| Literature DB >> 28692178 |
Veronika Kubaczkova1, David Vrabel2, Lenka Sedlarikova1, Lenka Besse3, Sabina Sevcikova1.
Abstract
Although tumor cells are the most reliable source of tumor DNA, biopsy of the tumor is an invasive procedure that should be avoided in some cases. The main limitation of any biopsy is sampling of one tumor site, which may not represent all malignant clones due to the heterogeneity of the tumor. These clones respond to treatment differently and thus directly influence survival of the patient. Circulating cell-free DNA (cfDNA) is released from multiple tumor sites, reflects overall heterogeneity of the tumor, and correlates with its progression. Detection of tumor-specific genetic and epigenetic aberrations in cfDNA could have a direct impact on molecular diagnosis, prognosis, follow-up of disease, monitoring of minimal residual disease, and response to treatment. While most cfDNA data are still experimental, they are very promising. This review focuses on cfDNA in hematological malignancies.Entities:
Keywords: acute lymphoblastic leukemia; acute myeloid leukemia; multiple myeloma; myelodysplastic syndromes
Mesh:
Substances:
Year: 2017 PMID: 28692178 DOI: 10.1111/ejh.12925
Source DB: PubMed Journal: Eur J Haematol ISSN: 0902-4441 Impact factor: 2.997