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Phase 2 trial of CPX-351, a fixed 5:1 molar ratio of cytarabine/ daunorubicin, vs cytarabine/daunorubicin in older adults with untreated AML

  • Jeffrey E. Lancet(corresponding author)
    ,
  • ,
  • Donna E. Hogge
    ,
  • Martin S. Tallman
    ,
  • Tibor J. Kovacsovics
    ,
  • Lloyd E. Damon
*Corresponding author for this work
  • Moffitt Cancer Center
    ,
  • University of Texas Health Science Center at Houston
    ,
  • Provincial Health Services Authority
    ,
  • Cornell University
    ,
  • Oregon Health and Science University
    ,
  • University of California at San Francisco
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

CPX-351 is a liposomal formulation of cytarabine:daunorubicin designed to deliver synergistic drug ratios to leukemia cells. In this phase 2 study, newly diagnosed older acute myeloid leukemia (AML) patients were randomized 2:1 to first-line CPX-351 or 7+3 treatment. The goal was to determine efficacy and identify patient subgroups that may benefit from CPX-351 treatment. Response rate (complete remission + incomplete remission) was the primary end point, with event-free survival (EFS) and overall survival (OS) as secondary end points. The 126 patients entered were balanced for disease and patient-specific risk factors. Overall, CPX-351 produced higher response rates (66.7% vs 51.2%,P=.07), meeting predefined criteria for success (P< .1). Differences in EFS andOS were not statistically significant.Aplanned analysis of the secondaryAMLsubgroup demonstrated an improved response rate (57.6% vs 31.6%, P= .06), and prolongation of EFS (hazard ratio [HR]= 0.59, P =.08) and OS (HR 50.46, P =.01). Recovery from cytopenias was slower after CPX-351 (median days to absolute neutrophil count ≥1000: 36 vs 32; platelets >100 000: 37 vs 28) with more grade 3-4 infections but without increase in infection-related deaths (3.5% vs 7.3%) or 60-day mortality (4.7% vs 14.6%), indicating acceptable safety. These results suggest a clinical benefit with CPX-351, particularly among patients with secondary AML, and provide the rationale for a phase 3 trial currently underway in newly diagnosed secondary AML patients. This study is registered at Clinicaltrials. gov as #NCT00788892.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 3239-3246 (8 pages)

Journal (Volume, Issue Number)

Blood (Volume 123, Issue 21)

Publication milestones

  • Published - 05/22/2014

Publication status

Published - 05/22/2014

ISSN

0006-4971

Publication IDs

  • Scopus: 84901412022
  • PubMed: 24687088
  • ORCID: /0000-0002-8636-1071/work/68887920

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Fractional count
1
Fractional count
0.08
Fractional count
12
Fractional count
0.92
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1
Fractional count
1
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citations
225
SciVal
FWCI
6.95
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Author count
13
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Paper percentile
99
SciVal
Top percentile
1
Scopus
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328
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Funding Details

FunderFunding number
NCI
P30CA016672