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Blood, 1 December 2004, Vol. 104, No. 12, pp. 3507-3512.
Prepublished online as a Blood First Edition Paper on August 17, 2004; DOI 10.1182/blood-2004-04-1389.


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Submitted April 12, 2004
Accepted July 9, 2004

Combination of intensive chemotherapy and imatinib can rapidly induce high-quality complete remission for a majority of patients with newly diagnosed BCR-ABL positive acute lymphoblastic leukemia

Masayuki Towatari, Masamitsu Yanada*, Noriko Usui, Jin Takeuchi, Isamu Sugiura, Makoto Takeuchi, Fumiharu Yagasaki, Yasukazu Kawai, Shuichi Miyawaki, Shigeki Ohtake, Itsuro Jinnai, Keitaro Matsuo, Tomoki Naoe, and Ryuzo Ohno

Department of Hematology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Jikei University School of Medicine, Tokyo, Japan
Nihon University School of Medicine, Tokyo, Japan
Toyohashi Municipal Hospital, Toyohashi, Japan
Minami-Okayama Medical Center, Okayama, Japan
Saitama Medical School, Saitama, Japan
Faculty of Medical Sciences, University of Fukui, Fukui, Japan
Saiseikai Maebashi Hospital, Maebashi, Japan
Kanazawa University School of Health Sciences, Kanazawa, Japan
Aichi Cancer Center, Nagoya, Japan

* Corresponding author; email: myanada{at}med.nagoya-u.ac.jp.

The outcome for adult patients with BCR-ABL positive acute lymphoblastic leukemia (ALL) remains dismal and long-term survival can hardly be achieved except by allogeneic hematopoietic stem cell transplantation (HSCT). The Japan Adult Leukemia Study Group (JALSG) has recently started a phase 2 trial with intensive chemotherapy and imatinib for newly diagnosed BCR-ABL positive ALL patients, and we present here the interim results for the first 24 patients. All patients except one case of early death (96%) attained complete remission (CR) after a single course of remission induction therapy. PCR negativity was achieved in 28% of the patients on day 28, in 50% on day 63, and in up to 78% during the follow-up period. The toxicity profile was almost similar to that with chemotherapy alone. As a result, 15 patients (63%) could receive allogeneic HSCT during their first CR. Although the number of patients is small and the observation period is too short, the combination therapy is very promising and produces high-quality CR for a majority of newly diagnosed patients with BCR-ABL positive ALL. This is especially useful because it provides the patients with a better chance to receive allogeneic HSCT.


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