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73_5_469.pdf 1.94 MB
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
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.
Keywords
peripheral T-cell lymphoma not otherwise specified
angioimmunoblastic T-cell lymphoma
gemcitabine
cisplatin, romidepsin
Amo Type
Clinical Study Protocol
Publication Title
Acta Medica Okayama
Published Date
2019-10
Volume
volume73
Issue
issue5
Publisher
Okayama University Medical School
Start Page
469
End Page
474
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
Copyright Holders
CopyrightⒸ 2019 by Okayama University Medical School
File Version
publisher
Refereed
True
PubMed ID
Web of Science KeyUT