晚期肉瘤中与免疫检查点抑制剂应答相关的组织学和免疫因素

IF 10 1区 医学 Q1 ONCOLOGY Clinical Cancer Research Pub Date : 2025-02-17 DOI:10.1158/1078-0432.CCR-24-3485
Alex Q Lee, Clara Hao, Minggui Pan, Kristen N Ganjoo, Nam Q Bui
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引用次数: 0

摘要

目的:研究晚期肉瘤患者对免疫检查点抑制剂(ICIs)应答的相关因素。实验设计:这是一项回顾性研究,纳入了2016-2023年间斯坦福医疗中心接受ICIs治疗的216例晚期肉瘤患者。通过组织学亚型、ICI方案、肿瘤突变负担(TMB)和PD-L1表达分析了总生存期(OS)、无进展生存期(PFS)、RECIST标准的客观缓解率(ORR)和ICI停止的原因。结果:该队列的总ORR为16.7%。ORR最高的组织学亚型为卡波西肉瘤(KS, 66.7%)、肺泡软组织肉瘤(aps, 50%)、血管肉瘤(AS, 33.3%)、黏液纤维肉瘤(MFS, 28.6%)和未分化多形性肉瘤(UPS, 27.8%)。ORR最低的亚型是骨肉瘤(0%)、滑膜肉瘤(0%)和脂肪肉瘤(3.7%)。中位PFS最高的亚型是KS(中位未达到,NR)、ASPS (NR)、MFS(27.4个月)和UPS(11.3个月)。PD-L1≥1%的肉瘤的ORR为27.8% (p=0.02),而TMB≥10突变/MB (mut/MB)的肉瘤的ORR为28.6% (p=0.20)。结论:不同肉瘤组织学亚型的ORR和PFS差异很大。在这项大型分析中,KS、asp、AS、MFS和UPS的ORR最高,PFS最长,而骨肉瘤、SS和LPS的ORR最低,PFS最短。PD-L1表达也与ORR升高有关。我们的研究结果为进一步了解与ICIs反应相对应的肉瘤组织学和免疫因素提供了进一步的见解。
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Histologic and Immunologic Factors Associated with Response to Immune Checkpoint Inhibitors in Advanced Sarcoma.

Purpose: To characterize factors associated with response to immune checkpoint inhibitors (ICI) in advanced sarcoma.

Experimental design: This is a retrospective study with a cohort of 216 patients with advanced sarcoma treated with ICI between 2016 and 2023 at Stanford Health Care. Overall survival, progression-free survival (PFS), objective response rates (ORR) per RECIST criteria, and reason for ICI discontinuation were analyzed across histologic subtypes, ICI regimens, tumor mutational burden, and PD-L1 expression.

Results: The overall ORR in the cohort was 16.7%. The histologic subtypes with the highest ORR were Kaposi sarcoma (KS, 66.7%), alveolar soft part sarcoma (ASPS, 50%), angiosarcoma (33.3%), myxofibrosarcoma (MFS, 28.6%), and undifferentiated pleomorphic sarcoma (UPS, 27.8%). The subtypes with the lowest ORR were osteosarcoma (0%), synovial sarcoma (0%), and liposarcoma (3.7%). The subtypes with the highest median PFS were KS (median not reached), ASPS (median not reached), MFS (27.4 months), and UPS (11.3 months). The ORR for sarcomas with PD-L1 ≥ 1% was 27.8% (P = 0.02), whereas the ORR for sarcomas with tumor mutational burden ≥10 mutations per megabase of DNA was 28.6% (P = 0.20).

Conclusions: ORR and PFS were highly variable across sarcoma histologic subtypes. In this large analysis, KS, ASPS, angiosarcoma, MFS, and UPS demonstrated the highest ORR and longest PFS while osteosarcoma, synovial sarcoma, and liposarcoma had the lowest ORR and shortest PFS. PD-L1 expression was also associated with increased ORR. Our findings provide further insight into understanding the sarcoma histologic and immunologic factors that correspond with response to ICI.

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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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