Table 2.
Skin toxicity grading scale
| Grade | Skin toxicity | Occurrence | Suggested modification |
|---|---|---|---|
| 1 | Numbness, dysesthesia, paresthesia, tingling, painless swelling, erythema, or discomfort of the hands or feet that does not disrupt the patient’s normal activities | Any occurrence | Continue treatment with sorafenib and consider topical therapy for symptomatic relief |
| 2 | Painful erythema and swelling of the hands or feet and/or discomfort affecting the patient’s normal activities | First occurrence | Continue treatment with sorafenib and consider topical therapy for symptomatic relief; if no improvement within 7 days, see below |
| No improvement within 7 days or second or third occurrence | Interrupt sorafenib treatment until toxicity resolves to grade 0–1; when resuming treatment, decrease dose by one dose level (400 mg daily or 400 mg every other day) | ||
| Fourth occurrence | Discontinue treatment | ||
| 3 | Moist desquamation, ulceration, blistering, or severe pain of the hands or feet, or severe discomfort that causes the patient to be unable to work or perform activities of daily living | First or second occurrence | Interrupt sorafenib treatment until toxicity resolves to grade 0–1; when resuming treatment, decrease dose by one dose level (400 mg daily or 400 mg every other day) |
| Third occurrence | Discontinue treatment |
From Nexavar® (sorafenib) [package insert]. West Haven, CT: Bayer Healthcare, 2005.