医学
全身疗法
临床终点
肿瘤科
内科学
乳腺癌
危险系数
烧蚀
放射治疗
随机对照试验
转移性乳腺癌
代理终结点
激素疗法
癌症
外科
放射外科
临床研究阶段
激素疗法
全身性疾病
比例危险模型
无进展生存期
耐火材料(行星科学)
原发性肿瘤
化疗
泌尿科
临床试验
总体生存率
放射科
乳腺
作者
Steven J. Chmura,Kathryn A. Winter,Wendy A. Woodward,Virginia F. Borges,Joseph Kamel Salama,Hania Al‐Hallaq,Martha M. Matuszak,Michael T. Milano,Nora T. Jaskowiak,Reshma Jagsi,Peter Kühn,Anthony Lucci,Salyna Meas,Stephanie N. Shishido,Jeremy M. Mason,Jose G. Bazan,Robert Nordal,David Y. Lee,Benjamin D. Smith,Zsolt Gabos
摘要
PURPOSE Metastasis-directed therapy is increasingly used for oligometastatic breast cancer, despite its uncertain benefit during first-line systemic therapy. We evaluated whether metastasis-directed ablation improves progression-free survival (PFS) compared with first-line systemic therapy alone in patients with oligometastatic breast cancer. METHODS NRG-BR002 is a randomized phase II/III trial across US/Canadian institutions. Participants had ≤4 metastases, controlled primary disease, ≤12 months of first-line systemic therapy without progression with all visible metastases amenable to stereotactic body radiation therapy (SBRT) or surgical resection and were randomly assigned 1:1 to systemic therapy alone (no ablation) or with metastasis-directed ablation (ablation). The primary end point was PFS, defined as time to progression or death. Secondary end points included overall survival (OS) and toxicity. Circulating tumor cells (CTCs) were evaluated as exploratory biomarkers. RESULTS From December 2014 to September 2019, 129 patients were enrolled; 125 were eligible for analysis. Median age was 54 years; 79% had hormone receptor–positive, human epidermal growth factor receptor 2‑negative disease, 60% solitary metastasis, 50% bone involvement, and 37% bone only. Ablation was delivered via SBRT for 93%. With 72 PFS events and a median follow-up of 29.9 months, median PFS was 23.0 months (no ablation) versus 19.5 months (ablation; hazard ratio [HR], 0.92 [70% CI, 0.71 to 1.17; 95% CI, 0.57 to 1.47]; one-sided P = .36; stratified P = .42). Thus, the trial did not proceed to phase III. OS did not differ significantly between arms (HR, 1.07 [95% CI, 0.60 to 1.89]; one-sided P = .41; stratified P = .52). No grade 5 toxicities occurred. Exploratory analysis suggested improved PFS with ablation in patients with low or absent pretreatment CTCs. CONCLUSION The addition of metastasis-directed ablation added to first-line systemic therapy did not improve PFS or OS in patients with oligometastatic breast cancer. Ablation should not be routinely used outside of clinical trials, except for palliation.
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