Petit T, Wilt M, Velten M, Millon R, Rodier J-F, Borel C, Mors R, Haegelé P, Eber M, Ghnassia J-P
Department of Medical Oncology, Centre de Lutte Contre le Cancer Paul Strauss, 3 rue de la Porte de l'Hôpital, 67065 Strasbourg Cedex, France.
Eur J Cancer. 2004 Jan;40(2):205-11. doi: 10.1016/s0959-8049(03)00675-0.
The aim of this study was to evaluate the predictive value of five different biological factors in breast cancer patients treated with neoadjuvant anthracycline-based chemotherapy: (1) tumour grade scored according to the Elston-Ellis classification, (2) hormonal receptor (HR) status; (3) tumour cell proliferation evaluated by Ki-67 staining, (4) HER-2 and topoisomerase II alpha (TopoIIalpha) expression evaluated by immunohistochemistry (IHC), (5) HER-2 and TopoIIalpha amplification evaluated by real-time polymerase chain reaction (PCR). 119 patients with operable breast cancer were treated with six cycles of FEC (100 5-fluorouracil (5-FU) 500 mg/m2, Epirubicin 100 mg/m2, Cyclophosphamide 500 mg/m2). Tumour response was assessed clinically and by computed tomography (CT) scan, then by pathological assessment. The clinical overall response (OR) was 80%, with 19% of complete responders (CR). The radiological OR was 71%, with 16% of CR. A pathological CR was demonstrated in 13% of the patients according to the Sataloff classification. In the multivariate analysis, the absence of HR expression and Ki-67 > or = 20% were predictive for a clinical CR. A high tumour grade was predictive for a pathological CR. Overexpression or amplification of HER2 or Topollcalpha were not predictive of response.
本研究旨在评估5种不同生物学因素对接受以蒽环类药物为基础的新辅助化疗的乳腺癌患者的预测价值:(1)根据Elston-Ellis分类法评定的肿瘤分级;(2)激素受体(HR)状态;(3)通过Ki-67染色评估的肿瘤细胞增殖;(4)通过免疫组织化学(IHC)评估的HER-2和拓扑异构酶IIα(TopoIIα)表达;(5)通过实时聚合酶链反应(PCR)评估的HER-2和TopoIIα扩增。119例可手术乳腺癌患者接受了6个周期的FEC方案化疗(氟尿嘧啶(5-FU)500mg/m²、表柔比星100mg/m²、环磷酰胺500mg/m²)。通过临床检查和计算机断层扫描(CT)评估肿瘤反应,随后进行病理评估。临床总缓解率(OR)为80%,其中完全缓解者(CR)占19%。影像学OR为71%,CR占16%。根据Sataloff分类,13%的患者出现病理CR。在多因素分析中,HR表达缺失和Ki-67≥20%可预测临床CR。高肿瘤分级可预测病理CR。HER2或TopoIIα的过表达或扩增不能预测疗效。