论

在选择的晚期 EOC 患者中,新辅助 CRS 和 HIPEC 联合治疗在预后方面提供了有前景的结果。与无 HIPEC 的积极细胞减灭术相比,其发病率相当。术后恢复延迟了辅助全身化疗的启动,但不足以对生存产生负面影响。这些数据需要在随机临床试验中进一步评估。

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