2017
Characteristics and outcome of patients with therapy-related acute promyelocytic leukemia front-line treated with or without arsenic trioxide
KAYSER, S.; J. KRZYKALLA; M.A. ELLIOTT; K. NORSWORTHY; P. GONZALES et. al.Základní údaje
Originální název
Characteristics and outcome of patients with therapy-related acute promyelocytic leukemia front-line treated with or without arsenic trioxide
Autoři
KAYSER, S.; J. KRZYKALLA; M.A. ELLIOTT; K. NORSWORTHY; P. GONZALES; R.K. HILLS; M.R. BAER; Zdeněk RÁČIL; Jiří MAYER; J. NOVAK; P. ZAK; T. SZOTKOWSKI; D. GRIMWADE; N.H. RUSSELL; R.B. WALTER; E.H. ESTEY; J. WESTERMANN; M. GORNER; A. BENNER; A. KRAMER; B.D. SMITH; A.K. BURNETT; C. THIEDE; C. ROLLIG; A.D. HO; G. EHNINGER; R.F. SCHLENK; M.S. TALLMAN; M.J. LEVIS a U. PLATZBECKER
Vydání
Leukemia, London, Nature Publishing Group, 2017, 0887-6924
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 10.023
Kód RIV
RIV/00216224:14110/17:00095682
Organizační jednotka
Lékařská fakulta
UT WoS
000414215400008
EID Scopus
2-s2.0-85017498433
Klíčová slova anglicky
promyelocytic leukemia
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 20. 3. 2018 16:56, Soňa Böhmová
Anotace
V originále
Therapy-related acute promyelocytic leukemia (t-APL) is relatively rare, with limited data on outcome after treatment with arsenic trioxide (ATO) compared to standard intensive chemotherapy (CTX). We evaluated 103 adult t-APL patients undergoing treatment with all-trans retinoic acid (ATRA) alone (n = 7) or in combination with ATO (n = 24), CTX (n = 53), or both (n = 19). Complete remissions were achieved after induction therapy in 57% with ATRA, 100% with ATO/ATRA, 78% with CTX/ATRA, and 95% with CTX/ATO/ATRA. Early death rates were 43% for ATRA, 0% for ATO/ATRA, 12% for CTX/ATRA and 5% for CTX/ATO/ATRA. Three patients relapsed, two developed therapy-related acute myeloid leukemia and 13 died in remission including seven patients with recurrence of the prior malignancy. Median follow-up for survival was 3.7 years. None of the patients treated with ATRA alone survived beyond one year. Event-free survival was significantly higher after ATO-based therapy (95%, 95% CI, 82-99%) as compared to CTX/ATRA (78%, 95% CI, 64-87%; P = 0.042), if deaths due to recurrence of the prior malignancy were censored. The estimated 2-year overall survival in intensively treated patients was 88% (95% CI, 80-93%) without difference according to treatment (P = 0.47). ATO when added to ATRA or CTX/ATRA is feasible and leads to better outcomes as compared to CTX/ATRA in t-APL.
Návaznosti
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