TY - JOUR
T1 - Prognostic and Predictive Molecular Biomarkers in Chronic Lymphocytic Leukemia
AU - Lee, Jimmy
AU - Wang, Y. Lynn
N1 - Publisher Copyright:
© 2020 Association for Molecular Pathology and American Society for Investigative Pathology
PY - 2020/9
Y1 - 2020/9
N2 - Chronic lymphocytic leukemia (CLL) is a malignancy of B cells with a variable clinical course. Prognostication is important to place patients into different risk categories for guiding decisions on clinical management, to treat or not to treat. Although several clinical, cytogenetic, and molecular parameters have been established, in the past decade, a tremendous understanding of molecular lesions has been obtained with the advent of high-throughput sequencing. Meanwhile, rapid advances in the understanding of the CLL oncogenic pathways have led to the development of small-molecule targeting signal transducers, Bruton tyrosine kinase and phosphatidylinositol 3-kinase, as well as anti-apoptotic protein BCL2 apoptosis regulator. After an initial response to these targeted therapies, some patients develop resistance and experience disease progression. Novel gene mutations have been identified that account for some of the drug resistance mechanisms. This article focuses on the prognostic and predictive molecular biomarkers in CLL relevant to the molecular pathology practice, beginning with a review of well-established prognostic markers that have already been incorporated into major clinical guidelines, which will be followed by a discussion of emerging biomarkers that are expected to impact clinical practice soon in the future. Special emphasis will be put on predictive biomarkers related to newer targeted therapies in hopes that this review will serve as a useful reference for molecular diagnostic professionals, clinicians, as well as laboratory investigators and trainees.
AB - Chronic lymphocytic leukemia (CLL) is a malignancy of B cells with a variable clinical course. Prognostication is important to place patients into different risk categories for guiding decisions on clinical management, to treat or not to treat. Although several clinical, cytogenetic, and molecular parameters have been established, in the past decade, a tremendous understanding of molecular lesions has been obtained with the advent of high-throughput sequencing. Meanwhile, rapid advances in the understanding of the CLL oncogenic pathways have led to the development of small-molecule targeting signal transducers, Bruton tyrosine kinase and phosphatidylinositol 3-kinase, as well as anti-apoptotic protein BCL2 apoptosis regulator. After an initial response to these targeted therapies, some patients develop resistance and experience disease progression. Novel gene mutations have been identified that account for some of the drug resistance mechanisms. This article focuses on the prognostic and predictive molecular biomarkers in CLL relevant to the molecular pathology practice, beginning with a review of well-established prognostic markers that have already been incorporated into major clinical guidelines, which will be followed by a discussion of emerging biomarkers that are expected to impact clinical practice soon in the future. Special emphasis will be put on predictive biomarkers related to newer targeted therapies in hopes that this review will serve as a useful reference for molecular diagnostic professionals, clinicians, as well as laboratory investigators and trainees.
KW - Adenine/analogs & derivatives
KW - Agammaglobulinaemia Tyrosine Kinase/antagonists & inhibitors
KW - Aged
KW - Animals
KW - Biomarkers, Tumor/genetics
KW - Drug Resistance, Neoplasm/genetics
KW - Female
KW - Humans
KW - Leukemia, Lymphocytic, Chronic, B-Cell/diagnosis
KW - Male
KW - Molecular Targeted Therapy/methods
KW - Mutation
KW - Piperidines/pharmacology
KW - Prognosis
KW - Treatment Outcome
UR - http://www.scopus.com/inward/record.url?scp=85089728739&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000569911300003&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1016/j.jmoldx.2020.06.004
DO - 10.1016/j.jmoldx.2020.06.004
M3 - Review article
C2 - 32615167
SN - 1525-1578
VL - 22
SP - 1114
EP - 1125
JO - Journal of Molecular Diagnostics
JF - Journal of Molecular Diagnostics
IS - 9
ER -