TY - JOUR
T1 - Detection of dormant chronic myeloid leukemia clones in the bone marrow of patients in complete molecular remission
AU - Quintás-Cardama, Alfonso
AU - Grgurevic, Srdana
AU - Rozovski, Uri
AU - Li, Ping
AU - Estrov, Zeev
AU - Cortes, Jorge
N1 - Funding Information:
J.C. received grant funding from Novartis and BMS. Rest of the authors declare no conflicts of interest.
PY - 2013/12
Y1 - 2013/12
N2 - Background Several methods are available to detect MRD in patients with CML in complete molecular remission (CMR) and taking tyrosine kinase inhibitor (TKI) therapy. Materials and Methods We performed clonogenic assays on mononuclear bone marrow cells from 14 patients. Of the 10 assessable samples, 6 were from patients in CMR and 4 from patients in complete cytogenetic remission but had detectable MRD using polymerase chain reaction (PCR) analysis (positive controls). At least 10 colonies per sample were microaspirated and individual colonies were subjected to PCR analysis. Results Of the 6 patients in CMR, 5 harbored breakpoint cluster region abelson (BCR-ABL1) negative colonies but in 1 sample, 1 of the 10 colonies analyzed was positive for BCR-ABL1. Of the 4 patients with evidence of MRD in peripheral blood, 2 had negative and 2 had positive BCR-ABL1 colonies. Conclusion MRD is still detectable using clonogenic assays in some patients with CML after achieving CMR using TKI therapy, which is likely responsible for relapse on TKI discontinuation. Because of the large number of single colonies that need to be analyzed, the use of clonogenic assays in clinical practice to determine the feasibility of TKI discontinuation is not recommended.
AB - Background Several methods are available to detect MRD in patients with CML in complete molecular remission (CMR) and taking tyrosine kinase inhibitor (TKI) therapy. Materials and Methods We performed clonogenic assays on mononuclear bone marrow cells from 14 patients. Of the 10 assessable samples, 6 were from patients in CMR and 4 from patients in complete cytogenetic remission but had detectable MRD using polymerase chain reaction (PCR) analysis (positive controls). At least 10 colonies per sample were microaspirated and individual colonies were subjected to PCR analysis. Results Of the 6 patients in CMR, 5 harbored breakpoint cluster region abelson (BCR-ABL1) negative colonies but in 1 sample, 1 of the 10 colonies analyzed was positive for BCR-ABL1. Of the 4 patients with evidence of MRD in peripheral blood, 2 had negative and 2 had positive BCR-ABL1 colonies. Conclusion MRD is still detectable using clonogenic assays in some patients with CML after achieving CMR using TKI therapy, which is likely responsible for relapse on TKI discontinuation. Because of the large number of single colonies that need to be analyzed, the use of clonogenic assays in clinical practice to determine the feasibility of TKI discontinuation is not recommended.
KW - BCR-ABL1
KW - Clonogenic assay
KW - Colony
KW - Minimal residual disease
KW - Tyrosine kinase inhibitor
UR - http://www.scopus.com/inward/record.url?scp=84888009697&partnerID=8YFLogxK
U2 - 10.1016/j.clml.2013.07.010
DO - 10.1016/j.clml.2013.07.010
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C2 - 24060288
AN - SCOPUS:84888009697
SN - 2152-2650
VL - 13
SP - 681
EP - 685
JO - Clinical Lymphoma, Myeloma and Leukemia
JF - Clinical Lymphoma, Myeloma and Leukemia
IS - 6
ER -