Stable Incidence and Poor Survival for HIV-Related Burkitt Lymphoma Among the US Veteran Population During the Antiretroviral Era.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 05 2020
Historique:
entrez: 7 4 2020
pubmed: 7 4 2020
medline: 11 11 2020
Statut: ppublish

Résumé

Despite advances in diagnosis and treatment of both HIV and Burkitt lymphoma (BL), persons living with HIV remain at high risk for BL. We conducted this study to evaluate if there have been any changes in the risk of or survival after BL diagnosis among persons living with HIV during the antiretroviral era. Veterans living with HIV (VLWH) and age-matched HIV-negative controls receiving care between 1999 and 2016 were retrospectively identified using Veterans Health Administration electronic medical records. We identified BL diagnoses through Veterans Health Administration Cancer Registry review and International Classification of Diseases, Ninth/Tenth Revisions, codes, and we extracted demographic, lifestyle, and clinical variables from electronic medical record. We estimated hazard ratios (HR) and 95% confidence intervals (CIs) for BL risk and survival using Cox proportional models. We identified 45,299 VLWH. Eighty-four developed BL (incidence rate = 21.2 per 100,000 person years; CI: 17.1 to 26.3). Median CD4 count at BL diagnosis was 238 cells per milliliter (SD: 324.74) and increased over time. Survival was truncated in VLWH with BL (P < 0.05). The risk of BL in VLWH was 38% less in blacks compared with whites (HR: 0.620; CI: 0.393 to 0.979; P = 0.0401). VLWH with an undetectable viral load for at least 40% of follow-up were 74% less likely to develop BL (HR: 0.261; CI: 0.143 to 0.478; P < 0.0001) and 86% less likely to die after diagnosis (HR: 0.141; CI: 0.058 to 0.348; P < 0.0001). BL incidence among VLWH did not improve between 2000 and 2016. Survival after BL diagnosis in VLWH remains dismal as compared with their HIV-negative counterparts, although veterans with prolonged periods of undetectable viral load had improved prognosis.

Sections du résumé

BACKGROUND
Despite advances in diagnosis and treatment of both HIV and Burkitt lymphoma (BL), persons living with HIV remain at high risk for BL. We conducted this study to evaluate if there have been any changes in the risk of or survival after BL diagnosis among persons living with HIV during the antiretroviral era.
SETTING
Veterans living with HIV (VLWH) and age-matched HIV-negative controls receiving care between 1999 and 2016 were retrospectively identified using Veterans Health Administration electronic medical records.
METHODS
We identified BL diagnoses through Veterans Health Administration Cancer Registry review and International Classification of Diseases, Ninth/Tenth Revisions, codes, and we extracted demographic, lifestyle, and clinical variables from electronic medical record. We estimated hazard ratios (HR) and 95% confidence intervals (CIs) for BL risk and survival using Cox proportional models.
RESULTS
We identified 45,299 VLWH. Eighty-four developed BL (incidence rate = 21.2 per 100,000 person years; CI: 17.1 to 26.3). Median CD4 count at BL diagnosis was 238 cells per milliliter (SD: 324.74) and increased over time. Survival was truncated in VLWH with BL (P < 0.05). The risk of BL in VLWH was 38% less in blacks compared with whites (HR: 0.620; CI: 0.393 to 0.979; P = 0.0401). VLWH with an undetectable viral load for at least 40% of follow-up were 74% less likely to develop BL (HR: 0.261; CI: 0.143 to 0.478; P < 0.0001) and 86% less likely to die after diagnosis (HR: 0.141; CI: 0.058 to 0.348; P < 0.0001).
CONCLUSIONS
BL incidence among VLWH did not improve between 2000 and 2016. Survival after BL diagnosis in VLWH remains dismal as compared with their HIV-negative counterparts, although veterans with prolonged periods of undetectable viral load had improved prognosis.

Identifiants

pubmed: 32251095
doi: 10.1097/QAI.0000000000002303
pii: 00126334-202005010-00004
pmc: PMC7793609
mid: NIHMS1549648
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

18-25

Subventions

Organisme : CSRD VA
ID : I01 CX001430
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA125123
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA206476
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA174647
Pays : United States

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Auteurs

Eva Clark (E)

Department of Medicine, Section of Infectious Diseases, Baylor College of Medicine, Houston, TX.
Section of Health Services Research, Michael E. DeBakey VA Health Services Research Center of Innovations (IQuESt), Houston, TX.

Kathryn E Royse (KE)

Section of Health Services Research, Michael E. DeBakey VA Health Services Research Center of Innovations (IQuESt), Houston, TX.
Department of Medicine, Section of Health Services Research, Baylor College of Medicine, Houston, TX.

Yongquan Dong (Y)

Section of Health Services Research, Michael E. DeBakey VA Health Services Research Center of Innovations (IQuESt), Houston, TX.
Department of Medicine, Section of Health Services Research, Baylor College of Medicine, Houston, TX.

Elaine Chang (E)

Section of Health Services Research, Michael E. DeBakey VA Health Services Research Center of Innovations (IQuESt), Houston, TX.
Department of Medicine, Section of Hematology and Oncology, Baylor College of Medicine, Houston, TX.

Suchismita Raychaudhury (S)

Section of Health Services Research, Michael E. DeBakey VA Health Services Research Center of Innovations (IQuESt), Houston, TX.
Department of Medicine, Section of Health Services Research, Baylor College of Medicine, Houston, TX.

Jennifer Kramer (J)

Section of Health Services Research, Michael E. DeBakey VA Health Services Research Center of Innovations (IQuESt), Houston, TX.
Department of Medicine, Section of Health Services Research, Baylor College of Medicine, Houston, TX.
Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX.

Donna L White (DL)

Department of Medicine, Section of Health Services Research, Baylor College of Medicine, Houston, TX.
Clinical Epidemiology and Comparative Effectiveness Program at Michael E. DeBakey VA Health Services Research Center of Innovations (IQuESt), Houston, TX; and.
Center for Translation in Inflammatory Diseases (CTRID), Michael E. DeBakey VA Medical Center, Houston, TX.

Elizabeth Chiao (E)

Department of Medicine, Section of Infectious Diseases, Baylor College of Medicine, Houston, TX.
Section of Health Services Research, Michael E. DeBakey VA Health Services Research Center of Innovations (IQuESt), Houston, TX.
Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX.

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