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. 2020 Feb;182(2):497-498.
doi: 10.1111/bjd.18522. Epub 2019 Oct 13.

A comparative analysis of histone deacetylase inhibitors for the treatment of mycosis fungoides and Sézary syndrome

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A comparative analysis of histone deacetylase inhibitors for the treatment of mycosis fungoides and Sézary syndrome

T Papps et al. Br J Dermatol. 2020 Feb.
No abstract available

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References

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    1. Piekarz RL, Frye R, Turner M et al. A multi-institutional phase II trial of the HDAC inhibitor romidepsin as monotherapy for patients with cutaneous T-cell lymphoma. J Clin Oncol 2009; 27:410-7.
    1. Duvic M, Dummer R, Becker JC et al. Panobinostat activity in both bexarotene-exposed and -naïve patients with refractory cutaneous T-Cell lymphoma: results of a phase II trial. Eur J Cancer 2013; 48:386-94.
    1. Dickinson M, Johnstone R, Prince HM. Histone deacetylase inhibitors: potential targets responsible for their anti-cancer effect. Invest New Drugs 2010; 28 (Suppl 1):S3-20.
    1. Hughes CF, Khot A, McCormack C et al. The lack of durable disease control with chemotherapy for mycosis fungoides and Sézary syndrome: a comparative study of systemic therapy. Blood 2015; 125:71-81.

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