Research Article
Outcome of childhood acute lymphoblastic leukemia with induction failure treated by the Japan Association of Childhood Leukemia Study (JACLS) ALL F-protocol
Article first published online: 7 OCT 2009
DOI: 10.1002/pbc.22217
Copyright © 2009 Wiley-Liss, Inc.
Additional Information
How to Cite
Suzuki, N., Yumura-Yagi, K., Yoshida, M., Hara, J., Nishimura, S., Kudoh, T., Tawa, A., Usami, I., Tanizawa, A., Hori, H., Ito, Y., Miyaji, R., Oda, M., Kato, K., Hamamoto, K., Osugi, Y., Hashii, Y., Nakahata, T. and Horibe, K. (2010), Outcome of childhood acute lymphoblastic leukemia with induction failure treated by the Japan Association of Childhood Leukemia Study (JACLS) ALL F-protocol. Pediatric Blood & Cancer, 54: 71–78. doi: 10.1002/pbc.22217
Publication History
- Issue published online: 9 NOV 2009
- Article first published online: 7 OCT 2009
- Manuscript Accepted: 29 JUN 2009
- Manuscript Received: 27 JAN 2009
Keywords:
- acute lymphoblastic leukemia;
- chemotherapy;
- childhood;
- hematopoietic cell transplantation;
- induction failure
Abstract
Background
Children with acute lymphoblastic leukemia (ALL) who fail to achieve complete remission (CR) after induction therapy (induction failure: IF) have a poor prognosis; however, there have been few prospective studies in patients with IF.
Patients and Methods
Between April 1997 and March 2005, 27 of 1,237 leukemic patients (2.2%) failed to achieve CR after four- or five-drug induction therapy. Twenty-three of these patients entered the F-protocol study, which mainly consisted of acute-myeloid-leukemia-oriented chemotherapy followed by scheduled hematopoietic cell transplantation (HCT).
Results
Seventeen (73.9%) of the 23 patients responded to re-induction chemotherapy with CR. Of note, 15 (93.8%) of 16 patients with Philadelphia-chromosome-negative (non-Ph+) ALL achieved CR; in contrast, only 2 (28.6%) of 7 Ph+ patients achieved CR. Fourteen (82.4%) of 17 patients remained in CR (CCR) until their scheduled HCT, 12 of the 14 with CCR underwent HCT as scheduled, and 6 patients remain in first CR after a median of 78 months (range, 49–107 months). The 5-year overall survival (OS) rates of 16 patients with non-Ph+ and 7 patients with Ph+ were 43.8 ± 12.4% and 14.3 ± 13.2%, respectively (P = 0.012). The 5-year OS rate of the 17 patients who obtained CR by re-induction therapy and the 6 who did not were 47.1 ± 12.1% and 0%, respectively (P < 0.001).
Conclusion
Acute-myeloid-leukemia-oriented chemotherapy followed by scheduled HCT is a promising treatment strategy for non-Ph+ ALL patients with IF. Pediatr Blood Cancer 2010; 54:71–78. © 2009 Wiley-Liss, Inc.

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