scholarly journals Atypical chronic myeloid leukemia is clinically distinct from unclassifiable myelodysplastic/myeloproliferative neoplasms

Blood ◽  
2014 ◽  
Vol 123 (17) ◽  
pp. 2645-2651 ◽  
Author(s):  
Sa A. Wang ◽  
Robert P. Hasserjian ◽  
Patricia S. Fox ◽  
Heesun J. Rogers ◽  
Julia T. Geyer ◽  
...  

Key Points Within MDS/MPN, the WHO 2008 criteria for aCML identify a subgroup of patients with aggressive clinical features distinct from MDS/MPN-U. The MDS/MPN-U category is heterogeneous, and patient risk can be further stratified by a number of clinicopathological parameters.

Blood ◽  
2015 ◽  
Vol 125 (3) ◽  
pp. 499-503 ◽  
Author(s):  
Carlo B. Gambacorti-Passerini ◽  
Carla Donadoni ◽  
Andrea Parmiani ◽  
Alessandra Pirola ◽  
Sara Redaelli ◽  
...  

Key Points Whole-exome sequencing reveals the presence of recurrent somatic mutations of ETNK1 in patients with atypical chronic myeloid leukemia. ETNK1 mutations impair the catalytic activity of the enzyme, causing a decrease in the intracellular levels of phosphoethanolamine.


2011 ◽  
Vol 1 (4) ◽  
pp. 232
Author(s):  
Ju Yeon Kim ◽  
Se Ryeon Lee ◽  
Myung-Hyun Nam ◽  
Soo-Young Yoon ◽  
Chae Seung Lim ◽  
...  

2017 ◽  
Vol 14 (3) ◽  
pp. 3717-3721
Author(s):  
Masahide Yamamoto ◽  
Sayaka Suzuki ◽  
Jun-Ichi Mukae ◽  
Keisuke Tanaka ◽  
Ken Watanabe ◽  
...  

2018 ◽  
Vol 10 (3) ◽  
Author(s):  
Aya Nakaya ◽  
Shinya Fujita ◽  
Atsushi Satake ◽  
Takahisa Nakanishi ◽  
Yoshiko Azuma ◽  
...  

Dasatinib is currently approved for clinical use as a first-line treatment agent for newly diagnosed chronic myeloid leukemia (CML). However, only a few clinical trials have been performed to evaluate dasatinibinduced PE following first-line therapy. We investigated the incidence and clinical features of dasatinib-induced PE following first-line therapy in Japanese CML patients of real world clinical practice settings. Among 22 patients, the median age of PEpositive patients was higher than that of PEnegative patients. Major molecular response was achieved in 75% of PE-positive patients and 50% of PE-negative patients. Most patients developed PE more than 1 year after treatment. Appearance of PE is associated with better clinical response during dasatinib treatment, however it is developed at any time. Elderly and high-risk patients tend to develop PE. The clinical features of dasatinib-induced PE following first-line therapy might be late onset and might not immediately follow the increasing of large granular lymphocyte.


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