TABLE 1.
Patients, n | 3946 |
Female sex | 49.0 (1934) |
Age, years, median (quartile 1–3) | 67 (59–74) |
Months since cancer diagnosis, median (quartile 1–3) | 16 (5–49) |
Medical anticancer treatment | |
PD‐1 inhibitor | 82.4 (3251) |
PD‐L1 inhibitor | 8.3 (326) |
CTLA4 inhibitor | 18.1 (715) |
Double checkpoint inhibitor treatment | 8.8 (346) |
Concomitant chemotherapy a | 6.7 (266) |
Any previous medical anticancer treatment b | 79.1 (3120) |
Khorana score level | |
0 | 36.0 (1421) |
1 | 34.6 (1366) |
2 | 19.6 (772) |
3 | 8.0 (315) |
4+ | 1.8 (72) |
Khorana risk category | |
Low risk (0) | 36.0 (1421) |
Intermediate risk (1–2) | 54.2 (2138) |
High risk (3+) | 9.8 (387) |
Khorana guideline threshold | |
0–1 | 70.6 (2787) |
2+ | 29.4 (1159) |
Khorana components | |
Cancer type | |
Stomach | 0.3 (12) |
Pancreatic | 1.9 (74) |
Lung | 39.1 (1543) |
Lymphoma | 0.7 (27) |
Gynecologic | 1.2 (48) |
Bladder | 3.5 (137) |
Testicular | n/a (<5) |
Pre‐treatment laboratory values | |
Hemoglobin level <10 g/dl or use of erythropoiesis stimulating agent | 8.7 (343) |
Platelet count ≥ 350 x 109/L | 30.1 (1189) |
Leukocyte count > 11 x 109/L | 16.4 (646) |
Body mass index ≥ 35 kg/m2 | 1.1 (43) |
Patients registered with a treatment code for chemotherapy ±7 days in relation to date of checkpoint inhibitor treatment.
Defined as any anticancer treatment given >30 days prior to checkpoint inhibitor treatment.