Literature DB >> 24295412

Romidepsin for cutaneous T-cell lymphoma.

H Miles Prince1, Michael Dickinson, Amit Khot.   

Abstract

Cutaneous T-cell lymphomas are relatively rare lymphomas and the most common form is mycosis fungoides. Its rare leukemic variant is Sezary syndrome. Advanced-stage disease is typically treated with bexarotene (a retinoid), IFN-α or conventional chemotherapeutic agents, but relapses are inevitable. Histone deacetylase inhibitors that modify the epigenome are an attractive addition to the armamentarium. Based on two large Phase II studies, the US FDA approved intravenous romidepsin for patients with relapsed/refractory cutaneous T-cell lymphomas. Romidepsin provides a subset of patients with an opportunity for prolonged clinical responses with a tolerable side-effect profile.

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Year:  2013        PMID: 24295412     DOI: 10.2217/fon.13.220

Source DB:  PubMed          Journal:  Future Oncol        ISSN: 1479-6694            Impact factor:   3.404


  3 in total

1.  Crosstalk among the proteome, lysine phosphorylation, and acetylation in romidepsin-treated colon cancer cells.

Authors:  Tian-Yun Wang; Yu-Rong Chai; Yan-Long Jia; Jian-Hui Gao; Xiao-Jun Peng; Hua-Feng Han
Journal:  Oncotarget       Date:  2016-08-16

2.  The histone deacetylase inhibitor Romidepsin induces as a cascade of differential gene expression and altered histone H3K9 marks in myeloid leukaemia cells.

Authors:  Kathryn Clarke; Christine Young; Fabio Liberante; Mary-Frances McMullin; Alexander Thompson; Ken Mills
Journal:  Oncotarget       Date:  2019-05-28

3.  Elucidating the mechanism of action of domatinostat (4SC-202) in cutaneous T cell lymphoma cells.

Authors:  Marion Wobser; Alexandra Weber; Amelie Glunz; Saskia Tauch; Kristina Seitz; Tobias Butelmann; Sonja Hesbacher; Matthias Goebeler; René Bartz; Hella Kohlhof; David Schrama; Roland Houben
Journal:  J Hematol Oncol       Date:  2019-03-18       Impact factor: 17.388

  3 in total

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