Palich Romain, Makinson Alain, Veyri Marianne, Guihot Amélie, Valantin Marc-Antoine, Brégigeon-Ronot Sylvie, Poizot-Martin Isabelle, Solas Caroline, Grabar Sophie, Martin-Blondel Guillaume, Spano Jean-Philippe
Department of Infectious Diseases, Pitié-Salpêtrière Hospital, AP-HP, Pierre Louis Epidemiology and Public Health Institute (iPLESP), INSERM U1136, Sorbonne University, 75013 Paris, France.
Infectious Diseases Department, INSERM U1175, University Hospital of Montpellier, 34000 Montpellier, France.
Cancers (Basel). 2021 Nov 15;13(22):5702. doi: 10.3390/cancers13225702.
Since the advent of highly effective combined antiretroviral treatment (cART), and with the implementation of large HIV testing programs and universal access to cART, the burden of AIDS-related comorbidities has dramatically decreased over time. The incidence of Kaposi's sarcoma (SK), strongly associated with HIV replication and CD4 immunosuppression, was greatly reduced. However, KS remains the most common cancer in patients living with HIV (PLHIV). HIV physicians are increasingly faced with KS in virally suppressed HIV-patients, as reflected by increasing description of case series. Though SK seem less aggressive than those in PLHIV with uncontrolled HIV-disease, some may require systemic chemotherapy. Persistent lack of specific anti-HHV-8 cellular immunity could be involved in the physiopathology of these KS. These clinical forms are a real therapeutic challenge without possible short-term improvement of anti-HHV-8 immunity, and no active replication of HIV to control. The cumulative toxicity of chemotherapies repeatedly leads to a therapeutic dead end. The introduction or maintenance of protease inhibitors in cART does not seem to have an impact on the evolution of these KS. Research programs in this emerging condition are important to consider new strategies.
自从高效联合抗逆转录病毒治疗(cART)出现以来,随着大规模HIV检测项目的实施以及cART的普遍可及,与艾滋病相关的合并症负担已随着时间大幅下降。与HIV复制和CD4免疫抑制密切相关的卡波西肉瘤(KS)发病率大幅降低。然而,KS仍然是HIV感染者(PLHIV)中最常见的癌症。正如病例系列描述的增加所反映的那样,HIV医生越来越多地在病毒抑制的HIV患者中遇到KS。尽管KS似乎比HIV疾病未得到控制的PLHIV中的KS侵袭性更小,但有些可能需要全身化疗。持续缺乏针对HHV-8的特异性细胞免疫可能与这些KS的病理生理有关。在无法短期内改善抗HHV-8免疫且无法控制HIV活跃复制的情况下,这些临床形式是一个真正的治疗挑战。化疗的累积毒性反复导致治疗陷入僵局。在cART中引入或维持蛋白酶抑制剂似乎对这些KS的进展没有影响。针对这种新出现情况的研究项目对于考虑新策略很重要。