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. 2023 Jan 16;46(2):64–73. doi: 10.1097/CJI.0000000000000451

TABLE 2.

Clinical features and treatment of CIP

Overall N=60 Nonrefractory CIP N=44 Refractory CIP N=16 P
Time to CIP (wk), n (%) 0.021
 <6 16 (26.7) 8 (18.2) 8 (50.0)
 ≥6 44 (73.3) 36 (81.8) 8 (50.0)
CTCAE grade, n (%) 0.211
 ≤2 36 (60.0) 29 (65.9) 7 (43.8)
 >2 24 (40.0 15 (34.1) 9 (56.2)
Symptoms, n (%) 0.025
 Shortness of breath 23 (38.3) 12 (27.3) 11 (68.8)
 Cough 21 (35.0) 19 (43.2) 2 (12.5)
 Fever 9 (15.0) 6 (13.6) 3 (18.8)
 Others 2 (3.3) 2 (4.5) 0 (0)
 No symptoms 5 (8.3) 5 (11.4) 0 (0)
Pneumonia, n (%) 0.407
 Yes 28 (46.7) 22 (50.0) 6 (37.5)
 Suspicious 6 (10.0) 3 (6.8) 3 (18.8)
 No 26 (43.3) 19 (43.2) 7 (43.8)
Starting dose of equivalent MP (mg/kg), n (%) 0.121
 <1 9 (15.0) 7 (15.9) 2 (12.5)
 1-2 19 (31.7) 17 (38.6) 2 (12.5)
 2-3 17 (28.3) 12 (27.3) 5 (31.2)
 ≥3 15 (25.0) 8 (18.2) 7 (43.8)
Antibiotic use, n (%) 1.000
 Yes 36 (60.0) 26 (59.1) 10 (62.5)
 No 24 (40.0) 18 (40.9) 6 (37.5)

Statistically significant P values are in bold.

CIP indicates checkpoint inhibitor-related pneumonitis; CTCAE, Common Toxicity Criteria for Adverse Events; MP, methylprednisolone.