Evidence map›Paper›PMID 33449813›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2021

Eprenetapopt (APR-246) and Azacitidine in

David A Sallman, Amy E DeZern, Guillermo Garcia-Manero, David P Steensma, Gail J Roboz, Mikkael A Sekeres, Thomas Cluzeau, Kendra L Sweet, Amy McLemore, Kathy L McGraw and 14 more

Open access · bronzeAbstract readClinical Trial, Phase IClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 304 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
304citing papers in PubMed, 2 pooled it
50.1field-weighted citation impact, top 1% 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

304 citing papers in PubMed, 2 syntheses or guidelines pooled it, 441 citations in OpenAlex.

  1. Pooled it
  2. Targeting p53 pathways: mechanisms, structures, and advances in therapy.Signal transduction and targeted therapy · 2023
    Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Review
  9. Revisiting tumor immunogenicity through the lens of mutant p53: Implications for cancer immunotherapy.Apoptosis : an international journal on programmed cell death · 2026
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Therapy of high-risk myelodysplastic syndromes.Bone marrow transplantation · 2026
    Review

244 more citing papers are in PubMed but not listed here.

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

24 authors at 8 institutions in 2 countries.

David A SallmanMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.ORCID 0000-0003-0504-8233
Amy E DeZernSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD.
Guillermo Garcia-ManeroDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-3631-2482
David P SteensmaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.ORCID 0000-0001-5130-9284
Gail J RobozWeill Cornell Medicine and The New York Presbyterian Hospital, New York, NY.ORCID 0000-0002-0384-3658
Mikkael A SekeresDepartment of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH.ORCID 0000-0003-2009-6524
Thomas CluzeauCote D'Azur University, Nice Sophia Antipolis University, Hematology Department, CHU Nice, Nice, France.ORCID 0000-0002-6745-1127
Kendra L SweetMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Amy McLemoreMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.ORCID 0000-0002-0155-502X
Kathy L McGrawMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
John PuskasMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Ling ZhangMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Jiqiang YaoDepartment of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Qianxing MoDepartment of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.ORCID 0000-0002-0021-7694
Lisa NardelliMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Najla H Al AliMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Eric PadronMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.ORCID 0000-0002-4707-7916
Greg KorbelAprea Therapeutics, Boston, MA.
Eyal C AttarAprea Therapeutics, Boston, MA.
Hagop M KantarjianDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX.
Jeffrey E LancetMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Pierre FenauxHospital St Louis, Assistance Publique-Hôpitaux de Paris, Paris, France.
Alan F ListMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Rami S KomrokjiMalignant Hematology Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.ORCID 0000-0002-1876-5269
Moffitt Cancer Center · USThe University of Texas MD Anderson Cancer Center · USAssistance Publique – Hôpitaux de Paris · FRCleveland Clinic · USHarvard University · USJohns Hopkins University · USNewYork–Presbyterian Hospital · USUniversité Côte d'Azur · FR

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI Christine O'Connell · 1998 to 2026
$93.5M
NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

purposeApproximately 20% of patients with

methodsThis was a phase Ib/II study to determine the safety, recommended phase II dose, and efficacy of eprenetapopt administered in combination with azacitidine in patients with

resultsFifty-five patients (40 MDS, 11 AML, and four MDS/myeloproliferative neoplasms) with at least one

conclusionCombination treatment with eprenetapopt and azacitidine is well-tolerated yielding high rates of clinical response and molecular remissions in patients with

Indexed as

MutationAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsAzacitidineBiomarkers, TumorFemaleHumansMaleMiddle AgedMyelodysplastic SyndromesQuinuclidinesTumor Suppressor Protein p53AzacitidineBiomarkers, TumoreprenetapoptQuinuclidinesTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID33449813
PMCPMC8099410
OpenAlexW3119649652

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.