File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Chemotherapy-free approaches to newly-diagnosed acute promyelocytic leukaemia: is oral-arsenic trioxide/all-trans retinoic acid/ascorbic acid the answer?

TitleChemotherapy-free approaches to newly-diagnosed acute promyelocytic leukaemia: is oral-arsenic trioxide/all-trans retinoic acid/ascorbic acid the answer?
Authors
Keywordsacute promyelocytic leukemia
all-trans retinoic acid
ascorbic acid
chemotherapy-free
Oral arsenic trioxide
Issue Date12-Aug-2024
PublisherTaylor and Francis Group
Citation
Expert Review of Hematology, 2024, v. 17, n. 10, p. 661-667 How to Cite?
Abstract

Introduction: Acute promyelocytic leukemia (APL) is a distinct form of acute myeloid leukemia characterized by the presence of t(15;17)(q24;21) and the PML:RARA gene fusion. Frontline use of intravenous arsenic trioxide (i.v.-ATO) and all-trans retinoic acid (ATRA) has vastly improved cure rates in APL. Researchers in Hong Kong invented the oral formulation of ATO (oral-ATO) and have confirmed a bioavailability comparable to i.v.-ATO. A plethora of studies have confirmed the safety and efficacy of oral-ATO-based regimens in the frontline and relapsed setting. Areas covered: Aspects on the development of oral-ATO-based regimens for APL in the frontline and relapsed setting are discussed. The short-term and long-term safety and efficacy of oral-ATO-based regimens are discussed. The frontline use of oral-ATO in combination with ATRA and ascorbic acid (AAA) induction in a ‘chemotherapy-free’ approach is highlighted. Expert opinion: Current and ongoing data on the use of oral-ATO-based regimens in APL support the use of oral-ATO as an alternative to i.v.-ATO allowing a more convenient and economical approach to the management of APL.


Persistent Identifierhttp://hdl.handle.net/10722/351514
ISSN
2023 Impact Factor: 2.3
2023 SCImago Journal Rankings: 0.699

 

DC FieldValueLanguage
dc.contributor.authorGill, Harinder-
dc.date.accessioned2024-11-21T00:35:11Z-
dc.date.available2024-11-21T00:35:11Z-
dc.date.issued2024-08-12-
dc.identifier.citationExpert Review of Hematology, 2024, v. 17, n. 10, p. 661-667-
dc.identifier.issn1747-4086-
dc.identifier.urihttp://hdl.handle.net/10722/351514-
dc.description.abstract<p>Introduction: Acute promyelocytic leukemia (APL) is a distinct form of acute myeloid leukemia characterized by the presence of t(15;17)(q24;21) and the PML:RARA gene fusion. Frontline use of intravenous arsenic trioxide (i.v.-ATO) and all-trans retinoic acid (ATRA) has vastly improved cure rates in APL. Researchers in Hong Kong invented the oral formulation of ATO (oral-ATO) and have confirmed a bioavailability comparable to i.v.-ATO. A plethora of studies have confirmed the safety and efficacy of oral-ATO-based regimens in the frontline and relapsed setting. Areas covered: Aspects on the development of oral-ATO-based regimens for APL in the frontline and relapsed setting are discussed. The short-term and long-term safety and efficacy of oral-ATO-based regimens are discussed. The frontline use of oral-ATO in combination with ATRA and ascorbic acid (AAA) induction in a ‘chemotherapy-free’ approach is highlighted. Expert opinion: Current and ongoing data on the use of oral-ATO-based regimens in APL support the use of oral-ATO as an alternative to i.v.-ATO allowing a more convenient and economical approach to the management of APL.</p>-
dc.languageeng-
dc.publisherTaylor and Francis Group-
dc.relation.ispartofExpert Review of Hematology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectacute promyelocytic leukemia-
dc.subjectall-trans retinoic acid-
dc.subjectascorbic acid-
dc.subjectchemotherapy-free-
dc.subjectOral arsenic trioxide-
dc.titleChemotherapy-free approaches to newly-diagnosed acute promyelocytic leukaemia: is oral-arsenic trioxide/all-trans retinoic acid/ascorbic acid the answer?-
dc.typeArticle-
dc.identifier.doi10.1080/17474086.2024.2391098-
dc.identifier.pmid39120131-
dc.identifier.scopuseid_2-s2.0-85201107545-
dc.identifier.volume17-
dc.identifier.issue10-
dc.identifier.spage661-
dc.identifier.epage667-
dc.identifier.eissn1747-4094-
dc.identifier.issnl1747-4094-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats