# Tofacitinib Use in a Patient With Rheumatoid Arthritis and Polycythemia Vera: A Case Report

**Authors:** Milan Bogojevic, Rifat Medjedovic, Milica Markovic, Nikola Bakic, Dragana Pravilovic Lutovac

PMC · DOI: 10.1002/ccr3.71730 · Clinical Case Reports · 2026-01-02

## TL;DR

Tofacitinib successfully treated rheumatoid arthritis in a patient with polycythemia vera without worsening blood conditions.

## Contribution

Demonstrates tofacitinib's efficacy for rheumatoid arthritis in a patient with polycythemia vera, highlighting its hematologic safety.

## Key findings

- Tofacitinib achieved clinical and ultrasonographic remission of rheumatoid arthritis within 3 months.
- Hematologic parameters remained stable during tofacitinib treatment.
- Tofacitinib had minimal impact on polycythemia vera-related erythrocytosis.

## Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by synovial inflammation and joint destruction, whereas polycythemia vera (PV) is a myeloproliferative neoplasm driven by the Janus kinase (JAK)2 V617F mutation, resulting in erythrocytosis and increased thromboembolic risk. Although JAK inhibitors are established in rheumatology, most selectively inhibit JAK1 and JAK3, sparing JAK2 activity, which is central to PV pathogenesis. We describe a 61‐year‐old woman with seropositive RA and JAK2 V617F‐positive PV. Treatment for polycythemia vera included hydroxyurea. Methotrexate and sulfasalazine were prescribed for rheumatoid arthritis but were withdrawn due to intolerance, and therapy was switched to tofacitinib 5 mg twice daily. Within 3 months, she achieved clinical and ultrasonographic remission of RA, with improvement of inflammatory markers. Hematologic parameters remained stable throughout follow‐up. After 6 months, a mild improvement allowed reduction in hydroxyurea dosing, although further tapering resulted in recurrence of erythrocytosis. After 12 months of therapy, RA remission persisted without adverse events or cytopenias. Tofacitinib demonstrated rheumatologic efficacy but minimal effect on PV‐related hematologic activity.

Tofacitinib effectively induced remission of rheumatoid arthritis in a patient with concomitant polycythemia vera, demonstrating strong rheumatologic efficacy while maintaining hematologic safety.Its limited impact on erythrocytosis underscores the need for JAK2‐directed therapies when treating patients with overlapping autoimmune and myeloproliferative diseases.

Tofacitinib effectively induced remission of rheumatoid arthritis in a patient with concomitant polycythemia vera, demonstrating strong rheumatologic efficacy while maintaining hematologic safety.

Its limited impact on erythrocytosis underscores the need for JAK2‐directed therapies when treating patients with overlapping autoimmune and myeloproliferative diseases.

## Linked entities

- **Genes:** JAK2 (Janus kinase 2) [NCBI Gene 3717]
- **Chemicals:** tofacitinib (PubChem CID 9926791), hydroxyurea (PubChem CID 3657), methotrexate (PubChem CID 4112), sulfasalazine (PubChem CID 5339)
- **Diseases:** rheumatoid arthritis (MONDO:0008383), polycythemia vera (MONDO:0009891)

## Full-text entities

- **Genes:** JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, JAK1 (Janus kinase 1) [NCBI Gene 3716] {aka AIIDE, JAK1A, JAK1B, JTK3}, JAK3 (Janus kinase 3) [NCBI Gene 3718] {aka JAK-3, JAK3_HUMAN, JAKL, L-JAK, LJAK}
- **Diseases:** joint destruction (MESH:D008105), RA (MESH:D001172), autoimmune disease (MESH:D001327), seropositive (MESH:D006679), PV (MESH:D011087), cytopenias (MESH:D006402), inflammatory (MESH:D007249), thromboembolic (MESH:D013923), erythrocytosis (MESH:D011086), myeloproliferative neoplasm (MESH:D009369)
- **Chemicals:** Tofacitinib (MESH:C479163), sulfasalazine (MESH:D012460), Methotrexate (MESH:D008727), hydroxyurea (MESH:D006918)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** JAK)2 V617F

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12758988/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12758988/full.md

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Source: https://tomesphere.com/paper/PMC12758988