Holánek Miloš, Bílek Ondřej, Nenutil Rudof, Kazda Tomáš, Selingerová Iveta, Zvaríková Mária, Palácová Markéta, Krásenská Marta, Vyzula Rostislav, Petráková Katarína
Klin Onkol. 2019 Summer;32(Supplementum2):31-35. doi: 10.14735/amko2019S31.
Mutations in the BRCA1 and BRCA2 genes are associated with a high risk of developing breast cancer. Tumors arising from this mutation are expected to be more sensitive to platinum-based drugs. The role of platinum-based drugs in systemic neoadjuvant BRCA1/2 breast cancer therapy, and its efficacy in increasing the probability of pathological complete remission (pCR) are discussed repeatedly; however, there are no clear recommendations.
We retrospectively evaluated the contribution of a platinum-based antineoplastic drug to the achievement of pCR in a set of patients with BRCA1/2 mutant breast cancer treated with neoadjuvant chemotherapy from 2010 to 2017. The response to neoadjuvant chemotherapy was evaluated by a pathologist using definitive surgical specimens. A pCR was defined as a condition in which complete invasive breast cancer, and (eventually) positive lymph nodes, had disappeared.
Of 76 patients (median age, 39 years; 62% with triple negative breast cancer (TNBC); 70% with BRCA1 positivity), 37 were treated with platinum-based drugs. More patients treated with platinum derivatives achieved pCR (57% vs. 23%, p = 0.005). Patients treated in a neoadjuvant setting with platinum-based antineoplastic drugs had a 4.4× greater chance of achieving pCR than those not treated with platinum, assuming the same tumor phenotype (TNBC or SR+/HER2).
Neoadjuvant platinum-based chemotherapy for patients with a BRCA1/2 mutation is associated with a higher probability of achieving pCR, which is important for subsequent prognosis. This treatment should be considered particularly for patients with BRCA1 mutation and a TNBC phenotype. This work was supported by grant of the Ministry of Health of the Czech Republic - Conceptual. Development of a Reaserch Organization (MMCI 00209805). This work was supported by grant of the Ministry of Education, Youth and Sport of the Czech Republic (NPU I - LO1413). The authors declare they have no potential confl icts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers. Submitted: 21. 3. 2019 Accepted: 14. 5. 2019.
BRCA1和BRCA2基因的突变与患乳腺癌的高风险相关。由这种突变引发的肿瘤预计对铂类药物更敏感。铂类药物在系统性新辅助BRCA1/2乳腺癌治疗中的作用及其提高病理完全缓解(pCR)概率的疗效已被反复讨论;然而,尚无明确建议。
我们回顾性评估了一组2010年至2017年接受新辅助化疗的BRCA1/2突变型乳腺癌患者中,铂类抗肿瘤药物对实现pCR的贡献。病理学家使用确定性手术标本评估新辅助化疗的反应。pCR定义为完全浸润性乳腺癌以及(最终)阳性淋巴结消失的情况。
76例患者(中位年龄39岁;62%为三阴性乳腺癌(TNBC);70%为BRCA1阳性)中,37例接受了铂类药物治疗。接受铂类衍生物治疗的患者实现pCR的比例更高(57%对23%,p = 0.005)。假设肿瘤表型相同(TNBC或SR+/HER2),在新辅助治疗中接受铂类抗肿瘤药物治疗的患者实现pCR的机会比未接受铂类治疗的患者高4.4倍。
BRCA1/2突变患者的新辅助铂类化疗与更高的pCR概率相关,这对后续预后很重要。对于BRCA1突变和TNBC表型的患者尤其应考虑这种治疗。本研究得到了捷克共和国卫生部 - 概念性研究组织发展基金(MMCI 00209805)的支持。本研究得到了捷克共和国教育、青年和体育部基金(NPU I - LO1413)的支持。作者声明他们在研究中使用的药物、产品或服务方面不存在潜在利益冲突。编辑委员会声明该手稿符合ICMJE对生物医学论文的建议。提交日期:2019年3月21日 接受日期:2019年5月14日。