Lurain Kathryn, Ramaswami Ramya, Mangusan Ralph, Widell Anaida, Ekwede Irene, George Jomy, Ambinder Richard, Cheever Martin, Gulley James L, Goncalves Priscila H, Wang Hao-Wei, Uldrick Thomas S, Yarchoan Robert
HIV and AIDS Malignancy Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA
HIV and AIDS Malignancy Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
J Immunother Cancer. 2021 Feb;9(2). doi: 10.1136/jitc-2020-002097.
Non-Hodgkin's lymphoma (NHL) is currently the most common malignancy among people living with HIV (PLWH) in the USA. NHL in PLWH is more frequently associated with oncogenic viruses than NHL in immunocompetent individuals and is generally associated with increased PD-1 expression and T cell exhaustion. An effective immune-based second-line approach that is less immunosuppressive than chemotherapy may decrease infection risk, improve immune control of oncogenic viruses, and ultimately allow for better lymphoma control.
We conducted a retrospective study of patients with HIV-associated lymphomas treated with pembrolizumab±pomalidomide in the HIV and AIDS Malignancy Branch, Center for Cancer Research, National Cancer Institute.
We identified 10 patients with stage IV relapsed and/or primary refractory HIV-associated NHL who were treated with pembrolizumab, an immune checkpoint inihibitor, with or without pomalidomide. Five patients had primary effusion lymphoma (PEL): one had germinal center B cell-like (GCB) diffuse large B cell lymphoma (DLBCL); two had non-GCB DLBCL; one had aggressive B cell lymphoma, not otherwise specified; and one had plasmablastic lymphoma. Six patients received pembrolizumab alone at 200 mg intravenously every 3 weeks, three received pembrolizumab 200 mg intravenously every 4 weeks plus pomalidomide 4 mg orally every day for days 1-21 of a 28-day cycle; and one sequentially received pembrolizumab alone and then pomalidomide alone. The response rate was 50% with particular benefit in gammaherpesvirus-associated tumors. The progression-free survival was 4.1 months (95% CI: 1.3 to 12.4) and overall survival was 14.7 months (95% CI: 2.96 to not reached). Three patients with PEL had leptomeningeal disease: one had a complete response and the other two had long-term disease control. There were four immune-related adverse events (irAEs), all CTCAEv5 grade 2-3; three of the four patients were able to continue receiving pembrolizumab. No irAEs occurred in patients receiving the combination of pembrolizumab and pomalidomide.
Treatment of HIV-associated NHL with pembrolizumab with or without pomalidomide elicited responses in several subtypes of HIV-associated NHL. This approach is worth further study in PLWH and NHL.
非霍奇金淋巴瘤(NHL)是目前美国人类免疫缺陷病毒(HIV)感染者(PLWH)中最常见的恶性肿瘤。与免疫功能正常个体的NHL相比,PLWH中的NHL更常与致癌病毒相关,并且通常与PD-1表达增加和T细胞耗竭有关。一种有效的基于免疫的二线治疗方法,其免疫抑制作用比化疗小,可能会降低感染风险,改善对致癌病毒的免疫控制,并最终更好地控制淋巴瘤。
我们在国立癌症研究所癌症研究中心的HIV和艾滋病恶性肿瘤科,对接受派姆单抗±泊马度胺治疗的HIV相关淋巴瘤患者进行了一项回顾性研究。
我们确定了10例IV期复发和/或原发性难治性HIV相关NHL患者,他们接受了免疫检查点抑制剂派姆单抗治疗,联合或不联合泊马度胺。5例患者患有原发性渗出性淋巴瘤(PEL):1例为生发中心B细胞样(GCB)弥漫性大B细胞淋巴瘤(DLBCL);2例为非GCB DLBCL;1例为未另行指定的侵袭性B细胞淋巴瘤;1例为浆母细胞淋巴瘤。6例患者每3周静脉注射200mg派姆单抗;3例患者每4周静脉注射200mg派姆单抗,外加每28天周期的第1-21天每天口服4mg泊马度胺;1例患者先后单独接受派姆单抗治疗,然后单独接受泊马度胺治疗。缓解率为50%,对γ疱疹病毒相关肿瘤有特别益处。无进展生存期为4.1个月(95%CI:1.3至12.4),总生存期为14.7个月(95%CI:2.96至未达到)。3例PEL患者有软脑膜疾病:1例完全缓解,另外2例病情长期得到控制。有4例免疫相关不良事件(irAEs),均为CTCAEv5 2-3级;4例患者中有3例能够继续接受派姆单抗治疗。接受派姆单抗和泊马度胺联合治疗的患者未发生irAEs。
派姆单抗联合或不联合泊马度胺治疗HIV相关NHL在几种HIV相关NHL亚型中引起了反应。这种方法值得在PLWH和NHL中进一步研究。