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. 2022 Oct 7;20(12):2921–2929. doi: 10.1111/jth.15883

TABLE 1.

Baseline characteristics of patients with cancer initiating treatment with an immune checkpoint inhibitor

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)
a

Patients registered with a treatment code for chemotherapy ±7 days in relation to date of checkpoint inhibitor treatment.

b

Defined as any anticancer treatment given >30 days prior to checkpoint inhibitor treatment.