Therapy type | Intravenous immunoglobulin | Infliximab | Combination |
Total patients, n (%) | 7 | 2 | 3 |
Baseline characteristics | |||
Age at ICI-pneumonitis diagnosis (mean, years) | 66 | 66 | 68 |
Sex | |||
Male | 4 (57) | 0 (0) | 2 (67) |
Female | 3 (43) | 2 (100) | 1 (33) |
Race | |||
Caucasian | 6 (86) | 2 (100) | 3 (100) |
African-American | 1 (14) | 0 (0) | 0 (0) |
Smoking status | |||
Never | 3 (43) | 0 (0) | 0 (0) |
Current/former | 4 (57) | 2 (100) | 3 (100) |
Pack year history (mean, years) | 29.4 | 37.5 | 32.5 |
Tumor histology | |||
Lung carcinoma | 5 (71) | 2 (100) | 2 (67) |
Non-small cell lung carcinoma | 4 (80) | 2 (100) | 2 (100) |
Small cell lung carcinoma | 1 (20) | 0 (0) | 0 (0) |
Oropharyngeal squamous cell carcinoma | 0 (0) | 0 (0) | 1 (33) |
Renal cell carcinoma | 0 (0) | 0 (0) | 0 (0) |
Pancreatic adenocarcinoma | 0 (0) | 0 (0) | 0 (0) |
Initial cancer stage* | |||
II | 1 (14) | 1 (50) | 1 (33) |
III | 3 (43) | 0 (0) | 0 (0) |
IV | 3 (43) | 1 (50) | 2 (67) |
Anticancer therapy | |||
Prior chemotherapy | 6 (86) | 2 (100) | 3 (100) |
Initial surgery | 1 (14) | 0 (0) | 1 (33) |
Prior chest radiation therapy† | 4 (57) | 1 (50) | 2 (67) |
PD-1/PD-L1 monotherapy | 2 (29) | 1 (50) | 3 (100) |
Durvalumab | 2 (100) | 0 (0) | 1 (33) |
Nivolumab | 0 (0) | 1 (100) | 1 (33) |
Pembrolizumab | 0 (0) | 0 (0) | 1 (33) |
PD-1/PD-L1-based combinations | 5 (71) | 1 (50) | 0 (0) |
Pembrolizumab+chemotherapy | 4 (80) | 0 (0) | 0 (0) |
Nivolumab+ipilimumab | 1 (20) | 1 (100) | 0 (0) |
ICI response at 3 months‡ | |||
Partial response | 1 (14) | 1 (50) | 1 (33) |
Stable disease | 4 (57) | 0 (0) | 0 (0) |
Progressive disease | 2 (29) | 1 (50) | 2 (67) |
*AJCC staging system.
†Dose of chest radiation in the range of 8–66 Gy given 276–739 days prior to steroid-refractory ICI-pneumonitis onset.
‡As defined by RECIST V.1.1 criteria.
ICI, immune-checkpoint inhibitor; PD, progressive disease.