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首页> 外文期刊>Oncology: International Journal of Cancer Research and Treatment >Phase II trial in Japan of sequential administration of weekly paclitaxel followed by FEC as neoadjuvant chemotherapy for locally advanced breast cancer (KBCSG0206 trial: Kinki Breast Cancer Study Group (KBCSG)).
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Phase II trial in Japan of sequential administration of weekly paclitaxel followed by FEC as neoadjuvant chemotherapy for locally advanced breast cancer (KBCSG0206 trial: Kinki Breast Cancer Study Group (KBCSG)).

机译:在日本进行的II期临床试验,依次给予每周紫杉醇,然后进行FEC作为局部晚期乳腺癌的新辅助化疗(KBCSG0206试验:近畿乳腺癌研究小组(KBCSG))。

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OBJECTIVE: We conducted a phase II trial in Japan to evaluate the efficacy and tolerability of weekly paclitaxel followed by fluorouracil, epirubicin, and cyclophosphamide (FEC) as neoadjuvant chemotherapy (NAC) for locally advanced breast cancer (LABC). METHODS: Patients with clinical stage IIIA-IIIB breast cancer received NAC consisting of 12 once-a-week cycles of paclitaxel followed by 4 once-every-third-week cycles of FEC. RESULTS: Fifty patients with LABC were enrolled, 47 of whom were administered paclitaxel followed by FEC as NAC. The clinical response rate for all chemotherapies was 85.1%, and the pathological complete response rate was 27.7%. Regarding toxicity, grade 3-4 neutropenia was observed in 10% of patients. No serious toxicities requiring the discontinuation of treatment were encountered. The rate of breast conservation surgery was 31.9%, median survival had not been reached at the time of conclusion of this study, and the 3-year survival rate was 85.1%. Median disease-free survival was 40.2 months, and the 3-year disease-free survival rate was 62.1%. CONCLUSIONS: Weekly paclitaxel followed by FEC demonstrated efficacy and tolerable toxicity in a neoadjuvant setting for LABC.
机译:目的:我们在日本进行了一项II期试验,以评估每周紫杉醇,氟尿嘧啶,表柔比星和环磷酰胺(FEC)作为局部晚期乳腺癌(LABC)的新辅助化疗(NAC)的疗效和耐受性。方法:IIIA-IIIB期临床乳腺癌患者接受NAC,包括12个每周一次的紫杉醇周期,以及4个每三周一次的FEC周期。结果:招募了50名LABC患者,其中47人接受了紫杉醇治疗,随后接受了FEC作为NAC。所有化学疗法的临床缓解率为85.1%,病理完全缓解率为27.7%。关于毒性,在10%的患者中观察到3-4级中性粒细胞减少。没有遇到需要中止治疗的严重毒性反应。保乳手术率为31.9%,在完成本研究时尚未达到中位生存期,3年生存率为85.1%。中位无病生存期为40.2个月,三年无病生存率为62.1%。结论:每周紫杉醇联合FEC在LABC的新辅助治疗中显示出疗效和可耐受的毒性。

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