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. 2015 Nov;3(19):284. doi: 10.3978/j.issn.2305-5839.2015.11.14

Table 1. Dose modification based on hematological, hepatic, and other toxicities.

Conditions Dose
Hematology: for both drugs (103/mL)
   Neutrophils (≥1.5) and platelets (≥90) 100%
   Neutrophils (1.0-1.49) or platelets (≥90) 75%
   Neutrophils (<1) or platelets (<100) Delay for 1 week (or longer if needed), till recovery, then give 75% dose, consider giving filgrastim for subsequent cycles
Febrile neutropenia 75% of dose for current and subsequent cycles, use G-CSF for 1st episode, and 50% of dose for 2nd episode
Creatinine clearance: for cyclophosphamide
   ≥10 100%
   <10 75%
Hepatic function tests
   For epirubicin
        ALT (<2 ULN) and total bilirubin (≤1.17 mg/dL) 100%
        ALT (2-4× ULN) and total bilirubin (1.23-2.92 mg/dL) 50%
        ALT (>4× ULN) and total bilirubin (>2.92 mg/dL) 25%
   For docetaxel
        ALT/AST (<1.5× ULN) and alkaline phosphatase (<2.5× UNL) 100 mg/m2
        ALT/AST (1.5-3.5 ULN) and alkaline phosphatase (2.5-6× UNL) 75 mg/m2
        ALT/AST (>3.5× ULN), total bilirubin (>ULN) and alkaline phosphatase (>6× UNL) Avoid use
Dose modification for other toxicities
   ≥grade 3 non-hematologic toxicities Paclitaxel dose: hold treatment, re-evaluate treatment plan, consider discontinuing treatment with this protocol