Literature DB >> 32145037

The multi-tyrosine kinase inhibitor ponatinib for chronic myeloid leukemia: Real-world data.

Luigia Luciano1, Mario Annunziata2, Immacolata Attolico3, Francesco Di Raimondo4, Alessandro Maggi5, Alessandra Malato6, Bruno Martino7, Fausto Palmieri8, Fabrizio Pane1, Nicola Sgherza9, Giorgina Specchia3.   

Abstract

Development of the highly selective targeted tyrosine kinase inhibitors (TKIs) has expanded the therapeutic options for chronic myeloid leukemia (CML). Patients undergoing TKI therapy should be closely monitored to ensure that the best therapeutic response and quality of life are achieved, and to control suboptimal responses and adverse events. Despite the high rate of response using current first-line TKIs, treatment failure may still occur, and resistance is considered a challenge in the treatment of patients with CML. The third-generation TKI, ponatinib, is a potent orally bioavailable pan BCR-ABL inhibitor that inhibits both wild-type and mutant BCR-ABL1 kinase, including the "gatekeeper" T315I mutation, which is resistant to all other currently available TKIs. This paper reviews the effectiveness, feasibility, and safety of ponatinib in the real-life clinical management of CML. Potential prognostic factors in identifying patients most likely to benefit from ponatinib treatment will be discussed, and case presentations illustrating situations encountered in real-life clinical practice are described. Ponatinib is effective in patients who have received prior TKIs in clinical studies as well as under real-life conditions. Nevertheless, the risk/benefit balance must be evaluated for each patient, particularly considering disease state, mutational status, treatment line, intolerance/resistance to prior TKIs, age, frailty, and specific comorbidities.
© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  chronic myeloid leukemia; elderly; frail; intolerant; ponatinib; resistant; tyrosine kinase inhibitors

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Year:  2020        PMID: 32145037     DOI: 10.1111/ejh.13408

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  3 in total

1.  RUNX1 transactivates BCR-ABL1 expression in Philadelphia chromosome positive acute lymphoblastic leukemia.

Authors:  Tatsuya Masuda; Shintaro Maeda; Sae Shimada; Naoya Sakuramoto; Ken Morita; Asami Koyama; Kensho Suzuki; Yoshihide Mitsuda; Hidemasa Matsuo; Hirohito Kubota; Itaru Kato; Kuniaki Tanaka; Junko Takita; Masahiro Hirata; Tatsuki R Kataoka; Tatsutoshi Nakahata; Souichi Adachi; Hideyo Hirai; Shuichi Mizuta; Kazuhito Naka; Yoichi Imai; Shinya Kimura; Hiroshi Sugiyama; Yasuhiko Kamikubo
Journal:  Cancer Sci       Date:  2021-12-28       Impact factor: 6.716

2.  New Imatinib Derivatives with Antiproliferative Activity against A549 and K562 Cancer Cells.

Authors:  Andressa Oliveira; Stefany Moura; Luiz Pimentel; João Neto; Rafael Dantas; Floriano Silva-Jr; Monica Bastos; Nubia Boechat
Journal:  Molecules       Date:  2022-01-24       Impact factor: 4.411

3.  Cardiovascular Toxicity of Tyrosine Kinase Inhibitors Used in Chronic Myeloid Leukemia: An Analysis of the FDA Adverse Event Reporting System Database (FAERS).

Authors:  Santa Cirmi; Asmae El Abd; Louis Letinier; Michele Navarra; Francesco Salvo
Journal:  Cancers (Basel)       Date:  2020-03-30       Impact factor: 6.639

  3 in total

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