Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Samsung Genome Institute, Samsung Medical Center, Seoul, Korea.
Cancer Res Treat. 2024 Apr;56(2):531-537. doi: 10.4143/crt.2023.996. Epub 2023 Nov 10.
This study aims to determine the association between pre- and postoperative radiotherapy (PORT) circulating tumor DNA (ctDNA) dynamics and oncological outcomes in patients with residual triple-negative breast cancer who underwent surgery after neoadjuvant chemotherapy (NAC).
Between March 2019 and July 2020, 11 nonmetastatic patients with residual disease who underwent surgery after NAC were prospectively enrolled. In each patient, tumor specimens obtained during surgery and blood samples collected at three time points during PORT (T0: pre-PORT, T1: 3 weeks after PORT, T2: 1 month after PORT) were sequenced, targeting 38 cancer-related genes. Disease-free survival (DFS) was evaluated and the association between DFS and ctDNA dynamics was analyzed.
At T0, ctDNA was detected in three (27.2%) patients. The ctDNA dynamics were as follows: two showed a decreasing ctDNA variant allele frequency (VAF) and reached zero VAF at T2, while one patient exhibited an increasing VAF during PORT and maintained an elevated VAF at T2. After a median follow-up of 48 months, two patients experienced distant metastasis without any locoregional failures. All failures occurred in patients with ctDNA positivity at T0 and a decreased VAF after PORT. The 4-year DFS rates according to the T0 ctDNA status were 67% (positive ctDNA) and 100% (negative ctDNA) (p=0.032).
More than a quarter of the patients with residual disease after post-NAC surgery exhibited pre-PORT ctDNA positivity, and ctDNA positivity was associated with poor DFS. For patients with pre-PORT ctDNA positivity, the administration of a more effective systemic treatment should be considered.
本研究旨在确定新辅助化疗(NAC)后接受手术的残余三阴性乳腺癌患者中,术前和术后放疗(PORT)循环肿瘤 DNA(ctDNA)动态与肿瘤学结局之间的关联。
2019 年 3 月至 2020 年 7 月,前瞻性纳入 11 例接受 NAC 后手术的残余疾病患者。对每位患者,在手术时获取肿瘤标本,并在 PORT 期间的三个时间点(T0:PORT 前,T1:PORT 后 3 周,T2:PORT 后 1 个月)采集血液样本,对 38 个癌症相关基因进行测序。评估无病生存期(DFS),并分析 DFS 与 ctDNA 动态之间的关系。
在 T0,有 3 例(27.2%)患者检测到 ctDNA。ctDNA 动态如下:2 例患者的 ctDNA 变异等位基因频率(VAF)逐渐降低,并在 T2 时降至零 VAF,而 1 例患者在 PORT 期间 VAF 增加,并在 T2 时维持升高的 VAF。中位随访 48 个月后,2 例患者发生远处转移,无局部区域失败。所有失败均发生在 T0 时 ctDNA 阳性且 PORT 后 VAF 降低的患者中。根据 T0 ctDNA 状态,4 年 DFS 率分别为 67%(ctDNA 阳性)和 100%(ctDNA 阴性)(p=0.032)。
NAC 后手术残余疾病患者中有超过四分之一的患者存在 PORT 前 ctDNA 阳性,ctDNA 阳性与较差的 DFS 相关。对于 PORT 前 ctDNA 阳性的患者,应考虑给予更有效的全身治疗。