Maintenance Decitabine (DAC) Improves Disease-Free (DFS) and Overall Survival (OS) after Intensive Therapy for Acute Myeloid Leukemia (AML) in Older Adults, Particularly in FLT3-ITD-Negative Patients: ECOG-ACRIN (E-A) E2906 Randomized Study

▪ Background: Relapse remains the most common cause of treatment failure after intensive induction and consolidation (CONS) therapy in older adults with AML. We therefore performed a prospective randomized phase II study to determine the safety and impact on DFS (relapse or death) and OS of DAC main...

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Veröffentlicht in:Blood 2019-11, Vol.134 (Supplement_1), p.115-115
Hauptverfasser: Foran, James M., Sun, Zhuoxin, Claxton, David F., Lazarus, Hillard M, Arber, Daniel A., Rowe, Jacob M., Paietta, Elisabeth, Racevskis, Janis, Altman, Jessica K., Luger, Selina M., Al-Kali, Aref, Zheng, Hong, Pratz, Keith W., Broun, Edward R., Powell, Bayard L, O'Dwyer, Kristen Marie, Godwin, John E., Ofran, Yishai, Litzow, Mark, Tallman, Martin S.
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Sprache:eng
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Zusammenfassung:▪ Background: Relapse remains the most common cause of treatment failure after intensive induction and consolidation (CONS) therapy in older adults with AML. We therefore performed a prospective randomized phase II study to determine the safety and impact on DFS (relapse or death) and OS of DAC maintenance using an abbreviated 3-day schedule administered every 4 weeks for 1 year (per Lubbert et al, Haematologica 97:393, 2012) vs. Observation (OBS) after intensive AML therapy, conducted in the large multi-center E-A E2906 Phase III trial in patients (pts) age ≥60 yrs. Methods: The design and primary clinical results for E2906 (n=727) have been reported previously (Foran et al, ASH #217a, 2015), demonstrating superior OS following ‘Standard’ 7&3 (Daunorubicin 60mg/m2) induction and intermediate dose Ara-C consolidation (CONS) vs. single agent Clofarabine (CLO, provided by SANOFI), despite similar CR/CRi (CR with incomplete CBC recovery) and induction mortality rates. All CR/CRi pts after induction (n=311) were assigned to 2 cycles CONS with either Ara-C (1.5g/m2 x 12 doses; 6 doses if age >/=70 yrs), or single agent CLO, based on induction randomization. Ongoing CR/CRi after recovery from CONS was confirmed with restaging BM biopsy, and eligible pts offered participation in the ‘Step 3‘ maintenance study, a 1:1 randomization (stratified by induction therapy, cytogenetic risk group, age
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2019-129876