Chronic Myeloid Leukemia, Version 1.2019, NCCN Clinical Practice Guidelines in Oncology

Jerald P. Radich, Michael W. Deininger, Camille N. Abboud(Fox Chase Cancer Center), Jessica K. Altman(Fox Chase Cancer Center), Ellin Berman, Ravi Bhatia, Bhavana Bhatnagar, Peter Curtin(Fox Chase Cancer Center), Daniel J. DeAngelo(Fox Chase Cancer Center), Jason Gotlib(Fox Chase Cancer Center), Gabriela Hobbs(Fox Chase Cancer Center), Madan Jagasia, Hagop M. Kantarjian(Fox Chase Cancer Center), Lori J. Maness(Fox Chase Cancer Center), Leland Metheny, Joseph O. Moore, Arnel Pallera(Fox Chase Cancer Center), Philip Pancari, Mrinal M. Patnaik, Enkhtsetseg Purev, Michal G. Rose, Neil P. Shah(Fox Chase Cancer Center), B. Douglas Smith(Memorial Sloan Kettering Cancer Center), David S. Snyder(Fox Chase Cancer Center), Kendra Sweet(Fox Chase Cancer Center), Moshe Talpaz, James E. Thompson(Fox Chase Cancer Center), David T. Yang, Kristina M. Gregory, Hema Sundar
Journal of the National Comprehensive Cancer Network
September 1, 2018
Cited by 281Open Access
Full Text

Abstract

Chronic myeloid leukemia (CML) is defined by the presence of Philadelphia chromosome (Ph), resulting from a reciprocal translocation between chromosomes 9 and 22 [t(9;22] that gives rise to a BCR-ABL1 fusion gene. CML occurs in 3 different phases (chronic, accelerated, and blast phase) and is usually diagnosed in the chronic phase. Tyrosine kinase inhibitor (TKI) therapy is a highly effective first-line treatment option for all patients with newly diagnosed chronic phase CML (CP-CML). The selection TKI therapy should be based on the risk score, toxicity profile of TKI, patient's age, ability to tolerate therapy, and the presence of comorbid conditions. This manuscript discusses the recommendations outlined in the NCCN Guidelines for the diagnosis and management of patients with CP-CML.


Related Papers

No related papers found

Powered by citation graph analysis