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. 2022 Oct 21;8(2):e002612. doi: 10.1136/rmdopen-2022-002612

Table 3.

Patient and irAE outcomes according to bDMARD/tsDMARD type

bDMARD/ tsDMARD Type of cancer Type of irAE DMARD duration (median, weeks) Association with ICI Safety Efficacy Cancer outcomes
Anti-IL-6R Lung (n=6)
Melanoma (n=6)
Renal (n=1)
RA-like (n=10) 17 (6 ongoing) Yes (n=3) 0 Partial improvement (n=3) Progression (n=2)
Stable (n=1)
PMR-like (n=2) No (10) Small intestine perforation (n=1)
Septic shock (n=1) (ongoing chemotherapy)
Resolution (n=3)
Partial improvement (n=5)
No efficacy (n=2)
Progression (n=4)
Stable (n=2)
Partial response (n=1)
Remission (n=3)
PsA-like (n=1)
TNF inhibitors Lung (n=4)
Lymphoma (n=1)
RA-like (n=5) 8 (2 ongoing) Yes (n=3) Diverticulitis (n=1)
Pneumonitis (n=1)
Resolution (n=1)
Partial improvement (n=1)
No efficacy (n=1)
Progression (n=3)
No (n=2) 0 Resolution (n=2) Remission (n=2)
Anakinra Melanoma RA-like (n=1) 1 Yes 0 No efficacy Stable
Baricitinib Lung RA-like (n=1) 78 (ongoing) No 0 Resolution Progression
Ustekinumab Lung PsA-like (n=1) 60 (ongoing) Yes 0 Partial improvement Stable

bDMARD, biologic disease-modifying antirheumatic drug; ICI, immune checkpoint inhibitor; irAE, immune-related adverse event; PMR, polymyalgia rheumatica; PsA, psoriatic arthritis; RA, rheumatoid arthritis; tsDMARD, targeted synthetic disease-modifying antirheumatic drug.