Efficacy of up-front 5-fluorouracil - Epidoxorubicin - cyclophosphamide (FEC) chemotherapy with an increased dose of epidoxorubicin in high-risk breast cancer patients

E. Van Der Wall, E. J.T. Rutgers, M. J. Holtkamp, J. W. Baars, J. H. Schornagel, J. L. Peterse, J. H. Beijnen, S. Rodenhuis

Research output: Contribution to journalArticlepeer-review

14 Scopus citations


The prognosis of patients with stage IIIB breast carcinoma with tumour spread to the apical axillary lymph nodes has hardly improved despite adequate locoregional control and the introduction of systemic adjuvant therapy. A combined modality regimen that includes anthracyclin-based chemotherapy, high-dose chemotherapy with peripheral stem cell support and radiation and hormonal therapy is currently under investigation in this subset of patients. The present study aims to document the efficacy and feasibility of dose-intensive epidoxorubicin in combination with a standard dose of 5-fluorouracil and cyclophosphamide as up-front chemotherapy in this setting. A preoperative chemotherapy regimen consisting of three courses of 5-fluorouracil 500 mg m 2, epidoxorubicin 120 mg m 2 and cyclophosphamide 500 mg m 2 (FE120C) was administered at 21 day intervals without haematopoietic growth factors to 70 patients with apex node-positive disease. All patients were below 60 years of age and had not had prior chemotherapy or radiotherapy. Sixty-six patients were evaluable for clinical response and histopathological examination could be performed in 62 of these. Thirteen patients achieved a clinical complete response (20%). Of these patients, microscopic examination of the mastectomy specimen revealed absence of malignant cells in two and exclusively ductal carcinoma in situ (DCIS) in another two patients. In addition, of the 46 patients (70%) with a clinical partial response, at pathological examination one patient had sclerosis only and four had DCIS. This results in a pathological complete response in three (5%) of all patients and absence of invasive carcinoma in 10%. None of the patients progressed during chemotherapy. The major toxicity was moderate bone marrow suppression with a median white blood count (WBC) nadir of 1800 μl 1 (range 500-4900). Other toxicities were mild. The full planned dose could be given without delays in 66 of 70 patients. FE120C is well tolerated and is highly effective as up-front chemotherapy in relatively young patients with high-risk breast cancer, with a 90% (CI 74 98%) clinical objective response rate.

Original languageEnglish (US)
Pages (from-to)1080-1085
Number of pages6
JournalBritish journal of cancer
Issue number9
StatePublished - 1996
Externally publishedYes


  • Breast cancer
  • High-dose epidoxorubicin
  • Up-front chemotherapy

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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