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Chidamide-BEAC plus autologous stem cell transplantation in high-risk non-Hodgkin lymphoma: a phase II clinical trial
Chidamide, a novel subtype-selective histone deacetylase inhibitor (HDACi), can directly inhibit tumor cell cycle progression, induce tumor cell apoptosis, and restore the sensitivity of drug-resistant tumor cells to drugs by loosening chromatin and exposing deoxyribonucleic acid (DNA). The protocol...
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Published in: | Chinese medical journal 2023-06, Vol.136 (12), p.1491-1493 |
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container_title | Chinese medical journal |
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creator | Xia, Yi Wang, Li Ding, Kaiyang Wu, Jiazhu Yin, Hua Hu, Maogui Shen, Haorui Liang, Jinhua Chen, Ruize Li, Yue Zhu, Huayuan Li, Jianyong Xu, Wei |
description | Chidamide, a novel subtype-selective histone deacetylase inhibitor (HDACi), can directly inhibit tumor cell cycle progression, induce tumor cell apoptosis, and restore the sensitivity of drug-resistant tumor cells to drugs by loosening chromatin and exposing deoxyribonucleic acid (DNA). The protocol of this study was approved by the Institutional Review Board of Jiangsu Province Hospital and Anhui Provincial Cancer Hospital (No. 2017-SR-271). [...]63 patients were included in the per-protocol set (PPS) [Supplementary Figure 1, http://links.lww.com/CM9/B617]. [...]chidamide with anti-programmed cell death protein 1 achieved an objective response rate of 58.3% and a CR rate of 44.4% in treating advanced and relapsed/refractory ENKTL. |
doi_str_mv | 10.1097/CM9.0000000000002636 |
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The protocol of this study was approved by the Institutional Review Board of Jiangsu Province Hospital and Anhui Provincial Cancer Hospital (No. 2017-SR-271). [...]63 patients were included in the per-protocol set (PPS) [Supplementary Figure 1, http://links.lww.com/CM9/B617]. [...]chidamide with anti-programmed cell death protein 1 achieved an objective response rate of 58.3% and a CR rate of 44.4% in treating advanced and relapsed/refractory ENKTL.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.1097/CM9.0000000000002636</identifier><identifier>PMID: 37036911</identifier><language>eng</language><publisher>China: Lippincott Williams & Wilkins</publisher><subject>Aminopyridines - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols ; Cell cycle ; Clinical trials ; Correspondence ; Hematology ; Hematopoietic Stem Cell Transplantation ; Humans ; Kinases ; Lymphoma ; Lymphoma, Non-Hodgkin - drug therapy ; Medical prognosis ; Patients ; Remission (Medicine) ; Stem cell transplantation ; T cell receptors ; Transplantation, Autologous</subject><ispartof>Chinese medical journal, 2023-06, Vol.136 (12), p.1491-1493</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>Copyright © 2023 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2023 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5485-3f37ef00920a55cf2baa74c47a4de4c0d2052fa9602aea506402fc77435368c83</citedby><cites>FETCH-LOGICAL-c5485-3f37ef00920a55cf2baa74c47a4de4c0d2052fa9602aea506402fc77435368c83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278685/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2827201788?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37036911$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xia, Yi</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Ding, Kaiyang</creatorcontrib><creatorcontrib>Wu, Jiazhu</creatorcontrib><creatorcontrib>Yin, Hua</creatorcontrib><creatorcontrib>Hu, Maogui</creatorcontrib><creatorcontrib>Shen, Haorui</creatorcontrib><creatorcontrib>Liang, Jinhua</creatorcontrib><creatorcontrib>Chen, Ruize</creatorcontrib><creatorcontrib>Li, Yue</creatorcontrib><creatorcontrib>Zhu, Huayuan</creatorcontrib><creatorcontrib>Li, Jianyong</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><title>Chidamide-BEAC plus autologous stem cell transplantation in high-risk non-Hodgkin lymphoma: a phase II clinical