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. 2020 Sep 17;26(1):21–29. doi: 10.1634/theoncologist.2020-0165

Table 1.

SUVmax among different groups of 108 patients with gastroenteropancreatic neuroendocrine tumors on SSA monotherapy

Baseline characteristics Patients, n Mean SUVmax ± SD p value a Effect size b (95% CI)
Gender
Male 81 57.9 ± 39.5 .56
Female 27 55.0 ± 40.5
Age, years
≤50 20 63.8 ± 45.1 .72
<50 and ≤60 38 56.0 ± 39.2
<60 and ≤70 32 53.2 ± 39.2
>70 18 53.7 ± 38.8
Tumor site
Gastrointestinal tract 81 45.8 ± 28.4 <.001 72.1% (57.1–88.4%)
Pancreas 27 87.6 ± 52.0
Tumor grade
1 53 57.7 ± 38.2 .36
2 46 56.1 ± 44.3
Ki67 index
≤5% 61 52.8 ± 35.6 .97
>5% 26 59.8 ± 49.2
Mitotic count
<2 per 10 HPFs 55 55.5 ± 39.8 .58
≥2 per 10 HPFs 22 59.9 ± 39.0
Germline mutation
Yes 9 53.5 ± 36.9 .89
No 99 56.5 ± 40.3
Functioning tumor
Yes 49 62.7 ± 31.7 .16
No 59 48.5 ± 44.9
Chromogranin A
Normal (≤95 ng/mL) 34 63.0 ± 46.0 .87
Elevated (>95 ng/mL) 71 53.4 ± 37.0
Urine 5‐HIAA
Normal (≤15 mg/day) 39 53.6 ± 38.2 .24
Elevated (>15 mg/day) 20 40.8 ± 20.8
SSA naïve
Yes 30 53.0 ± 36.1 .69
No 78 57.5 ± 41.4
a

Comparisons among groups were made using one‐way analysis of variance (ANOVA) on log‐transformed SUVmax data.

b

Effect size was estimated by taking antilog transformations of the ANOVA results.

Abbreviations: 5‐HIAA, 5‐hydroxyinidoleacetic acid; CI, confidence interval; HPF, high‐power field; SSA, somatostatin analog; SUVmax, maximum standardized uptake value.