Lurain Kathryn, Ramaswami Ramya, Ekwede Irene, Eulo Vanessa, Goyal Gaurav, Menon Manoj, Odeny Thomas A, Sharon Elad, Wagner Michael J, Wang Chia-Ching Jackie, Bhardwaj Nina, Friedlander Philip A, Abdul-Hay Maher, Cornejo Castro Elena M, Labo Nazzarena, Marshall Vickie Ann, Miley Wendell, Moore Kyle, Roshan Romin, Whitby Denise, Kask Angela Shaulov, Kaiser Judith, Han Emma, Wright Anna, Yarchoan Robert, Fling Steven P, Uldrick Thomas S
HIV and AIDS Malignancy Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.
University of Alabama at Birmingham, Birmingham, AL.
J Clin Oncol. 2025 Feb;43(4):432-442. doi: 10.1200/JCO.24.00640. Epub 2024 Oct 2.
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.
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.
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).
Pembrolizumab yielded a high rate of durable responses in HIV-associated KS. imAEs were successfully managed with standard guidelines.
癌症免疫治疗试验网络12证明了帕博利珠单抗治疗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,我们纳入了接受抗逆转录病毒治疗且CD4≥50细胞/μL、HIV血浆RNA<200拷贝/mL的HIV相关KS患者。每3周静脉注射一次帕博利珠单抗200mg,最多35个周期。主要终点是安全性,次要终点是根据改良的艾滋病临床试验组标准评估的KS反应。
32名顺性别男性入组,基线CD4 T细胞计数中位数为274细胞/µL。除9名参与者外,其余均接受过先前的系统性KS治疗。参与者接受帕博利珠单抗治疗的中位数为11个周期(范围为1 - 35个周期)。66%的患者出现≥1级治疗中出现的不良事件,包括1例因多克隆KS疱疹病毒相关B细胞淋巴增殖导致的死亡。31%的患者出现≥1次免疫介导的不良事件(imAE),其中25%需要全身使用类固醇。在29名可评估KS的参与者中,总体缓解率(ORR)为62.1%(95%CI,42.3至79.3),且不受CD4 T细胞计数的影响。8名既往未接受过KS治疗且可评估病情的参与者的ORR为87.5%(95%CI,47.3至99.7)。中位缓解持续时间(DOR)未达到,DOR≥12个月的Kaplan-Meier估计值为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至无法计算)。
帕博利珠单抗在HIV相关KS中产生了较高的持久缓解率。imAE通过标准指南成功管理。