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Updated: Jun 6, 2026

An Adoptive Transfer Model of Rheumatoid Arthritis in Mice
Published on: June 6, 2025
The risk of malignancies in RA patients treated with biologics
1Clinical Epidemiology Unit T2:01, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital Solna, 171 76, Stockholm, Schweden. johan.askling@ki.se
Abstract:
Ever since biologics were introduced in the treatment of RA around 10 years ago, concerns about their safety profiles, including cancer, have been raised. In the case of cancer, these concerns are based on our incomplete understanding of the full effects of these drugs, or the pathways that they inhibit, and their relation to cancer. Thus, it has been difficult to formulate specific hypotheses regarding what to expect (Which cancer types? In which patients? When?), and it will take time until we feel confident that all relevant risks are well characterized. Through RCT meta-analyses and observational studies including the biologics registers, some data have emerged. So far, but with exceptions both in terms of risks observed and absence of data, the emerging picture is reassuring rather than alarming.
Insights
Biologics used for rheumatoid arthritis (RA) treatment have raised cancer concerns. Current data from meta-analyses and observational studies suggest a generally reassuring safety profile, though further research is needed.
Area of Science:
- Rheumatology
- Oncology
- Pharmacology
Background:
- Biologic therapies have been used for rheumatoid arthritis (RA) for approximately a decade.
- Concerns regarding the safety profiles of biologics, particularly concerning cancer risk, have been raised.
- The precise relationship between biologic mechanisms and cancer development remains incompletely understood.
Purpose of the Study:
- To evaluate the available data on cancer risk associated with biologic treatments for RA.
- To assess the current understanding of the safety profile of biologics concerning oncogenesis.
- To determine if the emerging data supports or refutes initial safety concerns.
Main Methods:
- Systematic review and meta-analyses of randomized controlled trials (RCTs).
- Analysis of observational studies, including biologic treatment registers.
- Longitudinal data collection to characterize cancer risks over time.
Main Results:
- Emerging data from meta-analyses and observational studies have been analyzed.
- While some exceptions and data gaps exist, the overall picture regarding cancer risk appears reassuring.
- Specific cancer types, patient populations, and temporal relationships require further characterization.
Conclusions:
- The current evidence suggests that the cancer risk associated with biologic treatments for RA is not alarming.
- Continued monitoring and research are necessary to fully characterize the long-term safety of these therapies.
- Further studies should focus on identifying specific risk factors and cancer types potentially associated with biologics.
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