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首页> 外文期刊>Journal of Clinical Oncology >Phase III trial of concurrent or sequential adjuvant chemoradiotherapy after conservative surgery for early-stage breast cancer: final results of the ARCOSEIN trial.
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Phase III trial of concurrent or sequential adjuvant chemoradiotherapy after conservative surgery for early-stage breast cancer: final results of the ARCOSEIN trial.

机译:早期乳腺癌保守手术后同期或序贯辅助放化疗的III期试验:ARCOSEIN试验的最终结果。

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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.
机译:目的:1996年,我们启动了法国多中心III期随机试验,比较了保乳手术后I期和II期乳腺癌同时进行,序贯化疗(CT)和放疗(RT)对无病生存期(DFS)的影响癌症。该报告提供了中位随访60个月的临床结果。患者与方法:1996年2月至2000年4月,共有716例患者进入该试验。手术后6周内开始辅助治疗。将先给予CT后再行RT的顺序治疗与同时给予RT的CT同期治疗进行比较。在第1天,CT方案由米托蒽醌(12 mg / m2),氟尿嘧啶(500 mg / m2)和环磷酰胺(500 mg / m2)组成,每21天重复6个疗程。 RT被递送至乳房,并在指示时被递送至局部淋巴管。结果:5年DFS的治疗(两组均为80%; P = 0.83),局部无复发生存率(LRFS;顺序治疗为92%,同期为95%; P =)无统计学差异。 76),无转移生存率(连续生存率87%,同时发生率84%; P = .55)或总体生存率(连续生存率90%,同时发生率91%; P = 0.76)。然而,在淋巴结阳性亚组中,并发组的5年LRFS在统计学上更好(并发组97%,连续组91%; P = .02),对应于局部复发的风险降低了39%(危险比0.61; 95%CI 0.38至0.93)。结论:对于许多具有高复发风险的可手术乳腺癌的妇女,该治疗方案仍然是一种有吸引力的临床选择。乳腺癌与新药联合治疗是有必要的。

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