Tumor Necrosis Factor Inhibitors and the Risk of Cancer among Older Americans with Rheumatoid Arthritis.


Journal

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
ISSN: 1538-7755
Titre abrégé: Cancer Epidemiol Biomarkers Prev
Pays: United States
ID NLM: 9200608

Informations de publication

Date de publication:
11 2021
Historique:
received: 29 01 2021
revised: 28 04 2021
accepted: 09 08 2021
pubmed: 25 8 2021
medline: 10 2 2022
entrez: 24 8 2021
Statut: ppublish

Résumé

TNF inhibitors (TNFi) effectively treat rheumatoid arthritis but may increase patient risk of some malignancies, particularly lymphomas or skin cancers. We used Surveillance, Epidemiology, and End Results (SEER)-Medicare data to conduct a case-control study in patients with rheumatoid arthritis (2007-2015). Cases were individuals with a first cancer diagnosed in SEER registries (ages 66-99, 22 cancer sites, TNFi exposure was present in 16.2% of controls and 12.8% to 33.7% of cancer cases, varying by site. TNFi use was associated with increased risk of NMSC overall (aOR 1.32, 95% confidence interval 1.06-1.63), non-Hodgkin lymphoma (NHL) overall (1.28, 1.06-1.56) and, specifically, follicular lymphoma (2.63, 1.63-4.24). TNFi exposure was not associated with other SEER cancer sites, BCC or SCC specifically, or other common NHL subtypes. Among older adults with rheumatoid arthritis, TNFi exposure was associated with elevated risk of NMSC and NHL, driven specifically by follicular lymphoma. Exposure was not associated with increased risk for other cancer sites. Our results support a role for TNF in lymphomagenesis. Given the association with NMSC, patients initiating TNFi therapy may benefit from skin cancer screening and sun protection measures.

Sections du résumé

BACKGROUND
TNF inhibitors (TNFi) effectively treat rheumatoid arthritis but may increase patient risk of some malignancies, particularly lymphomas or skin cancers.
METHODS
We used Surveillance, Epidemiology, and End Results (SEER)-Medicare data to conduct a case-control study in patients with rheumatoid arthritis (2007-2015). Cases were individuals with a first cancer diagnosed in SEER registries (ages 66-99, 22 cancer sites,
RESULTS
TNFi exposure was present in 16.2% of controls and 12.8% to 33.7% of cancer cases, varying by site. TNFi use was associated with increased risk of NMSC overall (aOR 1.32, 95% confidence interval 1.06-1.63), non-Hodgkin lymphoma (NHL) overall (1.28, 1.06-1.56) and, specifically, follicular lymphoma (2.63, 1.63-4.24). TNFi exposure was not associated with other SEER cancer sites, BCC or SCC specifically, or other common NHL subtypes.
CONCLUSIONS
Among older adults with rheumatoid arthritis, TNFi exposure was associated with elevated risk of NMSC and NHL, driven specifically by follicular lymphoma. Exposure was not associated with increased risk for other cancer sites.
IMPACT
Our results support a role for TNF in lymphomagenesis. Given the association with NMSC, patients initiating TNFi therapy may benefit from skin cancer screening and sun protection measures.

Identifiants

pubmed: 34426413
pii: 1055-9965.EPI-21-0125
doi: 10.1158/1055-9965.EPI-21-0125
pmc: PMC8568666
mid: NIHMS1735680
doi:

Substances chimiques

Tumor Necrosis Factor Inhibitors 0

Types de publication

Journal Article Research Support, N.I.H., Intramural Comment

Langues

eng

Sous-ensembles de citation

IM

Pagination

2059-2067

Subventions

Organisme : Intramural NIH HHS
ID : Z99 CA999999
Pays : United States

Commentaires et corrections

Type : CommentOn

Informations de copyright

©2021 American Association for Cancer Research.

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Auteurs

Monica E D'Arcy (ME)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland. monica.d'arcy@nih.gov.

Daniel C Beachler (DC)

Healthcore Inc, Wilmington, Delaware.

Ruth M Pfeiffer (RM)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.

Jeffrey R Curtis (JR)

University of Alabama at Birmingham, Birmingham, Alabama.

Xavier Mariette (X)

Hôpital Bicêtre, Assistance Publique -Hôpitaux de Paris, Université Paris-Saclay, Le Kremlin Bicêtre, Paris, France.

Raphaele Seror (R)

Hôpital Bicêtre, Assistance Publique -Hôpitaux de Paris, Université Paris-Saclay, Le Kremlin Bicêtre, Paris, France.

Parag Mahale (P)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.

Donna R Rivera (DR)

Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, Maryland.

Elizabeth L Yanik (EL)

Washington University, St. Louis, Missouri.

Eric A Engels (EA)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.

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