High-dose chemotherapy with hematopoietic stem-cell rescue for high-risk breast cancer

被引:195
作者
Rodenhuis, S
Bontenbal, M
Beex, LVAM
Wagstaff, J
Richel, DJ
Nooij, MA
Voest, EE
Hupperets, P
van Tinteren, H
Peterse, HL
TenVergert, EM
de Vries, EGE
机构
[1] Netherlands Canc Inst, Dept Med Oncol, NL-1066 CX Amsterdam, Netherlands
[2] Erasmus Med Ctr, Dr Daniel den Hoed Canc Ctr, Rotterdam, Netherlands
[3] Univ Nijmegen Hosp, NL-6500 HB Nijmegen, Netherlands
[4] Free Univ Amsterdam, Med Ctr, Amsterdam, Netherlands
[5] Univ Hosp Maastricht, Maastricht, Netherlands
[6] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[7] Med Ctr Enschede, Enschede, Netherlands
[8] Univ Med Ctr Leiden, Leiden, Netherlands
[9] Univ Med Ctr Utrecht, Utrecht, Netherlands
[10] Univ Groningen Hosp, Groningen, Netherlands
关键词
D O I
10.1056/NEJMoa022794
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: The use of high-dose adjuvant chemotherapy for high-risk primary breast cancer is controversial. We studied its efficacy in patients with 4 to 9 or 10 or more tumor-positive axillary lymph nodes. METHODS: Patients younger than 56 years of age who had undergone surgery for breast cancer and who had no distant metastases were eligible if they had at least four tumor-positive axillary lymph nodes. Patients in the conventional-dose group received fluorouracil, epirubicin, and cyclophosphamide (FEC) every three weeks for five courses, followed by radiotherapy and tamoxifen. The high-dose treatment was identical, except that high-dose chemotherapy (6 g of cyclophosphamide per square meter of body-surface area, 480 mg of thiotepa per square meter, and 1600 mg of carboplatin per square meter) with autologous peripheral-blood hematopoietic progenitor-cell transplantation replaced the fifth course of FEC. RESULTS: Of the 885 patients, 442 were assigned to the high-dose group and 443 to the conventional-dose group. After a median follow-up of 57 months, the actuarial 5-year relapse-free survival rates were 59 percent in the conventional-dose group and 65 percent in the high-dose group (hazard ratio for relapse in the high-dose group, 0.83; 95 percent confidence interval, 0.66 to 1.03; P=0.09). In the group with 10 or more positive nodes, the relapse-free survival rates were 51 percent in the conventional-dose group and 61 percent in the high-dose group (P=0.05 by the log-rank test; hazard ratio for relapse, 0.71; 95 percent confidence interval, 0.50 to 1.00). CONCLUSIONS: High-dose alkylating therapy improves relapse-free survival among patients with stage II or III breast cancer and 10 or more positive axillary lymph nodes. This benefit may be confined to patients with HER-2/neu-negative tumors.
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收藏
页码:7 / 16
页数:10
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