Evidence map›Paper›PMID 41132245›Full record

ArticleHemaSphere2025

A Phase 2 study of CPX-351 in combination with venetoclax in patients with newly diagnosed high-risk acute myeloid leukemia.

Wei-Ying Jen, Jennifer Croden, Emmanuel Almanza-Huante, Courtney DiNardo, Kelly Chien, Danielle Hammond, Wei Qiao, Yesid Alvarado, Lucia Masarova, Andres E Quesada and 9 more

Abstract read
In one paragraph

Article in HemaSphere, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. AML, Myelodysplasia-Related: Beyond Classification-Toward Precision Decision-Making.Mediterranean journal of hematology and infectious diseases · 2026
    Review
  5. Article
  6. 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

19 authors.

Wei-Ying JenDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Jennifer CrodenDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.ORCID https://orcid.org/0000-0002-2634-4341
Emmanuel Almanza-HuanteDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Courtney DiNardoDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Kelly ChienDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Danielle HammondDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Wei QiaoDepartment of Biostatistics The University of Texas MD Anderson Cancer Center Houston Texas USA.
Yesid AlvaradoDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Lucia MasarovaDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Andres E QuesadaDepartment of Hematopathology The University of Texas MD Anderson Cancer Center Houston Texas USA.
Sherry PierceDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Alex BatallerDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Guillermo Garcia-ManeroDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Amin AlousiDepartment of Stem Cell Transplantation & Cellular Therapy The University of Texas MD Anderson Cancer Center Houston Texas USA.
Nicholas ShortDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Naval DaverDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Farhad RavandiDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Hagop KantarjianDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.
Tapan M KadiaDepartment of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Venetoclax has been combined with intensive chemotherapy regimens in the treatment of acute myeloid leukemia (AML). We aimed to investigate the safety and efficacy of venetoclax combined with full-dose CPX-351 (CPX + VEN) in newly diagnosed (ND) AML. Seventeen patients with a median age of 59 years (range, 43-69) were treated; 71% had secondary AML, 47% had prior hypomethylating agent (HMA) exposure, 59% had myelodysplastic syndrome (MDS)-related (MR) mutations, 47% had complex karyotype, and 29% were

Identifiers

PMID41132245
PMCPMC12542300

What Socratic 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 Socratic graph.