Literature DB >> 11331438

Risk/benefit profile of arsenic trioxide.

D M Rust1, S L Soignet.   

Abstract

Approximately 20%-30% of patients with acute promyelocytic leukemia (APL) who are treated with the current standard all-trans retinoic acid and anthracycline-based chemotherapy regimen suffer relapse. In the mid-1990s, studies from China reported the effective use of arsenic trioxide in achieving complete remission in patients with APL. In the United States, a multicenter trial of this agent in 40 patients with relapsed APL following conventional therapy confirmed the positive safety and efficacy outcomes of a smaller 12-patient pilot study. Common adverse events were hyperleukocytosis, APL differentiation syndrome, prolonged QT interval on electrocardiogram, skin rash, and hyperglycemia.

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Year:  2001        PMID: 11331438     DOI: 10.1634/theoncologist.6-suppl_2-29

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  12 in total

Review 1.  Drug-induced hypomagnesaemia : scope and management.

Authors:  Jacob Atsmon; Eran Dolev
Journal:  Drug Saf       Date:  2005       Impact factor: 5.606

2.  Arsenic exposure and toxicology: a historical perspective.

Authors:  Michael F Hughes; Barbara D Beck; Yu Chen; Ari S Lewis; David J Thomas
Journal:  Toxicol Sci       Date:  2011-07-12       Impact factor: 4.849

Review 3.  Pathophysiology, clinical features and radiological findings of differentiation syndrome/all-trans-retinoic acid syndrome.

Authors:  Luciano Cardinale; Francesco Asteggiano; Federica Moretti; Federico Torre; Stefano Ulisciani; Carmen Fava; Giovanna Rege-Cambrin
Journal:  World J Radiol       Date:  2014-08-28

Review 4.  QT Interval Prolongation Associated With Cytotoxic and Targeted Cancer Therapeutics.

Authors:  Sanjay Chandrasekhar; Michael G Fradley
Journal:  Curr Treat Options Oncol       Date:  2019-05-25

5.  Arsenate-induced maternal glucose intolerance and neural tube defects in a mouse model.

Authors:  Denise S Hill; Bogdan J Wlodarczyk; Laura E Mitchell; Richard H Finnell
Journal:  Toxicol Appl Pharmacol       Date:  2009-05-14       Impact factor: 4.219

6.  Oxidative stress induced by the chemotherapeutic agent arsenic trioxide.

Authors:  Mathews V Varghese; Alex Manju; M Abhilash; M V Sauganth Paul; S Abhilash; R Harikumaran Nair
Journal:  3 Biotech       Date:  2013-09-13       Impact factor: 2.406

7.  Arsenic trioxide inhibits glioma cell growth through induction of telomerase displacement and telomere dysfunction.

Authors:  Ye Cheng; Yunqian Li; Chengyuan Ma; Yang Song; Haiyang Xu; Hongquan Yu; Songbai Xu; Qingchun Mu; Haisong Li; Yong Chen; Gang Zhao
Journal:  Oncotarget       Date:  2016-03-15

Review 8.  On arsenic trioxide in the clinical treatment of acute promyelocytic leukemia.

Authors:  Peng Zhang
Journal:  Leuk Res Rep       Date:  2017-03-09

9.  HMGB1 promotes differentiation syndrome by inducing hyperinflammation via MEK/ERK signaling in acute promyelocytic leukemia cells.

Authors:  Lanlan Tang; Wenwen Chai; Fanghua Ye; Yan Yu; Lizhi Cao; Minghua Yang; Min Xie; Liangchun Yang
Journal:  Oncotarget       Date:  2017-04-18

Review 10.  Treatment of acute promyelocytic leukemia and other hematologic malignancies with arsenic trioxide: review of clinical and basic studies.

Authors:  Peng Liu; Zhong Chao Han
Journal:  Int J Hematol       Date:  2003-07       Impact factor: 2.319

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