Table S1. Capecitabine dose adjustments for non-hematologic AE’s.
AE incidence | Grade 2 | Grade 3 | Grade 4 |
---|---|---|---|
1st appearance | Interrupt treatment until resolved to grade 0–1, then continue at same dose with prophylaxis where possible | Interrupt treatment until resolved to grade 0–1, then continue at 75% of original dose with prophylaxis where possible | Discontinue treatment unless Investigator considers it to be in the best interests of the patient to continue at 50% of original dose, once toxicity has resolved to grade 0–1 |
2nd appearance of same toxicity | Interrupt treatment until resolved to grade 0–1, then continue at 75% of original dose |
Interrupt treatment until resolved to grade 0–1, then continue at 50% of original dose | – |
3rd appearance of same toxicity | Interrupt treatment until resolved to grade 0–1, then continue at 50% of original dose |
Discontinue treatment permanently (off study) unless it is considered to be by the investigator in the best interest of the patient to stay on treatment | – |
4th appearance of same toxicity | Discontinue treatment permanently (off study) unless it is considered to be by the investigator in the best interest of the patient to stay on treatment | – | – |