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Circulating Tumor DNA After Neoadjuvant Chemotherapy in Breast Cancer Is Associated With Disease Relapse

乳腺癌 医学 危险系数 内科学 肿瘤科 数字聚合酶链反应 比例危险模型 化疗 新辅助治疗 多路复用 癌症 循环肿瘤DNA 激素受体 阶段(地层学) 三阴性乳腺癌 置信区间 聚合酶链反应 生物 生物信息学 基因 生物化学 古生物学
作者
Frédéric Cailleux,Elisa Agostinetto,Matteo Lambertini,Françoise Rothé,Hsin-Ta Wu,Mustafa Balcioglu,Ekaterina Kalashnikova,Delphine Vincent,Giulia Viglietti,Andrea Gombos,Andreas Papagiannis,Isabelle Veys,Ahmad Awada,Himanshu Sethi,Alexey Aleshin,Denis Larsimont,Christos Sotiriou,David Venet,Michail Ignatiadis
出处
期刊:JCO precision oncology [Lippincott Williams & Wilkins]
卷期号:6 (6): e2200148-e2200148 被引量:72
标识
DOI:10.1200/po.22.00148
摘要

PURPOSE Detection of circulating tumor DNA (ctDNA) after neoadjuvant chemotherapy in patients with early-stage breast cancer may allow for early detection of relapse. In this study, we analyzed ctDNA using a personalized, tumor-informed multiplex polymerase chain reaction–based next-generation sequencing assay. METHODS Plasma samples (n = 157) from 44 patients were collected before neoadjuvant therapy (baseline), after neoadjuvant therapy and before surgery (presurgery), and serially postsurgery including a last follow-up sample. The primary end point was event-free survival (EFS) analyzed using Cox regression models. RESULTS Thirty-eight (86%), 41 (93%), and 38 (86%) patients had baseline, presurgical, and last follow-up samples, respectively. Twenty patients had hormone receptor–positive/human epidermal growth factor receptor 2–negative, 13 had triple-negative breast cancer, and 11 had human epidermal growth factor receptor 2–positive disease. Baseline ctDNA detection was observed in 22/38 (58%) patients and was significantly associated with Ki67 > 20% ( P = .036) and MYC copy-number gain ( P = .0025, false discovery rate = 0.036). ctDNA detection at presurgery and at last follow-up was observed in 2/41 (5%) and 2/38 (5%) patients, respectively. Eight relapses (seven distant and one local) were noted (median follow-up 3.03 years [range, 0.39-5.85 years]). After adjusting for pathologic complete response (pCR), ctDNA detection at presurgery and at last follow-up was associated with shorter EFS (hazard ratio [HR], 53; 95% CI, 4.5 to 624; P < .01, and HR, 31; 95% CI, 2.7 to 352; P < .01, respectively). Association between baseline detection and EFS was not observed (HR, 1.4; 95% CI, 0.3 to 5.9; P = .67). CONCLUSION The presence of ctDNA after neoadjuvant chemotherapy is associated with relapse in early-stage breast cancer, supporting interventional trials for testing the clinical utility of ctDNA monitoring in this setting.
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