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Author Pui, C.-H.; Relling, M.V.; Downing, J.R. url  doi
openurl 
  Title Acute lymphoblastic leukemia Type Journal Article
  Year 2004 Publication The New England Journal of Medicine Abbreviated Journal N Engl J Med  
  Volume 350 Issue 15 Pages 1535-1548  
  Keywords Age Factors; Genotype; Humans; Molecular Biology; Mutation; Pharmacogenetics; Polymorphism, Genetic; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy/*genetics; Prognosis; Translocation, Genetic  
  Abstract  
  Address Department of Hematology/Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. ching-hon.pui@stjude.org  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0028-4793 ISBN Medium  
  Area WP6 In vivo Expedition Conference  
  Notes PMID:15071128 Approved no  
  Call Number (up) CBM.UAM @ ccobaleda @ Serial 43  
Permanent link to this record
 

 
Author Pui, C.-H.; Robison, L.L.; Look, A.T. url  doi
openurl 
  Title Acute lymphoblastic leukaemia Type Journal Article
  Year 2008 Publication Lancet Abbreviated Journal Lancet  
  Volume 371 Issue 9617 Pages 1030-1043  
  Keywords Adolescent; Adult; Age Factors; Antineoplastic Agents/*therapeutic use; Child; Child, Preschool; Disease-Free Survival; Humans; Pharmacogenetics; *Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy/genetics/physiopathology; Randomized Controlled Trials as Topic; Risk Assessment; Translocation, Genetic/*genetics; Treatment Outcome  
  Abstract Acute lymphoblastic leukaemia, a malignant disorder of lymphoid progenitor cells, affects both children and adults, with peak prevalence between the ages of 2 and 5 years. Steady progress in development of effective treatments has led to a cure rate of more than 80% in children, creating opportunities for innovative approaches that would preserve past gains in leukaemia-free survival while reducing the toxic side-effects of current intensive regimens. Advances in our understanding of the pathobiology of acute lymphoblastic leukaemia, fuelled by emerging molecular technologies, suggest that drugs specifically targeting the genetic defects of leukaemic cells could revolutionise management of this disease. Meanwhile, studies are underway to ascertain the precise events that take place in the genesis of acute lymphoblastic leukaemia, to enhance the clinical application of known risk factors and antileukaemic agents, and to identify treatment regimens that might boost the generally low cure rates in adults and subgroups of children with high-risk leukaemia.  
  Address Department of Oncology, St Jude Children's Research Hospital and University of Tennessee Health Science Center, Memphis, TN 38105, USA. ching-hon.pui@stjude.org  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0140-6736 ISBN Medium  
  Area WP6 In vivo Expedition Conference  
  Notes PMID:18358930 Approved no  
  Call Number (up) CBM.UAM @ ccobaleda @ Serial 44  
Permanent link to this record
 

 
Author Schuz, J.; Ahlbom, A. url  doi
openurl 
  Title Exposure to electromagnetic fields and the risk of childhood leukaemia: a review Type Journal Article
  Year 2008 Publication Radiation Protection Dosimetry Abbreviated Journal Radiat Prot Dosimetry  
  Volume 132 Issue 2 Pages 202-211  
  Keywords Body Burden; Child; *Electromagnetic Fields; Environmental Exposure/*statistics & numerical data; Humans; Incidence; Leukemia, Radiation-Induced/*epidemiology; Radiation Monitoring/statistics & numerical data; Risk Assessment/methods; Risk Factors; Young Adult  
  Abstract Extremely low-frequency magnetic fields have been classified as possibly carcinogenic to humans, mainly based on epidemiological studies consistently showing an association between long-term average exposures to magnetic fields above 0.3/0.4 microT and the risk of childhood leukaemia. No mechanism to explain this finding has been established and no support for a causal link emerged from experimental studies. Chance or bias cannot be ruled out with reasonable confidence as an explanation for the observed association. If the association is causal, it explains only a small fraction of childhood leukaemia cases. There were some reports of childhood leukaemia clusters in the vicinity of high-power radio and television broadcast transmitters in studies in Australia and Italy. However, recent large-scale systematic studies in Korea and Germany show no association between exposure to radio frequency electromagnetic fields emitted from broadcast towers and childhood leukaemia risk. Studies on mobile phone use and leukaemia risk in adolescents and young adults may be indicated.  
  Address Institute of Cancer Epidemiology, Danish Cancer Society, Strandboulevarden 49, DK-2100 Copenhagen, Denmark. joachim@cancer.dk  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0144-8420 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:18927133 Approved no  
  Call Number (up) CBM.UAM @ ccobaleda @ Serial 45  
Permanent link to this record
 

