Table 3. National Cancer Institute Common Terminology Criteria for Adverse Events Chemotherapy-Induced Adverse Effects Scores for the Silymarin and Placebo Groups a.
| Variables | Nano-Silymarin Group (n = 30) | Placebo Group (n = 30) | P-Value b |
|---|---|---|---|
| Neuropathy, at the beginning of the study | 0 (0 - 0) | 0 (0 - 0) | 1 |
| Neuropathy, at the end of course 3 | 0 (0-0) | 1 (1 - 1) | < 0.001 c |
| Neuropathy, at the end of course 6 | 1 (0 - 2) | 1 (1 - 2) | 0.610 |
| HFS, at the beginning of the study | 0 (0 - 0) | 0 (0 - 0) | 1 |
| HFS, at the end of course 3 | 0 (0 - 0) | 1 (0 - 1) | < 0.001 c |
| HFS, at the end of course 6 | 1 (0 - 1) | 1 (0 - 1.25) | 0.022 c |
Abbreviations: NCI-CTCAE, National Cancer Institute-Common Terminology Criteria for Adverse Events; HFS, hand-foot syndrome.
a Values are expressed as median (quartile range).
b Mann–Whitney test.
c P < 0.05.