Literature DB >> 22215488

The role of therapeutic drug monitoring of imatinib in patients with chronic myeloid leukemia and metastatic or unresectable gastrointestinal stromal tumors.

Jennifer F T Teng1, Vincent H Mabasa, Mary H H Ensom.   

Abstract

Imatinib mesylate is a tyrosine kinase inhibitor used as first-line treatment in Philadelphia chromosome-positive chronic myeloid leukemia (Ph+ CML) and metastatic or unresectable gastrointestinal stromal tumors (GIST). Therapeutic drug monitoring (TDM) for imatinib has been suggested to improve efficacy, assess compliance, and evaluate drug-drug interactions. Imatinib has proven efficacy in improving treatment response and survival in patients with Ph+ CML and GIST. Several analytical methods are available to quantify total plasma imatinib concentrations. A good relationship exists between total imatinib plasma concentrations and pharmacologic response. Clinical evaluation of pharmacologic response to imatinib alone may be insufficient given the long duration of therapy before clinical response in patients with Ph+ CML and GIST. Thus, the authors have used a previously published 9-step decision-making algorithm to evaluate the utility of TDM for imatinib. The suggested trough concentrations for improved complete cytogenetic or major molecular response in patients with Ph+ CML and improved time to progression for patients with GIST are >1000 and >1100 ng/mL, respectively. Imatinib exhibits interindividual pharmacokinetic variability. Increased apparent clearance of imatinib has been observed in chronic phase chronic myeloid leukemia and increased body weight. Decreased apparent clearance has been observed in renal impairment and patients on concomitant medications with potent inhibition of cytochrome P450 3A4. Duration of therapy in patients with Ph+ CML and GIST is lifelong. Based on the available evidence, TDM for imatinib may provide additional information on efficacy, compliance, and safety than clinical evaluation alone. Patients with suboptimal response to treatment, treatment failure, rare adverse events, drug interactions, or suspected nonadherence will attain the greatest benefit from TDM.

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Year:  2012        PMID: 22215488     DOI: 10.1097/FTD.0b013e31823cdec9

Source DB:  PubMed          Journal:  Ther Drug Monit        ISSN: 0163-4356            Impact factor:   3.681


  14 in total

1.  Imatinib Pharmacokinetics in a Large Observational Cohort of Gastrointestinal Stromal Tumour Patients.

Authors:  Sheima Farag; Remy B Verheijen; J Martijn Kerst; Annemiek Cats; Alwin D R Huitema; Neeltje Steeghs
Journal:  Clin Pharmacokinet       Date:  2017-03       Impact factor: 6.447

Review 2.  Practical guidelines for therapeutic drug monitoring of anticancer tyrosine kinase inhibitors: focus on the pharmacokinetic targets.

Authors:  Huixin Yu; Neeltje Steeghs; Cynthia M Nijenhuis; Jan H M Schellens; Jos H Beijnen; Alwin D R Huitema
Journal:  Clin Pharmacokinet       Date:  2014-04       Impact factor: 6.447

3.  [Metastasized renal cell carcinoma. Measurement of plasma levels of the tyrosine kinase inhibitors sunitinib, sorafenib and pazopanib].

Authors:  C Keil; L Götze; P Olbert; R Hofmann; W A Nockher; A Hegele
Journal:  Urologe A       Date:  2015-06       Impact factor: 0.639

Review 4.  Treatment of Gastrointestinal Stromal Tumors (GISTs): A Focus on Younger Patients.

Authors:  Monika Dudzisz-Śledź; Anna Klimczak; Elżbieta Bylina; Piotr Rutkowski
Journal:  Cancers (Basel)       Date:  2022-06-08       Impact factor: 6.575

Review 5.  [Current diagnostic requirements in chronic myeloid leukemia].

Authors:  Thomas Lion; Gerald Webersinke; Ulrike Kastner; Christoph Seger; Gerlinde Mitterbauer-Hohendanner; Günther Gastl
Journal:  Wien Med Wochenschr       Date:  2013-10-01

6.  Comment on: Determination of serum levels of imatinib mesylate in patients with chronic myeloid leukemia: validation and application of a new analytical method to monitor treatment compliance.

Authors:  David C Simpson
Journal:  Rev Bras Hematol Hemoter       Date:  2013

7.  Determination of serum levels of imatinib mesylate in patients with chronic myeloid leukemia: validation and application of a new analytical method to monitor treatment compliance.

Authors:  Vinícius Marcondes Rezende; Ariane Julio Rivellis; Melissa Medrano Gomes; Felipe Augusto Dörr; Mafalda Megumi Yoshinaga Novaes; Luciana Nardinelli; Ariel Lais de Lima Costa; Dalton de Alencar Fisher Chamone; Israel Bendit
Journal:  Rev Bras Hematol Hemoter       Date:  2013

8.  Ultra High Performance Liquid Chromatography Method for the Determination of Two Recently FDA Approved TKIs in Human Plasma Using Diode Array Detection.

Authors:  Marwa Fouad; Maxime Helvenstein; Bertrand Blankert
Journal:  J Anal Methods Chem       Date:  2015-05-25       Impact factor: 2.193

9.  Comparative pharmacokinetic evaluation and bioequivalence study of three different formulations of Imatinib Mesylate in CML patients.

Authors:  Ehsan Mohajeri; Behjat Kalantari-Khandani; Abbas Pardakhty; Moeinadin Safavi; Mehdi Ansari
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2015-10-01

10.  Formulation and in vitro, in vivo evaluation of effervescent floating sustained-release imatinib mesylate tablet.

Authors:  Ali Kadivar; Behnam Kamalidehghan; Hamid Akbari Javar; Ehsan Taghizadeh Davoudi; Nurul Dhania Zaharuddin; Bahareh Sabeti; Lip Yong Chung; Mohamed Ibrahim Noordin
Journal:  PLoS One       Date:  2015-06-02       Impact factor: 3.752

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