Mamounas E P
National Surgical Adjuvant Breast and Bowel Project Operations Center, Pittsburgh, Pennsylvania, USA.
Oncology (Williston Park). 1997 Jun;11(6 Suppl 6):37-40.
Protocol B-27, conducted by the National Surgical Adjuvant Breast and Bowel Project (NSABP), is a phase III, randomized trial designed to evaluate whether sequencing docetaxel (Taxotere) to neoadjuvant doxorubicin/cyclophosphamide (Cytoxan, Neosar) prolongs disease-free and overall survival in patients with operable breast cancer. Patients are being randomized into three groups. The control group receives four 21-day courses of doxorubicin/cyclophosphamide chemotherapy with tamoxifen (Nolvadex), followed by breast surgery (and postoperative radiation for patients receiving breast-conserving surgery). Two experimental groups receive the same doxorubicin/cyclophosphamide chemotherapy and tamoxifen, followed by docetaxel--either before (preoperative group) or after (postoperative group) surgery. In the first 11 months of the study, 283 patients--of a projected 1,606 patients over a 5-year period--have been entered. Slightly more than half of the patients are younger than 50 years of age. Nearly half of the patients presented with tumors that were more than 4.0 cm in greatest diameter. Biopsy was performed by fine-needle aspiration slightly more than half of the time. Slightly more than two-thirds of the patients had clinically negative nodes. Lumpectomy was the proposed surgery at entry in 40% to 43% of the patients. As of November 1996, toxicity information is available on 29 patients in the preoperative docetaxel group and 23 patients in the postoperative docetaxel group. So far, there have been no unexpected toxicities, but the data are too preliminary to report in detail.
由美国国立乳腺癌和肠道外科辅助治疗项目(NSABP)开展的B - 27方案是一项III期随机试验,旨在评估多西他赛(泰索帝)序贯新辅助阿霉素/环磷酰胺(环磷酰胺、异环磷酰胺)是否能延长可手术乳腺癌患者的无病生存期和总生存期。患者被随机分为三组。对照组接受四个疗程、每疗程21天的阿霉素/环磷酰胺化疗加他莫昔芬(诺瓦得士),随后进行乳房手术(接受保乳手术的患者术后接受放疗)。两个试验组接受相同的阿霉素/环磷酰胺化疗和他莫昔芬,随后接受多西他赛治疗——术前组在手术前接受,术后组在手术后接受。在该研究的前11个月,已纳入计划在5年期间入组的1606例患者中的283例。略多于一半的患者年龄小于50岁。近一半的患者所患肿瘤最大直径超过4.0厘米。略多于一半的时间采用细针穿刺活检。略多于三分之二的患者临床检查淋巴结阴性。40%至43%的患者在入组时拟行保乳手术。截至1996年11月,可获得术前多西他赛组29例患者和术后多西他赛组23例患者的毒性信息。到目前为止,尚未出现意外毒性,但数据过于初步,无法详细报告。