ID | 57379 |
JaLCDOI | |
FullText URL | |
Author |
Yamasaki, Satoshi
Department of Hematology and Clinical Research Institute, NHO Kyushu Medical Cente
Kada, Akiko
Department of Clinical Trials and Research, Clinical Research Center, NHO Nagoya Medical Center
Nagai, Hirokazu
Department ofHematology and Oncology Research, NHO Nagoya Medical Center
Yoshida, Isao
Department of Hematologic Oncology, NHO Shikoku Cancer Center
Choi, Ilseung
Department of Hematology, NHO Kyushu Cancer Center
Saito, Akiko M.
Department of Clinical Trials and Research, Clinical Research Center, NHO Nagoya Medical Center
Iwasakia, Hiromi
Department of Hematology and Clinical Research Institute, NHO Kyushu Medical Cente
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Abstract | Romidepsin is an important therapeutic option for patients with peripheral T-cell lymphoma (PTCL). However, the timing of romidepsin administration remains controversial. Romidepsin was launched in Japan as a consolidation therapy agent after conventional salvage chemotherapy with gemcitabine, dexamethasone, and cisplatin (GDP). GDP therapy will be administered every 3 weeks. If complete response, partial response, or stable disease is confirmed after 2-4 GDP cycles, romidepsin will be administered every 4 weeks. The primary endpoint is a 2-year progression-free survival rate. Patients participating in this study and undergoing treatment can expect results similar to or better than those of conventional therapies.
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Keywords | peripheral T-cell lymphoma not otherwise specified
angioimmunoblastic T-cell lymphoma
gemcitabine
cisplatin, romidepsin
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Amo Type | Clinical Study Protocol
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Publication Title |
Acta Medica Okayama
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Published Date | 2019-10
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Volume | volume73
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Issue | issue5
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Publisher | Okayama University Medical School
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Start Page | 469
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End Page | 474
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ISSN | 0386-300X
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NCID | AA00508441
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Content Type |
Journal Article
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language |
English
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Copyright Holders | CopyrightⒸ 2019 by Okayama University Medical School
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File Version | publisher
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Refereed |
True
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PubMed ID | |
Web of Science KeyUT |