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. Author manuscript; available in PMC: 2020 Sep 8.
Published in final edited form as: J Surg Res. 2019 May 27;243:1–7. doi: 10.1016/j.jss.2019.04.086

Table 1 –

Univariable analysis comparing clinical and tumor characteristics of patients with benign disease versus those with malignant disease.

Characteristic Benign cohort, n = 25 (%) Malignant cohort, n = 10 (%) P-value
Gender 0.283
 Male 10 (40) 6 (60)
 Female 15 (60) 4 (40)
Race 0.717
 Caucasian 20 (80) 9 (90)
 African American 4 (16) 1 (10)
 Asian 1 (4) 0 (0)
 Unknown 0 (0) 0 (0)
Age at time of operation (y) 38 ± 20 38 ± 14 0.930
Primary tumor site 0.333
 Adrenal 17 (68) 7 (70)
 Periaortic 3 (12) 1 (10)
 Bladder 0 (0) 1 (10)
 Neck/paratracheal 1 (4) 1 (10)
 Retroperitoneal 4 (16) 0 (0)
Genetics 0.262
 No germline genetic mutation 13 (52) 2 (20)
 SDHB 6 (24) 4 (40)
 VHL 3 (12) 2 (20)
 MEN2A 1 (4) 0 (0)
 HIF2a 0 (0) 1 (10)
 MAX 0 (0) 1 (10)
 KIF1B 1 (4) 0 (0)
 NF1 1 (4) 0 (0)
Postoperative biochemical response 0.207
 Partial biochemical response 2 (8) 2 (20)
 Complete biochemical response 20 (80) 5 (50)
 Unknown 3 (12) 3 (30)
Body mass index at time of operation (kg/m2) 27.9 ± 8.4 29.1 ± 6.3 0.692
Serum miR-210 level (normalized) 3.0987 ± 1.2278 2.3299 ± 0.5078 0.013
Tumor size (cm) 4.1 ± 2.3 6.7 ± 5.0 0.03

Categorical values expressed as n (%) rounded to the nearest percentage. Continuous variables expressed as mean ± standard deviation. The miR-210 expression level is normalized.

SDHB = succinate dehydrogenase complex subunit B mutation; VHL = von Hippel-Lindau disease; MEN2A = multiple endocrine neoplasia type 2A; HIF2a = hypoxia-inducible factor a mutation; MAX = myc-associated factor X mutation; KIF1B = kinesin family member 1B mutation; NF1 = neurofibromatosis 1.