2022-RA-1415-ESGO Perspective on the future of the sentinel lymph node in cervical cancer

A. Manu, Diana-Elena Soare, Alexandra Irma Gabriela Bausic, C. Coroleucă, E. Brătilă
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Abstract

with recurrent/metastatic cervical cancer (r/mCC). Previous reports show potentially enhanced efficacy and tolerable safety with TV + pembrolizumab, carboplatin, or bevacizumab. We report interim safety and efficacy results from the dose-expansion cohorts evaluating 1L TV + pembrolizumab (1L-TP), 2/ 3L TV + pembrolizumab (2/3L-TP), and 1L TV + carboplatin (1L-TC) in patients with r/mCC. Methodology In the 1L-TP cohort, patients with r/mCC who had no prior systemic therapy (excluding chemoradiation) received TV 2.0 mg/kg + pembrolizumab 200 mg IV Q3W. In the 2/3L-TP cohort, patients with r/mCC who experienced disease progression on/after 1–2 prior systemic therapies received TV 2.0 mg/kg + pembrolizumab 200 mg IV Q3W. In the 1L-TC cohort, patients with r/mCC who had no prior systemic therapy (excluding chemoradiation) received TV 2.0 mg/kg + carboplatin AUC 5 IV Q3W. The primary end point was confirmed objective response rate (cORR) per RECIST v1.1. Results In the 1L-TP, 2/3L-TP, and 1L-TC cohorts, respectively, 33, 35, and 33 patients received treatment, and, at data cutoff, median follow-up was 18.8, 15.0, and 14.6 months. cORR was 41%, 38%, and 55%, with a median DOR of not reached, 14.0, and 8.6 months in the 1L-TP, 2/3L-TP, and 1LTC cohorts, respectively. Adverse events (AEs) of special interest in patients in the 1L-TP, 2/3L-TP, and 1L-TC cohorts (grade 1–2/grade 3) included ocular events (58/9; 51/3; 58/ 9), bleeding (61/6; 61/9; 52/6), and peripheral neuropathy (49/3; 37/3; 48/12), respectively; one patient in 2/3L-TP and one patient in 1L-TP experienced grade 4 and 5 treatmentrelated bleeding, respectively. Additional data will be presented at the meeting. Conclusion TV + pembrolizumab or carboplatin in patients with r/mCC demonstrated encouraging and durable antitumour activity, with tolerable safety profiles. © 2022 American Society of Clinical Oncology, Inc. Reused with permission. This abstract was accepted and previously presented at the 2022 ASCO Annual Meeting. All rights reserved.
展望宫颈癌前哨淋巴结的未来
复发/转移性宫颈癌(r/mCC)。先前的报告显示TV +派姆单抗、卡铂或贝伐单抗可能增强疗效和耐受安全性。我们报告了来自剂量扩展队列的中期安全性和有效性结果,评估了r/mCC患者1L TV +派姆单抗(1L- tp), 2/3L TV +派姆单抗(2/3L- tp)和1L TV +卡铂(1L- tc)。在1L-TP队列中,既往未接受过全身治疗(不包括放化疗)的r/mCC患者接受TV 2.0 mg/kg + pembrolizumab 200mg IV Q3W。在2/3L-TP队列中,既往1-2次全身治疗后出现疾病进展的r/mCC患者接受TV 2.0 mg/kg +派姆单抗200mg IV Q3W。在1L-TC队列中,既往未接受过全身治疗(不包括放化疗)的r/mCC患者接受TV 2.0 mg/kg +卡铂AUC 5 IV Q3W。主要终点是根据RECIST v1.1确定的客观缓解率(cORR)。结果在1L-TP、2/3L-TP和1L-TC组中,分别有33例、35例和33例患者接受了治疗,在数据截止时,中位随访时间分别为18.8、15.0和14.6个月。在1L-TP、2/3L-TP和1LTC组中,cORR分别为41%、38%和55%,未达到DOR的中位数分别为14.0和8.6个月。在1L-TP、2/3L-TP和1L-TC组(1-2级/3级)患者中,特别关注的不良事件(ae)包括眼部事件(58/9;51/3;58/ 9),出血(61/6);61/9;52/6),周围神经病变(49/3;37/3;分别为48/12);2/3L-TP组1例患者和1L-TP组1例患者分别出现4级和5级治疗相关出血。更多的数据将在会议上提出。结论TV +派姆单抗或卡铂在r/mCC患者中表现出令人鼓舞和持久的抗肿瘤活性,具有可耐受的安全性。©2022美国临床肿瘤学会,Inc。在获得许可的情况下重用。该摘要已被接受并在2022年ASCO年会上提交。版权所有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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