Philp L, Kanbergs A, Laurent J St, Growdon W B, Feltmate C, Goodman A
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Massachusetts General Hospital, Boston, MA, United States.
Department of Obstetrics and Gynecology, Massachusetts General Hospital and Brigham and Women's Hospital, Boston, MA, United States.
Gynecol Oncol Rep. 2021 Feb 8;36:100725. doi: 10.1016/j.gore.2021.100725. eCollection 2021 May.
The objective of this retrospective cohort study was to review the use of neoadjuvant chemotherapy followed by interval cytoreductive surgery in patients presenting with advanced, unresectable endometrial cancer at two large cancer centers. Patients with advanced endometrial cancer treated with neoadjuvant chemotherapy between 2008 and 2015 were identified from an institutional database. Clinical and surgical variables were analyzed and time to recurrence and death was calculated and compared between surgical groups. Thirty-three patients were identified (mean age 64.8 (range 42-86 years)). Overall, 28% of patients had endometrioid histology, 48% serous, 4% clear cell, 4% carcinosarcoma, 12% mixed and 4% other. Ineligibility for primary surgery was due to unresectable disease (85%), comorbidities (6%) and unknown reasons (9%). All patients received neoadjuvant chemotherapy with 91% of patients receiving carboplatin and paclitaxel. On reimaging, 12% of patients had progressed, 76% had a partial response and 3% had a complete response to chemotherapy. 76% of patients underwent interval surgery, with cytoreduction to no visible residual disease achieved in 52%. Overall, 91% of patients recurred and 85% died during follow-up. Patients undergoing surgery after chemotherapy had significantly longer progression-free survival (11.53 vs. 4.99 months, p = 0.0096) and overall survival (24.13 vs. 7.04 months, p = 0.0042) when compared to patients who did not have surgery. Neoadjuvant chemotherapy is a feasible treatment option to allow for interval cytoreductive surgery in patients with advanced endometrial cancer not amenable to primary debulking. Patients who undergo surgery after chemotherapy have significantly improved progression free and overall survival.
这项回顾性队列研究的目的是,在两家大型癌症中心,对晚期、无法切除的子宫内膜癌患者使用新辅助化疗后再进行间隔减瘤手术的情况进行回顾。从机构数据库中识别出2008年至2015年间接受新辅助化疗的晚期子宫内膜癌患者。分析临床和手术变量,计算手术组之间的复发时间和死亡时间并进行比较。共识别出33例患者(平均年龄64.8岁(范围42 - 86岁))。总体而言,28%的患者为子宫内膜样组织学类型,48%为浆液性,4%为透明细胞,4%为癌肉瘤,12%为混合型,4%为其他类型。无法进行初次手术的原因包括疾病无法切除(85%)、合并症(6%)和不明原因(9%)。所有患者均接受了新辅助化疗,91%的患者接受了卡铂和紫杉醇治疗。复查影像学检查时,12%的患者病情进展,76%的患者部分缓解,3%的患者完全缓解。76%的患者接受了间隔手术,其中52%的患者实现了减瘤至无可见残留病灶。总体而言,91%的患者在随访期间复发,85%的患者死亡。与未接受手术的患者相比,化疗后接受手术的患者无进展生存期显著延长(11.53个月对4.99个月,p = 0.0096),总生存期也显著延长(24.13个月对7.04个月,p = 0.0042)。新辅助化疗是一种可行的治疗选择,可使无法进行初次减瘤的晚期子宫内膜癌患者接受间隔减瘤手术。化疗后接受手术的患者无进展生存期和总生存期均有显著改善。