Molecular analysis of minimal residual disease in adult acute lymphoblastic leukaemia

Best Pract Res Clin Haematol. 2002 Mar;15(1):71-90. doi: 10.1053/beha.2002.0186.

Abstract

Despite intensive chemotherapy and stem cell transplantation (SCT) programmes, overall survival in adult acute lymphoblastic leukaemia (ALL) remains poor compared to that in childhood ALL. Despite clinical and morphological remission being achieved by over 80% of patients, 5-year survival is limited to 40% of patients, clearly indicating that morphology is insufficient in predicting future outcome. Molecular assessment of residual disease in bone marrow using immunoglobulin genes as markers of clonality has recently been evaluated in a large adult ALL study in our institution. Analysis of disease-free survival (DFS) rates for minimal residual disease-(MRD-) positive and -negative patients established that MRD positivity was associated with increased relapse rates at all times, being most significant at 3-5 months post-induction and beyond. Pre-autologous SCT tests are predictive of outcome, but for allogeneic SCT outcome is related to results of the tests after the procedure rather than before. The association of MRD test results and DFS was independent of, and greater than, other standard predictors of outcome and is therefore important in determining treatment for individual patients.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adult
  • Biomarkers, Tumor
  • Burkitt Lymphoma / diagnosis
  • Burkitt Lymphoma / mortality
  • Burkitt Lymphoma / therapy
  • Clone Cells / chemistry
  • Clone Cells / metabolism
  • Clone Cells / pathology
  • Humans
  • Neoplasm, Residual / diagnosis
  • Neoplasm, Residual / mortality
  • Neoplasm, Residual / therapy
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / diagnosis*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / mortality
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / therapy
  • Prognosis

Substances

  • Biomarkers, Tumor