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. Author manuscript; available in PMC: 2019 Jul 14.
Published in final edited form as: Oncologist. 2009 Aug 1;14(8):800–805. doi: 10.1634/theoncologist.2009-0088

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.