Militello Anna Maria, Zielli Teresa, Boggiani Daniela, Michiara Maria, Naldi Nadia, Bortesi Beatrice, Zanelli Paola, Uliana Vera, Giuliotti Sara, Musolino Antonino
Breast Unit and Cancer Genetics Service, University Hospital of Parma, Parma, Italy.
Medical Genetics Unit, University Hospital of Parma, Parma, Italy.
Front Oncol. 2019 Aug 13;9:759. doi: 10.3389/fonc.2019.00759. eCollection 2019.
Sensitivity to endocrine therapy of patients with estrogen receptor (ER)-positive metastatic breast cancer and germline mutations is not yet fully elucidated. Furthermore, the registration trials of CDK 4/6 inhibitors in combination with endocrine therapy lacked of a pre-specified subgroup analysis in mutation carriers. We report clinical history of two patients with BRCA-mutated, ER-positive metastatic breast cancer treated with letrozole plus the CDK 4/6 inhibitor palbociclib. Biological and clinical implications of the treatment outcome observed in the two cases are discussed with the knowledge of scientific evidence to date available. Overall, biological rationale, preclinical, and clinical data support the prominent role of CDK 4/6 inhibitors plus endocrine therapy, even in combination with PARP inhibitors, in the treatment of BRCA-mutated, ER-positive breast cancers. However, the interaction between Cyclin/CDK pathway, ER and BRCA is complex and evidences reported so far, albeit reliable, await confirmation in the context of future randomized clinical trials.
雌激素受体(ER)阳性转移性乳腺癌和胚系突变患者对内分泌治疗的敏感性尚未完全阐明。此外,CDK 4/6抑制剂与内分泌治疗联合应用的注册试验缺乏对突变携带者的预先指定亚组分析。我们报告了两名携带BRCA突变、ER阳性转移性乳腺癌患者接受来曲唑联合CDK 4/6抑制剂哌柏西利治疗的临床病史。结合目前可用的科学证据,讨论了这两例患者治疗结果的生物学和临床意义。总体而言,生物学原理、临床前和临床数据支持CDK 4/6抑制剂加内分泌治疗,甚至与PARP抑制剂联合应用,在治疗携带BRCA突变、ER阳性乳腺癌中发挥重要作用。然而,细胞周期蛋白/CDK通路、ER和BRCA之间的相互作用很复杂,目前报道的证据虽然可靠,但有待未来随机临床试验进一步证实。