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DOI 10.1007/s10147-018-1368-2

Медицинская библиотека · International journal of clinical oncology · 2018

Feasibility of the imatinib stop study in the Japanese clinical setting: delightedly overcome CML expert stop TKI trial (DOMEST Trial).

Fujisawa Shin, Ueda Yasunori, Usuki Kensuke, Kobayashi Hajime, Kondo Eisei, Doki Noriko, Nakao Takafumi, Kanda Yoshinobu, Kosugi Nobuharu, Kosugi Hiroshi, Kumagai Takashi, Harada Hiroshi, Shikami Masato, Maeda Yasuhiro, Sakura Toru, Inokuchi Koiti, Saito Akio, Nawa Yuichiro, Ogasawara Masahiro, Nishida Junji, Kondo Takeshi, Yoshida Chikashi, Kuroda Hiroyuki, Tabe Yoko, Maeda Yoshinobu, Imajo Kenji, Kojima Kensuke, Morita Satoshi, Komukai Sho, Kawaguchi Atsushi, Sakamoto Junichi, Kimura Shinya

Клиническое исследование II фазыСтатьяМногоцентровое исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Treatment-free remission (TFR), the ability to maintain a molecular response (MR), occurs in approximately 50% of patients with chronic myelogenous leukemia (CML) treated with tyrosine kinase inhibitors (TKIs).

METHODS

A multicenter phase 2 trial (Delightedly Overcome CML Expert Stop TKI Trial: DOMEST Trial) was conducted to test the safety and efficacy of discontinuing imatinib. Patients with CML with a sustained MR of 4.0 or MR4.0-equivalent for at least 2 years and confirmed MR4.0 at the beginning of the study were enrolled. In the TFR phase, the international scale (IS) was regularly monitored by IS-PCR testing. Molecular recurrence was defined as the loss of MR4.0. Recurrent patients were immediately treated with dasatinib or other TKIs including imatinib.

RESULTS

Of 110 enrolled patients, 99 were evaluable. The median time from diagnosis to discontinuation of imatinib was 103 months, and the median duration of imatinib therapy was 100 months. Molecular recurrence-free survival rates were 69.6%, 68.6% and 64.3% at 6, 12, and 24 months, respectively. After discontinuation of imatinib therapy, 26 patients showed molecular recurrence, and 25 re-achieved deep MR after dasatinib treatment. Molecular response MR4.0 was achieved in 23 patients within 6 months and 25 patients within 12 months. Multivariate analysis revealed that a longer time from diagnosis to discontinuation of imatinib therapy (p = 0.0002) and long duration of imatinib therapy (p = 0.0029) predicted a favorable prognosis.

CONCLUSIONS

This DOMEST Trial showed the feasibility of TKI discontinuation in a Japanese clinical setting.

Для цитирования: Fujisawa Shin, Ueda Yasunori, Usuki Kensuke, Kobayashi Hajime, Kondo Eisei, Doki Noriko, Nakao Takafumi, Kanda Yoshinobu, Kosugi Nobuharu, Kosugi Hiroshi, Kumagai Takashi, Harada Hiroshi, Shikami Masato, Maeda Yasuhiro, Sakura Toru, Inokuchi Koiti, Saito Akio, Nawa Yuichiro, Ogasawara Masahiro, Nishida Junji, Kondo Takeshi, Yoshida Chikashi, Kuroda Hiroyuki, Tabe Yoko, Maeda Yoshinobu, Imajo Kenji, Kojima Kensuke, Morita Satoshi, Komukai Sho, Kawaguchi Atsushi, Sakamoto Junichi, Kimura Shinya. Feasibility of the imatinib stop study in the Japanese clinical setting: delightedly overcome CML expert stop TKI trial (DOMEST Trial).. International journal of clinical oncology. 2018. DOI: 10.1007/s10147-018-1368-2.

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