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ID 57379
JaLCDOI
フルテキストURL
73_5_469.pdf 1.94 MB
著者
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
抄録
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.
キーワード
peripheral T-cell lymphoma not otherwise specified
angioimmunoblastic T-cell lymphoma
gemcitabine
cisplatin, romidepsin
Amo Type
Clinical Study Protocol
出版物タイトル
Acta Medica Okayama
発行日
2019-10
73巻
5号
出版者
Okayama University Medical School
開始ページ
469
終了ページ
474
ISSN
0386-300X
NCID
AA00508441
資料タイプ
学術雑誌論文
言語
英語
著作権者
CopyrightⒸ 2019 by Okayama University Medical School
論文のバージョン
publisher
査読
有り
PubMed ID
Web of Science KeyUT