Immunotherapy Rechallenge Is Effective for Most Patients With Late Progression After Initial Ipilimumab + Nivolumab Response

易普利姆玛 无容量 医学 肿瘤科 免疫疗法 内科学 黑色素瘤 联合疗法 转移性黑色素瘤 癌症 癌症研究
作者
Ethan Trim,Anita Giobbie‐Hurder,Tamara A. Sussman,David Liu,Megan L. Insco,Rizwan Haq,F. Stephen Hodi,Patrick A. Ott,Elizabeth I. Buchbinder
出处
期刊:Pigment Cell & Melanoma Research [Wiley]
卷期号:38 (4): e70023-e70023
标识
DOI:10.1111/pcmr.70023
摘要

Clinical benefit achieved with ipilimumab + nivolumab combination therapy is typically long lasting. However, late progression, after therapy completion, does occur in a subset of patients. At the time of late progression, immunotherapy options include anti-PD-1 monotherapy, anti-PD-1/LAG-3, repeat anti-PD-1/CTLA-4 therapy, or TIL therapy, but the efficacy of these approaches is unknown. To investigate, we evaluated 230 patients with advanced melanoma who received treatment with ipilimumab + nivolumab at Dana-Farber Cancer Institute between 2015 and 2022 as first-line treatment. Of these, 111 had an initial response of stable disease (SD) or better for 6 months or longer. Of the 111 deriving clinical benefit, 19 had late progression, 14 while off therapy. Ten of the 14 patients who had late progression off therapy were rechallenged with immune checkpoint inhibition (ICB), either as monotherapy or in combination. Eight out of those 10 patients had clinical benefit of SD or better upon ICB rechallenge. The two who did not benefit from rechallenge had mucosal melanoma (3 patients had mucosal, 7 had cutaneous). The data indicate that clinical benefit upon rechallenge with ICB can be achieved in the majority of patients, specifically those with the cutaneous subtype, although responses are mostly SD and are relatively short lived.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
潇洒的惋清应助kiluto采纳,获得10
1秒前
背后尔云发布了新的文献求助10
1秒前
熠云完成签到,获得积分10
2秒前
su完成签到,获得积分10
3秒前
DoctorSUN完成签到,获得积分10
4秒前
小镇做题家完成签到,获得积分20
4秒前
WENc完成签到,获得积分10
4秒前
芬芬发布了新的文献求助30
4秒前
LL完成签到,获得积分10
5秒前
5秒前
科研通AI6.4应助王老吉采纳,获得50
5秒前
槿裡完成签到 ,获得积分10
5秒前
liuy@完成签到,获得积分10
6秒前
Criminology34应助哇呜采纳,获得10
6秒前
7秒前
wxsmy完成签到,获得积分10
8秒前
8秒前
8秒前
美满的机器猫完成签到,获得积分10
8秒前
隐形曼青应助tinale_huang采纳,获得30
8秒前
百浪多息完成签到,获得积分10
8秒前
米线儿完成签到,获得积分10
9秒前
吴桂学完成签到 ,获得积分10
10秒前
10秒前
11秒前
gcyyyds发布了新的文献求助10
11秒前
百浪多息发布了新的文献求助10
11秒前
12秒前
科研通AI6.4应助刘浪采纳,获得10
12秒前
bkagyin应助liuy@采纳,获得10
12秒前
zrz完成签到,获得积分10
13秒前
SmallTang_123完成签到,获得积分10
13秒前
李铁梅发布了新的文献求助10
14秒前
梨凉发布了新的文献求助10
14秒前
15秒前
15秒前
ddk643完成签到 ,获得积分10
18秒前
研友_VZG7GZ应助福娃哇采纳,获得10
18秒前
19秒前
19秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
A Psychological Understanding of Criticism and Mental Health 600
Organizational Behavior 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7750531
求助须知:如何正确求助?哪些是违规求助? 9298071
关于积分的说明 20244372
捐赠科研通 7332430
什么是DOI,文献DOI怎么找? 3309630
关于科研通互助平台的介绍 2461212
邀请新用户注册赠送积分活动 2322107