TY - JOUR
T1 - Efficacy and safety of tyrosine kinase inhibitors for newly diagnosed chronic-phase chronic myeloid leukemia over a 5-year period
T2 - results from the Japanese registry obtained by the New TARGET system
AU - the New TARGET investigators
AU - Kizaki, Masahiro
AU - Takahashi, Naoto
AU - Iriyama, Noriyoshi
AU - Okamoto, Shinichiro
AU - Ono, Takaaki
AU - Usui, Noriko
AU - Inokuchi, Koiti
AU - Nakaseko, Chiaki
AU - Kurokawa, Mineo
AU - Sumi, Masahiko
AU - Nakamura, Fumihiko
AU - Kawaguchi, Tatsuya
AU - Suzuki, Ritsuro
AU - Yamamoto, Kazuhito
AU - Ohnishi, Kazunori
AU - Matsumura, Itaru
AU - Naoe, Tomoki
AU - Kizaki, M.
AU - Mori, S.
AU - Nemoto, T.
AU - Sagawa, M.
AU - Tabayashi, T.
AU - Tokuhira, M.
AU - Tomikawa, T.
AU - Watanabe, R.
AU - Hatta, Y.
AU - Inoue, Y.
AU - Iriyama, N.
AU - Kobayashi, S.
AU - Kobayashi, Y.
AU - Kurita, D.
AU - Karigane, D.
AU - Kasahara, H.
AU - Koda, Y.
AU - Miyakawa, Y.
AU - Murakami, K.
AU - Okamoto, S.
AU - Watanuki, S.
AU - Ono, T.
AU - Nagata, Y.
AU - Takeshita, A.
AU - Takahashi, N.
AU - Kameoka, Y.
AU - Yoshioka, T.
AU - Takahashi, S.
AU - Usui, N.
AU - Dan, K.
AU - Tomita, A.
AU - Yamamoto, H.
AU - Okamoto, M.
N1 - Funding Information:
Acknowledgements This study was supported by research funding from Novartis Pharmaceuticals and Bristol-Myers Squibb to JSH. The authors would like to thank all study participants and their families, and the study investigators at participating study sites. We also thank the New TARGET data center (EPS. Co.) for managing and monitoring the study. The following investigators and institutes participated in this study [Descending order of registered patient number (ITT)]: M. Kizaki, S. Mori, T. Nemoto, M. Sagawa, T. Tabayashi, M. Tokuhira, T. Tomikawa, R. Watanabe [Saitama Medical University Saitama Medical Center]; Y. Hatta, Y. Inoue, N. Iriyama, S. Kobayashi, Y. Kobayashi, D. Kurita [Nihon University Itabashi Hospital]; D. Karigane, H. Kasa-hara, Y. Koda, Y. Miyakawa, K. Murakami, S. Okamoto, S. Watanuki [Keio University Hospital]; T. Ono, Y. Nagata, A. Takeshita [Hama-matsu University Hospital]; N. Takahashi, Y. Kameoka, T. Yoshioka, S. Takahashi [Akita University Hospital]; N. Usui [The Jikei University Hospital]; K. Dan, K. Inokuchi, K. Nakamura [Nippon Medical School Hospital]; D. Abe, C. Nakaseko, C. Ohwada, E. Sakaida, N. Shimizu, M. Takeuchi [Chiba University Hospital]; S. Arai, Y. Kogure, A. Koya, Y. Masamoto, A. Masuda, K. Nakazaki, K. Toyama [Tokyo University Hospital]; Y. Hiroshima, N. Ichikawa, T. Kirihara, H. Kobayashi, I. Shimizu, M. Sumi, T. Ueki [Nagano Red Cross Hospital]; S. Hagi-wara, R. Hirai, T. Miwa, F. Nakamura, M. Nakamura, M. Takeshita, A. Tanimura [Center Hospital of National Center for Global Health and Medicine]; F. Hayakawa, Y. Ishikawa, H. Kiyoi, M. Murata, A. Tomita [Nagoya University Hospital]; T. Kurokawa, C. Sugimori [Toyama Red Cross Hospital]; A. Arai, O. Miura, M. Yamamoto [Tokyo Medical And Dental University, Medical Hospital]; K. Imai, N. Kobayashi, K. Minauchi, M. Obara, S. Ota [Sapporo Hokuyu Hospital]; T. Ikezoe, M. Mori, M. Sakai, A. Taniguchi, K. Togitani [Kochi Medical School Hospital]; H. Hayakawa, T. Kajiguchi, S. Kamoshita [Tosei General Hospital]; E. Otsuka, A. Nishida, M. Saburi, Y. Saburi [Oita Prefectural Hospital]; H. Iida, C. Kato, Y. Kojima, H. Ohashi, Y. Miyata, K. Sugimoto, H. Yamamoto, T. Yokozawa [National Hospital Organization Nagoya Medical Center]; T. Kamae, J. Kuyama, H. Mitsui, Y. Morikawa, Y. Uchida [Otemae Hospital]; T. Ashida, C. Hirase, K. Kawanishi, I. Matsumura, J. Miyatake, Y. Morita, T. Sano, T. Shi-mada, H. Tanaka, Y. Taniguchi, Y. Tatsumi, K. Yamaguchi [Kindai University Hospital]; F. Ishida, K. Momose, H. Nakazawa, S. Nishina, H. Sakai, N. Sekiguchi, [Shinshu University Hospital]; Y. Ito, K. Ohyashiki, T. Tauchi [Tokyo Medical University Hospital]; T. Hata, Y. Imaizumi, D. Imanishi, H. Itonaga, J. Makiyama, Y. Sawayama, J. Taguchi, M. Taguchi, H. Taniguchi [Nagasaki University Hospital]; G. Eguchi, M. Matsuda, N. Yamairi [PL General Hospital]; N. Fukushima, K. Ozeki, A. Kohno [Konan Kosei Hospital]; T. Sakura, S. Takada [Gunma Saiseikai Maebashi Hospital]; T. Kobayashi, H.
Publisher Copyright:
© 2019, Japanese Society of Hematology.
PY - 2019/4/5
Y1 - 2019/4/5
N2 - We report the results of a multicenter observational study using the New TARGET system, in which the effectiveness and safety of tyrosine kinase inhibitors (TKIs) were evaluated in newly diagnosed chronic-phase chronic myeloid leukemia (CML) patients. A total of 506 patients were enrolled between April 2010 and March 2013. Median age was 56 (range 18–92) years; 35% of patients were females. As the first-line therapy, 139 (27.9%), 169 (33.9%) and 144 (28.9%) patients were treated with imatinib, nilotinib, and dasatinib, respectively. Five-year progression-free survival (PFS) and overall survival (OS) were 93.8% and 94.5%, respectively. The OS curve was significantly superior for patients treated with second-generation TKIs than imatinib (P = 0.0068), and an early molecular response (EMR) at 3 months (BCR-ABL1 < 10%) was detected in 328 of 377 patients evaluated for molecular response. The PFS curve was significantly superior for patients with EMR than without (P < 0.0001). Although 12 patients experienced vascular adverse events, no new safety issues were observed in patients with adverse events. The results of this observational study demonstrated that treating newly diagnosed CML-CP patients with TKI results in satisfactory and reliable outcomes.
AB - We report the results of a multicenter observational study using the New TARGET system, in which the effectiveness and safety of tyrosine kinase inhibitors (TKIs) were evaluated in newly diagnosed chronic-phase chronic myeloid leukemia (CML) patients. A total of 506 patients were enrolled between April 2010 and March 2013. Median age was 56 (range 18–92) years; 35% of patients were females. As the first-line therapy, 139 (27.9%), 169 (33.9%) and 144 (28.9%) patients were treated with imatinib, nilotinib, and dasatinib, respectively. Five-year progression-free survival (PFS) and overall survival (OS) were 93.8% and 94.5%, respectively. The OS curve was significantly superior for patients treated with second-generation TKIs than imatinib (P = 0.0068), and an early molecular response (EMR) at 3 months (BCR-ABL1 < 10%) was detected in 328 of 377 patients evaluated for molecular response. The PFS curve was significantly superior for patients with EMR than without (P < 0.0001). Although 12 patients experienced vascular adverse events, no new safety issues were observed in patients with adverse events. The results of this observational study demonstrated that treating newly diagnosed CML-CP patients with TKI results in satisfactory and reliable outcomes.
UR - http://www.scopus.com/inward/record.url?scp=85061644674&partnerID=8YFLogxK
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U2 - 10.1007/s12185-019-02613-1
DO - 10.1007/s12185-019-02613-1
M3 - Article
C2 - 30762219
AN - SCOPUS:85061644674
SN - 0925-5710
VL - 109
SP - 426
EP - 439
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 4
ER -