Serum vascular endothelial growth factor-a levels during induction therapy in children with acute lymphoblastic

Manas Kalra1, Veronique Dinand, Sangeeta Choudhary

  • 1Pediatric Hematology Oncology and BMT, Department of Pediatrics, Institute of Child Health, India.

Indian Pediatrics
|March 19, 2013
PubMed

Insights

Children with acute lymphoblastic leukemia (ALL) have lower serum vascular endothelial growth factor (VEGF) levels before treatment. Chemotherapy for ALL increases VEGF to normal levels, indicating its potential role in leukemia.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Molecular Biology

Background:

  • Vascular Endothelial Growth Factor (VEGF) plays a crucial role in angiogenesis and tumor growth.
  • VEGF levels in pediatric malignancies, particularly Acute Lymphoblastic Leukemia (ALL), require further investigation.
  • Understanding VEGF kinetics during chemotherapy is essential for assessing treatment response.

Purpose of the Study:

  • To evaluate serum VEGF levels in children diagnosed with ALL.
  • To assess changes in serum VEGF during the induction phase of chemotherapy.
  • To correlate VEGF levels with tumor burden markers in pediatric ALL.

Main Methods:

  • Prospective hospital-based study over 18 months.
  • Inclusion of 30 children with ALL and 17 healthy controls.
  • Measurement of serum VEGF-A-165 isoform (s-VEGF) using ELISA at diagnosis and post-induction.

Main Results:

  • Untreated children with ALL exhibited significantly lower s-VEGF levels compared to controls (17.0 vs. 42.6 pg/mL).
  • s-VEGF levels showed a moderate correlation with White Blood Cell (WBC) count (r=-0.56) and Lactate Dehydrogenase (LDH) (r=-0.52) at diagnosis.
  • Following induction chemotherapy, s-VEGF levels significantly increased (median 44.2 pg/mL), nearing control levels.

Conclusions:

  • Children with ALL present with diminished s-VEGF concentrations prior to treatment.
  • Induction chemotherapy normalizes s-VEGF levels in pediatric ALL patients.
  • Further research is needed to elucidate the VEGF-VEGF receptor interactions in leukemia cells.
Abstract