TY - JOUR
T1 - Chronic Myeloid Leukemia, from Pathophysiology to Treatment-Free Remission
T2 - A Narrative Literature Review
AU - Rinaldi, Ikhwan
AU - Winston, Kevin
N1 - Funding Information:
The authors would like to express their gratitude to Yehezkiel Alexander Eduard George, MD, for his professional assistance in proofreading the galley proof of the manuscript.
Publisher Copyright:
© 2023 Rinaldi and Winston.
PY - 2023
Y1 - 2023
N2 - Chronic myeloid leukemia (CML) is one of the most common leukemias occurring in the adult population. The course of CML is divided into three phases: the chronic phase, the acceleration phase, and the blast phase. Pathophysiology of CML revolves around Philadelphia chromosome that constitutively activate tyrosine kinase through BCR-ABL1 oncoprotein. In the era of tyrosine kinase inhibitors (TKIs), CML patients now have a similar life expectancy to people without CML, and it is now very rare for CML patients to progress to the blast phase. Only a small proportion of CML patients have resistance to TKI, caused by BCR-ABL1 point mutations. CML patients with TKI resistance should be treated with second or third generation TKI, depending on the BCR-ABL1 mutation. Recently, many studies have shown that it is possible for CML patients who achieve a long-term deep molecular response to stop TKIs treatment and maintain remission. This review aimed to provide an overview of CML, including its pathophysiology, clinical manifestations, the role of stem cells, CML treatments, and treatment-free remission.
AB - Chronic myeloid leukemia (CML) is one of the most common leukemias occurring in the adult population. The course of CML is divided into three phases: the chronic phase, the acceleration phase, and the blast phase. Pathophysiology of CML revolves around Philadelphia chromosome that constitutively activate tyrosine kinase through BCR-ABL1 oncoprotein. In the era of tyrosine kinase inhibitors (TKIs), CML patients now have a similar life expectancy to people without CML, and it is now very rare for CML patients to progress to the blast phase. Only a small proportion of CML patients have resistance to TKI, caused by BCR-ABL1 point mutations. CML patients with TKI resistance should be treated with second or third generation TKI, depending on the BCR-ABL1 mutation. Recently, many studies have shown that it is possible for CML patients who achieve a long-term deep molecular response to stop TKIs treatment and maintain remission. This review aimed to provide an overview of CML, including its pathophysiology, clinical manifestations, the role of stem cells, CML treatments, and treatment-free remission.
KW - chronic myeloid leukemia
KW - remission
KW - tyrosine kinase inhibitor
UR - http://www.scopus.com/inward/record.url?scp=85153883193&partnerID=8YFLogxK
U2 - 10.2147/JBM.S382090
DO - 10.2147/JBM.S382090
M3 - Review article
AN - SCOPUS:85153883193
SN - 1179-2736
VL - 14
SP - 261
EP - 277
JO - Journal of Blood Medicine
JF - Journal of Blood Medicine
ER -