Cancer Immunotherapy Trials Network 12: Pembrolizumab in HIV-Associated Kaposi Sarcoma.

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2025-02-01 Epub Date: 2024-10-02 DOI:10.1200/JCO.24.00640
Kathryn Lurain, Ramya Ramaswami, Irene Ekwede, Vanessa Eulo, Gaurav Goyal, Manoj Menon, Thomas A Odeny, Elad Sharon, Michael J Wagner, Chia-Ching Jackie Wang, Nina Bhardwaj, Philip A Friedlander, Maher Abdul-Hay, Elena M Cornejo Castro, Nazzarena Labo, Vickie Ann Marshall, Wendell Miley, Kyle Moore, Romin Roshan, Denise Whitby, Angela Shaulov Kask, Judith Kaiser, Emma Han, Anna Wright, Robert Yarchoan, Steven P Fling, Thomas S Uldrick
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Abstract

Purpose: Cancer Immunotherapy Trials Network 12 demonstrated safety of pembrolizumab in treating advanced cancer in people with HIV. Here, we report results of the Kaposi sarcoma (KS) cohort.

Methods: In this multicenter phase I trial, we enrolled participants with HIV-associated KS on antiretroviral therapy with CD4+ ≥50 cells/μL and HIV plasma RNA <200 copies/mL. Pembrolizumab 200 mg intravenously was administered once every 3 weeks for up to 35 cycles. The primary end point was safety, and the secondary end point was KS response by modified AIDS Clinical Trials Group Criteria.

Results: Thirty-two cisgender men enrolled with baseline median CD4+ T-cell count of 274 cells/µL. All but nine participants had received previous systemic KS therapy. Participants received a median of 11 cycles of pembrolizumab (range, 1-35). Sixty-six percent had grade ≥1 treatment-emergent adverse events, including one death from polyclonal KS herpesvirus-related B-cell lymphoproliferation. Thirty-one percent had ≥one immune-mediated AEs (imAEs) with 25% requiring systemic steroids. In 29 participants with evaluable KS, the overall response rate (ORR) was 62.1% (95% CI, 42.3 to 79.3) and did not differ by CD4+ T-cell count. ORR in the eight participants with evaluable disease without previous KS therapy was 87.5% (95% CI, 47.3 to 99.7). Median duration of response (DOR) was not reached, and the Kaplan-Meier estimate of DOR of ≥12 months was 92.3% (95% CI, 56.6 to 98.8). Median progression-free survival was 28.2 months (95% CI, 4.2 to noncalculable).

Conclusion: Pembrolizumab yielded a high rate of durable responses in HIV-associated KS. imAEs were successfully managed with standard guidelines.

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癌症免疫疗法试验网络 12:Pembrolizumab 在 HIV 相关卡波西肉瘤中的应用。
目的:癌症免疫疗法试验网络12证明了pembrolizumab治疗HIV感染者晚期癌症的安全性。在此,我们报告卡波西肉瘤(KS)队列的结果:在这项多中心 I 期试验中,我们招募了正在接受抗逆转录病毒治疗、CD4+≥50 cells/μL 且血浆 RNA 为 HIV 的 HIV 相关 KS 患者:32 名男性患者的 CD4+ T 细胞计数中位数为 274 cells/μL。除 9 名患者外,其余患者均接受过系统的 KS 治疗。参与者接受了中位数为 11 个周期的 pembrolizumab 治疗(范围为 1-35)。66%的患者出现了≥1级的治疗突发不良事件,其中一人死于多克隆KS疱疹病毒相关的B细胞淋巴细胞增生。31%的患者发生了≥1次免疫介导的不良反应(imAEs),其中25%的患者需要全身使用类固醇。在29名可评估KS的参与者中,总应答率(ORR)为62.1%(95% CI,42.3至79.3),且不因CD4+ T细胞计数而异。8 名既往未接受过 KS 治疗、病情可评估的参与者的总应答率为 87.5%(95% CI,47.3 至 99.7)。未达到中位应答持续时间(DOR),Kaplan-Meier估计≥12个月的DOR为92.3%(95% CI,56.6至98.8)。中位无进展生存期为28.2个月(95% CI,4.2至不可计算):Pembrolizumab在HIV相关的KS中产生了较高的持久应答率。
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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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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