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Clinical experience with the BCL2-inhibitor venetoclax in combination therapy for relapsed and refractory acute myeloid leukemia and related myeloid malignancies

  • Courtney D. DiNardo(corresponding author)
    ,
  • Caitlin R. Rausch
    ,
  • Christopher Benton
    ,
  • Tapan Kadia
    ,
  • Nitin Jain
    ,
  • Naveen Pemmaraju
*Corresponding author for this work
  • University of Texas MD Anderson Cancer Center
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Introduction: Venetoclax (VEN), a selective BCL2 inhibitor, has single-agent activity in relapsed and refractory (R/R) acute myeloid leukemia (AML), and efficacy in lower intensity combinations for treatment-naïve elderly AML patients. VEN treatment combinations in R/R AML have not been previously reported. Methods: All R/R myeloid patients (including AML, myelodysplastic syndrome (MDS), and blastic plasmacytoid dendritic cell neoplasm (BPDCN)) treated with VEN combinations in the salvage setting were reviewed. Results: Forty-three patients with median age 68 (range, 25–83) were treated for AML (91%), MDS (5%), or BPDCN (5%). Most (n = 36, 84%) were ≥ salvage-2 treatment status, including prior hypomethylating agent (HMA) in 77%. In combination with VEN, most patients received HMA therapy (n = 31, 72%); eight (19%) received low-dose cytarabine (LDAC). Patients received a median of 2 treatment cycles (range, 1–4). Objective response was observed in 9 (21%) patients, including 2 complete responses (CR), 3 CRi, and 4 morphologic leukemia-free state (MLFS). Median survival was 3.0 months (range, 0.5–8.0), and estimated 6-month survival was 24%. Responses were observed in five (24%) of 21 patients with intermediate-risk cytogenetics, 3 (27%) of 11 IDH1/2-mutant, and 4 (50%) of 8 RUNX1-mutated patients. Two (20%) of 10 TP53-mutated patients responded; both had concurrent RUNX1 mutations. Of the 3 (15%) responding patients with adverse cytogenetics, all had concurrent RUNX1 mutations. Conclusion: Low-intensity chemotherapy, including HMAs or LDAC, in combination with VEN is a viable salvage option, even in multiply relapsed/refractory patients with AML, MDS, and BPDCN. Notable responses were identified in patients with diploid/intermediate cytogenetics, RUNX1, and/or IDH1/2 mutations.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 401-407 (7 pages)

Journal (Volume, Issue Number)

American Journal of Hematology (Volume 93, Issue 3)

Publication milestones

  • Published - 03/2018

Publication status

Published - 03/2018

ISSN

0361-8609

Publication IDs

  • Scopus: 85038936630
  • PubMed: 29218851
  • ORCID: /0000-0002-8636-1071/work/68811045

Publication metrics

Metrics

SciVal
FWCI
13.63
SciVal
Author count
17
SciVal
citations
167
SciVal
Paper percentile
99
SciVal
Top percentile
1
Fractional count
1
Fractional count
0.06
Fractional count
16
Fractional count
0.94
Fractional count
1
Fractional count
1
Scopus
citations

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2
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234
Citation count
405

Funding Details

This work was supported in part by the MD Anderson Cancer Center Support Grant (CCSG) CA016672, the Charif Souki Cancer Research Fund, and the MD Anderson Cancer Center Leukemia SPORE CA100632, and by the generous philanthropic contributions to MD Anderson's MDS/AML Moon Shot Program.