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Abstract

Dose-dense induction with the S-HAM regimen was compared to standard double induction therapy in adult patients with newly diagnosed acute myeloid leukemia. Patients were centrally randomized (1:1) between S-HAM (2nd chemotherapy cycle starting on day 8 = “dose-dense”) and double induction with TAD-HAM or HAM(-HAM) (2nd cycle starting on day 21 = “standard”). 387 evaluable patients were randomly assigned to S-HAM (N = 203) and to standard double induction (N = 184). The primary endpoint overall response rate (ORR) consisting of complete remission (CR) and incomplete remission (CRi) was not significantly different (P = 0.202) between S-HAM (77%) and double induction (72%). The median overall survival was 35 months after S-HAM and 25 months after double induction (P = 0.323). Duration of critical leukopenia was significantly reduced after S-HAM (median 29 days) versus double induction (median 44 days)—P < 0.001. This translated into a significantly shortened duration of hospitalization after S-HAM (median 37 days) as compared to standard induction (median 49 days)—P < 0.001. In conclusion, dose-dense induction therapy with the S-HAM regimen shows favorable trends but no significant differences in ORR and OS compared to standard double induction. S-HAM significantly shortens critical leukopenia and the duration of hospitalization by 2 weeks.

OriginalspracheEnglisch
ZeitschriftLeukemia
Jahrgang32
Ausgabenummer12
Seiten (von - bis)2558-2571
Seitenumfang14
ISSN0887-6924
DOIs
PublikationsstatusVeröffentlicht - 01.12.2018

Fördermittel

Conflict of interest Jan Braess has received research funding from Amgen and Janssen. Eva Elisabeth Lengfelder has received travel & accommodation expenses from Teva and Novartis. Ullrich Graeven has received honoraria from Amgen, Roche, Bayer, Sanofi, AbbVie, Servier, and Boehringer; has a consulting or advisory role in Baxalta, Servier, Roche, and Novartis; and has received travel & accommodation expenses from Merck and Sanofi. Dirk Behringer has a consulting or advisory role in Roche and BMS. Gero Massenkeil has received honoraria from Sanofi; has a consulting or advisory role in Sanofi; and is in speakers’ bureau in Sanofi. Stefan Bohlander has received honoraria from Roche. Wolfgang Hiddemann has received honoraria from Roche, Gilead, and Janssen; is in speakers’ bureau in Roche, Gilead, and Janssen; has received research funding from Amgen, Roche, Gilead, and Janssen; has received travel & accommodation expenses from Amgen, Roche, Gilead, and Janssen. All other authors declare that they have no conflict of interest.

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

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