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Circulating miRNA Signature Predicts Response to Preoperative Chemoradiotherapy in Locally Advanced Rectal Cancer.
Wada, Yuma; Shimada, Mitsuo; Morine, Yuji; Ikemoto, Tetsuya; Saito, Yu; Zhu, Zhongxu; Wang, Xin; Etxart, Ane; Park, Yangsoon; Bujanda, Luis; Park, In Ja; Goel, Ajay.
Affiliation
  • Wada Y; Department of Molecular Diagnostics and Experimental Therapeutics, Beckman Research Institute of City of Hope, Monrovia, CA.
  • Shimada M; Department of Surgery, Tokushima University, Tokushima, Japan.
  • Morine Y; Center for Gastrointestinal Research, Baylor Scott & White Research Institute and Charles A. Sammons Cancer Center, Baylor University Medical Center, Dallas, TX.
  • Ikemoto T; Department of Surgery, Tokushima University, Tokushima, Japan.
  • Saito Y; Department of Surgery, Tokushima University, Tokushima, Japan.
  • Zhu Z; Department of Surgery, Tokushima University, Tokushima, Japan.
  • Wang X; Department of Surgery, Tokushima University, Tokushima, Japan.
  • Etxart A; Department of Biomedical Sciences, City University of Hong Kong, Hong Kong, China.
  • Park Y; Department of Biomedical Sciences, City University of Hong Kong, Hong Kong, China.
  • Bujanda L; Department of Surgery, Donostia Hospital University, Instituto Biodonostia, San Sebastián, Spain.
  • Park IJ; Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
  • Goel A; Gastroenterology Department, Instituto Biodonostia, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Universidad del País Vasco (UPV/EHU), San Sebastián, Spain.
Article in En | MEDLINE | ID: mdl-34913022
ABSTRACT
Patients with locally advanced rectal cancer (LARC) are recommended to receive preoperative chemoradiotherapy (PCRT) followed by surgery. Response to PCRT varies widely 60%-70% of patients with LARC do not derive therapeutic benefit from PCRT, whereas 15%-20% of patients achieve pathologic complete response (pCR). We sought to develop a liquid biopsy assay for identifying response to PCRT in patients with LARC. MATERIALS AND

METHODS:

We analyzed two genome-wide microRNA (miRNA) expression profiling data sets from tumor tissue samples for in silico discovery (GSE68204) and validation (GSE29298). We prioritized biomarkers in pretreatment plasma specimens from clinical training (n = 41; 15 responders and 26 nonresponders) and validation (n = 65; 29 responders and 36 nonresponders) cohorts of patients with LARC. We developed an integrated miRNA panel and established a risk assessment model, which was combined with the miRNA panel and carcinoembryonic antigen levels.

RESULTS:

Our comprehensive discovery effort identified an 8-miRNA panel that robustly predicted response to PCRT, with an excellent accuracy in the discovery (area under the curve [AUC] = 0.95) and validation (AUC = 0.92) cohorts. We successfully established a circulating miRNA panel with remarkable diagnostic accuracy in the clinical training (AUC = 0.82) and validation (AUC = 0.81) cohorts. Moreover, the predictive accuracy of the panel was significantly superior to conventional clinical factors in both cohorts (P < .01) and the risk assessment model was superior (AUC = 0.83). Finally, we applied our model to detect patients with pathologic complete response and showed that it was dramatically superior to currently used pathologic features (AUC = 0.92).

CONCLUSION:

Our novel risk assessment signature for predicting response to PCRT has a potential for clinical translation as a liquid biopsy assay in patients with LARC.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rectal Neoplasms / MicroRNAs / Circulating MicroRNA Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: JCO Precis Oncol Year: 2021 Document type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rectal Neoplasms / MicroRNAs / Circulating MicroRNA Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: JCO Precis Oncol Year: 2021 Document type: Article Affiliation country: Canada