Chidamide in the treatment of peripheral T-cell lymphoma

Thomas S Chan, Eric Tse, Yok-Lam Kwong Department of Medicine, Queen Mary Hospital, Hong Kong, People’s Republic of China Abstract: Mature T-cell lymphomas are aggressive malignancies. Treatment outcome is poor with conventional chemotherapy. They are about twice as common in As...

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Main Authors: Chan TS, Tse E, Kwong YL
Format: Article
Language:English
Published: Dove Medical Press 2017-01-01
Series:OncoTargets and Therapy
Subjects:
Online Access:https://www.dovepress.com/chidamide-in-the-treatment-of-peripheral-t-cell-lymphoma-peer-reviewed-article-OTT
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spelling doaj-f79d598fe8904c0bb71896f15ef3020f2020-11-24T23:14:57ZengDove Medical PressOncoTargets and Therapy1178-69302017-01-01Volume 1034735230831Chidamide in the treatment of peripheral T-cell lymphomaChan TSTse EKwong YLThomas S Chan, Eric Tse, Yok-Lam Kwong Department of Medicine, Queen Mary Hospital, Hong Kong, People’s Republic of China Abstract: Mature T-cell lymphomas are aggressive malignancies. Treatment outcome is poor with conventional chemotherapy. They are about twice as common in Asia as compared with other non-Asian countries. Histone proteins form the basic structure of chromatin, and their acetylation at lysine residues relaxes chromatin structure, facilitating gene transcription. Conversely, histone deacetylation, catalyzed by histone deacetylases, compacts chromatin and represses gene transcription. Histone deacetylase inhibitors are an important class of antineoplastic agents. Chidamide is a novel orally active benzamide-type histone deacetylase inhibitor that has shown in vitro activities against a wide array of neoplasms. In Phase I trials, chidamide showed preferential efficacy in mature T-cell lymphomas. In a pivotal Phase II trial of chidamide in 79 patients with relapsed or refractory mature T-cell lymphomas, an overall response rate of 28% (complete remission/complete remission unconfirmed: 14%) was achieved, with most responses occurring within the first 6 weeks of treatment. The median duration of response (DOR) was 9.9 (1.1–40.8) months. Of 22 responders, 19 patients (86%) had a DOR of ≥3 months and eight patients (36%) had a DOR of >12 months. Angioimmunoblastic T-cell lymphoma and anaplastic large cell lymphoma (anaplastic lymphoma kinase-negative) showed better response rates, with the most durable responses observed in angioimmunoblastic T-cell lymphoma patients. Safety profile was favorable, with very few cases of grade 3/4 toxicities observed. Chidamide is approved by the China Food and Drug Administration for the treatment of relapsed and refractory peripheral T-cell lymphomas. Keywords: chidamide, peripheral T-cell lymphoma, benzamide, histone deacetylase inhibitorshttps://www.dovepress.com/chidamide-in-the-treatment-of-peripheral-t-cell-lymphoma-peer-reviewed-article-OTTchidamideperipheral T-cell lymphomabenzamidehistone deacetylase inhibitors
collection DOAJ
language English
format Article
sources DOAJ
author Chan TS
Tse E
Kwong YL
spellingShingle Chan TS
Tse E
Kwong YL
Chidamide in the treatment of peripheral T-cell lymphoma
OncoTargets and Therapy
chidamide
peripheral T-cell lymphoma
benzamide
histone deacetylase inhibitors
author_facet Chan TS
Tse E
Kwong YL
author_sort Chan TS
title Chidamide in the treatment of peripheral T-cell lymphoma
title_short Chidamide in the treatment of peripheral T-cell lymphoma
title_full Chidamide in the treatment of peripheral T-cell lymphoma
title_fullStr Chidamide in the treatment of peripheral T-cell lymphoma
title_full_unstemmed Chidamide in the treatment of peripheral T-cell lymphoma
title_sort chidamide in the treatment of peripheral t-cell lymphoma
publisher Dove Medical Press
series OncoTargets and Therapy
issn 1178-6930
publishDate 2017-01-01
description Thomas S Chan, Eric Tse, Yok-Lam Kwong Department of Medicine, Queen Mary Hospital, Hong Kong, People’s Republic of China Abstract: Mature T-cell lymphomas are aggressive malignancies. Treatment outcome is poor with conventional chemotherapy. They are about twice as common in Asia as compared with other non-Asian countries. Histone proteins form the basic structure of chromatin, and their acetylation at lysine residues relaxes chromatin structure, facilitating gene transcription. Conversely, histone deacetylation, catalyzed by histone deacetylases, compacts chromatin and represses gene transcription. Histone deacetylase inhibitors are an important class of antineoplastic agents. Chidamide is a novel orally active benzamide-type histone deacetylase inhibitor that has shown in vitro activities against a wide array of neoplasms. In Phase I trials, chidamide showed preferential efficacy in mature T-cell lymphomas. In a pivotal Phase II trial of chidamide in 79 patients with relapsed or refractory mature T-cell lymphomas, an overall response rate of 28% (complete remission/complete remission unconfirmed: 14%) was achieved, with most responses occurring within the first 6 weeks of treatment. The median duration of response (DOR) was 9.9 (1.1–40.8) months. Of 22 responders, 19 patients (86%) had a DOR of ≥3 months and eight patients (36%) had a DOR of >12 months. Angioimmunoblastic T-cell lymphoma and anaplastic large cell lymphoma (anaplastic lymphoma kinase-negative) showed better response rates, with the most durable responses observed in angioimmunoblastic T-cell lymphoma patients. Safety profile was favorable, with very few cases of grade 3/4 toxicities observed. Chidamide is approved by the China Food and Drug Administration for the treatment of relapsed and refractory peripheral T-cell lymphomas. Keywords: chidamide, peripheral T-cell lymphoma, benzamide, histone deacetylase inhibitors
topic chidamide
peripheral T-cell lymphoma
benzamide
histone deacetylase inhibitors
url https://www.dovepress.com/chidamide-in-the-treatment-of-peripheral-t-cell-lymphoma-peer-reviewed-article-OTT
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