Brief Report: Long-Term Follow-Up of Adjuvant Pembrolizumab After Locally Ablative Therapy for Oligometastatic NSCLC

David J. Cantor MD, PhD , Christiana Davis MD , Christine Ciunci MD, MSCE , Charu Aggarwal MD, MPH , Tracey Evans MD , Roger B. Cohen MD , Joshua M. Bauml MD , Corey J. Langer MD
{"title":"Brief Report: Long-Term Follow-Up of Adjuvant Pembrolizumab After Locally Ablative Therapy for Oligometastatic NSCLC","authors":"David J. Cantor MD, PhD ,&nbsp;Christiana Davis MD ,&nbsp;Christine Ciunci MD, MSCE ,&nbsp;Charu Aggarwal MD, MPH ,&nbsp;Tracey Evans MD ,&nbsp;Roger B. Cohen MD ,&nbsp;Joshua M. Bauml MD ,&nbsp;Corey J. Langer MD","doi":"10.1016/j.jtocrr.2024.100667","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Patients with oligometastatic NSCLC benefit from locally ablative therapies (LAT); the role of adjuvant systemic therapies, however, remains less clear. In a single-arm, phase II clinical trial, we found that patients with oligometastatic NSCLC treated with a year of pembrolizumab after LAT had superior progression-free survival (PFS) compared with a historical control cohort. Herein, we present long-term follow-up on PFS and overall survival (OS).</p></div><div><h3>Methods</h3><p>From February 1, 2015, to September 30, 2017, 45 patients with synchronous or metachronous oligometastatic (≤4 metastatic sites) NSCLC treated with LAT to all sites received adjuvant pembrolizumab every 21 days for up to 16 cycles. The primary efficacy end point was PFS from the start of pembrolizumab. Secondary end points included OS and safety. Median duration of follow-up was 66 months, and data cutoff was December 1, 2022.</p></div><div><h3>Results</h3><p>A total of 45 patients were enrolled and treated with pembrolizumab after LAT (median age, 64 y [range, 46–82]; 21 women [47%]; 31 with a solitary oligometastatic site [69%]). At the data cutoff, 32 patients had progressive disease, 19 patients had died, and 13 patients had no evidence of relapse. Median PFS was 19.7 months (95% confidence interval: 7.6–31.7 mo); median OS was not reached (95% confidence interval: 37.7 mo–not reached). OS at 5 years was 60.0% (SE, 7.4%). Metachronous oligometastatic disease was associated with improved OS and PFS through Cox proportional hazard models.</p></div><div><h3>Conclusions</h3><p>Pembrolizumab after LAT for oligometastatic NSCLC results in promising PFS and OS with a tolerable safety profile.</p></div>","PeriodicalId":17675,"journal":{"name":"JTO Clinical and Research Reports","volume":"5 6","pages":"Article 100667"},"PeriodicalIF":3.0000,"publicationDate":"2024-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666364324000377/pdfft?md5=0687f20c1fa0d78bc4ac583db50c81dd&pid=1-s2.0-S2666364324000377-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JTO Clinical and Research Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666364324000377","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Patients with oligometastatic NSCLC benefit from locally ablative therapies (LAT); the role of adjuvant systemic therapies, however, remains less clear. In a single-arm, phase II clinical trial, we found that patients with oligometastatic NSCLC treated with a year of pembrolizumab after LAT had superior progression-free survival (PFS) compared with a historical control cohort. Herein, we present long-term follow-up on PFS and overall survival (OS).

Methods

From February 1, 2015, to September 30, 2017, 45 patients with synchronous or metachronous oligometastatic (≤4 metastatic sites) NSCLC treated with LAT to all sites received adjuvant pembrolizumab every 21 days for up to 16 cycles. The primary efficacy end point was PFS from the start of pembrolizumab. Secondary end points included OS and safety. Median duration of follow-up was 66 months, and data cutoff was December 1, 2022.

Results

A total of 45 patients were enrolled and treated with pembrolizumab after LAT (median age, 64 y [range, 46–82]; 21 women [47%]; 31 with a solitary oligometastatic site [69%]). At the data cutoff, 32 patients had progressive disease, 19 patients had died, and 13 patients had no evidence of relapse. Median PFS was 19.7 months (95% confidence interval: 7.6–31.7 mo); median OS was not reached (95% confidence interval: 37.7 mo–not reached). OS at 5 years was 60.0% (SE, 7.4%). Metachronous oligometastatic disease was associated with improved OS and PFS through Cox proportional hazard models.

Conclusions

Pembrolizumab after LAT for oligometastatic NSCLC results in promising PFS and OS with a tolerable safety profile.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
简要报告:寡转移性 NSCLC 局部消融治疗后 Pembrolizumab 辅助治疗的长期随访
导言少转移性 NSCLC 患者可从局部消融治疗(LAT)中获益;然而,辅助性全身治疗的作用仍不十分明确。在一项单臂 II 期临床试验中,我们发现寡转移性 NSCLC 患者在局部消融治疗后接受一年的 pembrolizumab 治疗,其无进展生存期(PFS)优于历史对照组。方法从2015年2月1日至2017年9月30日,45名接受LAT治疗至所有部位的同步或近同步寡转移(≤4个转移部位)NSCLC患者接受了每21天一次的pembrolizumab辅助治疗,最多16个周期。主要疗效终点是开始使用 pembrolizumab 后的 PFS。次要终点包括OS和安全性。中位随访时间为66个月,数据截止日期为2022年12月1日。结果共有45名患者入组,并在LAT后接受了pembrolizumab治疗(中位年龄为64岁[46-82岁];21名女性[47%];31名患者为单发少转移部位[69%])。数据截止时,32 名患者病情进展,19 名患者死亡,13 名患者无复发迹象。中位 PFS 为 19.7 个月(95% 置信区间:7.6-31.7 个月);未达到中位 OS(95% 置信区间:37.7 个月-未达到)。5年的OS为60.0%(SE,7.4%)。通过 Cox 比例危险模型,近端寡转移性疾病与 OS 和 PFS 的改善相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
4.20
自引率
0.00%
发文量
145
审稿时长
19 weeks
期刊最新文献
First Report of Response to Tarlatamab in a Patient With DLL3-Positive Pulmonary Carcinoid: Case Report A Response to the Letter to the Editor: “Heart and Lung Dose as Predictors of Overall Survival in Patients With Locally Advanced Lung Cancer: A National Multicenter Study” Racial Differences in Systemic Immune Parameters in Individuals With Lung Cancer Brief Report of a New Anatomical Region at Risk in Thoracic Radiotherapy: From Discovery to Implementation Entrectinib-Induced Myocarditis and Acute Heart Failure Responding to Steroid Treatment: A Case Report
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1