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早期乳腺癌保乳手术后同步或序贯辅助放化疗的Ⅲ期试验:ARCOSEIN试验的最终结果

Phase III trial of concurrent or sequential adjuvant chemoradiotherapy after conservative surgery for early-stage breast cancer: final results of the ARCOSEIN trial.

作者信息

Toledano Alain, Azria David, Garaud Pascal, Fourquet Alain, Serin Daniel, Bosset Jean-François, Miny-Buffet Joelle, Favre Anne, Le Floch Olivier, Calais Gilles

机构信息

Department of Radiation Oncology, Henry Kaplan, Hôpital Bretonneau, Tours, France.

出版信息

J Clin Oncol. 2007 Feb 1;25(4):405-10. doi: 10.1200/JCO.2006.07.8576.

Abstract

PURPOSE

In 1996, we initiated the French multicenter phase III randomized trial to compare the effect on disease-free survival (DFS) of concurrent versus sequential chemotherapy (CT) and radiotherapy (RT) after breast-conserving surgery for stages I and II breast cancer. This report presents the clinical results with a median follow-up of 60 months.

PATIENTS AND METHODS

Between February 1996 and April 2000, 716 patients were entered onto this trial. Adjuvant treatment began within 6 weeks after surgery. Sequential treatment of CT administered first followed by RT was compared with concurrent treatment of CT administered with RT. The CT regimen consisted of mitoxantrone (12 mg/m2), fluorouracil (500 mg/m2), and cyclophosphamide (500 mg/m2) on day 1, and it was repeated every 21 days for six courses. RT was delivered to the breast and, when indicated, to the regional lymphatics.

RESULTS

There was no statistically significant difference in treatment in the 5-year DFS (80% in both groups; P = .83), locoregional recurrence-free survival (LRFS; 92% in sequential v 95% in concurrent; P = .76), metastasis-free survival (87% in sequential v 84% in concurrent; P = .55), or overall survival (90% in sequential v 91% in concurrent; P = .76). Nevertheless, in the node-positive subgroup, the 5-year LRFS was statistically better in the concurrent arm (97% in concurrent v 91% in sequential; P = .02), corresponding to a risk of locoregional recurrence decreased by 39% (hazard ratio, 0.61; 95% CI, 0.38 to 0.93).

CONCLUSION

This treatment protocol remains an appealing clinical option for many women with operable breast cancer at a high risk of recurrence. Combination treatments with new drugs for breast cancer are warranted.

摘要

目的

1996年,我们启动了一项法国多中心III期随机试验,以比较保乳手术后I期和II期乳腺癌同步化疗(CT)与序贯化疗(CT)及放疗(RT)对无病生存期(DFS)的影响。本报告展示了中位随访60个月的临床结果。

患者与方法

1996年2月至2000年4月期间,716例患者纳入该试验。辅助治疗在术后6周内开始。将先进行CT序贯治疗随后进行RT与CT和RT同步治疗进行比较。CT方案为第1天给予米托蒽醌(12 mg/m²)、氟尿嘧啶(500 mg/m²)和环磷酰胺(500 mg/m²),每21天重复一次,共六个疗程。对乳房进行放疗,必要时对区域淋巴结进行放疗。

结果

两组的5年DFS(均为80%;P = 0.83)、局部区域无复发生存期(LRFS;序贯组为92%,同步组为95%;P = 0.76)、无转移生存期(序贯组为87%,同步组为84%;P = 0.55)或总生存期(序贯组为90%,同步组为91%;P = 0.76)均无统计学显著差异。然而,在淋巴结阳性亚组中,同步治疗组的5年LRFS在统计学上更好(同步组为97%,序贯组为91%;P = 0.02),对应局部区域复发风险降低39%(风险比,0.61;95% CI,0.38至0.93)。

结论

该治疗方案对于许多有复发高风险的可手术乳腺癌女性而言仍是一个有吸引力的临床选择。有必要采用新药进行联合治疗。

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