医学
肿瘤科
循环肿瘤DNA
生物标志物
乳腺癌
临床试验
循环肿瘤细胞
微小残留病
内科学
观察研究
液体活检
疾病
个性化医疗
前瞻性队列研究
新辅助治疗
精密医学
癌症
临床意义
临床研究设计
转移性乳腺癌
生物信息学
心理干预
梅德林
重症监护医学
阶段(地层学)
伴生诊断
临床研究
生物标志物发现
化疗
临床实习
靶向治疗
曲妥珠单抗
作者
Ilana Schlam,S M Tolaney,Nancy U. Lin,Heather Parsons,Stefania Morganti
出处
期刊:JAMA Oncology
[American Medical Association]
日期:2026-05-28
卷期号:12 (7): 773-773
被引量:2
标识
DOI:10.1001/jamaoncol.2026.1465
摘要
Importance: Circulating tumor DNA (ctDNA) has emerged as a noninvasive biomarker with the potential to detect minimal residual disease (MRD), monitor treatment response, and identify recurrence (eg, molecular relapse) earlier than conventional clinical or imaging approaches. Although ctDNA-based MRD assays have demonstrated prognostic value in early breast cancer, their optimal clinical utility remains uncertain. Observations: This review summarizes the current data on ctDNA MRD assays in early breast cancer. Although these assays have established analytical and clinical validity, their clinical utility remains uncertain. Dynamics of ctDNA during neoadjuvant therapy are associated with pathologic complete response and long-term outcomes. Following completion of curative-intent therapy, ctDNA positivity (eg, presence of MRD) is strongly associated with future distant recurrence. Similarly, the emergence of ctDNA during surveillance precedes the clinical diagnosis of overt metastatic disease. Although observational studies and meta-analyses have supported ctDNA as a complementary biomarker for established risk-stratification tools, evidence that demonstrates improved outcomes with ctDNA-guided management remains limited. Furthermore, the optimal timing and frequency of testing remain unknown, and studies comparing assays are lacking. Multiple ongoing prospective interventional trials are evaluating whether ctDNA-guided treatment escalation or de-escalation can improve patient outcomes and support the routine implementation of ctDNA assays in clinical practice. Conclusions and Relevance: ctDNA-based MRD assays hold promise for refining risk stratification, enabling earlier detection of recurrence, and informing treatment decisions in patients with early breast cancer, but clinical utility has not yet been demonstrated. Prospective trials are essential to determine whether ctDNA-guided interventions improve outcomes beyond standard management. Clinicians should understand the strengths, limitations, and evolving evidence base of ctDNA assays, as well as patient preferences, prior to incorporating them into patient care.
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