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. Author manuscript; available in PMC: 2021 Mar 1.
Published in final edited form as: Immunol Rev. 2020 Jan 13;294(1):106–123. doi: 10.1111/imr.12832

Table 1:

Comparison of clinical features between ICI-IA, RA, and SpA

RA SpA* ICI-IA

Epidemiology 2–3 times more common in women AS more common in men Even gender distribution
Incidence peaks in 30s-50s Axial SpA most commonly presents before age 40 Adults 30s-80s exposed to ICI therapy
Time from exposure to development ranges from weeks-years

Risk Factors Tobacco smoke GI/GU infections (ReA) Largely unclear
Periodontal disease Obesity (PsA) Combination or long duration ICI therapy, multiple irAEs (persistent ICI-IA)

Joint involvement Small and large joints; classically MCPs, PIPs, wrists Some subtypes have oligoarthritis, lower extremity predominant Various subtypes: polyarthritis, large joint oligoarthritis
Axial disease rare except for C1–2 Axial disease can be seen in all subtypes Rare reports of axial disease (sacroiliitis)

Imaging findings Ultrasound: synovitis (Doppler positive); small and large joint effusions; tenosynovitis MRI: Sacroiliitis with bone marrow edema, erosions, and sclerosis Ultrasound: synovitis (Doppler positive); small and large joint effusions; enthesitis; enthesophytes
Radiographs: erosions and joint space narrowing Radiographs: facet or SI joint ankylosis; syndesmophytes; juxta-articular bone formation (PsA) Radiographs: erosions can be observed within months of symptoms (rare)

Extra-articular disease Interstitial lung disease common, can be subclinical Some subtypes associated with GI inflammation (IBD associated, ReA) Concurrent colitis reported in those on combination ICI therapy
Increased risk for lymphoma, lung cancer Skin psoriasis can be seen in all subtypes Multiple irAEs common
Ocular: scleritis Ocular: uveitis Ocular: uveitis, may not be concurrent with IA

Prognosis Chronic; requires long term treatment with DMARDs Most subtypes are chronic Varies: some self-limited but others persist
Common to have disability in 2–3 years if untreated ReA self-limited in > 90% Bone damage within months of symptom onset reported
*

Includes AS (ankylosing spondylitis) as well as axial, IBD (inflammatory bowel disease)-associated, and undifferentiated SpA (spondyloarthritis), ReA (reactive arthritis), and PsA (psoriatic arthritis); RA (rheumatoid arthritis); ICI-IA (immune checkpoint inhibitor-induced inflammatory arthritis); irAE (immune related adverse event); DMARD (disease modifying anti-rheumatic drug); MRI (magnetic resonance imaging)