VRÁBEL, Dávid, Jana GREGOROVÁ, Lenka SEDLAŘÍKOVÁ, Martina ALMÁŠI, Renata BEZDĚKOVÁ, Martin ŠTORK, Marta KREJČÍ, Zdeněk ADAM, Luděk POUR, Roman HAJEK and Sabina ŠEVČÍKOVÁ. Tumor Specific cfDNA Predicts Treatment Response of Multiple Myeloma Patients. In 60th Annual Meeting of the American-Society-of-Hematology (ASH). 2018. ISSN 0006-4971. Available from: https://dx.doi.org/10.1182/blood-2018-99-114793.
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Basic information
Original name Tumor Specific cfDNA Predicts Treatment Response of Multiple Myeloma Patients
Authors VRÁBEL, Dávid (703 Slovakia, belonging to the institution), Jana GREGOROVÁ (203 Czech Republic, belonging to the institution), Lenka SEDLAŘÍKOVÁ (203 Czech Republic, belonging to the institution), Martina ALMÁŠI (203 Czech Republic), Renata BEZDĚKOVÁ (203 Czech Republic), Martin ŠTORK (203 Czech Republic), Marta KREJČÍ (203 Czech Republic), Zdeněk ADAM (203 Czech Republic), Luděk POUR (203 Czech Republic), Roman HAJEK (203 Czech Republic) and Sabina ŠEVČÍKOVÁ (203 Czech Republic, belonging to the institution).
Edition 60th Annual Meeting of the American-Society-of-Hematology (ASH), 2018.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 30205 Hematology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 16.601
RIV identification code RIV/00216224:14110/18:00120122
Organization unit Faculty of Medicine
ISSN 0006-4971
Doi http://dx.doi.org/10.1182/blood-2018-99-114793
UT WoS 000454842801007
Keywords in English cell-free dna; multiple myeloma; neoplasms; immunoglobulin heavy chains; polymerase chain reaction; liquid biopsy; massively-parallel genome sequencing; molecule; biopsy; bone marrow specimen
Tags rivok
Tags International impact
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 23/8/2021 11:09.
Abstract
Great progress achieved in treatment of multiple myeloma (MM) over the past decade changed overall perception of importance of minimal residual disease (MRD) assessment. Since new drugs induce deep responses, MRD must be evaluated using sensitive techniques, such as allele specific PCR (ASO-PCR), next-generation sequencing (NGS) or flow cytometry. MM is a genetically heterogeneous cancer of plasma cells characterized by multiple focal lesions in the bone marrow (BM). Hence, a single-site biopsy can create a sampling bias. In spite of this, BM samples are typically used for MRD analysis, but currently an alternative approach called liquid biopsies, which utilizes body fluids for analysis of various molecules and cells, is intensively studied. Cell-free DNA (cfDNA) as one type of the molecule which can be analyzed using liquid biopsy approach showed promising results previously. In our study, patient-specific, clonotypic rearrangement of immunoglobulin heavy chain (IgH) gene, identified in bone marrow samples, was used for qPCR analysis of cfDNA samples from peripheral blood. We demonstrate that dynamics and quantity of patient-specific, clonotypic IgH rearrangement found in cfDNA can predict the outcomes and response of MM patients.
Links
NV17-29343A, research and development projectName: Analýza mikroprostředí kostní dřeně u extramedulárního relapsu mnohočetného myelomu
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