Department of Radiation Oncology, Weill Cornell Medical College, New York, New York.
Department of Pathology, Weill Cornell Medical College, New York, New York.
Clin Cancer Res. 2021 Apr 1;27(7):1855-1863. doi: 10.1158/1078-0432.CCR-20-3871. Epub 2021 Jan 25.
Recent preclinical data suggest that cyclin-dependent kinase 4/6 (CDK4/6) inhibition may be harnessed to sensitize estrogen receptor-positive (ER) breast cancer to radiotherapy. However, these findings were obtained in human ER breast cancer cell lines exposed to subclinical doses of CDK4/6 inhibitors with limited attention to treatment schedule. We investigated the activity of radiotherapy combined with the prototypic CDK4/6 inhibitor palbociclib placing emphasis on therapeutic schedule.
We combined radiotherapy and palbociclib in various doses and therapeutic schedules in human and mouse models of ER and ER-negative (ER) breast cancer, including an immunocompetent mouse model that recapitulates key features of human luminal B breast cancer in women. We assessed proliferation, cell death, cell-cycle control, and clonogenic survival , as well as tumor growth, overall survival, and metastatic dissemination .
Radiotherapy and palbociclib employed as standalone agents had partial cytostatic effects , correlating with suboptimal tumor control . However, while palbociclib delivered before focal radiotherapy provided minimal benefits as compared with either treatment alone, delivering focal radiotherapy before palbociclib mediated superior therapeutic effects, even in the absence of p53. Such superiority manifested with enhanced cytostasis and loss of clonogenic potential, as well as with improved local and systemic tumor control.
Our preclinical findings demonstrate that radiotherapy delivered before CDK4/6 inhibitors mediates superior antineoplastic effects compared with alternative treatment schedules, calling into question the design of clinical trials administering CDK4/6 inhibitors before radiotherapy in women with ER breast cancer.
最近的临床前数据表明,细胞周期蛋白依赖性激酶 4/6(CDK4/6)抑制可能被利用来使雌激素受体阳性(ER)乳腺癌对放疗敏感。然而,这些发现是在人类 ER 乳腺癌细胞系中获得的,这些细胞系暴露于 CDK4/6 抑制剂的亚临床剂量下,且对治疗方案的关注有限。我们研究了将放射治疗与原型 CDK4/6 抑制剂 palbociclib 联合使用的效果,重点关注治疗方案。
我们在人类和小鼠的 ER 和 ER 阴性(ER)乳腺癌模型中,以各种剂量和治疗方案组合了放射治疗和 palbociclib,包括一个免疫功能正常的小鼠模型,该模型再现了女性中腔 B 型乳腺癌的关键特征。我们评估了增殖、细胞死亡、细胞周期控制和克隆形成存活,以及肿瘤生长、总生存和转移扩散。
放射治疗和 palbociclib 作为单一药物使用时具有部分细胞静止作用,与肿瘤控制不理想相关。然而,虽然与单独使用任何一种药物相比,在局部放射治疗前使用 palbociclib 提供的益处最小,但在缺乏 p53 的情况下,在 palbociclib 前进行局部放射治疗可介导更好的治疗效果。这种优越性表现为增强的细胞静止和丧失克隆形成潜力,以及改善的局部和全身肿瘤控制。
我们的临床前研究结果表明,与替代治疗方案相比,放射治疗在前的 CDK4/6 抑制剂治疗方案介导了更好的抗肿瘤效果,这对在 ER 乳腺癌女性中进行 CDK4/6 抑制剂在前的放射治疗临床试验的设计提出了质疑。