Li Shunying, Lai Hongna, Liu Jieqiong, Liu Yujie, Jin Liang, Li Yudong, Liu Fengtao, Gong Yuhua, Guan Yanfang, Yi Xin, Shi Qianfeng, Cai Zijie, Li Qian, Li Ying, Zhu Mengdi, Wang Jingru, Yang Yaping, Wei Wei, Yin Dong, Song Erwei, Liu Qiang
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
JCO Precis Oncol. 2020 Mar 27;4. doi: 10.1200/PO.19.00292. eCollection 2020.
Many patients with breast cancer still relapse after curative treatment. How to identify the ones with high relapse risk remains a critical problem. Circulating tumor DNA (ctDNA) has recently become a promising marker to monitor tumor burden. Whether ctDNA can be used to predict the response and prognosis in patients with breast cancer receiving neoadjuvant chemotherapy (NAC) is unknown. Our study aimed to evaluate the clinical value of the presence and dynamic change of ctDNA to predict the tumor response and prognosis in patients with breast cancer treated with NAC.
Fifty-two patients with early breast cancer who underwent NAC were prospectively enrolled. Serial plasma samples before, during, and after NAC and paired tumor biopsies were harvested and subjected to deep targeted sequencing using a large next-generation sequencing panel that covers 1,021 cancer-related genes.
Positive baseline ctDNA was detected in 21 of 44 patients before NAC. Most patients with positive ctDNA had one or more mutations confirmed in paired primary tumor. The ctDNA level after 2 cycles of NAC was predictive of local tumor response after all cycles of NAC (area under the curve, 0.81; 95% CI, 0.61 to 1.00). ctDNA tracking during NAC outperformed imaging in predicting the overall response to NAC. More importantly, positive baseline ctDNA is significantly associated with worse disease-free survival ( = .011) and overall survival ( = .004) in patients with early breast cancer, especially in estrogen receptor-negative patients.
Our study demonstrated that ctDNA can be used to predict tumor response to NAC and prognosis in early breast cancer, providing information to tailor an individual's therapeutic regimen.
许多乳腺癌患者在根治性治疗后仍会复发。如何识别高复发风险患者仍然是一个关键问题。循环肿瘤DNA(ctDNA)最近已成为监测肿瘤负荷的一个有前景的标志物。ctDNA是否可用于预测接受新辅助化疗(NAC)的乳腺癌患者的反应和预后尚不清楚。我们的研究旨在评估ctDNA的存在和动态变化对预测接受NAC治疗的乳腺癌患者肿瘤反应和预后的临床价值。
前瞻性纳入52例接受NAC的早期乳腺癌患者。收集NAC前、中、后的系列血浆样本以及配对的肿瘤活检组织,使用覆盖1021个癌症相关基因的大型二代测序面板进行深度靶向测序。
44例患者在NAC前有21例检测到基线ctDNA阳性。大多数ctDNA阳性患者在配对的原发肿瘤中确认有一个或多个突变。NAC 2个周期后的ctDNA水平可预测NAC所有周期后的局部肿瘤反应(曲线下面积,0.81;95%CI,0.61至1.00)。NAC期间的ctDNA追踪在预测对NAC的总体反应方面优于影像学检查。更重要的是,基线ctDNA阳性与早期乳腺癌患者较差的无病生存期(P = 0.011)和总生存期(P = 0.004)显著相关,尤其是在雌激素受体阴性患者中。
我们的研究表明,ctDNA可用于预测早期乳腺癌对NAC的肿瘤反应和预后,为制定个体化治疗方案提供信息。