hiv相关淋巴瘤的临床治疗进展

J. Khwaja, J. E. Burns, N. Ahmed, K. Cwynarski
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引用次数: 2

摘要

人类免疫缺陷病毒(HIV)和淋巴瘤之间的联系早在20世纪80年代的HIV流行中就被观察到。淋巴瘤的发病率仍然明显高于一般人群。以前艾滋病毒感染者(PLWH)有晚期免疫抑制,器官功能障碍,因此表现不佳(PS)。抗逆转录病毒联合治疗(ART)的出现改善了免疫重建,显著改善了PLWH的前景,影响了淋巴瘤亚型的发病率,提高了治疗的耐受性。然而,淋巴瘤仍然是癌症相关死亡的最常见原因。我们描述了hiv相关淋巴瘤的多学科管理,并概述了最近的进展。面临的挑战包括发病晚期、中枢神经系统(CNS)等结外部位的倾向、潜在的药物相互作用和机会性感染(OIs)的发生率增加。总体管理现在较少关注艾滋病毒相关因素,而更多关注淋巴瘤特征,结果良好。然而,在淋巴瘤临床试验中缺乏代表性,因为阳性血清状态是大多数人的排除标准。罕见亚型的数据很少。一些小型I/II期试验已经成功招募了艾滋病毒感染者。免疫治疗试验和安全性数据对于了解这种有前景的靶向治疗的毒性和有效性至关重要。我们欢迎最近更宽松的临床试验纳入标准,并支持扩大研究不足的靶向治疗,特别是针对罕见亚型。扩大获取途径将为艾滋病毒感染者提供更好的公平待遇。
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HIV-associated lymphoma—advances in clinical management
The association between human immunodeficiency virus (HIV) and lymphoma was observed early in the HIV epidemic in the 1980s. Lymphoma incidence remains significantly higher than in the general population. Previously people living with HIV (PLWH) had advanced immune suppression, organ dysfunction and consequently poor performance status (PS). The advent of combination antiretroviral therapy (ART) has led to improved immune reconstitution and significantly enhanced the outlook of PLWH, influenced the incidence of lymphoma subtypes and improved tolerability of treatment. However lymphoma still remains the most common cause of cancer related death. We describe the multidisciplinary management of HIV-associated lymphomas and outline recent advances. Challenges include the advanced stage at presentation, propensity for extranodal sites including the central nervous system (CNS), potential drug interactions and increased incidence of opportunistic infections (OIs). Overall management now focusses less on HIV-related factors and more on lymphoma characteristics, with favourable outcomes. Representation in lymphoma clinical trials however is lacking, as a positive serostatus is an exclusion criterion for the majority. Data is scant for the rarer subtypes. A number of small phase I/II trials have successfully recruited patients living with HIV. Immunotherapy trial and safety data will be essential in understanding toxicity and efficacy of this promising targeted treatment. We welcome the recent more permissive inclusion criteria for clinical trials and support the expansion of understudied targeted therapies particularly for rarer subtypes. Broadening access will provide better equity for those living with HIV.
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