Literature DB >> 28482729

Treatment of chronic myeloid leukemia: assessing risk, monitoring response, and optimizing outcome.

Naranie Shanmuganathan1,2,3,4, Devendra Keshaorao Hiwase1,2,3,4, David Morrall Ross1,2,3,4,5.   

Abstract

Over the past two decades, tyrosine kinase inhibitors have become the foundation of chronic myeloid leukemia (CML) treatment. The choice between imatinib and newer tyrosine kinase inhibitors (TKIs) needs to be balanced against the known toxicity and efficacy data for each drug, the therapeutic goal being to maximize molecular response assessed by BCR-ABL RQ-PCR assay. There is accumulating evidence that the early achievement of molecular targets is a strong predictor of superior long-term outcomes. Early response assessment provides the opportunity to intervene early with the aim of ensuring an optimal response. Failure to achieve milestones or loss of response can have diverse causes. We describe how clinical and laboratory monitoring can be used to ensure that each patient is achieving an optimal response and, in patients who do not reach optimal response milestones, how the monitoring results can be used to detect resistance and understand its origins.

Entities:  

Keywords:  BCR-ABL; Chronic myeloid leukemia; minimal residual disease; resistance

Mesh:

Year:  2017        PMID: 28482729     DOI: 10.1080/10428194.2017.1312377

Source DB:  PubMed          Journal:  Leuk Lymphoma        ISSN: 1026-8022


  7 in total

1.  Early molecular response in East African Philadelphia chromosome-positive chronic myeloid leukaemia patients treated with Imatinib and barriers to access treatment.

Authors:  Oliver Henke; Priscus John Mapendo; Elifuraha Wilson Mkwizu; Philipp le Coutre
Journal:  Ecancermedicalscience       Date:  2020-08-18

2.  Budget impact analysis of treatment-free remission in nilotinib-treated Japanese chronic myeloid leukemia patients.

Authors:  Kiyotaka Yamazaki; Naohito Inagaki; Daniel Moldaver; Ricardo Viana; Shinya Kimura
Journal:  Cancer Sci       Date:  2020-05-23       Impact factor: 6.716

3.  HucMSC exosomes promoted imatinib-induced apoptosis in K562-R cells via a miR-145a-5p/USP6/GLS1 axis.

Authors:  Xiaowen Chen; Yixin Chen; Min Zhang; Hui Cheng; Huirong Mai; Meng Yi; Huanli Xu; Xiuli Yuan; Sixi Liu; Feiqiu Wen
Journal:  Cell Death Dis       Date:  2022-01-28       Impact factor: 9.685

4.  Knockdown of ADORA2A antisense RNA 1 inhibits cell proliferation and enhances imatinib sensitivity in chronic myeloid leukemia.

Authors:  Yabo Liu; Huibo Li; Yanqiu Zhao; Dandan Li; Qian Zhang; Jinyue Fu; Shengjin Fan
Journal:  Bioengineered       Date:  2022-02       Impact factor: 3.269

5.  A systematic review and meta-analysis on the risk factors of acute myeloid leukemia.

Authors:  Yanrong Guo; Wenwen Wang; Huali Sun
Journal:  Transl Cancer Res       Date:  2022-04       Impact factor: 1.241

6.  Anticancer potential of mebendazole against chronic myeloid leukemia: in silico and in vitro studies revealed new insights about the mechanism of action.

Authors:  Julio Paulino Daniel; Felipe Pantoja Mesquita; Emerson Lucena Da Silva; Pedro Filho Noronha de Souza; Luina Benevides Lima; Lais Lacerda Brasil de Oliveira; Maria Elisabete Amaral de Moraes; Caroline de Fátima Aquino Moreira-Nunes; Rommel Mario Rodríguez Burbano; Geancarlo Zanatta; Raquel Carvalho Montenegro
Journal:  Front Pharmacol       Date:  2022-08-25       Impact factor: 5.988

7.  A Rare Chromosome Abnormality with der(16)t(1;16)(q12;q11.2) in Blast Crisis of Chronic Myeloid Leukemia.

Authors:  Ryo Yanagiya; Daisuke Ishikawa; Tomomi Toubai; Tsubasa Ichikawa; Naofumi Kawaguchi; Kunie Sugasawa; Kenichi Ishizawa; Soichi Saito
Journal:  Case Rep Oncol       Date:  2020-08-27
  7 in total

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