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.; Jan MUŽÍK; K. INDRAK; P. ZAK; F. A. SABTY; T. KOZAK; Petr CETKOVSKY; V. KOZA; M. KARAS; L. RAIDA a T. SZOTKOWSKI
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
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/13:00069888
Organizační jednotka
Lékařská fakulta
UT WoS
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.