2013
The outcome of allogeneic HSCT in older AML patients is determined by disease biology and not by the donor type: An analysis of 96 allografted AML patients >= 50 years from the Czech acute leukaemia clinical register (alert)
JINDRA, P., Jan MUŽÍK, K. INDRAK, P. ZAK, F. A. SABTY et. al.Základní údaje
Originální název
The outcome of allogeneic HSCT in older AML patients is determined by disease biology and not by the donor type: An analysis of 96 allografted AML patients >= 50 years from the Czech acute leukaemia clinical register (alert)
Autoři
JINDRA, P. (203 Česká republika), Jan MUŽÍK (203 Česká republika, garant, domácí), K. INDRAK (203 Česká republika), P. ZAK (203 Česká republika), F. A. SABTY (203 Česká republika), T. KOZAK (203 Česká republika), Petr CETKOVSKY (203 Česká republika), V. KOZA (203 Česká republika), M. KARAS (203 Česká republika), L. RAIDA (203 Česká republika) a T. SZOTKOWSKI (203 Česká republika)
Vydání
Neoplasma, BRATISLAVA, Slovenská akademie vied, 2013, 0028-2685
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Slovensko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.642
Kód RIV
RIV/00216224:14110/13:00069888
Organizační jednotka
Lékařská fakulta
UT WoS
000322501800015
Klíčová slova anglicky
AML; allogeneic HSCT; age; donor
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 25. 10. 2013 11:08, Soňa Böhmová
Anotace
V originále
Older patients with AML have poor prognosis after chemotherapy and allo-SCT was historically limited to the young patients. In the multicentre retrospective study we analyzed 96 consecutive AML patients >= 50 years allografted with related (n=59) or unrelated (n=37) donor. The 2- year OS and DFS rates were 45 % and 42 % for the whole group. The corresponding figures for related patients were 48% and 42% whereas for unrelated 42% and 42%, respectively (OS p=0,721, DFS p = 0,896). The cumulative incidences of relapse (28% of all patients) and NRM mortality (26%) were low with no significant differences among related and unrelated cohorts. Multivariate analysis revealed the only major independent variables associated with an inferior OS were unfavourable cytogenetics (RR 3.36; CI 1.66-6.83; p=0.001) and advanced disease status (RR 2.30; CI 1.21-4.37; p=0.011). Unfavourable cytogenetics (RR 3.00; CI 1.50-5.99; p=0.002) and advanced disease at SCT (RR 2.27; CI 1.22-4.22; p=0.009) were also the only independent variables associated with inferior DFS. In conclusion, our analysis indicates that outcomes of allografted AML patients aged >= 50 years are determined by cytogenetic risk category and disease status at transplantation and not by the type of donor.