Adverse Events | TRT Group (n = 99) | non-TRT Group (n = 98) | P value |
---|---|---|---|
Any Grades | 81 (81.8%) | 82 (83.7%) | 0.874 |
G3-4 Totally | 28 (28.3%) | 27 (27.6%) | 0.909 |
Leucopenia /White-cell count decreased | 4 (4.0%) | 2 (2.0%) | 0.683 |
Neutropenia /Neutrophil count decreased | 8 (8.1%) | 12(12.2%) | 0.356 |
Thrombocytopenia /Platelet count decreased | 1 (1.0%) | 2 (2.0%) | 0.621 |
Anaemia | 1 (1.0%) | 2 (2.0%) | 0.621 |
Nausea | 4 (4.0%) | 7 (7.1%) | 0.373 |
Decreased appetite | 1 (1.0%) | 3 (3.1%) | 0.369 |
Constipation | 0 (0%) | 0 (0%) | / |
Diarrhea | 0 (0%) | 2 (2.0%) | 0.246 |
Radiation esophagitis | 4 (4.0%) | / | / |
Pneumonitis | 6 (6.1%) | 3 (3.1%) | 0.498 |
Myocarditis | 3 (2.0%) | 0 (0%) | 0.497 |
Hypothyroid | 1 (1.0%) | 0 (0%) | 1.000 |
Atrial fibrillation | 0 (0%) | 1 (1.0%) | 0.497 |