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铂敏感复发性卵巢癌中手术与非手术治疗的比较:SOC-1 随机 3 期试验的最终总生存分析。

Surgery versus no surgery in platinum-sensitive relapsed ovarian cancer: final overall survival analysis of the SOC-1 randomized phase 3 trial.

机构信息

Institute for Ovarian Cancer, Fudan University & Department of Gynecologic Oncology, Cancer Center, Fudan University Zhongshan Hospital, Shanghai, China.

Department of Gynecologic Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Centre for Cancer Medicine, Sun Yat-sen University Cancer Centre, Guangzhou, China.

出版信息

Nat Med. 2024 Aug;30(8):2181-2188. doi: 10.1038/s41591-024-02981-0. Epub 2024 Jun 1.

Abstract

Surgery for platinum-sensitive, relapsed ovarian cancer (PSROC) is widely practiced but had contradictory survival outcomes in previous studies. In this multicenter, open-label, phase 3 trial, women with PSROC, and having had one previous therapy and no platinum-based chemotherapy (platinum-free interval) of 6 months or more, were randomly assigned to either the surgery group (182 patients) or the no-surgery group (control) (175 patients). Patients with resectable diseases were eligible according to the international model (iMODEL), combined with a positron emission tomography-computed tomography imaging. Overall survival (OS) and progression-free survival were coprimary endpoints in hierarchical testing, and a significantly longer progression-free survival with surgery was previously reported. Final analysis of OS was planned at data maturity of 59%. Between 19 July 2012 and 3 June 2019, 357 patients were enrolled. Median follow-up was 82.5 months. Median OS was 58.1 months with surgery and 52.1 months for control (hazard ratio (HR) 0.80, 95% confidence interval (CI) 0.61-1.05, P = 0.11). The predefined threshold for statistical significance was not met, but prespecified sensitivity analysis was performed. Overall, 61 of 175 (35%) patients in control had crossed over to surgery following subsequent relapse, and adjusted HR for death in the surgery group compared with control was 0.76, 95% CI 0.58-0.99. In subgroup analysis of relapse sites by imaging, median survival was not estimable in the surgery group and was 69.5 months in control in patients with <20 sites (HR 0.69, 95% CI 0.46-1.03). Patients with a complete resection had the most favorable outcome, with a median OS of 73.0 months. Twenty-four of 182 (13.2%) patients remained relapse free and alive >60 months in the surgery group as compared with five of 175 (2.9%) patients in the control group. In patients with PSROC, surgery did not increase OS in the intention-to-treat population but resulted in a prolongation of survival following adjustment of crossover.ClinicalTrials.gov registration: NCT01611766 .

摘要

铂敏感复发性卵巢癌(PSROC)的手术广泛应用,但在之前的研究中生存结果存在矛盾。在这项多中心、开放标签、3 期试验中,铂类无化疗间期(platinum-free interval)≥6 个月且有铂类敏感复发卵巢癌病史和一次既往治疗的女性患者被随机分配到手术组(182 例患者)或非手术组(对照组)(175 例患者)。根据国际模型(iMODEL)并结合正电子发射断层扫描计算机断层扫描(PET-CT)成像,有可切除疾病的患者符合入组标准。分层检验的主要终点为总生存(OS)和无进展生存(PFS),之前报道手术可显著延长 PFS。OS 的最终分析计划在数据成熟度为 59%时进行。2012 年 7 月 19 日至 2019 年 6 月 3 日,共纳入 357 例患者。中位随访时间为 82.5 个月。手术组中位 OS 为 58.1 个月,对照组为 52.1 个月(风险比(HR)0.80,95%置信区间(CI)0.61-1.05,P=0.11)。未达到统计学意义的预设阈值,但进行了预设的敏感性分析。总体而言,对照组中有 61 例(35%)患者在后续复发后交叉至手术组,手术组与对照组相比,死亡的调整 HR 为 0.76,95%CI 为 0.58-0.99。在根据影像学进行的复发部位亚组分析中,手术组中位生存期无法评估,对照组中有<20 个部位的患者中位生存期为 69.5 个月(HR 0.69,95%CI 0.46-1.03)。完全切除的患者预后最佳,中位 OS 为 73.0 个月。手术组有 24 例(13.2%)患者无复发且>60 个月存活,对照组有 5 例(2.9%)患者符合这一标准。对于铂敏感复发性卵巢癌患者,手术并未增加意向治疗人群的 OS,但在交叉调整后可延长生存。临床试验注册:NCT01611766。

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