Heller W, Mazhar D, Ward R, Sinnett H D, Lowdell C, Phillips R, Shousha S, Fayaz A, Palmieri C, Coombes R C
Department of Medical Oncology, Cancer Research UK Laboratories, Faculty of Medicine, Imperial College London, London W6 8RF, UK.
Oncol Rep. 2007 Jan;17(1):253-9. doi: 10.3892/or.17.1.253.
The objective of this study was to evaluate the clinical response of locally advanced breast cancer (LABC) to neoadjuvant (NA) chemotherapy with 5-fluorouracil, epirubicin and cyclophosphamide (FEC) and to study the role of docetaxel in patients who fail to respond to first-line chemotherapy. Patients were enrolled who had primary tumours without distant metastasis that were too extensive for conservative surgery. All underwent NA chemotherapy for breast cancer and thereafter surgery and/or radical radiotherapy. NA chemotherapy with FEC was administered to 88 patients between February 1998 and June 2005. A median of 6 cycles of FEC (range 1-8) was given, followed in 21 cases by a median of 4 cycles (range 2-6) of docetaxel. Where clinically established, with FEC the clinical complete response (cCR) was 22/81 (27%), clinical partial response (cPR) 41/81 (51%), clinical stable disease (cSD) 18/81 (22%). In patients where the response to FEC was regarded as insufficient, docetaxel was given. Response rates were cCR 3/21 (14%); cPR 10/21 (48%), cSD 8/21 (38%). There were 11 cases of pathological complete response (pCR), 9 in the FEC-only group and 2 in the docetaxel group. Following chemotherapy 49 (56%) patients underwent mastectomy, 32 (36%) breast conserving surgery and 5 (6%) radical radiotherapy, giving a breast conservation rate of 42%. Two patients died before receiving surgery or radical radiotherapy. The results show that neoadjuvant FEC is a reasonable NA therapy in breast cancer and that docetaxel is effective in FEC refractory cases. Only 8 of 81 (10%) assessable patients did not respond to any chemotherapy, giving an overall clinical response rate of 90%, which is comparable to studies in which taxanes were given irrespective of response to preceding therapy with antracycline including regimes.
本研究的目的是评估局部晚期乳腺癌(LABC)对含5-氟尿嘧啶、表柔比星和环磷酰胺(FEC)的新辅助化疗(NA)的临床反应,并研究多西他赛在一线化疗无反应患者中的作用。纳入的患者患有原发性肿瘤,无远处转移,但肿瘤范围过大无法进行保守手术。所有患者均接受乳腺癌新辅助化疗,之后进行手术和/或根治性放疗。1998年2月至2005年6月期间,88例患者接受了FEC新辅助化疗。FEC化疗的中位周期数为6个周期(范围1 - 8个周期),其中21例患者在FEC化疗后中位接受了4个周期(范围2 - 6个周期)的多西他赛化疗。在临床评估中,接受FEC化疗的患者临床完全缓解(cCR)为22/81(27%),临床部分缓解(cPR)为41/81(51%),临床疾病稳定(cSD)为18/81(22%)。对于FEC化疗反应不足的患者,给予多西他赛化疗。其反应率为cCR 3/21(14%);cPR 10/21(48%),cSD 8/21(38%)。有11例病理完全缓解(pCR),仅接受FEC化疗组9例,多西他赛组2例。化疗后,49例(56%)患者接受了乳房切除术,32例(36%)患者接受了保乳手术,5例(6%)患者接受了根治性放疗,保乳率为42%。2例患者在接受手术或根治性放疗前死亡。结果表明,新辅助FEC是乳腺癌合理的新辅助治疗方法,多西他赛对FEC难治性病例有效。81例可评估患者中只有8例(10%)对任何化疗均无反应,总体临床反应率为90%,这与不考虑对先前蒽环类药物治疗反应而给予紫杉烷类药物的研究结果相当。