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帕博利珠单抗与盆腔放化疗联合治疗局部晚期宫颈癌的一项研究的早期安全性分析结果

Results of an early safety analysis of a study of the combination of pembrolizumab and pelvic chemoradiation in locally advanced cervical cancer.

作者信息

Duska Linda R, Scalici Jennifer M, Temkin Sarah M, Schwarz Julie K, Crane Erin K, Moxley Katherine M, Hamilton Chad A, Wethington Stephanie L, Petroni Gina R, Varhegyi Nikole E, Clift Sheena H, Bullock Timothy N J, Showalter Timothy N

机构信息

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Virginia School of Medicine, Charlottesville, Virginia.

Mitchell Cancer Institute, USA Health, Mobile, Alabama.

出版信息

Cancer. 2020 Nov 15;126(22):4948-4956. doi: 10.1002/cncr.33136. Epub 2020 Sep 10.

Abstract

BACKGROUND

Immune checkpoint inhibitors are being considered for locally advanced cervical cancer (LACC) together with standard-of-care pelvic chemoradiation (CRT). However, the safety of the combination and its optimal schedule are unknown. Defining the safety of the combination is a primary objective of a study examining concurrent and sequential schedules. This article presents a safety analysis that was fully accrued and met reporting requirements.

METHODS

Pembrolizumab was given after CRT (arm 1) or during CRT (arm 2) according to a randomized phase 2 design. Patients who were 18 years old or older and had LACC (stages IB-IVA according to the 2009 International Federation of Gynecology and Obstetrics system) were randomized 1:1 to the treatment regimens. The CRT was identical in the 2 arms. Pembrolizumab was administered every 3 weeks for 3 doses; no maintenance was allowed. All patients receiving any treatment were evaluated for safety. Safety assessments included the incidence and severity of adverse events (AEs) and the occurrence of protocol-defined dose-limiting toxicity (DLT) through 30 days after the last pembrolizumab infusion.

RESULTS

As of August 2019, 52 of the 88 planned patients had completed treatment and were evaluable for toxicity. Treatment-related grade 2 or higher toxicity was experienced by 88%; 11 had at least 1 grade 4 AE, and another 23 had at least 1 grade 3 AE. Grade 1 or higher diarrhea was reported in 34 patients (65%; 50% of these were grade 1), and there was no difference between arms (63% in arm 1 vs 68% in arm 2). Two patients experienced 3 DLTs. Most patients completed cisplatin (100% in arm 1 vs 82% in arm 2); 83% in both arms completed all pembrolizumab.

CONCLUSIONS

Preliminary results support the safety and feasibility of adding pembrolizumab to pelvic CRT concurrently or sequentially.

LAY SUMMARY

Pembrolizumab is a humanized antibody against programmed cell death protein 1 that is used in cancer immunotherapy. Preliminary data suggest that pembrolizumab can be safely combined with chemotherapy and pelvic radiation in the treatment of locally advanced cervical cancer. Future studies of the addition of immunotherapy to traditional chemoradiation are planned to determine the best way to deliver the treatment and whether any improvement is seen with the addition of immunotherapy to traditional therapy.

摘要

背景

免疫检查点抑制剂正与标准治疗方案盆腔放化疗(CRT)一起被考虑用于局部晚期宫颈癌(LACC)。然而,联合治疗的安全性及其最佳方案尚不清楚。确定联合治疗的安全性是一项研究同步和序贯方案的主要目标。本文介绍了一项已完全入组并符合报告要求的安全性分析。

方法

根据随机2期设计,帕博利珠单抗在CRT后(1组)或CRT期间(2组)给药。年龄在18岁及以上且患有LACC(根据2009年国际妇产科联盟系统为IB-IVA期)的患者按1:1随机分配至各治疗方案。两组的CRT相同。帕博利珠单抗每3周给药1次,共3剂;不允许维持治疗。对所有接受任何治疗的患者进行安全性评估。安全性评估包括不良事件(AE)的发生率和严重程度,以及至最后一次帕博利珠单抗输注后30天内方案定义的剂量限制性毒性(DLT)的发生情况。

结果

截至2019年8月,88例计划患者中有52例完成治疗并可进行毒性评估。88%的患者经历了与治疗相关的2级或更高毒性;11例至少有1次4级AE,另有23例至少有1次3级AE。34例患者(65%)报告了1级或更高的腹泻(其中50%为1级),两组之间无差异(1组为63%,2组为68%)。2例患者经历了3次DLT。大多数患者完成了顺铂治疗(1组为100%,2组为82%);两组均有83%的患者完成了所有帕博利珠单抗治疗。

结论

初步结果支持同步或序贯将帕博利珠单抗添加到盆腔CRT中的安全性和可行性。

简述

帕博利珠单抗是一种用于癌症免疫治疗的抗程序性细胞死亡蛋白1的人源化抗体。初步数据表明,帕博利珠单抗可安全地与化疗和盆腔放疗联合用于治疗局部晚期宫颈癌。计划对在传统放化疗中添加免疫治疗进行进一步研究,以确定最佳治疗方式,以及在传统治疗中添加免疫治疗是否能带来任何改善。

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