Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Clin Cancer Res. 2021 Jun 15;27(12):3469-3477. doi: 10.1158/1078-0432.CCR-20-4300. Epub 2021 May 5.
This study analyzes the potential of stromal platelet-derived growth factor receptor-beta (PDGFRb) expression as biomarker for radiotherapy (RT) benefit on ipsilateral breast events (IBE) in ductal carcinoma (DCIS). Improved identification of DCIS patients refractory to adjuvant whole-breast RT is needed. Predictive biomarker studies in DCIS have focused on tumor cell features rather than the tumor-associated stroma, despite growing evidence of its influence on therapy efficiency.
Samples from the Swedish randomized radiotherapy DCIS trial (SweDCIS) were subjected to IHC analysis for stromal PDGFRb expression. IBE incidence at 10 years after breast-conserving surgery was the primary endpoint. Interactions between marker and treatment were analyzed.
PDGFRb score was predictive for RT benefit with regard to IBE ( = 0.002 and = 0.008 adjusted multivariably). Patients of the PDGFRb group had a strong benefit from RT regarding IBE risk [HR, 0.23; 95% confidence interval (CI), 0.12-0.45; < 0.001] with an absolute risk reduction of 21% (cumulative risk 7% vs. 28%) at 10 years. No significant risk reduction by RT was observed for patients of the PDGFRb group (HR, 0.83; 0.51-1.34; = 0.444; cumulative risk 22% vs. 25%). The RT response-predictive effect of stromal PDGFRb was equally strong in analyses for and invasive IBE when analyzed separately ( IBE: = 0.029; invasive IBE: = 0.044).
Results suggest high stromal PDGFRb expression as a novel biomarker identifying DCIS patients who are refractory to standard whole-breast adjuvant RT. The data imply previously unrecognized fibroblast-mediated modulation of radiosensitivity of DCIS, which should be further explored from mechanistic and targeting perspectives.
本研究分析了间质血小板衍生生长因子受体-β(PDGFRb)表达作为导管癌(DCIS)同侧乳腺事件(IBE)放疗获益的生物标志物的潜力。需要更好地识别对辅助全乳放疗有抵抗性的 DCIS 患者。预测性生物标志物研究在 DCIS 中集中于肿瘤细胞特征,而不是肿瘤相关的基质,尽管越来越多的证据表明其对治疗效果有影响。
对瑞典随机放疗 DCIS 试验(SweDCIS)的样本进行了免疫组化分析,以检测间质 PDGFRb 的表达。乳腺保留手术后 10 年的 IBE 发生率是主要终点。分析了标志物与治疗之间的相互作用。
PDGFRb 评分对 IBE 有预测放疗获益的作用( = 0.002 和 = 0.008 经多变量调整)。PDGFRb 组的患者在 IBE 风险方面从放疗中获益显著[风险比(HR),0.23;95%置信区间(CI),0.12-0.45; < 0.001],10 年时绝对风险降低 21%(累积风险 7%对 28%)。PDGFRb 组的患者未观察到放疗的显著风险降低(HR,0.83;0.51-1.34; = 0.444;累积风险 22%对 25%)。当分别分析时,间质 PDGFRb 对放疗反应的预测作用在 和浸润性 IBE 分析中同样强烈(IBE: = 0.029;浸润性 IBE: = 0.044)。
结果表明,高间质 PDGFRb 表达可作为一种新的生物标志物,识别对标准全乳辅助放疗有抵抗性的 DCIS 患者。这些数据表明,以前未被认识到的成纤维细胞介导的 DCIS 放射敏感性的调节,应从机制和靶向的角度进一步探索。