Clinical significance of deletions of chromosome arm 6q in childhood acute lymphoblastic leukemia: A report from the children's cancer group Academic Article uri icon


MeSH Major

  • Chromosome Deletion
  • Chromosomes, Human, Pair 6
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma


  • We have compared outcome for 167 (9.0%) children with a del(6q) and 1713 (91%) children without a del(6q) treated on Children's Cancer Group (CCG) risk-adjusted treatment protocols for acute lymphoblastic leukemia (ALL). Thirty-three patients had a del(6q) as the sole aberration; 22 patients had a del(6q) only as a secondary abnormality. Thirty-six cases had a del(6q) and high hyperdiploidy (>50 chromosomes). Six patients with a del(6q) also had +16 and 8 patients had loss of a sex chromosome. Frequent recurring breakpoints were q13, q15, q21, q23, and q25. Patients with a del(6q) were more likely to have T-lineage ALL (p < 0.001), a mediastinal mass (p = 0.01), and higher WBC counts (p = 0.04), although only half of these patients were classified as poor risk. Event-free survival at 6 years was similar for patients with or without a del(6q), with estimates of 77% (SD = 5%) and 74% (SD = 2%), respectively (p = 0.44). This finding was also observed within NCI poor and standard risk groups. Thus, cytogenetically detectable del(6q) is not associated with adverse risk in pediatric ALL.

publication date

  • March 2000



  • Academic Article



  • eng

PubMed ID

  • 10784391

Additional Document Info

start page

  • 467

end page

  • 78


  • 36


  • 5-6