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. 2022 Nov 28;12:20495. doi: 10.1038/s41598-022-23319-1

Table 4.

Prevalence of high tumour mutational burden (≥ 10 mutations/Mb) in adult solid tumours by cancer type and stage.

Cancer Prevalence from random-effect model (95% CI)a
Overall Early stage Advanced stage
Gastrointestinal cancers
Anal cancer 15.7% (8.8–24.1%)
Appendiceal cancer
Colon cancerc
Colorectal cancerc 8.5% (7.1–10.1%)
Esophageal cancer 32.9% (26.9–39.2%)
Gastric cancer 13.9% (10.9–17.1%) 44.2% (17.3–73.0%), I2 = 0.9b
Liver cancer 1.4% (0.2–3.6%) 3.5% (0.0–11.2%), I2 = 0.93b
Pancreatic cancer 0.0% (0.0–1.7%)
Rectal cancerc
Small bowel cancer 19.1% (11.8–27.8%)
Genitourinary tract cancers
Bladder/urothelial cancer 38.1% (21.4–56.4%), I2 = 0.98b 60.3% (53.3–67.1%) 43.6% (21.9–66.7%), I2 = 0.96b
Kidney cancer
Penile cancer
Prostate cancer 4.0% (2.3–6.3%), I2 = 0.91b 7.1% (3.9–11.2%)
Testicular cancer 3.7% (0.8–8.3%)
Breast and gynaecological cancers
Breast cancer 7.2% (1.6–16.4%), I2 = 1b 9.4% (7.6–11.2%), I2 = 0.77b
Cervical cancer 23.7% (20.1–27.5%) 21.3% (12.7–31.4%)
Endometrial cancer (EC) 43.0% (39.1–46.9%) 18.3% (10.6–27.5%)
Ovarian cancer 1.6% (0.0–6.6%)
Uterine cancer (excl. EC)
Vulvar cancer 16.9% (9.0–26.6%)
Thoracic cancers
Lung cancer 27.5% (16.0–40.8%), I2 = 0.99b 58.7% (52.4–65.0%) 29.0% (20.1–38.7%), I2 = 0.97b
Thymic malignancy
Biliary tract cancers
Ampullary cancer
Bile duct/gallbladder 9.5% (3.3–18.2%) 0.0% (0.0–2.7%)
Head and neck cancers, sarcomas, and skin cancers
Head and neck cancers 8.6% (1.8–19.4%), I2 = 0.95b 3.7% (0.5–9.1%)
Sarcomas 1.7% (0.4–3.6%), I2 = 0.14
Skin cancers 52.6% (49.7–55.5%) 42.5% (15.5–72.0%), I2 = 0.92b
Central nervous system tumours, endocrine tumours, neuroendocrine tumours, and other cancers
Brain tumours 2.8% (0.0–8.3%)
Endocrine tumours 5.8% (3.8–8.2%) 2.5% (0.0–7.4%)
Neuroendocrine tumours 24.8% (22.9–26.7%) 5.7% (1.7–11.8%)
Other cancersd

aHeterogeneity across studies was presented based on the point estimate of I2 score and heterogeneity test, if ≥ 2 records were available for each cancer type and stage group.

bStatistically significant heterogeneity across studies (p < 0.05).

cWe analysed the pooled prevalence of pan-tumour biomarkers separately based on estimates including (1) colon cancer only, (2) rectal cancer only, and (3) tumours at any sites in the colon and the rectum, obtaining pooled prevalence estimates described as “colon cancer”, “rectal cancer”, and “colorectal cancer”, respectively.

dOther caners include cancer of unknown primary, cancer of unknown primary-neuro, germ cell tumour, peritoneal cancer, and underspecified cancer.

See Supplementary Tables S7 and S12 for the number of records included in the analysis and the references.