Division of Gynecologic Oncology, Obstetrics, Gynecology, Women's Health Institute, Cleveland Clinic, Desk A81, 9500 Euclid Avenue, Cleveland, OH 44195, United States.
Department of Qualitative Health Sciences, Cleveland Clinic, Cleveland, OH 44195, United States.
Gynecol Oncol. 2021 May;161(2):389-395. doi: 10.1016/j.ygyno.2021.01.039. Epub 2021 Feb 5.
OBJECTIVE(S): To identify recurrence patterns and outcomes in women with advanced or recurrent epithelial ovarian cancer (EOC) after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC).
This is an IRB-approved single-institution cohort study of women who underwent CRS+HIPEC for advanced or recurrent EOC followed in a prospective registry from 1/12/2014-3/1/2020. Recurrence locations were defined as pelvic, upper abdominal (UA) and/or extra-peritoneal (EP). Univariate analysis assessed associations between recurrence location, progression-free survival (PFS), and overall survival (OS).
In total, 92 women with EOC underwent interval (56.5%; n=52) or recurrent CRS+HIPEC (43.5%; n=40). For interval CRS+HIPEC, recurrence locations were pelvic in 50.0% (n=15), UA in 23.3% (n=7) and EP in 56.7% (n=17); 40.0% (n=12) were EP alone. Similarly, for recurrent CRS+HIPEC, recurrence locations were pelvic (22.5%, n=9), UA (5.0%, n=2) and EP (60.0%, n=24); 66.7% (n=20) were EP alone. For both interval and recurrent CRS+HIPEC, median PFS was 10.5 vs. 13.0 months for pelvic and UA vs. EP only recurrences (p=0.02). Similarly, median OS was 29.2 months for pelvic and UA and not reached for EP only (p=0.05). For interval CRS+HIPEC, there was no difference in median PFS (10.6 vs. 11.7 months, p=0.68) and OS (27.1 vs. 24.8 months, p=0.96) for pelvic and UA vs EP alone. However, for recurrent CRS+HIPEC, pelvic and UA sites of recurrence were associated with reduced PFS (10.0 vs. 18.1 months, p=0.03) and OS (33.6 months vs. not reached, p=0.02) vs. EP only.
In women with advanced or recurrent EOC undergoing CRS+HIPEC, one-half of patients experience their first recurrence outside of the peritoneal cavity. Providers must be aware of the risk of EP failure in patients treated with CRS+HIPEC.
确定接受细胞减灭术(CRS)和腹腔内热化疗(HIPEC)治疗的晚期或复发性上皮性卵巢癌(EOC)女性的复发模式和结局。
这是一项经过机构审查委员会批准的单机构队列研究,纳入了 2014 年 1 月 12 日至 2020 年 3 月 1 日期间在前瞻性登记处接受 CRS+HIPEC 治疗的晚期或复发性 EOC 女性。复发部位定义为盆腔、上腹部(UA)和/或腹膜外(EP)。单因素分析评估了复发部位、无进展生存期(PFS)和总生存期(OS)之间的关联。
共有 92 名 EOC 女性接受了间隔期(56.5%;n=52)或复发性 CRS+HIPEC(43.5%;n=40)。对于间隔期 CRS+HIPEC,盆腔复发占 50.0%(n=15),UA 占 23.3%(n=7),EP 占 56.7%(n=17);40.0%(n=12)为 EP 单独复发。同样,对于复发性 CRS+HIPEC,盆腔(22.5%,n=9)、UA(5.0%,n=2)和 EP(60.0%,n=24)为复发部位;66.7%(n=20)为 EP 单独复发。对于间隔期和复发性 CRS+HIPEC,盆腔和 UA 仅复发的患者的中位 PFS 分别为 10.5 个月和 13.0 个月(p=0.02)。同样,盆腔和 UA 仅复发患者的中位 OS 为 29.2 个月,而 EP 仅复发患者未达到(p=0.05)。对于间隔期 CRS+HIPEC,盆腔和 UA 与 EP 单独复发的中位 PFS(10.6 比 11.7 个月,p=0.68)和 OS(27.1 比 24.8 个月,p=0.96)无差异。然而,对于复发性 CRS+HIPEC,盆腔和 UA 部位的复发与 PFS(10.0 比 18.1 个月,p=0.03)和 OS(33.6 个月比未达到,p=0.02)缩短相关,而仅 EP 复发。
在接受 CRS+HIPEC 治疗的晚期或复发性 EOC 女性中,有一半患者首次复发发生在腹膜腔外。治疗医生必须意识到接受 CRS+HIPEC 治疗的患者 EP 失败的风险。