Expression of CD66c and CD25 in acute lymphoblastic leukemia as a predictor of the presence of BCR/ABL rearrangement

Hematol Oncol Stem Cell Ther. 2008 Jan-Mar;1(1):34-7. doi: 10.1016/s1658-3876(08)50058-6.

Abstract

Background: Expression of myeloid or T cell lymphoid in precursor B cell acute lymphoblastic leukemia (pre-B cell ALL), which is referred to as aberrant expression, is quite a common phenomenon. CD66c is a myeloid marker which has aberrant expression in pre-B cell ALL, with strong correlation with non-random genetic changes (BCR/ABL rearrangement). Another leukemia associated marker (CD25) is frequently expressed in pre-B cell ALL. The frequency of CD25-expressing lymphoblasts has been found to be significantly higher in BCR/ABL-positive vs. BCR/ABL-negative patients.

Methods: In a cohort of 103 patients diagnosed with pre-B cell ALL or biphenotypic leukemia and studied for expression of CD66c and CD25 at presentation, we evaluated the frequency of expression of either or both in BCR/ABL positive cases.

Results: Surface CD66c was expressed by 70 cases (68%) and CD25 was expressed by 33 cases (32%) while both were expressed together on 29 cases (28%). BCR/ABL was positive in 18/103 patients. All BCR/ABL positive cases were positive for surface CD66c and CD25.

Conclusion: Positivity for both leukemia-associated antigens CD66c and CD25 in combination can predict the presence of BCR/ABL rearrangement in pre-B cell ALL. While this finding does not replace the detection of BCR/ABL abnormality by cytogenetic or molecular techniques, it does provide an early and handy tool for prediction and management of high-risk cases of pre-B cell ALL, especially in centers with limited laboratory facilities.

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / biosynthesis*
  • Biomarkers, Tumor / analysis
  • Cell Adhesion Molecules / biosynthesis*
  • Child
  • Child, Preschool
  • Female
  • Fusion Proteins, bcr-abl / genetics
  • Fusion Proteins, bcr-abl / metabolism*
  • GPI-Linked Proteins
  • Humans
  • Immunophenotyping
  • In Situ Hybridization, Fluorescence
  • Interleukin-2 Receptor alpha Subunit / biosynthesis*
  • Male
  • Middle Aged
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Translocation, Genetic
  • Young Adult

Substances

  • Antigens, CD
  • Biomarkers, Tumor
  • CEACAM6 protein, human
  • Cell Adhesion Molecules
  • GPI-Linked Proteins
  • Interleukin-2 Receptor alpha Subunit
  • Fusion Proteins, bcr-abl