ReviewFrontiers in oncology2026
ctDNA-based detection of residual disease: implications for management of non-metastatic NSCLC.
Review in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Despite advancements in perioperative and consolidative immunotherapy in early-stage to locally advanced non-small cell lung cancer (NSCLC), recurrence rates remain substantial. In this context, liquid biopsy has transformed the oncological landscape by enabling the non-invasive detection of tumor-derived components, including DNA, cells, and proteins, from biological fluids. Although plasma-based circulating tumor DNA (ctDNA) analysis is routinely used in metastatic NSCLC to identify actionable genomic alterations at diagnosis and mechanisms of acquired resistance to targeted therapies, its application in non-metastatic disease represents a pivotal challenge. Leveraging minimal residual disease (MRD) detection through ctDNA offers the potential for early risk stratification, enabling the identification of patients who may benefit from treatment escalation, such as intensified adjuvant or consolidative regimens, while sparing low-risk patients from unnecessary toxicity through de-escalation strategies. This review summarizes the biological and technological foundations underlying ctDNA-based MRD detection, including tumor-informed and non-tumor-informed approaches, and examines the current evidence supporting its clinical utility in non-metastatic NSCLC. We also highlight key technical and clinical challenges and discuss future perspectives to optimize integration of ctDNA MRD assessment into routine clinical practice.
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