Outcomes after Induction Failure in Childhood Acute Lymphoblastic Leukemia

Martin Schrappe(University Medical Center), Stephen P. Hunger(Children's Hospital Colorado), Ching‐Hon Pui(St. Jude Children's Research Hospital), Vaskar Saha(Manchester Academic Health Science Centre), Paul S. Gaynon(Children's Hospital of Los Angeles), André Baruchel(Université Paris Cité), Valentino Conter(Azienda Ospedaliero Universitaria Ospedali Riuniti), Jacques Otten(Universitair Ziekenhuis Brussel), Akira Ohara(Toho University), Anne Birgitta Versluys(University Medical Center Utrecht), Gabriele Escherich(Universität Hamburg), Mats Heyman(Karolinska Institutet), Lewis B. Silverman(Dana-Farber Cancer Institute), Keizo Horibe(Nagoya Medical Center), Georg Mann(St Anna Children's Hospital), Bruce M. Camitta(Children's Hospital of Wisconsin), Jochen Harbott(Justus-Liebig-Universität Gießen), Hansjörg Riehm(Medizinische Hochschule Hannover), Sue Richards(University of Oxford), Meenakshi Devidas(University of Florida), Martin Zimmermann(Medizinische Hochschule Hannover)
New England Journal of Medicine
April 11, 2012
Cited by 295Open Access
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Abstract

BACKGROUND: Failure of remission-induction therapy is a rare but highly adverse event in children and adolescents with acute lymphoblastic leukemia (ALL). METHODS: We identified induction failure, defined by the persistence of leukemic blasts in blood, bone marrow, or any extramedullary site after 4 to 6 weeks of remission-induction therapy, in 1041 of 44,017 patients (2.4%) 0 to 18 years of age with newly diagnosed ALL who were treated by a total of 14 cooperative study groups between 1985 and 2000. We analyzed the relationships among disease characteristics, treatments administered, and outcomes in these patients. RESULTS: Patients with induction failure frequently presented with high-risk features, including older age, high leukocyte count, leukemia with a T-cell phenotype, the Philadelphia chromosome, and 11q23 rearrangement. With a median follow-up period of 8.3 years (range, 1.5 to 22.1), the 10-year survival rate (±SE) was estimated at only 32±1%. An age of 10 years or older, T-cell leukemia, the presence of an 11q23 rearrangement, and 25% or more blasts in the bone marrow at the end of induction therapy were associated with a particularly poor outcome. High hyperdiploidy (a modal chromosome number >50) and an age of 1 to 5 years were associated with a favorable outcome in patients with precursor B-cell leukemia. Allogeneic stem-cell transplantation from matched, related donors was associated with improved outcomes in T-cell leukemia. Children younger than 6 years of age with precursor B-cell leukemia and no adverse genetic features had a 10-year survival rate of 72±5% when treated with chemotherapy only. CONCLUSIONS: Pediatric ALL with induction failure is highly heterogeneous. Patients who have T-cell leukemia appear to have a better outcome with allogeneic stem-cell transplantation than with chemotherapy, whereas patients who have precursor B-cell leukemia without other adverse features appear to have a better outcome with chemotherapy. (Funded by Deutsche Krebshilfe and others.).


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