4.7 Article

Clinical Impact of Presurgery Circulating Tumor DNA after Total Neoadjuvant Treatment in Locally Advanced Rectal Cancer: A Biomarker Study from the GEMCAD1402 Trial

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CLINICAL CANCER RESEARCH
卷 27, 期 10, 页码 2890-2898

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-20-4769

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  1. Instituto de Salud Carlos III -FEDER [PI18/00031]
  2. Fundacion CRIS [19-30]
  3. SEOM grant
  4. TTD grant
  5. ISCIII (Juan Rodes Research Contract) [JR18/00003]

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The study showed that in patients with LARC undergoing TNT, the detection of presurgery ctDNA identified individuals at high risk of systemic recurrence, with shorter disease-free survival and overall survival. This sets the foundation for future clinical trials using liquid biopsy to personalize treatment post TNT.
Purpose: Total neoadjuvant treatment (TNT) is a valid strategy for patients with high-risk locally advanced rectal cancer (LARC). Biomarkers of response to TNT are an unmet clinical need. We aimed to determine the value of circulating tumor DNA(ctDNA) to predict tumor response, recurrence, and survival in patients with LARC treated with TNT. Experimental Design: The GEMCAD 1402 was a phase II randomized, multicentric clinical trial that randomized 180 patients with LARC to modified schedule of fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) +/- aflibercept, followed by chemoradiation and surgery. Plasma samples were collected at baseline and after TNT within 48 hours before surgery (presurgery). An ultra-sensitive assay that integrates genomic and epigenomic cancer signatures was used to assess ctDNA status. ctDNA results were correlated with variables of local tumor response in the surgery sample, local/systemic recurrence, and survival. Results: A total of 144 paired plasma samples from 72 patients were included. ctDNA was detectable in 83% of patients at baseline and in 15% following TNT (presurgery). No association was found between ctDNA status and pathologic response. Detectable presurgery ctDNA was significantly associated with systemic recurrence, shorter disease-free survival (HR, 4; P = 0.033), and shorter overall survival (HR, 23; P < 0.0001). Conclusions: In patients with LARC treated with TNT, presurgery ctDNA detected minimal metastatic disease identifying patients at high risk of distant recurrence and death. This study sets the basis for prospective clinical trials that use liquid biopsy to personalize the therapeutic approach following TNT.

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