Real-world treatment outcomes for Hodgkin lymphoma in South Africa: a prospective observational study.

Bone marrow involvement HIV Hodgkin lymphoma Overall survival Tuberculosis

Journal

Infectious agents and cancer
ISSN: 1750-9378
Titre abrégé: Infect Agent Cancer
Pays: England
ID NLM: 101276559

Informations de publication

Date de publication:
27 Sep 2024
Historique:
received: 29 08 2024
accepted: 18 09 2024
medline: 28 9 2024
pubmed: 28 9 2024
entrez: 28 9 2024
Statut: epublish

Résumé

Prospective data from sub-Saharan Africa suggests that treatment outcomes for people living with HIV (PWH) with Hodgkin lymphoma (HL) are similar to those without HIV. However, real-world data from high-resource settings and retrospective studies from sub-Saharan Africa, suggest inferior outcomes. We set out to evaluate the real-world treatment outcomes for HL in South Africa to better understand the disparate outcomes. We established a prospective, observational cohort of newly diagnosed, adult (≥ 18 years) HL cases recruited from Chris Hani Baragwanath Academic and Netcare Olivedale Hospitals in Johannesburg, South Africa between March 2021 and March 2023. Participants were followed for up to 18 months after enrollment with data censored on December 23rd, 2023. The primary endpoint was 1-year overall survival. We enrolled 47 participants with HL including 31 PWH and 16 HIV-negative. Advanced stage disease and B symptoms were common at time of diagnosis irrespective of HIV status. Bone marrow biopsy, performed during the work-up and evaluation of cytopenias, provided the initial diagnosis of HL in 16/31 (52%) PWH. HIV status and bone marrow involvement were associated with early mortality (within 3 months of diagnosis) and a poorer 1-year overall survival from diagnosis (HIV: 55% vs. 88%; p = 0.03; bone marrow involvement: 50% vs. 80%; p = 0.02). Among evaluable participants, those that received at least 6 cycles of chemotherapy and underwent response assessment, there was no difference between those with and without HIV. Traditional laboratory markers of poor prognosis including anemia, lymphopenia and hypoalbuminemia were more common among PWH and those with bone marrow involvement and suggest high risk disease. A better understanding of the drivers of these aggressive presentations is warranted to ensure more PWH are able to tolerate chemotherapy.

Sections du résumé

BACKGROUND BACKGROUND
Prospective data from sub-Saharan Africa suggests that treatment outcomes for people living with HIV (PWH) with Hodgkin lymphoma (HL) are similar to those without HIV. However, real-world data from high-resource settings and retrospective studies from sub-Saharan Africa, suggest inferior outcomes. We set out to evaluate the real-world treatment outcomes for HL in South Africa to better understand the disparate outcomes.
METHODS METHODS
We established a prospective, observational cohort of newly diagnosed, adult (≥ 18 years) HL cases recruited from Chris Hani Baragwanath Academic and Netcare Olivedale Hospitals in Johannesburg, South Africa between March 2021 and March 2023. Participants were followed for up to 18 months after enrollment with data censored on December 23rd, 2023. The primary endpoint was 1-year overall survival.
RESULTS RESULTS
We enrolled 47 participants with HL including 31 PWH and 16 HIV-negative. Advanced stage disease and B symptoms were common at time of diagnosis irrespective of HIV status. Bone marrow biopsy, performed during the work-up and evaluation of cytopenias, provided the initial diagnosis of HL in 16/31 (52%) PWH. HIV status and bone marrow involvement were associated with early mortality (within 3 months of diagnosis) and a poorer 1-year overall survival from diagnosis (HIV: 55% vs. 88%; p = 0.03; bone marrow involvement: 50% vs. 80%; p = 0.02). Among evaluable participants, those that received at least 6 cycles of chemotherapy and underwent response assessment, there was no difference between those with and without HIV.
CONCLUSION CONCLUSIONS
Traditional laboratory markers of poor prognosis including anemia, lymphopenia and hypoalbuminemia were more common among PWH and those with bone marrow involvement and suggest high risk disease. A better understanding of the drivers of these aggressive presentations is warranted to ensure more PWH are able to tolerate chemotherapy.

Identifiants

pubmed: 39334203
doi: 10.1186/s13027-024-00612-4
pii: 10.1186/s13027-024-00612-4
doi:

Types de publication

Journal Article

Langues

eng

Pagination

46

Subventions

Organisme : FIC NIH HHS
ID : R25TW009340
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NCI NIH HHS
ID : 5T32 CA09071; R01CA250069; R21CA232891; P30CA006973, P30AI094189
Pays : United States
Organisme : NIH HHS
ID : UM1CA121947
Pays : United States
Organisme : NIH HHS
ID : UM1CA121947
Pays : United States

Informations de copyright

© 2024. The Author(s).

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Auteurs

Samantha L Vogt (SL)

Department of Medicine, Johns Hopkins School of Medicine, Division of Hematology, 4940 Eastern Ave, Rm 4500, Baltimore, MD, 21224, USA. svogt2@jhmi.edu.
Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD, USA. svogt2@jhmi.edu.
Perinatal HIV Research Unit (PHRU), Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa. svogt2@jhmi.edu.

Garrick Laudin (G)

Clinical Haematology Unit, Department of Medicine, Chris Hani Baragwanath Academic Hospital and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Marianna Zahurak (M)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Jenifer Vaughan (J)

Department of Molecular Medicine and Haematology, Faculty of Health Sciences, National Health Laboratory Service, University of the Witwatersrand, Johannesburg, South Africa.

Atul Lakha (A)

Clinical Haematology Unit, Department of Medicine, Chris Hani Baragwanath Academic Hospital and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Sugeshnee Pather (S)

Division of Anatomical Pathology, Faculty of Health Sciences, National Health Laboratory Service, University of the Witwatersrand, Johannesburg, South Africa.

Ziyaad Waja (Z)

Perinatal HIV Research Unit (PHRU), Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Deshan Chetty (D)

Perinatal HIV Research Unit (PHRU), Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Tanvier Omar (T)

Division of Anatomical Pathology, Faculty of Health Sciences, National Health Laboratory Service, University of the Witwatersrand, Johannesburg, South Africa.

Wendy Stevens (W)

Wits Diagnostic Innovation Hub, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Philippa Ashmore (P)

Clinical Haematology, Netcare Olivedale Hospital, Johannesburg, South Africa.

Kennedy Otwombe (K)

Perinatal HIV Research Unit (PHRU), Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
School of Public Health, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Khuthadzo Hlongwane (K)

Perinatal HIV Research Unit (PHRU), Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Ravi Varadhan (R)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Moosa Patel (M)

Clinical Haematology Unit, Department of Medicine, Chris Hani Baragwanath Academic Hospital and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Richard F Ambinder (RF)

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Department of Pathology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Neil A Martinson (NA)

Department of Medicine, Johns Hopkins School of Medicine, Division of Hematology, 4940 Eastern Ave, Rm 4500, Baltimore, MD, 21224, USA.
Perinatal HIV Research Unit (PHRU), Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Rena R Xian (RR)

Department of Pathology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Vinitha Philip (V)

Clinical Haematology Unit, Department of Medicine, Chris Hani Baragwanath Academic Hospital and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Classifications MeSH