Title of article :
Tailored fluorouracil, epirubicin, and cyclophosphamide compared with marrow-supported high-dose chemotherapy as adjuvant treatment for high-risk breast cancer: a randomised trial
Author/Authors :
Jonas Bergh، نويسنده , , Tom Wiklund، نويسنده , , Bj?rn Erikstein، نويسنده , , Elisabet Lidbrink، نويسنده , , Henrik Lindman، نويسنده , , Per Malmstr?m، نويسنده , , Pirkko Kellokumpu-Lehtinen، نويسنده , , Nils-Olof Bengtsson، نويسنده , , Gustaf S?derlund، نويسنده , , Gun Anker، نويسنده , , Erik Wist، نويسنده , , Susanne Ottosson، نويسنده , , Eeva Salminen، نويسنده , , Per Ljungman، نويسنده , , Harald Holte، نويسنده , , Wendy Kress and Jonas Nilsson، نويسنده , , Carl Blomqvist، نويسنده , , Nils Wilking and Scandinavian Breast Group 9401 study، نويسنده ,
Abstract :
Background
Chemotherapy drug distribution varies greatly among individual patients. Therefore, we developed an individualised fluorouracil, epirubicin, cyclophosphamide (FEC) regimen to improve outcomes in patients with high-risk early breast cancer. We then did a randomised trial to compare this individually tailored FEC regimen with conventional adjuvant chemotherapy followed by consolidation with high-dose chemotherapy with stem-cell support.
Methods
525 women younger than 60 years of age with highrisk primary breast cancer were randomised after surgery to receive nine cycles of tailored FEC to haematological equitoxicity with granulocyte colony-stimulating factor (G-CSF) support (n=251), or three cycles of FEC at standard doses followed by high-dose chemotherapy with cyclophosphamide, thiotepa, and carboplatin (CTCb), and peripheral-blood stemcell or bone-marrow support (n=274). Both groups received locoregional radiation therapy and tamoxifen for 5 years. The primary outcome measure was relapse-free survival, and analysis was by intention to treat.
Findings
At a median follow-up of 34·3 months, there were 81 breast-cancer relapses in the tailored FEC group versus 113 in the CTCb group (double triangular method p=0·04). 60 deaths occurred in the tailored FEC group and 82 in the CTCb group (log-rank p=0·12). Patients in the CTCb group experienced more grade 3 or 4 acute toxicity compared with the tailored FEC group (p<0·0001). Two treatment-related deaths (0·7%) occurred in the CTCb group. Six patients in the tailored FEC group developed acute myeloid leukaemia and three developed myelodysplastic syndrome.
Interpretation
Tailored FEC with G-CSF support resulted in a significantly improved relapse-free survival and fewer grade 3 and 4 toxicities compared with marrow-supported high-dose chemotherapy with CTCb as adjuvant therapy of women with high-risk primary breast cancer.
