Phase II Evaluation of Ultra-Hypofractionated Postoperative Radiation Therapy for Breast Cancer: Toxicity and Efficacy in a Single-Center Nonrandomized Prospective Study.

IF 3 Q2 ONCOLOGY
JCO Global Oncology Pub Date : 2025-03-01 Epub Date: 2025-03-07 DOI:10.1200/GO-24-00277
Marcel Fang, Vinicius de Carvalho Gico, Lucas Casimiro, Bruno Takatsu, Elson Santos Neto, Rossana Veronica Mendoza Lopez, Gustavo Vilela Costa Pinto, Gustavo Nader Marta
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引用次数: 0

Abstract

Purpose: To evaluate the toxicity profile and efficacy of postoperative ultra-hypofractionated radiation therapy in elderly patients with breast cancer.

Materials and methods: This is a nonrandomized, single-center, prospective Phase II trial. Patients with breast cancer older than 65 years were treated with ultra-hypofractionated radiation therapy in 5 fractions of 5.7 Gy on alternate days in the breast or chest wall, or regional lymph nodes. The primary end point was acute toxicity.

Results: A total of 60 patients were analyzed, with a median follow-up of 42.5 months (range, 13.8-66.2). Most patients presented pathologic stage I (56.6%, n = 34) or stage II (33.3%, n = 20) disease. Regional lymph node irradiation was performed in 22% (n = 13) of patients. During treatment, 51% (n = 31) of patients experienced grade 1 or 2 acute toxicity, with no cases of grade 3 acute toxicity reported. Late toxicity included 1.7% (n = 1) of patients developing grade 3 fibrosis and 1.7% (n = 1) developing grade 3 pneumonitis. Regional lymph node irradiation was not associated with a statistically significant increase in toxicity risk (P = .194). Cosmesis evaluations revealed no significant changes when comparing pretreatment assessments with evaluations at 10 weeks (P = .223) and 26 weeks (P = .615) post-treatment. Quality of life was not adversely affected, regardless of whether regional lymph nodes were irradiated. Recurrence rates included two patients with both locoregional and distant recurrence and five patients with distant recurrence. The 3-year disease-free survival probability was 81.7%, and the 3-year overall survival probability was 86.7%.

Conclusion: This study demonstrates the safety of ultra-hypofractionated radiation therapy in terms of toxicity in patients with breast cancer. The findings for side effects, cosmesis, quality of life, and survival outcomes are consistent with those observed in moderately hypofractionated radiation therapy regimens, suggesting its use as a viable treatment option in this demographic.

乳腺癌术后超低分割放疗的II期评价:单中心非随机前瞻性研究的毒性和疗效。
目的:评价老年乳腺癌术后超低分割放疗的毒副作用及疗效。材料和方法:这是一项非随机、单中心、前瞻性II期试验。65岁以上的乳腺癌患者在乳房或胸壁或区域淋巴结进行5次超低分割放射治疗,每次5.7 Gy,隔天进行。主要终点为急性毒性。结果:共分析60例患者,中位随访42.5个月(范围13.8-66.2)。大多数患者表现为病理I期(56.6%,n = 34)或II期(33.3%,n = 20)。22% (n = 13)的患者接受了局部淋巴结放疗。在治疗期间,51% (n = 31)的患者出现了1级或2级急性毒性,没有3级急性毒性的病例报道。晚期毒性包括1.7% (n = 1)的患者发展为3级纤维化,1.7% (n = 1)的患者发展为3级肺炎。区域淋巴结照射与毒性风险增加无统计学意义(P = 0.194)。治疗后10周(P = .223)和26周(P = .615)的美容评估结果显示,治疗前评估与治疗后10周(P = .223)和26周(P = .615)的评估没有显著变化。无论局部淋巴结是否照射,生活质量均未受到不良影响。复发率包括2例局部和远处复发,5例远处复发。3年无病生存率为81.7%,3年总生存率为86.7%。结论:本研究从毒性方面证明了超低分割放疗对乳腺癌患者的安全性。副作用、美容、生活质量和生存结果的研究结果与中度低分割放射治疗方案的观察结果一致,表明其可作为这一人群的可行治疗选择。
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
JCO Global Oncology
JCO Global Oncology Medicine-Oncology
CiteScore
6.70
自引率
6.70%
发文量
310
审稿时长
7 weeks
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