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  • Toft, N (author)

Results of NOPHO ALL2008 treatment for patients aged 1-45 years with acute lymphoblastic leukemia.

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2017-08-18
  • Springer Science and Business Media LLC,2018

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/259793
  • https://gup.ub.gu.se/publication/259793URI
  • https://doi.org/10.1038/leu.2017.265DOI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-146231URI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-343170URI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:137798036URI

Supplementary language notes

  • Language:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Adults with acute lymphoblastic leukemia (ALL) do worse than children. From 7/2008 to 12/2014, Nordic and Baltic centers treated 1509 consecutive patients aged 1-45 years with Philadelphia chromosome-negative ALL according to the NOPHO ALL2008 without cranial irradiation. Overall, 1022 patients were of age 1-9 years (A), 266 were 10-17 years (B) and 221 were 18-45 years (C). Sixteen patients (three adults) died during induction. All others achieved remission after induction or 1-3 intensive blocks. Subsequently, 45 patients (12 adults) died, 122 patients relapsed (32 adults) with a median time to relapse of 1.6 years and 13 (no adult) developed a second malignancy. Median follow-up time was 4.6 years. Among the three age groups, older patients more often had higher risk ALL due to T-ALL (32%/25%/9%, P<0.001), KMT2A rearrangements (6%/5%/3%, P<0.001) and higher day 29 residual leukemia for B-lineage (P<0.001), but not T-ALL (P=0.53). Event-free survival rates (pEFS5y) were 89±1% (A), 80±3% (B) and 74±4% (C) with significant differences only for non-high risk groups. Except for thrombosis, pancreatitis and osteonecrosis, the risk of 19 specified toxicities was not enhanced by age above 10 years. In conclusion, a pediatric-based protocol is tolerable and effective for young adults, despite their increased frequency of higher risk features.Leukemia advance online publication, 22 September 2017; doi:10.1038/leu.2017.265.

Subject headings and genre

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  • Birgens, H (author)
  • Abrahamsson, Jonas,1954Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics(Swepub:gu)xabrjo (author)
  • Griškevičius, L (author)
  • Hallböök, HeleneUppsala universitet,Hematologi(Swepub:uu)helehall (author)
  • Heyman, MKarolinska Institutet (author)
  • Klausen, T W (author)
  • Jónsson, Ó G (author)
  • Palk, K (author)
  • Pruunsild, K (author)
  • Quist-Paulsen, P (author)
  • Vaitkeviciene, G (author)
  • Vettenranta, K (author)
  • Åsberg, A (author)
  • Frandsen, T L (author)
  • Marquart, H V (author)
  • Madsen, H O (author)
  • Norén-Nyström, UlrikaUmeå universitet,Pediatrik(Swepub:umu)kagr0007 (author)
  • Schmiegelow, K (author)
  • Göteborgs universitetInstitutionen för kliniska vetenskaper, Avdelningen för pediatrik (creator_code:org_t)

Related titles

  • In:Leukemia: Springer Science and Business Media LLC32, s. 606-6151476-55510887-6924

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