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Retinoic Acid, All-trans Retinoic Acid (ATRA), and Tamibarotene

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Chemotherapy for Leukemia

Abstract

Retinoids, all-trans retinoic acid (ATRA), and tamibarotene can induce differentiation of leukemic cells that carry t(15;17) and potentially lead to complete remission (CR) in patients with acute promyelocytic leukemia (APL). Although introduction of ATRA as a differentiating agent has been a major breakthrough in the treatment of APL, ATRA is currently recognized as a molecular-targeted therapy directed at the PML-RARα chimeric protein, which is generated by the specific chromosomal translocation t(15;17). In several multicenter trials, more than 90% of newly diagnosed APL patients treated with ATRA and chemotherapy achieved CR, of whom 20–30% subsequently relapsed, and then approximately 80% of patients had overall survival. However, several problems still account for treatment failure including early death, death during consolidation, and disease relapse. Tamibarotene demonstrated efficacy in both untreated APL patients and relapsed patients who have been treated with ATRA and chemotherapy. Retinoids are a model of the development of new molecular-targeted agents for other malignant tumors.

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Acknowledgments

The author declares no potential conflicts of interest. This work was supported in part by Grants-in-Aid for Scientific Research from the Japanese Ministry of Education, Culture, Sport, Science, and Technology (JSPS KAKENHI Grant number 26461431); by the National Cancer Center Research and Development Fund (26-A-24); by Grants-in-Aid from the Cancer Research from the Japanese Ministry of Health, Labor and Welfare (Clinical Cancer Research 23-004); by the MHLW KAKENHI Grant Number H26-Kakushintekigan-Ippan-133; by Grants-in-Aid from the Project for Development of Innovative Research on Cancer Therapeutics (P-Direct); and by the Japan Leukaemia Research Fund.

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Asou, N. (2017). Retinoic Acid, All-trans Retinoic Acid (ATRA), and Tamibarotene. In: Ueda, T. (eds) Chemotherapy for Leukemia. Springer, Singapore. https://doi.org/10.1007/978-981-10-3332-2_11

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