Use of Biologic or Targeted Synthetic Disease-Modifying Antirheumatic Drugs and Cancer Risk

In this cohort study of individuals with RA and new biologic or targeted synthetic DMARD exposures, individuals initiating rituximab, abatacept, and JAKis demonstrated higher incidence rates and statistically significantly increased risks of incident cancers compared with those initiating TNFis in the first 2 years after initiation of biologic or targeted synthetic DMARDs. Given the limitations of administrative claims data and confounding by indication, it is likely that these patients may have a higher disease burden, resulting in channeling bias. To better understand these associations, larger studies with longer follow-up time are needed.

Authors

Institutions

Publication Details

Journal
JAMA Network Open
Published
2024-11-20
DOI
https://doi.org/10.1001/jamanetworkopen.2024.46336
Citations
7
Primary Topic
Rheumatoid Arthritis Research and Therapies
Type
article
Field-Weighted Citation Impact
3.29

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Use of Biologic or Targeted Synthetic Disease-Modifying Antirheumatic Drugs and Cancer Risk

Mathilde H. Pioro, Jeffrey A. Sparks, James S. Andrews, Radjiv Goulabchand et al.
7 citations
JAMA Network Open
Rheumatoid Arthritis Research and Therapies
3.29
article

Use of Biologic or Targeted Synthetic Disease-Modifying Antirheumatic Drugs and Cancer Risk

Mathilde H. Pioro, Jeffrey A. Sparks, James S. Andrews, Radjiv Goulabchand, Laura S. Gold, Maureen Dubreuil, David Liew, Jeffrey G. Jarvik, Pankti Reid, Jean W. Liew, Xavier Sendaydiego, Grant C. Hughes, Abha G. Singh, Siddharth Singh, Namrata Singh
article en
7 citations

Abstract

In this cohort study of individuals with RA and new biologic or targeted synthetic DMARD exposures, individuals initiating rituximab, abatacept, and JAKis demonstrated higher incidence rates and statistically significantly increased risks of incident cancers compared with those initiating TNFis in the first 2 years after initiation of biologic or targeted synthetic DMARDs. Given the limitations of administrative claims data and confounding by indication, it is likely that these patients may have a higher disease burden, resulting in channeling bias. To better understand these associations, larger studies with longer follow-up time are needed.

JAMA Network OpenVol. 7(11)
Boston University (US), Brigham and Women's Hospital (US), Harvard University (US), Inserm (FR), The University of Melbourne (AU), Université de Montpellier (FR), University of Washington (US), VA Boston Healthcare System (US), University of Alabama at Birmingham (US), University of California San Diego (US), University of Chicago Medical Center (US), Geriatric Research Education and Clinical Center (US), Washington Center (US), Austin Health (AU), Université de Nîmes (FR)
George Gund Foundation, Amgen, Bristol-Myers Squibb, Pfizer, AstraZeneca, Rheumatology Research Foundation, University of Washington, Australian Government, National Institutes of Health
Openalex Percentile: Top 8%
Rheumatoid Arthritis Research and Therapies
3.29
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.