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. 2022 Jun 10;12:876732. doi: 10.3389/fonc.2022.876732

Table 1.

Clinicopathological description of the optimization and validation cohorts.

Optimization cohort (n = 5 samples)
Cases Description
Sample #1 37 years, Seminoma, Stage I
Sample #2 28 years, Seminoma, Stage I
Sample #3 37 years, Embryonal carcinoma, Stage II
Sample #4 34 years, Embryonal carcinoma, stage III
Sample #5 44 years, healthy blood donor
Validation cohort summary (n= 107 samples)
TGCT samples 56
 Pre-orchiectomy 31
 First follow-up timing 15
 Second follow-up timing 9
 Third follow-up timing 1
Non-TGCT testicular mass samples 3
Male healthy blood donors 47
Non-testicular tumor with elevated AFP (hepatocarcinoma) 1
TGCT patients—clinicopathological features
Age (years [median, interquartile range]) 33 (8.5)
Size of tumor mass (cm [mean, interquartile range]) 5.7 (3.95)
Histology (n, %)
 Seminoma 19/31 (61.3)
 Embryonal carcinoma 2/31 (6.5)
 Mixed tumor 9/31 (29.0)
 Postpubertal-type yolk sac tumor 1/31 (3.2)
Stage (n, %)
 I 19/31 (61.3)
 II 6/31 (19.4)
 III 6/31 (19.4)
AFP positive (n, %) 9/31 (29.0)
HCG positive (n, %) 12/31 (38.7)
LDH positive (n, %) 14/31 (45.2)
Either AFP or HCG or LDH positive (n, %) 20/31 (64.5)

AFP, alpha fetoprotein; HCG, human chorionic gonadotropin; LDH, lactate dehydrogenase.