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Patient stratification based on prednisolone-vincristine-asparaginase resistance profiles in children with acute lymphoblastic leukemia

  • M L Den Boer
  • , D O Harms
  • , R Pieters
  • , K M Kazemier
  • , U Gobel
  • , D Körholz
  • , U Graubner
  • , R J Haas
  • , N Jorch
  • , H J Spaar
  • , G J L Kaspers
  • , W A Kamps
  • , A Van der Does-Van den Berg
  • , E R Van Wering
  • , A J P Veerman
  • , G E Janka-Schaub

Research output: Contribution to journalArticlepeer-review

163 Citations (Scopus)

Abstract

PURPOSE: To confirm the prognostic value of a drug resistance profile combining prednisolone, vincristine, and l-asparaginase (PVA) cytotoxicity in an independent group of children with acute lymphoblastic leukemia (ALL) treated with a different protocol and analyzed at longer follow-up compared with our previous study of patients treated according to the Dutch Childhood Leukemia Study Group (DCLSG) ALL VII/VIII protocol.

PATIENTS AND METHODS: Drug resistance profiles were determined in 202 children (aged 1 to 18 years) with newly diagnosed ALL who were treated according to the German Cooperative Study Group for Childhood Acute Lymphoblastic Leukemia (COALL)-92 protocol.

RESULTS: At a median follow-up of 6.2 years (range, 4.1 to 9.3 years), the 5-year disease-free survival probability (pDFS) rate +/- SE was 69% +/- 7.0%, 83% +/- 4.4%, and 84% +/- 6.8% for patients with resistant (PVA score 7 to 9), intermediate-sensitive (PVA score 5 to 6), and sensitive (SPVA score 3 to 4) profiles, respectively (sensitive and intermediate-sensitive v resistant, P </=.05). Resistant patients were at increased risk of an early event (nonresponse or relapse within 2.5 years of diagnosis) compared with sensitive and intermediate-sensitive patients (P =.03). The profile did not identify patients at higher risk of late relapse, which was also observed for DCLSG ALL-VII/VIII patients now analyzed at a median of 7.5 years of follow-up (range, 4.4 to 10.8 years). Despite being nondiscriminative for late relapses, the resistant profile was still the strongest prognostic factor for COALL-92 patients in a multivariate analysis including known risk factors (P =.07).

CONCLUSION: Drug resistance profiles identify patients at higher risk of early treatment failures and may, therefore, be used to improve risk-group stratification of children with ALL.

Original languageEnglish
Pages (from-to)3262-8
Number of pages7
JournalJournal of clinical oncology : official journal of the American Society of Clinical Oncology
Volume21
Issue number17
DOIs
Publication statusPublished - 1 Sept 2003
Externally publishedYes

Keywords

  • Adolescent
  • Antineoplastic Agents, Hormonal/administration & dosage
  • Antineoplastic Agents, Phytogenic/administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols/therapeutic use
  • Asparaginase/administration & dosage
  • Chi-Square Distribution
  • Child
  • Child, Preschool
  • Disease-Free Survival
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm
  • Drug Screening Assays, Antitumor/standards
  • Female
  • Humans
  • Infant
  • Male
  • Patient Selection
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy
  • Predictive Value of Tests
  • Prednisolone/administration & dosage
  • Risk
  • Statistics, Nonparametric
  • Vincristine/administration & dosage

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