Evidence map›Paper›PMID 39562780›Full record

ReviewBlood cancer journal2024

Frontline Ph-negative B-cell precursor acute lymphoblastic leukemia treatment and the emerging role of blinatumomab.

Elias J Jabbour, Hagop M Kantarjian, Nicola Goekbuget, Bijal D Shah, Sabina Chiaretti, Jae H Park, Anita W Rijneveld, Lia Gore, Shaun Fleming, Aaron C Logan and 6 more

Abstract readReview
In one paragraph

Review in Blood cancer journal, 2024. 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
–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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Posttransplant cells for the win? DLI and adoptive cell therapy to eradicate MRD.Hematology. American Society of Hematology. Education Program · 2025
    Review
  6. Review
  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

16 authors.

Elias J JabbourDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. ejabbour@mdanderson.org.ORCID 0000-0003-4465-6119
Hagop M KantarjianDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-1908-3307
Nicola GoekbugetDepartment of Medicine II, Goethe University, University Hospital, Frankfurt, Germany.
Bijal D ShahDepartment of Malignant Hematology, Moffitt Cancer Center, Tampa, FL, USA.
Sabina ChiarettiHematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
Jae H ParkLeukemia Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0002-2903-5130
Anita W RijneveldErasmus MC Cancer Institute, Rotterdam, Netherlands.
Lia GoreChildren's Hospital Colorado and the University of Colorado School of Medicine, University of Colorado Cancer Center, Aurora, CO, USA.
Shaun FlemingDepartment of Clinical Haematology, Alfred Hospital, Melbourne, VIC, Australia, and Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Aaron C LoganHematology, Blood and Marrow Transplant, and Cellular Therapy Program, Division of Hematology/Oncology, University of California San Francisco, San Francisco, CA, USA.
Josep M RiberaICO-Hospital Germans Trias I Pujol. Josep Carreras Research Institute, Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID 0000-0003-1042-6024
Tobias F MenneThe Newcastle upon Tyne Hospitals and Newcastle University, Newcastle upon Tyne, UK.
Khalid MezziAmgen Inc, Thousand Oaks, CA, USA.
Faraz ZamanAmgen Inc, Thousand Oaks, CA, USA.
Kelly VelascoAmgen Inc, Thousand Oaks, CA, USA.
Nicolas BoisselDivision of Hematology, EA3518 Saint-Louis Institute for Research, Saint-Louis Hospital, Paris, France.ORCID 0000-0003-2091-7927

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Amgen (Amgen Inc.) No grantNCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

This narrative review seeks to summarize chemotherapeutic regimens commonly used for patients with newly diagnosed Philadelphia (Ph) chromosome-negative B-cell precursor acute lymphoblastic leukemia (BCP-ALL) in the frontline setting and to describe the latest clinical research using the bispecific T-cell-engaging immunotherapy blinatumomab in the first-line treatment setting. Current standard-of-care chemotherapeutic backbones for newly diagnosed Ph-negative BCP-ALL are based on the same overarching treatment principle: to reduce disease burden to undetectable levels and maintain lasting remission. The adult treatment landscape has progressively evolved following the adoption of pediatric-inspired regimens. However, these intense regimens are not tolerated by all, and high-risk patients still have inferior outcomes. Therefore, designing more effective and less toxic strategies remains key to further improving efficacy and safety outcomes. Overall, the treatment landscape is evolving in the frontline, and integration of blinatumomab into different standard frontline regimens may improve overall outcomes with a favorable safety profile.

Indexed as

Antibodies, BispecificPrecursor B-Cell Lymphoblastic Leukemia-LymphomaHumansPhiladelphia ChromosomeAntibodies, Bispecificblinatumomab

Identifiers

PMID39562780
PMCPMC11577064

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.