Department of Gastroenterology, Chiba Cancer Center, Chiba, Japan.
Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Br J Cancer. 2024 Oct;131(7):1237-1245. doi: 10.1038/s41416-024-02834-0. Epub 2024 Aug 28.
Identification of homologous recombination deficiency (HRD) remains a challenge in advanced pancreatic cancer (APC). We investigated the utility of circulating tumour DNA (ctDNA) profiling in the assessment of BRCA1/2 and ATM mutation status and treatment selection in APC.
We analysed clinical and ctDNA data of 702 patients with APC enroled in GOZILA, a ctDNA profiling study using Guardant360.
Inactivating BRCA1/2 and ATM mutations were detected in 4.8% (putative germline, 3.7%) and 4.4% (putative germline, 0.9%) of patients, respectively. Objective response (63.2% vs. 16.2%) and PFS (HR 0.55, 95% CI 0.32-0.93) on platinum-containing chemotherapy were significantly better in patients with putative germline BRCA1/2 (gBRCA) mutation than those without. In contrast, putative gBRCA mutation had no impact on the efficacy of gemcitabine plus nab-paclitaxel. In 2 patients treated with platinum-containing therapy, putative BRCA2 reversion mutations were detected. Three of seven patients with somatic BRCA mutations responded to platinum-containing therapy, while only one of four with putative germline ATM mutations did. One-third of somatic ATM mutations were in genomic loci associated with clonal haematopoiesis.
Comprehensive ctDNA profiling provides clinically relevant information regarding HRD status. It can be a practical, convenient option for HRD screening in APC.
在晚期胰腺导管腺癌(APC)中,同源重组缺陷(HRD)的鉴定仍然具有挑战性。我们研究了循环肿瘤 DNA(ctDNA)分析在评估 APC 中 BRCA1/2 和 ATM 突变状态和治疗选择中的作用。
我们分析了 702 例 APC 患者的临床和 ctDNA 数据,这些患者均参加了使用 Guardant360 进行 ctDNA 分析的 GOZILA 研究。
分别在 4.8%(假定种系,3.7%)和 4.4%(假定种系,0.9%)的患者中检测到失活的 BRCA1/2 和 ATM 突变。在含铂化疗中,有假定种系 BRCA1/2(gBRCA)突变的患者的客观缓解率(63.2% vs. 16.2%)和无进展生存期(HR 0.55,95%CI 0.32-0.93)明显更好,而无 gBRCA 突变的患者则无明显差异。相比之下,假定 gBRCA 突变对吉西他滨联合 nab-紫杉醇的疗效没有影响。在接受含铂治疗的 2 例患者中,检测到假定的 BRCA2 回复突变。7 例具有体细胞 BRCA 突变的患者中有 3 例对含铂治疗有反应,而 4 例具有假定种系 ATM 突变的患者中仅有 1 例有反应。三分之一的体细胞 ATM 突变位于与克隆性造血相关的基因组位置。
全面的 ctDNA 分析提供了有关 HRD 状态的临床相关信息。它可能是 APC 中 HRD 筛查的一种实用、方便的选择。