Early induction intensification with cladribine, cytarabine, and mitoxantrone (CLAM) in AML patients treated with the DAC induction regimen: a prospective, non-randomized, phase II study of the Polish Adult Leukemia Group (PALG).
Agnieszka PlutaTadeusz RobakKamil BrzozowskiKonrad StepkaEwa WawrzyniakAnna KrawczynskaMagdalena CzemerskaAnna Szmigielska-KaplonOlga Grzybowska-IzydorczykMateusz NowickiPiotr StelmachMarta KuydowiczTomasz GromekMarek HusGrzegorz HelbigSebastian GrosickiEwa BodzentaMałgorzata RaznyKarol WojcikLukasz BolkunJanusz KloczkoWanda Knopinska-PoslusznyAgnieszka PiekarskaAndrzej HellmanMarta Anna SobasTomasz WrobelElzbieta PatkowskaEwa Lech-MarandaKrzysztof WarzochaJerzy HolowieckiSebastian GiebelAgnieszka WierzbowskaPublished in: Leukemia & lymphoma (2019)
We present the results of a prospective, non-randomized phase 2 trial in which 253 AML patients (pts) under 60 years old received DAC (Daunorubicin + AraC + Cladribine) as first induction followed by CLAM (Cladribine + AraC + Mitoxantrone) as early second induction on day 16 based on bone marrow (BM) blasts on day 14 (D14). The CR/CRi rate after a single course of DAC was 83% for pts with D14 BM blasts less than 10%. Forty-six pts had >10% BM blasts on D14, of whom 35 received CLAM with rates of CR/CRi 60% and early death (ED) 23%. The remaining 11 pts were not fit to receive CLAM, with rates of CR/CRi 28%, PR 18%, and ED 18%. Median OS was 7.2 versus 7.5 months, respectively. The overall CR/CRi rate was 77% after the first induction, with final CR/CRi rate 80% after DAC reinduction for pts who achieved PR with initial DAC course. CLAM used as early second induction might improve CR/CRi rates for younger AML pts with poor early response to DAC induction, but may be associated with higher mortality.
Keyphrases
- acute myeloid leukemia
- bone marrow
- open label
- phase ii study
- emergency department
- double blind
- placebo controlled
- end stage renal disease
- type diabetes
- clinical trial
- squamous cell carcinoma
- ejection fraction
- cardiovascular disease
- high dose
- allogeneic hematopoietic stem cell transplantation
- phase ii
- peritoneal dialysis
- young adults