Dana-Farber Cancer Institute, Boston, MA.
Yale University School of Medicine, New Haven, CT.
J Clin Oncol. 2023 Jul 20;41(21):3712-3723. doi: 10.1200/JCO.22.02459. Epub 2023 May 16.
Compared with people living without HIV (PWOH), people living with HIV (PWH) and cancer have traditionally been excluded from immune checkpoint inhibitor (ICI) trials. Furthermore, there is a paucity of real-world data on the use of ICIs in PWH and cancer.
This retrospective study included PWH treated with anti-PD-1- or anti-PD-L1-based therapies for advanced cancers. Kaplan-Meier method was used to estimate overall survival (OS) and progression-free survival (PFS). Objective response rates (ORRs) were measured per RECIST 1.1 or other tumor-specific criteria, whenever feasible. Restricted mean survival time (RMST) was used to compare OS and PFS between matched PWH and PWOH with metastatic NSCLC (mNSCLC).
Among 390 PWH, median age was 58 years, 85% (n = 331) were males, 36% (n = 138) were Black; 70% (n = 274) received anti-PD-1/anti-PD-L1 monotherapy. Most common cancers were NSCLC (28%, n = 111), hepatocellular carcinoma ([HCC]; 11%, n = 44), and head and neck squamous cell carcinoma (HNSCC; 10%, n = 39). Seventy percent (152/216) had CD4+ T cell counts ≥200 cells/µL, and 94% (179/190) had HIV viral load <400 copies/mL. Twenty percent (79/390) had any grade immune-related adverse events (irAEs) and 7.7% (30/390) had grade ≥3 irAEs. ORRs were 69% (nonmelanoma skin cancer), 31% (NSCLC), 16% (HCC), and 11% (HNSCC). In the matched mNSCLC cohort (61 PWH 110 PWOH), 20% (12/61) PWH and 22% (24/110) PWOH had irAEs. Adjusted 42-month RMST difference was -0.06 months (95% CI, -5.49 to 5.37; = .98) for PFS and 2.23 months (95% CI, -4.02 to 8.48; = .48) for OS.
Among PWH, ICIs demonstrated differential activity across cancer types with no excess toxicity. Safety and activity of ICIs were similar between matched cohorts of PWH and PWOH with mNSCLC.
与未感染 HIV 的人群(PWOH)相比,HIV 感染者(PWH)和癌症患者通常被排除在免疫检查点抑制剂(ICI)试验之外。此外,关于 PWH 和癌症患者使用 ICI 的真实世界数据也很少。
本回顾性研究纳入了接受抗 PD-1 或抗 PD-L1 为基础的治疗方案治疗晚期癌症的 PWH。采用 Kaplan-Meier 法估计总生存期(OS)和无进展生存期(PFS)。尽可能按照 RECIST 1.1 或其他肿瘤特异性标准,测量客观缓解率(ORR)。采用受限平均生存时间(RMST)比较匹配的转移性非小细胞肺癌(mNSCLC)患者的 PWH 和 PWOH 的 OS 和 PFS。
在 390 例 PWH 中,中位年龄为 58 岁,85%(n=331)为男性,36%(n=138)为黑人;70%(n=274)接受抗 PD-1/抗 PD-L1 单药治疗。最常见的癌症为非小细胞肺癌(28%,n=111)、肝细胞癌(11%,n=44)和头颈部鳞状细胞癌(HNSCC;10%,n=39)。70%(152/216)的 CD4+T 细胞计数≥200 个/µL,94%(179/190)的 HIV 病毒载量<400 拷贝/ml。20%(79/390)有任何级别的免疫相关不良事件(irAEs),7.7%(30/390)有≥3 级的 irAEs。ORR 分别为:非黑色素瘤皮肤癌 69%(n=49)、非小细胞肺癌 31%(n=21)、肝细胞癌 16%(n=10)和头颈部鳞状细胞癌 11%(n=7)。在匹配的 mNSCLC 队列(61 例 PWH 110 例 PWOH)中,20%(12/61)的 PWH 和 22%(24/110)的 PWOH 有 irAEs。调整后的 42 个月 RMST 差异为 -0.06 个月(95%CI:-5.49 至 5.37; =.98)的 PFS 和 2.23 个月(95%CI:-4.02 至 8.48; =.48)的 OS。
在 PWH 中,ICI 在不同癌症类型中显示出不同的活性,且没有额外的毒性。在匹配的 mNSCLC 患者的 PWH 和 PWOH 队列中,ICI 的安全性和活性相似。