Literature DB >> 26709030

Swallowing a bitter pill-oral arsenic trioxide for acute promyelocytic leukemia.

Pallawi Torka1, Omar Al Ustwani2, Meir Wetzler3, Eunice S Wang4, Elizabeth A Griffiths5.   

Abstract

Parenteral arsenic trioxide (ATO) has been firmly established as a standard therapy for acute promyelocytic leukemia (APL). Despite widespread use of oral arsenicals in medicine historically, they had disappeared from modern pharmacopeia until oral ATO was redeveloped in Hong Kong in 2000. Since then, over 200 patients with leukemia (predominantly APL) have been treated with oral ATO in Hong Kong and China. Oral arsenic trioxide and other formulations of arsenic appear to have a clinical efficacy comparable to that of IV formulations. These drugs given orally also appear to have a slightly better safety profile, lower operational costs and improved convenience for patients. The clinical experience with oral ATO has previously been reported piecemeal as case series, pilot studies or subgroup analyses rather than in a comprehensive cohort. In this report we attempt to synthesize the published English language literature on oral arsenicals and present the argument for further development of these compounds. Systematic study of this drug with well-designed randomized multi-center clinical trials is needed to accelerate its development and incorporation into clinical practice.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Acute promyelocytic leukemia; Hematologic malignancies; Leukemia; Oral arsenic trioxide; Oral arsenicals; Realgar

Mesh:

Substances:

Year:  2015        PMID: 26709030     DOI: 10.1016/j.blre.2015.11.004

Source DB:  PubMed          Journal:  Blood Rev        ISSN: 0268-960X            Impact factor:   8.250


  7 in total

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5.  Exploring the Mechanism of Realgar against Esophageal Cancer Based on Ferroptosis Induced by ROS-ASK1-p38 MAPK Signaling Pathway.

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6.  Personalized therapy: CNS HGNET-BCOR responsiveness to arsenic trioxide combined with radiotherapy.

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Journal:  Oncotarget       Date:  2017-12-11

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  7 in total

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