trial</title><title>Chinese medical journal</title><addtitle>Chin Med J (Engl)</addtitle><description>Chidamide, a novel subtype-selective histone deacetylase inhibitor (HDACi), can directly inhibit tumor cell cycle progression, induce tumor cell apoptosis, and restore the sensitivity of drug-resistant tumor cells to drugs by loosening chromatin and exposing deoxyribonucleic acid (DNA). The protocol of this study was approved by the Institutional Review Board of Jiangsu Province Hospital and Anhui Provincial Cancer Hospital (No. 2017-SR-271). [...]63 patients were included in the per-protocol set (PPS) [Supplementary Figure 1, http://links.lww.com/CM9/B617]. [...]chidamide with anti-programmed cell death protein 1 achieved an objective response rate of 58.3% and a CR rate of 44.4% in treating advanced and relapsed/refractory ENKTL.</description><subject>Aminopyridines - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols</subject><subject>Cell cycle</subject><subject>Clinical trials</subject><subject>Correspondence</subject><subject>Hematology</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Humans</subject><subject>Kinases</subject><subject>Lymphoma</subject><subject>Lymphoma, Non-Hodgkin - drug therapy</subject><subject>Medical prognosis</subject><subject>Patients</subject><subject>Remission (Medicine)</subject><subject>Stem cell transplantation</subject><subject>T cell receptors</subject><subject>Transplantation, Autologous</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkkFv1DAQhSMEokvhHyAUiQuXFMeOHZsLKlGhKxVxgbM160w23nXiYCet-u_xsqW09cXWzPOnN0-TZW9LclYSVX9svqsz8uBQwcSzbEV5RQsuqvJ5tiJMiEIopU6yVzHukobzWrzMTlidWqosV9nS9LaFwbZYfLk4b_LJLTGHZfbOb316xhmH3KBz-RxgjJODcYbZ-jG3Y97bbV8EG_f56Mfi0rfbfaq622Hq_QCfcsinHiLm63VunB2tgQPGgnudvejARXxzd59mv75e_Gwui6sf39bN-VVheCV5wTpWY0eIogQ4Nx3dANSVqWqoWqwMaSnhtAMlCAUETkRFaGfqumKcCWkkO83WR27rYaenYAcIt9qD1X8LPmw1hNkah5qmSBBbJjrESoEEJsqaEikN2aBAlVifj6xp2QzYGhxTIu4R9HFntL3e-mtdElpLIXkifLgjBP97wTjrwcZDtjBiyjpZUEpSxQRJ0vdPpDu_hDFlpamkyVdZy8N41VFlgo8xYHfvpiT6sCQ6LYl-uiTp27uHk9x_-rcV_7k33s0Y4t4tNxh0j-Dm_sBLJhkpKKGMCEpIkUolZ38AEfjG7w</recordid><startdate>20230620</startdate><enddate>20230620</enddate><creator>Xia, Yi</creator><creator>Wang, Li</creator><creator>Ding, Kaiyang</creator><creator>Wu, Jiazhu</creator><creator>Yin, Hua</creator><creator>Hu, Maogui</creator><creator>Shen, Haorui</creator><creator>Liang, Jinhua</creator><creator>Chen, Ruize</creator><creator>Li, Yue</creator><creator>Zhu, Huayuan</creator><creator>Li, Jianyong</creator><creator>Xu, Wei</creator><general>Lippincott Williams & Wilkins</general><general>Lippincott Williams & Wilkins Ovid Technologies</general><general>Wolters Kluwer</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230620</creationdate><title>Chidamide-BEAC plus autologous stem cell transplantation in high-risk non-Hodgkin lymphoma: a phase II clinical trial</title><author>Xia, Yi ; 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The protocol of this study was approved by the Institutional Review Board of Jiangsu Province Hospital and Anhui Provincial Cancer Hospital (No. 2017-SR-271). [...]63 patients were included in the per-protocol set (PPS) [Supplementary Figure 1, http://links.lww.com/CM9/B617]. [...]chidamide with anti-programmed cell death protein 1 achieved an objective response rate of 58.3% and a CR rate of 44.4% in treating advanced and relapsed/refractory ENKTL.</abstract><cop>China</cop><pub>Lippincott Williams & Wilkins</pub><pmid>37036911</pmid><doi>10.1097/CM9.0000000000002636</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aminopyridines - therapeutic use Antineoplastic Combined Chemotherapy Protocols Cell cycle Clinical trials Correspondence Hematology Hematopoietic Stem Cell Transplantation Humans Kinases Lymphoma Lymphoma, Non-Hodgkin - drug therapy Medical prognosis Patients Remission (Medicine) Stem cell transplantation T cell receptors Transplantation, Autologous |
title | Chidamide-BEAC plus autologous stem cell transplantation in high-risk non-Hodgkin lymphoma: a phase II clinical trial |
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