Berthet Julie, Kime Amel, Borghese Bruno, De Percin Sixtine, Gaudet-Chardonnet Antoine, Alexandre Jerome, Beinse Guillaume
Department of Medical Oncology, Hopital Cochin, Sorbonne Université, Institut du Cancer Paris CARPEM, AP-HP, Paris, France.
Department of Pathology, Hopital Cochin, Institut du Cancer Paris CARPEM, AP-HP, Paris, France.
J Gynecol Oncol. 2025 Jul;36(4):e64. doi: 10.3802/jgo.2025.36.e64. Epub 2025 Mar 23.
Uterine and ovarian carcinosarcomas (OCSs) are rare and aggressive neoplasms. We assessed whether progression free survival after initial treatment (PFS1) was associated with the clinical benefit of chemotherapy after progression, estimated as overall survival (OS) after progression/relapse.
All consecutive patients treated with chemotherapy for stage I-IV uterine/OCS in Cochin University Hospital between 2010 and 2022 were included in this retrospective cohort. Association between PFS1 and OS after progressive disease (PD) was determined by Cox regression. Optimal PFS1 threshold for OS after PD prediction was determined by a time-dependent receiver operating characteristic-curve analysis.
Forty patients treated for endometrial (n=32) or OCS (n=8) were included. Median PFS1 and OS after PD were 16 months 95% confidence interval (95% CI=11-not available [NA]) and 6 months (95% CI=2-15). In patients who relapsed/progressed (n=20), OS after PD was anticipated by PFS1 (Pearson r=0.61; area under the curve=0.79; 95% CI=0.6-1). At the threshold of PFS1 ≤/>9 months (n=6/n=7), median OS post PD were 2 months (0.1-NA) and 15 months (6-NA), for patients treated with platinum/anthracycline based chemotherapy in second line. Patients receiving best supportive care alone (n=7) had a median OS post PD of 8 months (1.3-NA).
Our results highlight that a subgroup of carcinosarcomas patients exhibits a durable benefit from chemotherapy in the relapse settings, and suggest the use of PFS1, as a proxy of platinum-sensitivity, to select patients who might derive higher clinical benefit of a 2nd line of chemotherapy.
子宫和卵巢癌肉瘤(OCS)是罕见的侵袭性肿瘤。我们评估了初始治疗后的无进展生存期(PFS1)是否与进展后化疗的临床获益相关,进展后化疗的临床获益以进展/复发后的总生存期(OS)来估计。
纳入2010年至2022年在科钦大学医院接受化疗的所有连续的I-IV期子宫/OCS患者,组成该回顾性队列。通过Cox回归确定PFS1与疾病进展(PD)后的OS之间的关联。通过时间依赖性受试者工作特征曲线分析确定预测PD后OS的最佳PFS1阈值。
纳入了40例接受子宫内膜癌(n=32)或OCS(n=8)治疗的患者。PD后的中位PFS1和OS分别为16个月(95%置信区间[95%CI]=11-不可用[NA])和6个月(95%CI=2-15)。在复发/进展的患者(n=20)中,PD后的OS可由PFS1预测(Pearson相关系数r=0.61;曲线下面积=0.79;95%CI=0.6-1)。在PFS1≤/>9个月的阈值时(n=6/n=7),二线接受铂类/蒽环类化疗的患者PD后的中位OS分别为2个月(0.1-NA)和15个月(6-NA)。仅接受最佳支持治疗的患者(n=7)PD后的中位OS为8个月(1.3-NA)。
我们的结果表明,一部分癌肉瘤患者在复发情况下从化疗中表现出持久的获益,并建议使用PFS1作为铂敏感性的替代指标,以选择可能从二线化疗中获得更高临床获益的患者。