# Risk of Cancer in Patients with Rheumatoid Arthritis Compared with the General Population: A Nationwide Cohort Study in Lithuania

**Authors:** Vaida Gedvilaitė, Augustė Kačėnienė, Gintarė Jonušienė, Jolanta Dadonienė, Dalia Miltinienė, Giedrė Deresevičienė, Giedrė Smailytė

PMC · DOI: 10.3390/medicina62020290 · Medicina · 2026-02-01

## TL;DR

This study finds that people with rheumatoid arthritis in Lithuania have a higher cancer risk compared to the general population, especially for certain cancers like lymphoma and skin cancer.

## Contribution

The study provides updated population-specific cancer risk data for rheumatoid arthritis patients in Lithuania, highlighting elevated risks for specific cancer types.

## Key findings

- Patients with rheumatoid arthritis had a 17% higher overall cancer risk compared to the general population.
- Hematological cancers and nonmelanoma skin cancers were most common in rheumatoid arthritis patients.
- Colorectal and mouth/pharynx cancers were significantly less common in rheumatoid arthritis patients.

## Abstract

Background and Objectives: Rheumatoid arthritis (RA) is a multisystem autoimmune disease that needs immunosuppressive treatment. Previously, studies have shown an increased risk of cancer in patients with RA compared with the general population. The purpose of this study was to explore the associations between RA and cancer risk, providing updated insights into the incidence of specific cancers in patients with RA. Materials and Methods: A total of 746 cancer cases were observed, with the most common types being nonmelanoma skin cancer (139 cases), breast cancer (87 cases), lung cancer (47 cases), and Hodgkin lymphoma (43 cases). Results: Compared with the general Lithuanian population, patients with RA had an increased overall cancer risk, with an SIR of 1.17 and 95% CI of 1.09–1.26. Hematological cancers and nonmelanoma skin cancers were the most common types of cancer in the RA population, and patients with RA had a significantly greater risk of site-specific cancers (non-Hodgkin lymphoma: SIR 4.19, 95% CI 1.57–11.18; Hodgkin lymphoma: SIR 3.03, 95% CI 2.11–4.36; myeloma: SIR 3.00, 95% CI 1.84–4.90; leukemia: SIR 2.39, 95% CI 1.62–3.54; and skin nonmelanoma: SIR 1.54, 95% CI 1.27–1.83). Male patients with RA had an increased risk of prostate and kidney cancer (SIR 1.40, 95% CI 1.12–1.75; SIR 1.85, 95% CI 1.11–3.06). Our study revealed a significantly lower risk of colorectal cancer among patients with RA. Additionally, we observed a statistically significant reduction in the risk of mouth and pharynx cancers; however, this finding was based on only three observed cases. Conclusions: Patients with RA remain particularly affected by an increased cancer risk. Knowing these risks, we need clear recommendations for specific screenings in patients with RA, which could allow for early diagnosis and better cancer treatment in the early stages.

## Linked entities

- **Diseases:** rheumatoid arthritis (MONDO:0008383), nonmelanoma skin cancer (MONDO:0002656), breast cancer (MONDO:0004989), lung cancer (MONDO:0005138), Hodgkin lymphoma (MONDO:0004952), non-Hodgkin lymphoma (MONDO:0018908), myeloma (MONDO:0009693), leukemia (MONDO:0004355), colorectal cancer (MONDO:0005575), prostate cancer (MONDO:0005159), kidney cancer (MONDO:0002367)

## Full-text entities

- **Genes:** IL6R (interleukin 6 receptor) [NCBI Gene 3570] {aka CD126, HIES5, IL-1Ra, IL-6R, IL-6R-1, IL-6RA}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** Hodgkin lymphoma (MESH:D006689), mouth and pharynx cancer (MESH:D009062), Autoimmune diseases (MESH:D001327), nonmelanoma skin cancer (MESH:D012878), hematologic malignancies (MESH:D019337), kidney cancer (MESH:D007680), cervical cancer (MESH:D002583), skin nonmelanoma (MESH:D012871), coeliac disease (MESH:D004194), injury to (MESH:D014947), autoimmune and inflammatory disorder (MESH:D007249), prostate cancer (MESH:D011471), intestinal tract carcinoma (MESH:D007414), asthma (MESH:D001249), rectal cancer (MESH:D012004), multiple myeloma (MESH:D009101), lung cancer (MESH:D008175), Cancer (MESH:D009369), type 1 diabetes (MESH:D003922), non-Hodgkin lymphoma (MESH:D008228), lymphoma (MESH:D008223), T-cell or B-cell dysfunction (MESH:D016393), inflammatory bowel disease (MESH:D015212), chronic pain (MESH:D059350), breast cancer (MESH:D001943), prostate carcinoma (MESH:D011472), diffuse large B-cell lymphomas (MESH:D016403), death (MESH:D003643), endometrial cancer (MESH:D016889), colon cancer (MESH:D015179), leukemia (MESH:D007938), breast and endometrial cancers (MESH:C537243), RA (MESH:D001172), joint damage (MESH:D007592), autoimmune rheumatic disease (MESH:D012216)
- **Chemicals:** methotrexate (MESH:D008727), methylprednisolone (MESH:D008775), adalimumab (MESH:D000068879), infliximab (MESH:D000069285), tocilizumab (MESH:C502936), azathioprine (MESH:D001379), hydrochloroquine (-), prednisolone (MESH:D011239), sulfasalazine (MESH:D012460), leflunomide (MESH:D000077339), rituximab (MESH:D000069283)
- **Species:** Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376]

## Full text

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942537/full.md

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Source: https://tomesphere.com/paper/PMC12942537