Preoperative and perioperative chemotherapy with 5-fluorouracil as continuous infusion in operable breast cancer expressing a high proliferation fraction:: cytotoxic treatment during the surgical phase

被引:9
作者
Colleoni, M
Curigliano, G
Minchella, I
Peruzzotti, G
Nolè, F
Mazzarol, G
Renne, G
Orlando, L
Rocca, A
Veronesi, P
Intra, M
Viale, G
Sandri, MT
Severi, G
Goldhirsch, A
机构
[1] European Inst Oncol, Dept Med, Div Med Oncol, I-20141 Milan, Italy
[2] European Inst Oncol, Div Pathol & Lab Med, I-20141 Milan, Italy
[3] Univ Milan, Sch Med, European Inst Oncol, Milan, Italy
[4] European Inst Oncol, Div Senol, I-20141 Milan, Italy
[5] European Inst Oncol, Div Epidemiol, I-20141 Milan, Italy
关键词
fluorouracil; operable breast cancer; perioperative chemotherapy;
D O I
10.1093/annonc/mdg411
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Experimental data on perioperative chemotherapy (PeCT) indicate that its initiation might be most useful if administered as close as possible to the time of first 'disturbance of the tumour'. Regimens including 5-fluorouracil (5-FU) as continuous infusion are commonly used in the preoperative setting, especially for large tumours and locally advanced disease. We therefore evaluated the role of PeCT with 5-FU as continuous infusion after preoperative chemotherapy (PreCT), covering the surgical phase and acute wound healing period, in patients with breast cancer too large to attempt breast-conserving surgery upon diagnosis. Patients and methods: Breast cancer patients, clinical stages T2-T3, N0-N2, M0, and Ki-67 labelling index greater than or equal to20%. were treated every 3 weeks with a maximum of six courses of vinorelbine 20 mg total dose intravenously (i.v.) on days 1 and 3, cisplatin 60 mg/m(2) i.v. on day 1 and 5-FU 200 mg/m(2)/day as a continuous infusion (ViFuP regimen). Patients who achieved a clinical and radiological objective remission with PreCT were also treated with perioperative 5-FU that was continued until 30 min before, and restarted immediately after surgery, prolonging infusion until 15 days after surgery. Results: Following preoperative treatment, 39 of 49 evaluable patients [80%; 95% confidence interval (0) 70% to 90%] had an objective response. Pathological complete remission (pCR) was achieved in 14 (29%) patients. No relevant clinical or haematological toxicity due to PeCT was observed. In 36 patients submitted to PeCT the rate of pCR was 33% (95% CI 18% to 48%). The highest response of the primary tumour to PreCT and PeCT was observed in women with tumours not expressing estrogen and progesterone receptors (pCR 46%; 95% CI 19% to 73%). Conclusions: Preoperative therapy can be protracted into the surgical (and wound healing) period without significant additional short-term toxicity. Proper selection of patients according to biological features might improve the therapeutic yield of preoperative therapies.
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页码:1477 / 1483
页数:7
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