Breast Cancer Clinical Trial
Official title:
SBG 2000-1. Individually Dose-adjusted FEC Compared to Standard FEC as Adjuvant Chemotherapy for Node Positive or High-risk Node Negative Breast Cancer. A Randomized Study by the Scandinavian Breast Group
This is an open randomized phase III study. The primary objective of this study is to compare FEC adjuvant chemotherapy in operable breast cancer given either as fixed doses calculated according to the patients surface area or with doses adjusted according to leukopenia after course one in order to achieve hematological equitoxicity. The main aim of the study is to test whether chemotherapy dosage aimed at hematological equitoxicity will improve the effect of adjuvant chemotherapy.
Group A, FECStandard(standard FEC) is given 7 courses of 5-fluorouracil-epirubicin
(Farmorubicin)-cyclophosphamide with doses based on the patient's surface area. Leukocyte
nadir values at day 10, 12 or 13 and 15 are measured. Dose-reductions of one step according
to table 8.2.1 are performed in case of leukopenic fever or grade 4 leukopenia.
Group B FECTailored(Tailored FEC) receives course one at identical doses to group A.
Leukocyte nadir values at day 10,12 or 13 and 15 are measured. Doses of subsequent courses
are adjusted to achieve grade 3 leukopenia (leukocyte nadir 1.0 to 2.0) in patients
experiencing only grade 0 to 2 leukopenia after course one.
Dose-reductions of one step according to table 8.2.1 are performed in case of leukopenic
fever or grade 4 leukopenia .
Patients achieving only grade 0-2 leukopenia at the first course will be randomized into
continued treatment at standard doses (Group A) or to doses tailored to achieve grade 3
leukopenia (Group B). The primary comparisons will be made between these two groups of
patients.
Patients with grade 3-4 leukopenia after the first course not be randomized but followed
according to the protocol and received treatment as group A, FECStandard.
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