| Literature DB >> 29801428 |
Ciprian Tomuleasa1,2, Cristina Selicean1, Sonia Cismas3,4, Anca Jurj5, Mirela Marian1, Delia Dima1, Sergiu Pasca5, Bobe Petrushev5, Vlad Moisoiu5, Wilhelm-Thomas Micu5, Anna Vischer4, Kanza Arifeen4, Sonia Selicean4, Mihnea Zdrenghea1,4, Horia Bumbea6,7, Alina Tanase8, Ravnit Grewal9, Laura Pop5, Carmen Aanei10, Ioana Berindan-Neagoe5.
Abstract
Chronic lymphocytic leukemia (CLL) is a malignancy defined by the accumulation of mature lymphocytes in the lymphoid tissues, bone marrow, and blood. Therapy for CLL is guided according to the Rai and Binet staging systems. Nevertheless, state-of-the-art protocols in disease monitoring, diagnostics, and prognostics for CLL are based on the assessment of minimal residual disease (MRD). MRD is internationally considered to be the level of disease that can be detected by sensitive techniques and represents incomplete treatment and a probability of disease relapse. MRD detection has been continuously improved by the quick development of both flow cytometry and molecular biology technology, as well as by next-generation sequencing. Considering that MRD detection is moving more and more from research to clinical practice, where it can be an independent prognostic marker, in this paper, we present the methodologies by which MRD is evaluated, from translational research to clinical practice.Entities:
Keywords: Chronic lymphocytic leukemia; clinical relevance; minimal residual disease
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Year: 2018 PMID: 29801428 DOI: 10.1080/10408363.2018.1463508
Source DB: PubMed Journal: Crit Rev Clin Lab Sci ISSN: 1040-8363 Impact factor: 6.250