TY - JOUR
T1 - Telomerase activity is prognostic in pediatric patients with acute myeloid leukemia
T2 - Comparison with adult acute myeloid leukemia
AU - Verstovsek, Srdan
AU - Manshouri, Taghi
AU - Smith, Franklin O.
AU - Giles, Francis J.
AU - Cortes, Jorge
AU - Estey, Elihu
AU - Kantarjian, Hagop
AU - Keating, Michael
AU - Jeha, Sima
AU - Albitar, Maher
PY - 2003/5/1
Y1 - 2003/5/1
N2 - BACKGROUND. Significantly elevated telomerase activity (TA) has been found in samples from patients with almost all malignant hematologic diseases. The impact of elevated TA on the course of pediatric patients with acute myeloid leukemia (P-AML) is unknown. METHODS. Using a modified polymerase chain reaction-based, telomeric repeat-amplification protocol assay, the authors measured TA in bone marrow samples from 40 patients with P-AML and, for comparison, in 65 adult patients with AML (A-AML), excluding patients with French-American-British M3 disease. The results were correlated with patient characteristics and survival. RESULTS. TA in patients with P-AML was significantly lower compared with TA in patients with A-AML (P = 0.005). Patients who had P-AML with low TA had a projected 5-year survival rate of 88%, whereas patients who had P-AML with high TA had a projected 5-year survival rate of 43% (P = 0.009). Conversely, patients who had A-AML with very high TA (upper quartile) had significantly longer survival compared with patients who had A-AML with lower TA (P = 0.03). There was no correlation between complete remission rate or disease free survival and TA in P-AML or A-AML. In the A-AML group, when patients were separated by cytogenetic findings (poor prognosis vs. others), it was found that TA was significantly lower in patients with a poor prognosis, but the prognostic value of TA was not independent of cytogenetic status. CONCLUSIONS. The current results suggest, that for patients with P-AML, bone marrow TA is a highly significant prognostic factor.
AB - BACKGROUND. Significantly elevated telomerase activity (TA) has been found in samples from patients with almost all malignant hematologic diseases. The impact of elevated TA on the course of pediatric patients with acute myeloid leukemia (P-AML) is unknown. METHODS. Using a modified polymerase chain reaction-based, telomeric repeat-amplification protocol assay, the authors measured TA in bone marrow samples from 40 patients with P-AML and, for comparison, in 65 adult patients with AML (A-AML), excluding patients with French-American-British M3 disease. The results were correlated with patient characteristics and survival. RESULTS. TA in patients with P-AML was significantly lower compared with TA in patients with A-AML (P = 0.005). Patients who had P-AML with low TA had a projected 5-year survival rate of 88%, whereas patients who had P-AML with high TA had a projected 5-year survival rate of 43% (P = 0.009). Conversely, patients who had A-AML with very high TA (upper quartile) had significantly longer survival compared with patients who had A-AML with lower TA (P = 0.03). There was no correlation between complete remission rate or disease free survival and TA in P-AML or A-AML. In the A-AML group, when patients were separated by cytogenetic findings (poor prognosis vs. others), it was found that TA was significantly lower in patients with a poor prognosis, but the prognostic value of TA was not independent of cytogenetic status. CONCLUSIONS. The current results suggest, that for patients with P-AML, bone marrow TA is a highly significant prognostic factor.
KW - Adult acute myeloid leukemia
KW - Pediatric acute myeloid leukemia (AML)
KW - Prognosis
KW - Telomerase activity
UR - https://www.scopus.com/pages/publications/0345381983
U2 - 10.1002/cncr.11313
DO - 10.1002/cncr.11313
M3 - Article
C2 - 12712473
AN - SCOPUS:0345381983
SN - 0008-543X
VL - 97
SP - 2212
EP - 2217
JO - Cancer
JF - Cancer
IS - 9
ER -