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  • Frost, Britt-MarieUppsala universitet,Institutionen för kvinnors och barns hälsa,Barnonkologisk forskning/Lönnerholm (author)

Increased in vitro cellular drug resistance is related to poor outcome in high-risk childhood acute lymphoblastic leukaemia

  • Article/chapterEnglish2003

Publisher, publication year, extent ...

  • 2003-07-23
  • Wiley,2003
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-89993
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-89993URI
  • https://doi.org/10.1046/j.1365-2141.2003.04442.xDOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:1940100URI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-64728URI

Supplementary language notes

  • Language:English
  • Summary in:English

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Classification

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

Notes

  • On behalf of the Nordic Society for Paediatric Haematology and Oncology
  • Summary. We determined the in vitro cellular drug resistance in 370 children with newly diagnosed acute lymphoblastic leukaemia (ALL). The resistance to each of 10 drugs was measured by the fluorometric microculture cytotoxicity assay (FMCA) and was related to clinical outcome. The median follow-up time was 41 months. Risk-group stratified analyses indicated that in vitro resistance to dexamethasone, doxorubicin and amsacrine were each significantly related to the probability of disease-free survival. In the high-risk (HR) group, increased in vitro resistance to dexamethasone (P = 0·014), etoposide (P = 0·025) and doxorubicin (P = 0·05) was associated with a worse clinical outcome. Combining the results for these drugs provided a drug resistance score with an independent prognostic significance superior to that of any other factor studied, with a relative risk of relapse in the most resistant group 9·8 times that in the most sensitive group (P = 0·007). The results in the intermediate-risk (IR) and standard-risk (SR) groups were less clear cut. In conclusion, our data indicate that in vitro testing of cellular drug resistance can be used to predict the clinical outcome in HR ALL, while the final evaluation of the results in IR and SR patients must await longer follow-up.

Added entries (persons, corporate bodies, meetings, titles ...)

  • Nygren, PeterUppsala universitet,Institutionen för onkologi, radiologi och klinisk immunologi,Cancer Pharmacology and Informatics(Swepub:uu)peterng (author)
  • Gustafsson, GUppsala universitet,Karolinska Institutet,Institutionen för kvinnors och barns hälsa,Barnonkologisk forskning/Lönnerholm (author)
  • Forestier, E (author)
  • Jonsson, O G (author)
  • Kanerva, J (author)
  • Nygaard, R (author)
  • Schmiegelow, K (author)
  • Larsson, RolfUppsala universitet,Klinisk farmakologi,Institutionen för medicinska vetenskaper,Cancer Pharmacology and Informatics(Swepub:uu)rolflars (author)
  • Lönnerholm, GudmarUppsala universitet,Institutionen för kvinnors och barns hälsa(Swepub:uu)gudmarlh (author)
  • Uppsala universitetInstitutionen för kvinnors och barns hälsa (creator_code:org_t)

Related titles

  • In:British Journal of Haematology: Wiley122, s. 376-0007-10481365-2141
  • In:Br J Haematol: Wiley122, s. 376-

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