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Tailored versus high-dose chemotherapy as adjuvant breast cancer treatment
- Richard De Boer1
© Current Science Ltd 2000
- Published: 1 December 2000
- breast cancer
- high-dose chemotherapy
Efforts to improve the efficacy of adjuvant chemotherapy in patients with high risk EBC include the use of increased doses, both within the conventional dose range and at high doses, where the associated haematological toxicity necessitates bone marrow support. Whether adjuvant HDC impacts upon survival remains controversial, with recent publications generally not supporting superiority over standard therapies. Patients receiving standard chemotherapy all receive the same mg/m2 dose, but it has been shown that drug distribution varies greatly among individual patients. Thus, some patients may be overdosed while others may be under-dosed. The authors developed an individualised FEC regimen in an attempt to improve outcomes in these patients. The treatment was tailored to achieve haematologic equitoxicity between patients, using this as a surrogate marker for equieffective doses.
To compare TFEC regimen with conventional therapy followed by consolidation with HDC with stem cell support.
Patients <60 years of age with high-risk primary BC were randomised after surgery to receive either nine cycles of TFEC (3-weekly) to haematological equitoxicity with granulocyte colony-stimulating factor (G-CSF) support, or three cycles of standard 3-weekly FEC followed by HDC with cyclophosphamide, thiotepa, and carboplatin, with bone-marrow or peripheral-blood stem-cell support. There were six defined dose levels in the TFEC schedule. All patients received the same dose for cycle 1 and then were either dose-escalated, -unchanged or -decreased depending upon haematologic parameters. Following chemotherapy, patients in both groups received radiation and tamoxifen for 5 years. The primary outcome measure was RFS, and analysis was by intention to treat.
Between 1994-98, 525 patients were divided into two treatment groups, TFEC (n = 251) and HDC (n = 274). In the TFEC group, 244 patients received at least six cycles of treatment (214 received all nine). In the HDC group, 266 patients received at least three cycles of FEC and 264 received HDC. At a median follow-up of 34?3 months, there were 81 BC relapses in the TFEC group versus 113 in the HDC group (P = 0.04). The 3 year RFS rates were estimated at 72% and 63%, respectively. In the TFEC group, 60 patients died, compared with 82 in the HDC group and the calculated 3 year overall survival rates were 83% and 77%, respectively (P = 0.12). Seven patients in the TFEC group died of AML or MDS. The estimated Kaplan-Meier risk at 3.2 years was 4.55%. Patients who received HDC experienced more grade 3 and 4 toxicities, including anorexia, diarrhoea, infections, nausea, and stomatitis (P<0.0001). Seven patients in the TFEC group and five in the HDC group were treated for cardiac symptoms.
Tailored FEC with G-CSF support resulted in a significantly improved RFS and fewer grade 3 and 4 toxicities compared with marrow-supported HDC as adjuvant therapy for women with high-risk EBC. However, the TFEC regimen was associated with an increased risk of AML and MDS. It is too early to determine if there is a difference in overall survival, although the calculated 3 year survival was not statistically significant. Subanalysis of the tailored arm showed that RFS rates were virtually identical among different FEC doses.
- Bergh J, Wiklund T, Erikstein B, Lidbrink E, Lindman H, Malmstrom P, Kellokumpu-Lehtinen P, Bengtsson N-O, Soderlund G, Anker G, Wist E, Ottosson S, Salminen E, Ljungman P, Holte H, Nilsson J, Blomqvist C, Wilking N: Tailored fluorouracil, epirubicin, and cyclophosphamide compared with marrow-supported high-dose chemotherapy as adjuvant treatment for high-risk breast cancer: a randomised trial. Lancet. 2000, 356: 1384-1391.View ArticlePubMedGoogle Scholar