TY - JOUR
T1 - The use of cell free DNA (cfDNA) for mutational screening of multiple myeloma
AU - Marivel, A. M.Joëlle
AU - Ma, Yafeng
AU - Becker, Therese M.
AU - Verma, Anvita
AU - Trieu, Steven
AU - Roberts, Tara L.
AU - Ling, Silvia C.W.
N1 - Publisher Copyright:
© 2023
PY - 2023
Y1 - 2023
N2 - Multiple myeloma (MM) is an incurable haematological malignancy which relies heavily on bone marrow biopsies for disease monitoring and prediction of treatment response. In recent years, liquid biopsy derived cell-free DNA (cfDNA) has emerged as alternative for invasive biopsies. This pilot study aimed to evaluate the feasibility of using cfDNA for the detection of oncogenic mutations in the mitogen-activated protein kinase (MAPK) pathway genes NRAS, KRAS, and BRAF in MM patients. Matched peripheral blood and bone marrow aspirates were collected from thirteen MM patients at various disease stages. cfDNA was isolated using the Qiagen Circulating Nucleic Acid Kit while bone marrow DNA was extracted using the Maxwell Promega platform. The presence of NRAS, KRAS, and BRAF mutations was analysed by ddPCR and compared between the cfDNA and gDNA samples. Although our data come from a small patient cohort, mutations were detected, which supports cfDNA utility for mutational screening and prognostication in MM.
AB - Multiple myeloma (MM) is an incurable haematological malignancy which relies heavily on bone marrow biopsies for disease monitoring and prediction of treatment response. In recent years, liquid biopsy derived cell-free DNA (cfDNA) has emerged as alternative for invasive biopsies. This pilot study aimed to evaluate the feasibility of using cfDNA for the detection of oncogenic mutations in the mitogen-activated protein kinase (MAPK) pathway genes NRAS, KRAS, and BRAF in MM patients. Matched peripheral blood and bone marrow aspirates were collected from thirteen MM patients at various disease stages. cfDNA was isolated using the Qiagen Circulating Nucleic Acid Kit while bone marrow DNA was extracted using the Maxwell Promega platform. The presence of NRAS, KRAS, and BRAF mutations was analysed by ddPCR and compared between the cfDNA and gDNA samples. Although our data come from a small patient cohort, mutations were detected, which supports cfDNA utility for mutational screening and prognostication in MM.
UR - http://www.scopus.com/inward/record.url?scp=85174526239&partnerID=8YFLogxK
U2 - 10.1016/j.lrr.2023.100393
DO - 10.1016/j.lrr.2023.100393
M3 - Article
AN - SCOPUS:85174526239
SN - 2213-0489
VL - 20
JO - Leukemia Research Reports
JF - Leukemia Research Reports
M1 - 100393
ER -