Prognostic implications of mutations in NOTCH1 and FBXW7 in childhood T-all treated according to the NOPHO ALL-1992 and ALL-2000 protocols-Reference-Cited by-同舟云学术

Prognostic implications of mutations in NOTCH1 and FBXW7 in childhood T-all treated according to the NOPHO ALL-1992 and ALL-2000 protocols

Published:2013-10-08 Issue:3 Volume:61 Page:424-430
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Fogelstrand Linda¹,Staffas Anna¹,Wasslavik Carina¹,Sjögren Helene¹,Söderhäll Stefan²,Frost Britt-Marie³,Forestier Erik⁴,Degerman Sofie⁵,Behrendtz Mikael⁶,Heldrup Jesper⁷,Karrman Kristina⁸,Johansson Bertil⁸,Heyman Mats⁹,Abrahamsson Jonas¹⁰,Palmqvist Lars¹

Affiliation:

1. Department of Clinical Chemistry and Transfusion Medicine; Institute of Biomedicine, Sahlgrenska Academy at University of Gothenburg; Gothenburg Sweden

2. Childhood Cancer Research Unit, Department of Women and Child Health; Astrid Lindgren Children's Hospital; Stockholm Sweden

3. Department of Women's and Children's Health; Institute of Paediatric; Uppsala Sweden

4. Department of Medical Biosciences; Clinical Genetics, Umeå University; Umeå Sweden

5. Department of Medical Biosciences; Pathology; Umeå University; Umeå Sweden

6. Department of Paediatrics; University Hospital Linköping; Linköping Sweden

7. Department of Pediatrics; Skåne University Hospital, Lund University; Lund Sweden

8. Department of Clinical Genetics; University and Regional Laboratories, Lund University; Lund Sweden

9. Department of Woman and Child Health; Karolinska Institute; Stockholm Sweden

10. Department of Pediatrics; Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg; Gothenburg Sweden

Funder

The Swedish Childhood Cancer Foundation

The Swedish Cancer Society

Lions Cancer Research Foundation at Umea University

Vasterbotten County Council

Sahlgrenska University Hospital

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.24803/fullpdf

Reference39 articles.

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2. Late MRD response determines relapse risk overall and in subsets of childhood T-cell ALL: Results of the AIEOP-BFM-ALL 2000 study;Schrappe;Blood,2011

3. Detection of minimal residual disease identifies differences in treatment response between T-ALL and precursor B-ALL;Willemse;Blood,2002

4. Minimal residual disease assessment in childhood acute lymphoblastic leukaemia: A swedish multi-centre study comparing real-time polymerase chain reaction and multicolour flow cytometry;Thorn;Br J Haematol,2011

5. Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome;Karrman;Genes Chromosomes Cancer,2009

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