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Guadecitabine vs treatment choice in newly diagnosed acute myeloid leukemia: a global phase 3 randomized study
P. Fenaux, M. Gobbi, PL. Kropf, JJ. Issa, GJ. Roboz, J. Mayer, J. Krauter, T. Robak, H. Kantarjian, J. Novak, WW. Jedrzejczak, X. Thomas, M. Ojeda-Uribe, Y. Miyazaki, YH. Min, SP. Yeh, J. Brandwein, L. Gercheva-Kyuchukova, J. Demeter, E....
Jazyk angličtina Země Spojené státy americké
Typ dokumentu klinické zkoušky, fáze III, randomizované kontrolované studie, časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2016
PubMed Central
od 2016
Europe PubMed Central
od 2016
ROAD: Directory of Open Access Scholarly Resources
od 2016
- MeSH
- akutní myeloidní leukemie * diagnóza farmakoterapie MeSH
- azacytidin * škodlivé účinky MeSH
- cytarabin škodlivé účinky MeSH
- lidé MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
This phase 3 study evaluated the efficacy and safety of the new hypomethylating agent guadecitabine (n = 408) vs a preselected treatment choice (TC; n = 407) of azacitidine, decitabine, or low-dose cytarabine in patients with acute myeloid leukemia unfit to receive intensive induction chemotherapy. Half of the patients (50%) had poor Eastern Cooperative Oncology Group Performance Status (2-3). The coprimary end points were complete remission (19% and 17% of patients for guadecitabine and TC, respectively [stratified P = .48]) and overall survival (median survival 7.1 and 8.5 months for guadecitabine and TC, respectively [hazard ratio, 0.97; 95% confidence interval, 0.83-1.14; stratified log-rank P = .73]). One- and 2-year survival estimates were 37% and 18% for guadecitabine and 36% and 14% for TC, respectively. A large proportion of patients (42%) received <4 cycles of treatment in both the arms. In a post hoc analysis of patients who received ≥4 treatment cycles, guadecitabine was associated with longer median survival vs TC (15.6 vs 13.0 months [hazard ratio, 0.78; 95% confidence interval, 0.64-0.96; log-rank P = .02]). There was no significant difference in the proportion of patients with grade ≥3 adverse events (AEs) between guadecitabine (92%) and TC (88%); however, grade ≥3 AEs of febrile neutropenia, neutropenia, and pneumonia were higher with guadecitabine. In conclusion, no significant difference was observed in the efficacy of guadecitabine and TC in the overall population. This trial was registered at www.clinicaltrials.gov as #NCT02348489.
Astex Pharmaceuticals Inc Pleasanton CA
China Medical University Hospital Taichung City Taiwan
Coriell Institute for Medical Research Camden NJ
Fakultní Nemocnice Brno Česká Republika
GHR Mulhouse Sud Alsace Mulhouse France
Hôpital Lyon Sud Pierre Bénite France
Hôpital Saint Louis Paris France
Hospital St Marina EAD Varna Bulgaria
Medical University of Lodz and Copernicus Memorial Hospital Lodz Poland
Nagasaki University Hospital Nagasaki Japan
Novant Health Cancer Institute Elizabeth Charlotte NC
Ospedale Policlinico San Martino Genova Italy
Princess Margaret Cancer Centre Toronto ON Canada
Roswell Park Comprehensive Cancer Institute Buffalo NY
Samodzielny Publiczny Centralny Szpital Kliniczny Warszawa Poland
Semmelweis Egyetem Budapest Hungary
Severance Hospital Yonsei University Health System Seoul Republic of Korea
Städtisches Klinikum Braunschweig gGmbH Braunschweig Germany
The University of Texas MD Anderson Cancer Center Houston TX
Ulm University Hospital Ulm Germany
University of Alberta Hospital Edmonton Canada
Citace poskytuje Crossref.org
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