HIV and Hodgkin Lymphoma Survival: A Prospective Study in Botswana

Author:

Moahi Kaelo12ORCID,Ralefala Tlotlo3ORCID,Nkele Isaac4,Triedman Scott5ORCID,Sohani Aliyah67ORCID,Musimar Zola3ORCID,Efstathiou Jason8ORCID,Armand Philipe9ORCID,Lockman Shahin41011ORCID,Dryden-Peterson Scott41011ORCID

Affiliation:

1. Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA

2. Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA

3. Princess Marina Hospital, Ministry of Health and Wellness, Gaborone, Botswana

4. Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana

5. Department of Radiation Oncology, Warren Alpert Medical School, Providence, RI

6. Department of Pathology, Massachusetts General Hospital, Boston, MA

7. Department of Pathology, Harvard Medical School, Boston, MA

8. Department of Radiation Oncology, Massachusetts General Hospital, Boston, MA

9. Department of Medical Oncology/Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA

10. Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA

11. Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA

Abstract

PURPOSE People living with HIV (PLWH) experience increased risk of Hodgkin lymphoma (HL) despite effective initiation of antiretroviral therapy (ART). In high-income countries, outcomes following HIV HL have been reported to be non-differential, or inferior for PLWH. We sought to assess the effect of HIV on HL survival in Botswana, an African country with a generalized HIV epidemic and high ART coverage, to describe a context more reflective of global HIV populations. PATIENTS AND METHODS In the Thabatse Cancer Cohort, consenting participants initiating treatment for HL at one of four cancer centers in Botswana were enrolled from 2010 to 2020. Patients were followed quarterly for up to 5 years. The impact of HIV on survival following treatment initiation was assessed using an inverse probability–weighted Cox marginal structural model adjusted for age, performance status, and disease stage. RESULTS Seventy-eight new HL cases were enrolled, 47 (60%) were PLWH and 31 (40%) were HIV-uninfected. Baseline characteristics were similar between groups. The majority (61%) of patients presented with regional disease (stage I or II) with no statistically significant difference by HIV status ( P = .38). Nearly all (87%) PLWH participants were on ART before their HL diagnosis (median ART duration 42 months), and median CD4 count was 413 cells/μL (interquartile range 253-691). Survival, in unadjusted analyses, was lower among patients without HIV compared with PLWH (log rank P = .021). In adjusted analysis, HIV infection was not significantly associated with survival in inverse probability–weighted Cox model (hazard ratio 0.43; 95% CI, 0.16 to 1.16; P = .094). CONCLUSION In this cohort of patients treated for HL in Botswana, survival in PLWH (87% on long-standing ART) was at least as good as in individuals without HIV.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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