Circulating miRNA Signature Predicts Response to Preoperative Chemoradiotherapy in Locally Advanced Rectal Cancer

被引:6
|
作者
Wada, Yuma [1 ,2 ,3 ,4 ]
Shimada, Mitsuo [2 ]
Morine, Yuji [2 ]
Ikemoto, Tetsuya [2 ]
Saito, Yu [2 ]
Zhu, Zhongxu [5 ]
Wang, Xin [5 ]
Etxart, Ane [6 ]
Park, Yangsoon [7 ]
Bujanda, Luis [8 ]
Park, In Ja [9 ]
Goel, Ajay [1 ,3 ,4 ,10 ]
机构
[1] City Hope Natl Med Ctr, Dept Mol Diagnost & Expt Therapeut, Beckman Res Inst, Monrovia, CA 91016 USA
[2] Tokushima Univ, Dept Surg, Tokushima, Japan
[3] Baylor Univ, Med Ctr, Ctr Gastrointestinal Res, Baylor Scott & White Res Inst, Dallas, TX USA
[4] Baylor Univ, Med Ctr, Charles A Sammons Canc Ctr, Dallas, TX USA
[5] City Univ Hong Kong, Dept Biomed Sci, Hong Kong, Peoples R China
[6] Donostia Hosp Univ, Inst Biodonostia, Dept Surg, San Sebastian, Spain
[7] Univ Ulsan, Asan Med Ctr, Dept Pathol, Coll Med, Seoul, South Korea
[8] Univ Basque Country, Ctr Invest Biomed Red Enfermedades Hepat & Digest, Inst Biodonostia, Gastroenterol Dept,UPV EHU, San Sebastian, Spain
[9] Univ Ulsan, Asan Med Ctr, Dept Surg, Div Colon & Rectal Surg,Coll Med, Seoul, South Korea
[10] City Hope Comprehens Canc Ctr, Duarte, CA USA
基金
美国国家卫生研究院;
关键词
PATHOLOGICAL COMPLETE RESPONSE; TUMOR-REGRESSION GRADE; NEOADJUVANT CHEMORADIOTHERAPY; POSTOPERATIVE CHEMORADIOTHERAPY; PROGNOSTIC-SIGNIFICANCE; MICRORNA EXPRESSION; FOLLOW-UP; PHASE-II; CHEMORADIATION; THERAPY;
D O I
10.1200/PO.21.00015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE 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. (C) 2021 by American Society of Clinical Oncology
引用
收藏
页码:1788 / 1801
页数:14
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