Detailed Information on Publication Record
2021
An Independent Validation Study of Candidate microRNAs as Predictive Biomarkers for Bevacizumab-based Therapy in Patients With Metastatic Colorectal Cancer
KISS, David, Táňa MACHÁČKOVÁ, Kamila SOUČKOVÁ, Pavel FABIAN, Iveta KŘEPELKOVÁ et. al.Basic information
Original name
An Independent Validation Study of Candidate microRNAs as Predictive Biomarkers for Bevacizumab-based Therapy in Patients With Metastatic Colorectal Cancer
Authors
KISS, David (203 Czech Republic), Táňa MACHÁČKOVÁ (203 Czech Republic, belonging to the institution), Kamila SOUČKOVÁ (203 Czech Republic, belonging to the institution), Pavel FABIAN (203 Czech Republic), Iveta KŘEPELKOVÁ (203 Czech Republic), M. SVOBODA and Igor KISS (203 Czech Republic, guarantor, belonging to the institution)
Edition
In vivo, ATHENS, Greece : International Institute of Anticancer Research, 2021, 0258-851X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30204 Oncology
Country of publisher
Greece
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.406
RIV identification code
RIV/00216224:14740/21:00120233
Organization unit
Central European Institute of Technology
UT WoS
000691746000013
Keywords in English
Bevacizumab; metastatic colorectal cancer; microRNA; progression-free survival; predictive biomarker; validation
Tags
International impact, Reviewed
Změněno: 15/10/2024 14:27, Ing. Martina Blahová
Abstract
V originále
Background/Aim: The monoclonal antibody bevacizumab is a standard drug used in combination with oxaliplatin (FOLFOX) or irinotecan (FOLFIRI) based chemotherapy in the first or second-line treatment of metastatic colorectal cancer (mCRC). Our previous study identified and subsequently validated 4 microRNAs in a small group of patients as predictors of the therapeutic response to bevacizumab combined with chemotherapy. The aim of this follow-up study is to confirm the predictive ability of these tissue miRNAs in a larger independent cohort of mCRC patients. Patients and Methods: The retrospective study included 92 patients with generalized-radically inoperable tumors treated with the combined therapy of bevacizumab/FOLFOX in a standard regimen. Results: Expression levels of candidate miRNA biomarkers (miR-92b3p, miR-3156-5p, miR-10a-5p and miR-125a-5p) were determined in tumor tissue specimens and statistically evaluated. MiR-92b-3p and miR-125a-5p were confirmed to be associated with radiological response according to RECIST criteria (p=0.005 and 0.05, respectively) and to be up-regulated in responders to bevacizumab/FOLFOX therapy. Higher levels of miR-92b-3p were also significantly associated with extended progression-free survival
Links
NU20-03-00127, research and development project |
| ||
90091, large research infrastructures |
|