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. 2020 May 30;8(1):e000469. doi: 10.1136/jitc-2019-000469

Table 1.

Adrenocortical carcinoma: patients’ and tumor characteristics

N Age
(years)
Sex
(male/female (n))
Size of tumor (cm) Ki67 index (%) Glucocorticoids
+/−other steroids
Only sex hormones Other steroid pattern No steroid excess Hormone profile n/a
All ACC samples 146 47 (18–77) 45/101 10.0
(0.5–30.0)
10 (0–80) 63 (36/27) 12 7 31 33
Primary tumors 107 47 (18–77) 32/75 11.8
(3.3–30.0)
10 (0–80) 44 (29/15) 9 4 23 27
 ENSAT I/II* 47 46 (18–77) 13/34 12.0
(3.3–28.0)
10 (0–50) 17 (10/7) 6 3 14 7
 ENSAT III* 38 47 (18–75) 13/25 10.3
(5.0–30.0)
20 (1–80) 16 (10/6) 3 1 7 11
 ENSAT IV* 20 47.5 (24–72) 6/14 13.0
(7.0–25.0)
10 (1–30) 11 (9/2) 0 0 3 6
Local recurrences 16 44 (20–70) 6/10 4.5
(1.5–9.4)
12.5 (5–20) 6 (2/4) 2 2 3 3
Distant metastases 23 41 (19–72) 7/16 1.7
(0.5–4.0)
17.5 (5–40) 13 (8/5) 1 1 4 4

Data represent median values with ranges or total numbers.

*Tumor stage at the time of diagnosis according to the European Network for the Study of Adrenal Tumors (ENSAT) classification.40

†In patients who experienced local recurrences or distant metastases during mitotane treatment, endocrine activity was classified according the information available at primary diagnosis.

ACC, adrenocortical carcinoma.