Characteristics (N = 527) | Value No. (%) |
---|---|
Sex | Â |
 Male/Female | 381 (72.3)/146 (27.7) |
Age at start of first ICI cycle (in years) | 70 [17-90] |
Primary tumor localization | Â |
 Respiratory tract/Head and neck/Digestive tract | 214/88/70 |
 Urinary tract/Hepatocellular, Biliary Tract/Female genital organs | 67/35/24 |
 Skin/Breast/Others | 15/11/3 |
Comorbidities* (prior to the initiation of ICI therapy) | 315 (59.8) |
Immune-related comorbidities** (prior to initiation of ICI therapy) | 62 (11.8) |
ICI treatment line | Â |
 First or adjuvant | 291 (55.2) |
 Second | 151 (28.7) |
 Third or later | 85 (16.2) |
ICI agent | Â |
 Anti-PD-1 antibody (nivolumab/pembrolizumab) | 216/204 |
 Anti-PD-L1 antibody (atezolizumab/durvalumab/avelumab) | 106/15/6 |
 Anti-CTLA-4 antibody (ipilimumab) | 56 |
ICI Combination regimen | Â |
 Anti-PD-(L)1 antibody Monotherapy | 302 |
 Anti-PD-(L)1 antibody and Chemotherapy | 192 |
 Anti-CTLA-4 antibody and Anti-PD-(L)1 antibody | 56 |
 Anti-CTLA-4 antibody and Anti-PD-(L)1 antibody and Chemotherapy | 23 |
ICI Combination regimen; Chemotherapy | Â |
 Cytotoxic Drugs; platinum/taxane/5-FU   pemetrexed/etoposide | 137/37/30 46/30 |
 Antiangiogenic Agents; bevacizumab/lenvatinib/axitinib | 44/14/2 |