Literature DB >> 22535155

Romidepsin for cutaneous T-cell lymphoma.

H Miles Prince1, Michael Dickinson.   

Abstract

Cutaneous T-cell lymphomas (CTCL) are relatively rare lymphomas with an annual incidence of approximately 0.2 to 0.8/100,000 and comprise a variety of clinical entities; mycosis fungoides or its leukemic variant Sezary syndrome account for the majority of cases. Advanced-stage disease is typically treated with bexarotene (a retinoid), interferon, or conventional chemotherapeutic agents, but relapses are inevitable. Histone deacetylase inhibitors, which modify the epigenome, are an attractive addition to the armamentarium. On the basis of 2 large phase II studies, the U.S. Food and Drug Administration approved intravenous romidepsin for patients with relapsed and/or refractory CTCL. Romidepsin provides a subset of patients with an opportunity for prolonged clinical responses with a tolerable side effect profile. ©2012 AACR.

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Year:  2012        PMID: 22535155     DOI: 10.1158/1078-0432.CCR-11-3144

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  23 in total

1.  Phase 1/2 study of mogamulizumab, a defucosylated anti-CCR4 antibody, in previously treated patients with cutaneous T-cell lymphoma.

Authors:  Madeleine Duvic; Lauren C Pinter-Brown; Francine M Foss; Lubomir Sokol; Jeffrey L Jorgensen; Pramoda Challagundla; Karen M Dwyer; Xiaoping Zhang; Michael R Kurman; Rocco Ballerini; Li Liu; Youn H Kim
Journal:  Blood       Date:  2015-01-20       Impact factor: 22.113

Review 2.  Sézary Syndrome: Clinical and Biological Aspects.

Authors:  Rebecca Kohnken; Stephanie Fabbro; Justin Hastings; Pierluigi Porcu; Anjali Mishra
Journal:  Curr Hematol Malig Rep       Date:  2016-12       Impact factor: 3.952

3.  LSD1 Substrate Binding and Gene Expression Are Affected by HDAC1-Mediated Deacetylation.

Authors:  Dhanusha A Nalawansha; Mary Kay H Pflum
Journal:  ACS Chem Biol       Date:  2016-12-15       Impact factor: 5.100

4.  Selective inhibition of esophageal cancer cells by combination of HDAC inhibitors and Azacytidine.

Authors:  Theresa D Ahrens; Sylvia Timme; Jens Hoeppner; Jenny Ostendorp; Sina Hembach; Marie Follo; Ulrich T Hopt; Martin Werner; Hauke Busch; Melanie Boerries; Silke Lassmann
Journal:  Epigenetics       Date:  2015       Impact factor: 4.528

5.  The structural requirements of histone deacetylase inhibitors: SAHA analogs modified at the C5 position display dual HDAC6/8 selectivity.

Authors:  Ahmed T Negmeldin; Mary Kay H Pflum
Journal:  Bioorg Med Chem Lett       Date:  2017-06-13       Impact factor: 2.823

6.  Trichostatin A, a histone deacetylase inhibitor, induces synergistic cytotoxicity with chemotherapy via suppression of Raf/MEK/ERK pathway in urothelial carcinoma.

Authors:  Wei-Chou Lin; Fu-Shun Hsu; Kuan-Lin Kuo; Shing-Hwa Liu; Chia-Tung Shun; Chung-Sheng Shi; Hong-Chiang Chang; Yu-Chieh Tsai; Ming-Chieh Lin; June-Tai Wu; Yu Kuo; Po-Ming Chow; Shih-Ming Liao; Shao-Ping Yang; Jo-Yu Hong; Kuo-How Huang
Journal:  J Mol Med (Berl)       Date:  2018-10-04       Impact factor: 4.599

Review 7.  Trials with 'epigenetic' drugs: an update.

Authors:  Angela Nebbioso; Vincenzo Carafa; Rosaria Benedetti; Lucia Altucci
Journal:  Mol Oncol       Date:  2012-10-06       Impact factor: 6.603

8.  A Bim-targeting strategy overcomes adaptive bortezomib resistance in myeloma through a novel link between autophagy and apoptosis.

Authors:  Shuang Chen; Yu Zhang; Liang Zhou; Yun Leng; Hui Lin; Maciej Kmieciak; Xin-Yan Pei; Richard Jones; Robert Z Orlowski; Yun Dai; Steven Grant
Journal:  Blood       Date:  2014-09-10       Impact factor: 22.113

9.  Synergy of BCL2 and histone deacetylase inhibition against leukemic cells from cutaneous T-cell lymphoma patients.

Authors:  Benoit M Cyrenne; Julia M Lewis; Jason G Weed; Kacie R Carlson; Fatima N Mirza; Francine M Foss; Michael Girardi
Journal:  Blood       Date:  2017-10-02       Impact factor: 22.113

10.  One-pot, multi-component synthesis and structure-activity relationships of peptoid-based histone deacetylase (HDAC) inhibitors targeting malaria parasites.

Authors:  Daniela Diedrich; Katharina Stenzel; Eva Hesping; Yevgeniya Antonova-Koch; Tamirat Gebru; Sandra Duffy; Gillian Fisher; Andrea Schöler; Stephan Meister; Thomas Kurz; Vicky M Avery; Elizabeth A Winzeler; Jana Held; Katherine T Andrews; Finn K Hansen
Journal:  Eur J Med Chem       Date:  2018-09-07       Impact factor: 6.514

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