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タイトル: Final 3-year Results of the Dasatinib Discontinuation Trial in Patients With Chronic Myeloid Leukemia Who Received Dasatinib as a Second-line Treatment
著者: Okada, Masaya
Imagawa, Jun
Tanaka, Hideo
Nakamae, Hirohisa
Hino, Masayuki
Murai, Kazunori
Ishida, Yoji
Kumagai, Takashi
Sato, Seiichi
Ohashi, Kazuteru
Sakamaki, Hisashi
Wakita, Hisashi
Uoshima, Nobuhiko
Nakagawa, Yasunori
Minami, Yosuke
Ogasawara, Masahiro
Takeoka, Tomoharu
Akasaka, Hiroshi
Utsumi, Takahiko
Uike, Naokuni
Sato, Tsutomu
Ando, Sachiko
Usuki, Kensuke
Mizuta, Syuichi
Hashino, Satoshi
Nomura, Tetsuhiko
Shikami, Masato
Fukutani, Hisashi
Ohe, Yokiko
Kosugi, Hiroshi
Shibayama, Hirohiko
Maeda, Yasuhiro
Fukushima, Toshihiro
Yamazaki, Hirohito
Tsubaki, Kazuo
Kukita, Toshimasa
Adachi, Yoko
Nataduka, Toshiki
Sakoda, Hiroto
Yokoyama, Hisayuki
Okamoto, Takahiro
Shirasugi, Yukari
Onishi, Yasushi
Nohgawa, Masaharu
Yoshihara, Satoshi
Morita, Satoshi  kyouindb  KAKEN_id
Sakamoto, Junichi
Kimura, Shinya
DADI Trial Group, Japan
著者名の別形: 森田, 智視
キーワード: CML
DADI
Natural killer cell
Stop trial
Treatment-free remission
発行日: May-2018
出版者: Elsevier BV
誌名: Clinical Lymphoma Myeloma and Leukemia
巻: 18
号: 5
開始ページ: 353
終了ページ: 360.e1
抄録: Introduction: We previously reported an interim analysis of the DADI (dasatinib discontinuation) trial. The results showed that 48% of patients with chronic myeloid leukemia in the chronic phase who maintained a deep molecular response (DMR) for ≥ 1 year could discontinue second- or subsequent-line dasatinib treatment safely at a median follow-up of 20 months. However, the results from longer follow-up periods would be much more useful from a clinical perspective. Patients and Methods: The DADI trial was a prospective, multicenter trial conducted in Japan. After confirming a stable DMR for ≥ 1 year, dasatinib treatment subsequent to imatinib or nilotinib was discontinued. After discontinuation, the loss of DMR (even of 1 point) was defined as stringent molecular relapse, thereby triggering therapy resumption. The predictive factors of treatment-free remission (TFR) were analyzed. Results: The median follow-up period was 44.0 months (interquartile range, 40.5-48.0 months). The estimated overall TFR rate at 36 months was 44.4% (95% confidence interval, 32.0%-56.2%). Only 2 patients developed a molecular relapse after the 1-year cutoff point. The presence of imatinib resistance was a significant risk factor for molecular relapse. Moreover, high natural killer cell and low γδ+ T-cell and CD4+ regulatory T-cell (CD25+CD127low) counts before discontinuation correlated significantly with successful therapy discontinuation. Conclusion: These findings suggest that discontinuation of second- or subsequent-line dasatinib after a sustained DMR of ≥ 1 year is feasible, especially for patients with no history of imatinib resistance. In addition, the natural killer cell count was associated with the TFR.
著作権等: © 2018 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
URI: http://hdl.handle.net/2433/230949
DOI(出版社版): 10.1016/j.clml.2018.03.004
PubMed ID: 29610029
出現コレクション:学術雑誌掲載論文等

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