Detailed Information on Publication Record
2021
Evaluation of two CE-IVD tests for BCR-ABL1 transcript monitoring of chronic myeloid leukemia patients
FOLTA, Adam, Tomas JURCEK, Blanka KUBESOVA, Daniela ŽÁČKOVÁ, Lukáš SEMERÁD et. al.Basic information
Original name
Evaluation of two CE-IVD tests for BCR-ABL1 transcript monitoring of chronic myeloid leukemia patients
Authors
FOLTA, Adam (203 Czech Republic), Tomas JURCEK (203 Czech Republic), Blanka KUBESOVA (203 Czech Republic), Daniela ŽÁČKOVÁ (203 Czech Republic, belonging to the institution), Lukáš SEMERÁD (203 Czech Republic, belonging to the institution), Jiří MAYER (203 Czech Republic, belonging to the institution) and Ivana JEŽÍŠKOVÁ (203 Czech Republic, guarantor, belonging to the institution)
Edition
LEUKEMIA & LYMPHOMA, LONDON, INFORMA HEALTHCARE, 2021, 1042-8194
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30205 Hematology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.996
RIV identification code
RIV/00216224:14110/21:00120995
Organization unit
Faculty of Medicine
UT WoS
000603914300001
Keywords in English
CE-IVD tests; BCR-ABL1 transcript monitoring; chronic myeloid leukemia
Tags
International impact, Reviewed
Změněno: 14/7/2021 07:11, Mgr. Tereza Miškechová
Abstract
V originále
According to European Leukemia Network (ELN) recommendations, real-time quantitative PCR (qRT-PCR) is a conventional strategy for long-term BCR-ABL1 transcript monitoring in patients with chronic myeloid leukemia (CML) both during tyrosine kinase inhibitor (TKI) therapy and its discontinuation [1–5]. However, with the new Regulation (EU) 2017/746 coming, health institutions will have to start using CE-marked IVD (CE-IVD) devices (including kits, reagents, calibrators, etc.) for analyses. Thus, commercial CE-IVD tests will also enter into routine CML diagnostics in the near future.
Links
MUNI/A/1395/2019, interní kód MU |
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