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. 2021 Feb 2;12(3):199–208. doi: 10.18632/oncotarget.27876

Table 2. Additional clinical information of the patients with previously normal testosterone who subsequently developed low testosterone after treatment with immunotherapy.

Clinical information of patients with normal T who developed low T after immunotherapy
Pt Age at diagnosis Immunotherapy Agent(s) Baseline T Lowest T value Resolution of low T Comorbidities Radiation Clinical trial Endocrine dysfunction during tx
1 50 Ipilimumab, Pembrolizumab Normal (314) 55 No Heart disease Local - -
2 72 Ipilimumab Normal (498) 78 No - - - -
3 66 Pembrolizumab Normal (319) 144 No Heart disease Brain - Pituitary, adrenal
4 61 Ipilimumab, Pembrolizumab Normal (338) 69 No Obese, heart disease, diabetes, hypothyroid Brain Yes -
5 82 Pembrolizumab Normal (399) 181 No Heart disease, diabetes - - -
6 59 Ipilimumab, Pembrolizumab Normal (419) < 5 No Obesity, heart disease Local - Hypophysitis
7 35 Ipilimumab, Pembrolizumab Normal (524) 170 Yes Obesity Brain Yes Pituitary, thyroid
8 85 Pembrolizumab Normal (351) 206 Yes Obesity, heart disease, previous prostate cancer - - Pituitary, adrenal
9 46 Pembrolizumab Normal (369) 22 Yes - - - Adrenal
10 52 Pembrolizumab Normal (456) 133 Yes Obesity, heart disease, OSA, previous melanoma Local - Pituitary, adrenal, and thyroid
Avg: 60.8 398.7 105.8

While these patients had diverse treatment courses, most of these patients had multiple comorbidities prior to their development of low testosterone.