{"title":"HIV infection and survival in Hodgkin lymphoma: a real-world analysis of a multicenter research network.","authors":"Shih-Ping Lin, Tsung-Han Yen, Jian-Ri Li, Cheng-Wei Chou","doi":"10.1093/jncics/pkag076","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Despite effective antiretroviral therapy, people living with human immunodeficiency virus (HIV) (PLWH) remain at a higher risk of developing Hodgkin lymphoma (HL). Further, survival disparities persist despite similar treatment recommendations.</p><p><strong>Methods: </strong>Herein, we present a global retrospective cohort study including data of adults (≥18 years) diagnosed with HL between 2015 and 2025 from the TriNetX database to evaluate the survival outcomes of Hodgkin lymphoma in HIV-infected vs non-HIV-infected patients and analyze the associated risk factors. Patients were stratified according to HIV status and matched 1:1 for age, sex, race, and comorbidities. Overall survival (OS) was analyzed using Kaplan-Meier and Cox proportional hazards models.</p><p><strong>Results: </strong>A total of 927 matched HIV-infected and non-HIV-infected patients were included. Overall, HIV-positive status was associated with significantly inferior OS (HR 1.42; 95% CI 1.10-1.84; P = .033). Among PLWH, cerebrovascular disease, hepatitis C virus infection, and chronic kidney disease independently predicted increased mortality. In a matched subgroup of patients treated with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) chemotherapy (n = 154 per group), OS did not differ significantly between the HIV-positive and HIV-negative groups (HR 1.37; 95% CI 0.73-2.56; P = .247).</p><p><strong>Conclusion: </strong>In conclusion, HIV-infected patients with HL experienced worse OS compared with non-HIV-infected individuals, but the outcomes were comparable when treated with ABVD chemotherapy, highlighting the importance of optimal treatment delivery and comorbidity management in PLWH.</p>","PeriodicalId":14681,"journal":{"name":"JNCI Cancer Spectrum","volume":" ","pages":""},"PeriodicalIF":4.8000,"publicationDate":"2026-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13499626/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JNCI Cancer Spectrum","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/jncics/pkag076","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Despite effective antiretroviral therapy, people living with human immunodeficiency virus (HIV) (PLWH) remain at a higher risk of developing Hodgkin lymphoma (HL). Further, survival disparities persist despite similar treatment recommendations.
Methods: Herein, we present a global retrospective cohort study including data of adults (≥18 years) diagnosed with HL between 2015 and 2025 from the TriNetX database to evaluate the survival outcomes of Hodgkin lymphoma in HIV-infected vs non-HIV-infected patients and analyze the associated risk factors. Patients were stratified according to HIV status and matched 1:1 for age, sex, race, and comorbidities. Overall survival (OS) was analyzed using Kaplan-Meier and Cox proportional hazards models.
Results: A total of 927 matched HIV-infected and non-HIV-infected patients were included. Overall, HIV-positive status was associated with significantly inferior OS (HR 1.42; 95% CI 1.10-1.84; P = .033). Among PLWH, cerebrovascular disease, hepatitis C virus infection, and chronic kidney disease independently predicted increased mortality. In a matched subgroup of patients treated with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) chemotherapy (n = 154 per group), OS did not differ significantly between the HIV-positive and HIV-negative groups (HR 1.37; 95% CI 0.73-2.56; P = .247).
Conclusion: In conclusion, HIV-infected patients with HL experienced worse OS compared with non-HIV-infected individuals, but the outcomes were comparable when treated with ABVD chemotherapy, highlighting the importance of optimal treatment delivery and comorbidity management in PLWH.
尽管抗逆转录病毒治疗有效,但人类免疫缺陷病毒(HIV) (PLWH)感染者发展为霍奇金淋巴瘤(HL)的风险仍然较高。此外,尽管有类似的治疗建议,生存差异仍然存在。在此,我们提出了一项全球回顾性队列研究,包括来自TriNetX数据库的2015年至2025年间诊断为HL的成人(≥18岁)的数据,以评估hiv感染与非hiv感染的霍奇金淋巴瘤患者的生存结果,并分析相关危险因素。患者根据HIV状况分层,并按年龄、性别、种族和合并症1:1匹配。采用Kaplan-Meier和Cox比例风险模型分析总生存期(OS)。共纳入927例匹配的hiv感染者和非hiv感染者。总体而言,hiv阳性状态与明显较差的OS相关(HR 1.42; 95% CI 1.10-1.84; p = 0.033)。在PLWH中,脑血管疾病、丙型肝炎病毒感染和慢性肾脏疾病独立预测死亡率增加。在接受阿霉素、博来霉素、长春碱和达卡巴嗪(ABVD)化疗的患者的匹配亚组中(每组n = 154), hiv阳性组和hiv阴性组之间的OS无显著差异(HR 1.37; 95% CI 0.73-2.56; p = 0.247)。总之,与非hiv感染者相比,hiv感染的HL患者经历了更糟糕的OS,但当接受ABVD化疗时,结果是相当的,这突出了PLWH中最佳治疗交付和合并症管理的重要性。