Circulating tumor DNA to anticipate loco-regional recurrence in early-stage breast cancer: a proof-of-concept study.

IF 3.5 3区 医学 Q2 ONCOLOGY
Frontiers in Oncology Pub Date : 2025-09-11 eCollection Date: 2025-01-01 DOI:10.3389/fonc.2025.1621322
Valentina Appierto, Elena Tamborini, Paola Tiberio, Adele Busico, Loris De Cecco, Marco Silvestri, Cinzia De Marco, Elena Cavadini, Maria Carmen De Santis, Secondo Folli, Gianfranco Scaperrotta, Rebecca Manitto, Andrea Vingiani, Giancarlo Pruneri, Serena Di Cosimo
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引用次数: 0

Abstract

Background: Loco-regional recurrence (LRR) poses a clinical challenge for the follow-up of patients treated with curative intent for early-stage breast cancer (EBC). While circulating tumor DNA (ctDNA) has been shown to predict distant metastases, its value for LRR is less characterized.

Methods: Starting from an index case with documented LRR and available tumor and plasma samples, we report the analysis of the prospective phase III fenretinide prevention trial, which primarily aimed to assess the incidence of second malignancy in women with T1-T2 N0 EBC. Patients were eligible if they had FFPE and/or frozen tissue from primary or recurrent invasive tumor for next generation sequencing, and at least three serial plasma samples for ctDNA analysis by digital PCR.

Results: The TP53 R196* mutation was identified in the primary tumor of the index case with a variant allele frequency (VAF) of 29%, and in the LRR with a VAF of 58%. The same mutation was also detected in plasma prior to both the primary and LRR surgeries with VAFs of 0.19% and 0.12%, respectively. Following treatment, the mutation became undetectable in plasma samples during follow-up, consistent with the absence of recurrence. Among 40 eligible patients from the fenretinide prevention trial, 27 (67.5%) had primary tumor somatic variants trackable in plasma. Median age was 55 years (range, 35-78); stage I (16, 59%) and stage II (11, 41%); mostly luminal-like (19, 70%); median follow-up 173 months (range, 98-193); common mutations included PIK3CA (50%), TP53 (30.7%), and PTEN (5.9%). Six patients developed LRR as first event; 4 distant metastases. In all LRR cases, except one, ctDNA was detected prior to surgery and anticipated the clinical diagnosis up to 28 months. Three patients with LRR developed distant metastases 1 to 2 years later.

Conclusion: These findings show the potential of ctDNA for the early detection of LRR in EBC, and its promise as a tool for timely interventions and personalized surveillance strategies.

循环肿瘤DNA预测早期乳腺癌局部区域复发:一项概念验证研究
背景:局部区域复发(LRR)对早期乳腺癌(EBC)患者的随访提出了临床挑战。虽然循环肿瘤DNA (ctDNA)已被证明可以预测远处转移,但其对LRR的价值尚不明确。方法:从有LRR记录和可获得肿瘤和血浆样本的指标病例开始,我们报告了前瞻性III期芬瑞啶预防试验的分析,该试验主要旨在评估T1-T2 N0型EBC女性第二恶性肿瘤的发生率。如果患者有来自原发性或复发性侵袭性肿瘤的FFPE和/或冷冻组织进行下一代测序,并且至少有三个连续血浆样本用于数字PCR的ctDNA分析,则符合条件。结果:TP53 R196*突变在原发性肿瘤中发现,变异等位基因频率(VAF)为29%,在LRR中发现变异等位基因频率(VAF)为58%。在原发性和LRR手术前的血浆中也检测到相同的突变,VAFs分别为0.19%和0.12%。治疗后,在随访期间血浆样本中检测不到突变,与没有复发相一致。在芬维啶预防试验的40例符合条件的患者中,27例(67.5%)在血浆中有可追踪的原发性肿瘤体细胞变异。中位年龄55岁(范围35-78岁);I期(16.59%)和II期(11.41%);大部分是发光的(19.70%);中位随访173个月(范围98-193);常见突变包括PIK3CA(50%)、TP53(30.7%)和PTEN(5.9%)。6例患者首次发生LRR;4例远处转移。在所有LRR病例中,除一例外,ctDNA在手术前检测,并在临床诊断前28个月检测。3例LRR患者在1至2年后发生远处转移。结论:这些发现表明ctDNA在EBC中早期检测LRR的潜力,以及它作为及时干预和个性化监测策略的工具的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Oncology
Frontiers in Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
6.20
自引率
10.60%
发文量
6641
审稿时长
14 weeks
期刊介绍: Cancer Imaging and Diagnosis is dedicated to the publication of results from clinical and research studies applied to cancer diagnosis and treatment. The section aims to publish studies from the entire field of cancer imaging: results from routine use of clinical imaging in both radiology and nuclear medicine, results from clinical trials, experimental molecular imaging in humans and small animals, research on new contrast agents in CT, MRI, ultrasound, publication of new technical applications and processing algorithms to improve the standardization of quantitative imaging and image guided interventions for the diagnosis and treatment of cancer.
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