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
{"title":"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。","authors":"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","doi":"10.1200/JCO.24.00640","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>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.</p><p><strong>Methods: </strong>In this multicenter phase I trial, we enrolled participants with HIV-associated KS on antiretroviral therapy with CD4<sup>+</sup> ≥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.</p><p><strong>Results: </strong>Thirty-two cisgender men enrolled with baseline median CD4<sup>+</sup> 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<sup>+</sup> 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).</p><p><strong>Conclusion: </strong>Pembrolizumab yielded a high rate of durable responses in HIV-associated KS. imAEs were successfully managed with standard guidelines.</p>","PeriodicalId":15384,"journal":{"name":"Journal of Clinical Oncology","volume":" ","pages":"432-442"},"PeriodicalIF":42.1000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11779594/pdf/","citationCount":"0","resultStr":"{\"title\":\"Cancer Immunotherapy Trials Network 12: Pembrolizumab in HIV-Associated Kaposi Sarcoma.\",\"authors\":\"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\",\"doi\":\"10.1200/JCO.24.00640\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Cancer Immunotherapy Trials Network 12 demonstrated safety of pembrolizumab in treating advanced cancer in people with HIV. 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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<sup>+</sup> 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). 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引用次数: 0
摘要
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。
Cancer Immunotherapy Trials Network 12: Pembrolizumab in HIV-Associated Kaposi Sarcoma.
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.
期刊介绍:
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