Detailed Information on Publication Record
2017
High levels of FLT3-ligand in bone marrow and peripheral blood of patients with advanced multiple myeloma
STEINER, Normann, Roman HAJEK, Sabina ŠEVČÍKOVÁ, Bojana BORJAN, Karin JÖHRER et. al.Basic information
Original name
High levels of FLT3-ligand in bone marrow and peripheral blood of patients with advanced multiple myeloma
Authors
STEINER, Normann (40 Austria), Roman HAJEK (203 Czech Republic), Sabina ŠEVČÍKOVÁ (203 Czech Republic, guarantor, belonging to the institution), Bojana BORJAN (40 Austria), Karin JÖHRER (40 Austria), Georg GÖBEL (40 Austria), Gerold UNTERGASSER (40 Austria) and Eberhard GUNSILIUS (40 Austria)
Edition
Plos one, San Francisco, Public Library of Science, 2017, 1932-6203
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30205 Hematology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.766
RIV identification code
RIV/00216224:14110/17:00097567
Organization unit
Faculty of Medicine
UT WoS
000406634500078
Keywords in English
Multiple myeloma
Tags
Tags
International impact, Reviewed
Změněno: 20/3/2018 18:33, Soňa Böhmová
Abstract
V originále
Introduction Multiple myeloma (MM) is still incurable due to resistance against various therapies. Thus, the identification of biomarkers predicting progression is urgently needed. Here, we evaluated four biomarkers in bone marrow and peripheral blood of MM patients for their prognostic significance. Materials & methods Bone marrow- and peripheral blood plasma levels of FLT3-L, soluble TIE2, endostatin, and osteoactivin were determined in patients with monoclonal gammopathy of undetermined significance (MGUS, n = 14/n = 4), patients with newly diagnosed MM (NDMM, n = 42/n = 31) and patients with relapsed/refractory MM (RRMM, n = 27/n = 16) by sandwich ELISA. Results Median FLT3-L expression increased from MGUS (58.77 pg/ml in bone marrow; 80.40 pg/ml in peripheral blood) to NDMM (63.15 pg/ml in bone marrow; 85.05 pg/ml in peripheral blood) and was maximal in RRMM (122 pg/ml in bone marrow; 160.47 pg/ml in peripheral blood; NDMM vs. RRMM p<0.001). A cut-off value of FLT3-L >92 pg/ml in bone marrow and >121 pg/ml in peripheral blood was associated with relapse or refractoriness in MM patients. FLT3-L was found to be a high predictive marker for discrimination between NDMM and RRMM as well in bone marrow as in peripheral blood (AUC 0.75 in bone marrow; vs 0.84 in peripheral blood). Conclusion High levels of FLT3-L in bone marrow and peripheral blood of MM patients identify patients with progressive disease and are associated with relapse or refractoriness in MM patients. FLT3-L could be useful as a marker to identify RRMM patients and should be evaluated as target for future therapies.