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Review
. 2020 May;32(3):315-320.
doi: 10.1097/BOR.0000000000000701.

Treatment of immune checkpoint inhibitor-induced inflammatory arthritis

Affiliations
Review

Treatment of immune checkpoint inhibitor-induced inflammatory arthritis

Susanna Jeurling et al. Curr Opin Rheumatol. 2020 May.

Abstract

Purpose of review: This review summarizes the current evidence on treatment strategies for inflammatory arthritis because of cancer treatment with immune checkpoint inhibitors (ICI), prognosis of ICI-induced arthritis, and management of patients with preexisting inflammatory arthritis receiving ICI therapy.

Recent findings: Inflammatory arthritis is the most common rheumatic immune-related adverse event observed in patients receiving ICI therapy. Most patients can successfully be treated with low doses of corticosteroids or conventional synthetic disease modifying anti-rheumatic drugs (DMARDs). A small minority will develop severe symptoms requiring biologic therapy including TNF inhibitors and IL-6 receptor inhibitors. Many cases of inflammatory arthritis will resolve with cessation of ICI therapy. Some patients will develop persistent arthritis despite discontinuation. Patients with preexisting inflammatory arthritis (e.g. rheumatoid arthritis) commonly flare on ICI therapy, but can usually be managed with corticosteroids.

Summary: Inflammatory arthritis following ICI therapy for cancer is relatively common and the practicing rheumatologist should be able to recognize and manage it in conjunction with Oncology. The majority of patients respond to corticosteroids, but some will need treatment with conventional synthetic or biologic DMARDs. Additional studies should investigate the effects of immunosuppression on tumor response and the use of ICI therapy in patients with preexisting autoimmune disease.

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Conflict of interest statement

Conflicts of interest

L.C.C.: research funding from Bristol-Myers Squibb, consulting for Regeneron/Sanofi. S.J. has no conflicts of interest.

References

    1. Larkin J, Chiarion-Sileni V, Gonzalez R, et al. Five-year survival with combined nivolumab and ipilimumab in advanced melanoma. N Engl J Med 2019; 381:1535–1546. - PubMed
    1. Reck M, Rodriguez-Abreu D, Robinson AG, et al., KEYNOTE-024 Investigators. Pembrolizumab versus chemotherapy for PD-L1-positive non-small-cell lung cancer. N Engl J Med 2016; 375:1823–1833. - PubMed
    1. Motzer RJ, Escudier B, McDermott DF, et al., CheckMate 025 Investigators. Nivolumab versus everolimus in advanced renal-cell carcinoma. N Engl J Med 2015; 373:1803–1813. - PMC - PubMed
    1. Lemery S, Keegan P, Pazdur R. First FDA approval agnostic of cancer site — when a biomarker defines the indication. N Engl J Med 2017; 377: 1409–1412. - PubMed
    1. Puhr HC, Ilhan-Mutlu A. New emerging targets in cancer immunotherapy: the role of LAG3. ESMO Open 2019; 4:; e000482. - PMC - PubMed

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