 
Author Sherborne, A.L.; Hosking, F.J.; Prasad, R.B.; Kumar, R.; Koehler, R.; Vijayakrishnan, J.; Papaemmanuil, E.; Bartram, C.R.; Stanulla, M.; Schrappe, M.; Gast, A.; Dobbins, S.E.; Ma, Y.; Sheridan, E.; Taylor, M.; Kinsey, S.E.; Lightfoot, T.; Roman, E.; Irving, J.A.E.; Allan, J.M.; Moorman, A.V.; Harrison, C.J.; Tomlinson, I.P.; Richards, S.; Zimmermann, M.; Szalai, C.; Semsei, A.F.; Erdelyi, D.J.; Krajinovic, M.; Sinnett, D.; Healy, J.; Gonzalez Neira, A.; Kawamata, N.; Ogawa, S.; Koeffler, H.P.; Hemminki, K.; Greaves, M.; Houlston, R.S. url  doi
openurl 
  Title Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk Type Journal Article
  Year 2010 Publication Nature Genetics Abbreviated Journal Nat Genet  
  Volume 42 Issue 6 Pages 492-494  
  Keywords Case-Control Studies; *Chromosomes, Human, Pair 9; *Genes, p16; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics  
  Abstract Using data from a genome-wide association study of 907 individuals with childhood acute lymphoblastic leukemia (cases) and 2,398 controls and with validation in samples totaling 2,386 cases and 2,419 controls, we have shown that common variation at 9p21.3 (rs3731217, intron 1 of CDKN2A) influences acute lymphoblastic leukemia risk (odds ratio = 0.71, P = 3.01 x 10(-11)), irrespective of cell lineage.  
  Address Section of Cancer Genetics, Institute of Cancer Research, Sutton, Surrey, UK  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1061-4036 ISBN Medium  
  Area WP6 In vivo Expedition Conference  
  Notes PMID:20453839 Approved no  
  Call Number (up) CBM.UAM @ ccobaleda @ Serial 46  
Permanent link to this record
 

 
Author Steliarova-Foucher, E.; Stiller, C.; Kaatsch, P.; Berrino, F.; Coebergh, J.-W.; Lacour, B.; Parkin, M. url  doi
openurl 
  Title Geographical patterns and time trends of cancer incidence and survival among children and adolescents in Europe since the 1970s (the ACCISproject): an epidemiological study Type Journal Article
  Year 2004 Publication Lancet Abbreviated Journal Lancet  
  Volume 364 Issue 9451 Pages 2097-2105  
  Keywords Adolescent; Adult; Age of Onset; Child; Child, Preschool; Europe/epidemiology; Humans; Incidence; Infant; Neoplasms/*epidemiology/mortality; Registries; Survival Rate  
  Abstract BACKGROUND: Cancer is rare before age 20 years. We aimed to use the European database of childhood and adolescent cancer cases, within the Automated Childhood Cancer Information System project, to estimate patterns and trends of incidence and survival within Europe. METHODS: Comparable, high-quality data from 63 European population-based cancer registries consisted of 113000 tumours in children and 18243 in adolescents diagnosed in 1970-99. Incidence rates and survival were compared by region (east vs west), period, and malignant disease. FINDINGS: In the 1990s, age-standardised incidence rates were 140 per million for children (0-14 years) and 157 per million for ages 0-19 years. Over the three decades, overall incidence increased by 1.0% per year (p<0.0001) in children (increases for most tumour types), and by 1.5% (p<0.0001) in adolescents (15-19 years; notable increases were recorded for carcinomas, lymphomas, and germ-cell tumours). Overall 5-year survival for children in the 1990s was 64% in the east and 75% in the west, with differences between regions for virtually all tumour groups; 5-year survival was much the same in adolescents. Survival has improved dramatically since the 1970s in children and adolescents, more so in the west than in the east. INTERPRETATION: Our results are clear evidence of an increase of cancer incidence in childhood and adolescence during the past decades, and of an acceleration of this trend. Geographical and temporal patterns suggest areas for further study into causes of these neoplasms, as well as providing an indicator of progress of public-health policy in Europe.  
  Address International Agency for Research on Cancer, Lyon, France. steliarova@iarc.fr  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0140-6736 ISBN Medium  
  Area WP9 Epidemiology Expedition Conference  
  Notes PMID:15589307 Approved no  
  Call Number (up) CBM.UAM @ ccobaleda @ Serial 47  
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