Markedly improved outcomes and acceptable toxicity in adolescents and young adults with acute lymphoblastic leukemia following treatment with a pediatric protocol: a phase II study by the Japan Adult Leukemia Study Group

Fumihiko Hayakawa(Nagoya University), Toru Sakura(Gunma Saiseikai Maebashi Hospital), Toshiaki Yujiri(Yamaguchi University), Eisei Kondo(Okayama University), Katsumichi Fujimaki(Fujisawa City Hospital), Osamu Sasaki(Miyagi Prefectural Hospital Organization), J. Miyatake(Kindai University), Hiroshi Handa(Gunma University), Yasunori Ueda(Kurashiki Central Hospital), Yasutaka Aoyama(Fuchu Hospital), Satoru Takada(Gunma Saiseikai Maebashi Hospital), Yoshinori Tanaka(Yamaguchi University), Noriko Usui(Jikei University School of Medicine), Shuichi Miyawaki(Tokyo Metropolitan Ohtsuka Hospital), Souichi Suenobu(Oita University), Keizo Horibe(National Hospital Organization), Hitoshi Kiyoi(Nagoya University), Kazunori Ohnishi(Hamamatsu University School of Medicine), Yasushi Miyazaki(Nagasaki University), Shigeki Ohtake(Kanazawa University), Yukio Kobayashi, Keitaro Matsuo(Kyushu University), T Naoe(National Hospital Organization), for the Japan Adult Leukemia Study Group (JALSG)
Blood Cancer Journal
October 17, 2014
Cited by 105Open Access
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Abstract

The superiority of the pediatric protocol for adolescents with acute lymphoblastic leukemia (ALL) has already been demonstrated, however, its efficacy in young adults remains unclear. The ALL202-U protocol was conducted to examine the efficacy and feasibility of a pediatric protocol in adolescents and young adults (AYAs) with BCR-ABL-negative ALL. Patients aged 15-24 years (n=139) were treated with the same protocol used for pediatric B-ALL. The primary objective of this study was to assess the disease-free survival (DFS) rate and its secondary aims were to assess toxicity, the complete remission (CR) rate and the overall survival (OS) rate. The CR rate was 94%. The 5-year DFS and OS rates were 67% (95% confidence interval (CI) 58-75%) and 73% (95% CI 64-80%), respectively. Severe adverse events were observed at a frequency that was similar to or lower than that in children treated with the same protocol. Only insufficient maintenance therapy significantly worsened the DFS (hazard ratio 5.60, P<0.001). These results indicate that this protocol may be a feasible and highly effective treatment for AYA with BCR-ABL-negative ALL.


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