Hypofractionated Versus Conventionally Fractionated Postmastectomy Radiotherapy With Internal Mammary Node Irradiation for High-Risk Breast Cancer (HypoMast-IMNI): A Randomized Phase III Trial.

IF 44.7 1区 医学 Q1 ONCOLOGY
Xiaofang Wang, Xiaomeng Zhang, Xingxing Chen, Zhaozhi Yang, Xin Mei, Li Zhang, Jin Meng, Wei Shi, Jurui Luo, Kairui Jin, Yu Gu, Miao Mo, Zhen Zhang, Keda Yu, Guangyu Liu, Jiong Wu, Zhimin Shao, Xiaomao Guo, Xiaoli Yu, Jinli Ma
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引用次数: 0

Abstract

Purpose: When coverage of internal mammary nodes (IMN) is required, the efficacy and safety of hypofractionated regimens within postmastectomy radiotherapy (PMRT) remain to be established. This study evaluated hypofractionated radiotherapy (HypoRT) in patients with high-risk, operable breast cancer undergoing PMRT with IMN irradiation (IMNI).

Methods: In this phase III noninferiority trial, eligible patients with high-risk disease after mastectomy (including pT1-4N2-3, pT3-4N1, or pT1-2N1 disease with additional high-risk factors) were randomly assigned (1:1) to HypoRT (42.56 Gy in 16 fractions) or conventionally fractionated radiotherapy (ConvRT; 50 Gy in 25 fractions), both targeting the chest wall and regional lymph nodes, including the IMN. The primary end point was locoregional recurrence (LRR). Secondary end points were distant metastasis-free survival (DMFS), breast cancer recurrence-free survival (BCRFS), disease-free survival (DFS), overall survival (OS), and treatment-related toxicity. The trial is registered with ClinicalTrial.gov (identifier: NCT03856372).

Results: Between September 2018 and July 2022, 1,494 patients were randomly assigned. After a median follow-up of 58.1 months in the modified intention-to-treat population (n = 1,429), the 5-year cumulative incidence of LRR was 1.7% (95% CI, 0.9 to 2.9) with HypoRT and 2.2% (95% CI, 1.3 to 3.5) with ConvRT (hazard ratio, 0.69 [95% CI, 0.32 to 1.51]), meeting the noninferiority criterion (P = .017). No significant differences were observed in 5-year DMFS, BCRFS, DFS, or OS. Grade 3 acute skin toxicity was significantly lower with HypoRT (1.7% v 12.2%, P < .001). The incidence of grade ≥2 radiation pneumonitis and pulmonary fibrosis was low and comparable between arms, with no ischemic cardiac events recorded.

Conclusion: For patients with high-risk, operable breast cancer requiring PMRT with IMNI, the 16-fraction HypoRT regimen is noninferior to ConvRT for locoregional control, offers a superior acute toxicity profile, and demonstrates excellent cardiopulmonary safety.

低分割与常规分割乳房切除术后放疗加内乳结照射治疗高危乳腺癌(HypoMast-IMNI):一项随机III期试验
目的:当需要覆盖乳腺内淋巴结(IMN)时,在乳房切除术后放疗(PMRT)中使用低分割方案的有效性和安全性仍有待确定。本研究评估了低分割放疗(HypoRT)在高风险、可手术的乳腺癌患者行PMRT + IMN照射(IMNI)的疗效。方法:在这项III期非效性试验中,符合条件的乳房切除术后高危疾病患者(包括pT1-4N2-3、pT3-4N1或pT1-2N1伴有其他高危因素的疾病)被随机(1:1)分配到HypoRT (42.56 Gy / 16组)或常规分级放疗(ConvRT; 50 Gy / 25组),均针对胸壁和区域淋巴结,包括IMN。主要终点为局部复发(LRR)。次要终点是远端无转移生存期(DMFS)、乳腺癌无复发生存期(BCRFS)、无病生存期(DFS)、总生存期(OS)和治疗相关毒性。该试验已在ClinicalTrial.gov注册(标识符:NCT03856372)。结果:在2018年9月至2022年7月期间,随机分配了1494名患者。在修改意向治疗人群(n = 1429)中位随访58.1个月后,HypoRT的5年累积LRR发生率为1.7% (95% CI, 0.9 ~ 2.9), ConvRT的5年累积LRR发生率为2.2% (95% CI, 1.3 ~ 3.5)(风险比0.69 [95% CI, 0.32 ~ 1.51]),符合非劣效性标准(P = 0.017)。5年DMFS、BCRFS、DFS或OS均无显著差异。HypoRT组3级急性皮肤毒性显著降低(1.7% vs 12.2%, P < 0.001)。≥2级放射性肺炎和肺纤维化的发生率较低,两组间相当,无缺血性心脏事件记录。结论:对于需要PMRT合并IMNI的高风险可手术乳腺癌患者,16组分HypoRT方案在局部区域控制方面不逊于ConvRT,具有优越的急性毒性,并显示出良好的心肺安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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