Seminars in Hematology
Volume 46, Issue 1 , Pages 52-63, January 2009

Treatment of Childhood Acute Lymphoblastic Leukemia

  • Martin Stanulla
  • ,
  • Martin Schrappe

      Affiliations

    • Corresponding Author InformationAddress correspondence to Martin Schrappe, MD, Children's Hospital at the University Medical Center Schleswig-Holstein, Campus Kiel, Schwanenweg 20, 24105 Kiel, Germany

Department of Pediatrics, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany

Childhood acute lymphoblastic leukemia (ALL) is the most common malignancy of childhood. Studies in ALL have been a model for clinical and basic research beyond pediatric hemato-oncology. As a result of sustained and well-organized research efforts since the early 1960s, childhood ALL now can be successfully treated in about 80% of patients by the application of intensive combination chemotherapy regimens, which in specific patient subgroups may need to be supplemented with radiation therapy and/or hematopoietic stem cell transplantation. Triggered by the observation of specific clinical presenting features, biological characteristics, and early treatment response being associated with treatment outcome, therapy intensity in contemporary ALL protocols is adjusted according to prognostic factors predicting the risk of relapse. While the goal of effective therapy for the majority of children with ALL has been achieved, significant numbers of patients still die due to recurrent disease or the toxicity of treatment. Thus, future research must extend our molecular understanding of leukemia and host factors in order to even more specifically identify the mechanisms underlying the differences in treatment response and outcome, and to finally address the therapeutic needs of the individual child.

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 Supported by the Deutsche Krebshilfe, the Bundesministerium für Bildung und Forschung, the Madeleine Schickedanz Kinderkrebsstiftung, and the Deutsche José Carreras-Leukämie-Stiftung.

PII: S0037-1963(08)00150-9

doi:10.1053/j.seminhematol.2008.09.007

Seminars in Hematology
Volume 46, Issue 1 , Pages 52-63, January 2009