Evidence map›Paper›PMID 34563945›Full record

ArticleLeukemia research2021

Phase 1 study of the histone deacetylase inhibitor entinostat plus clofarabine for poor-risk Philadelphia chromosome-negative (newly diagnosed older adults or adults with relapsed refractory disease) acute lymphoblastic leukemia or biphenotypic leukemia.

Hetty E Carraway, Yazeed Sawalha, Ivana Gojo, Min-Jung Lee, Sunmin Lee, Yusuke Tomita, Akira Yuno, Jackie Greer, B Douglas Smith, Keith W Pratz and 10 more

Open access · greenAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Leukemia research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Mechanisms of HDACs in cancer development.Frontiers in immunology · 2025
    Review
  4. Epigenetics-targeted drugs: current paradigms and future challenges.Signal transduction and targeted therapy · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 8 institutions in 1 country.

Hetty E CarrawayHematology Oncology Program, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, United States. Electronic address: carrawh@ccf.org.
Yazeed SawalhaArthur G. James Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Ivana GojoSidney Kimmel Comprehensive Cancer Center at Johns Hopkins Hospital, Baltimore, MD, United States.
Min-Jung LeeDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, United States.
Sunmin LeeDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, United States.
Yusuke TomitaDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, United States.
Akira YunoDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, United States.
Jackie GreerSidney Kimmel Comprehensive Cancer Center at Johns Hopkins Hospital, Baltimore, MD, United States.
B Douglas SmithSidney Kimmel Comprehensive Cancer Center at Johns Hopkins Hospital, Baltimore, MD, United States.
Keith W PratzThe University of Pennsylvania, Philadelphia, Pennsylvania.
Mark J LevisSidney Kimmel Comprehensive Cancer Center at Johns Hopkins Hospital, Baltimore, MD, United States.
Steven D GoreCancer Therapy Evaluation Program (CTEP), National Cancer Institute, NIH, Bethesda, MD, United States.
Nilanjan GhoshAtrium Health, Carolinas HealthCare System, Charlotte, NC, United States.
Amy DezernSidney Kimmel Comprehensive Cancer Center at Johns Hopkins Hospital, Baltimore, MD, United States.
Amanda L BlackfordSidney Kimmel Comprehensive Cancer Center at Johns Hopkins Hospital, Baltimore, MD, United States.
Maria R BaerUniversity of Maryland Greenebaum Comprehensive Cancer Center, Baltimore, MD, United States.
Lia GoreUniversity of Colorado Cancer Center, Aurora, CO, United States.
Richard PiekarzCancer Therapy Evaluation Program (CTEP), National Cancer Institute, NIH, Bethesda, MD, United States.
Jane B TrepelDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, United States.
Judith E KarpSidney Kimmel Comprehensive Cancer Center at Johns Hopkins Hospital, Baltimore, MD, United States.
Johns Hopkins Hospital · USNational Cancer Institute · USCarolinas Healthcare System · USCleveland Clinic · USThe Ohio State University Wexner Medical Center · USUniversity of Colorado Cancer Center · USUniversity of Maryland, Baltimore · USUniversity of Pennsylvania · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
The Johns Hopkins Translational Science Team for the ET-CTNUM1CA186691 · NCI · JOHNS HOPKINS UNIVERSITY · PI Jan Hendrik Beumer, Michael A Carducci · 2014 to 2026
$21.9M
NCI ET-CTN with Phase i Emphasis at UPCIUM1CA186690 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD, Farshid Dayyani · 2014 to 2026
$9.1M
PHASE I TRIALS OF ANTICANCER AGENTSU01CA070095 · NCI · JOHNS HOPKINS UNIVERSITY · PI CARDUCCI, MICHAEL A · 1995 to 2013
$8.6M
NCATS NIH HHS UL1 TR001863NCI NIH HHS U01 CA070095NCI NIH HHS UM1 CA186690NCI NIH HHS UM1 CA186691
6 · The paper itself

Abstract

purposeDespite advances in immunotherapies, the prognosis for adults with Philadelphia chromosome-negative, newly diagnosed (ND) or relapsed/refractory (R/R) acute lymphoblastic leukemia/acute biphenotypic leukemia (ALL/ABL) remains poor. The benzamide derivative entinostat inhibits histone deacetylase and induces histone hyperacetylation. The purine nucleoside analogue clofarabine is FDA-approved for R/R ALL in children 1-21 years of age. Low doses of clofarabine have been reported to induce DNA hypomethylation. We conducted a phase 1 study of low dose clofarabine with escalating doses of entinostat in adults with ND or R/R ALL/ABL. EXPERIMENTAL

designAdults ≥60 years with ND ALL/ABL or ≥21 years with R/R ALL/ABL received repeated cycles every 3 weeks of entinostat (4 mg, 6 mg or 8 mg orally days 1 and 8) and clofarabine (10 mg/m

resultsTwenty-eight patients were treated at three entinostat dose levels with the maximum administered dose being entinostat 8 mg. The regimen was well tolerated with infectious and metabolic derangements more common in the older population versus the younger cohort. There was no severe hyperglycemia and no peripheral neuropathy in this small study. There were 2 deaths (1 sepsis, 1 intracranial bleed). Overall response rate was 32 %; it was 50 % for ND ALL/ABL. Entinostat increased global protein acetylation and inhibited immunosuppressive monocyte subpopulations, while clofarabine induced DNA damage in all cell subsets examined.

conclusionEntinostat plus clofarabine appears to be tolerable and active in older adults with ND ALL/ABL, but less active in R/R patients. Further evaluation of this regimen in ND ALL/ABL appears warranted.

Indexed as

Cell LineageDrug Resistance, NeoplasmPhiladelphia ChromosomeAdultAgedAntineoplastic Combined Chemotherapy ProtocolsBenzamidesClofarabineFemaleFollow-Up StudiesHistone Deacetylase InhibitorsHumansMaleMaximum Tolerated DoseMiddle AgedNeoplasm Recurrence, LocalBenzamidesClofarabineentinostatHistone Deacetylase InhibitorsPyridinesAcetylationAcute lymphoblastic leukemiaClofarabineEntinostatHDAC inhibition

Identifiers

PMID34563945
PMCPMC8915247
OpenAlexW3200224382

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.