Evidence map›Paper›PMID 41367923›Full record

ArticleHemaSphere2025

Harmonization on defining B-cell recovery post CD19-CAR T-cell therapy in B-cell acute lymphoblastic leukemia: An international consensus statement.

Adam Lamble, Sandra D Bohling, Kara L Davis, Aimee C Talleur, Kevin O McNerney, Swati Naik, Priya Kumar, Rebecca Thomas, Hao-Wei Wang, Constance M Yuan and 7 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Concurrent MLL-AF4Frontiers in pediatrics · 2026
    Article
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

17 authors.

Adam LambleDivision of Hematology and Oncology, Seattle Children's Hospital University of Washington Seattle Washington United States.ORCID https://orcid.org/0000-0002-7781-2918
Sandra D BohlingDepartments of Laboratory Medicine and Pathology Seattle Children's Hospital University of Washington Seattle Washington United States.
Kara L DavisDepartment of Pediatrics Stanford University School of Medicine, Division of Pediatric Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine Stanford California United States.
Aimee C TalleurDepartment of Bone Marrow Transplantation and Cellular Therapy St. Jude Children's Research Hospital Memphis Tennessee United States.
Kevin O McNerneyDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois United States.
Swati NaikDepartment of Bone Marrow Transplantation and Cellular Therapy St. Jude Children's Research Hospital Memphis Tennessee United States.
Priya KumarDepartment of Pathology St. Jude Children's Research Hospital Memphis Tennessee United States.
Rebecca ThomasDepartment of Haematology UCL Great Ormond Street Institute of Child Health London United Kingdom.
Hao-Wei WangLaboratory of Pathology National Cancer Institute, NIH Bethesda Maryland United States.
Constance M YuanLaboratory of Pathology National Cancer Institute, NIH Bethesda Maryland United States.
Elad JacobyThe Edmond and Lily Safra Children's Hospital, Sheba Medical Center and Tel Aviv University Division of Pediatric Hematology and Oncology Tel Aviv Israel.
Andre BaruchelPediatric Hematology and Immunology Department Robert-Debré Hospital (Assistance Publique-Hôpitaux de Paris [APHP]) Paris France.
Sara GhorashianDepartment of Haematology UCL Great Ormond Street Institute of Child Health London United Kingdom.
Michael A PulsipherIntermountain Primary Children's Hospital, Spencer Fox Eccles School of Medicine at the University of Utah, Division of Hematology and Oncology Huntsman Cancer Institute Salt Lake City Utah United States.
Liora SchultzDepartment of Pediatrics Stanford University School of Medicine, Division of Pediatric Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine Stanford California United States.
Rebecca A GardnerDepartment of Bone Marrow Transplantation and Cellular Therapy St. Jude Children's Research Hospital Memphis Tennessee United States.
Nirali N ShahPediatric Oncology Branch, Center for Cancer Research National Cancer Institute Bethesda Maryland United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Relapse following CD19-targeting chimeric antigen receptor T-cell therapy (CD19-CAR) remains a major barrier to long-term cure in relapsed/refractory B-cell acute lymphoblastic leukemia, with nearly 50% of patients relapsing within 6 months. Early B-cell recovery (BCR), as detected by the re-emergence of CD19-positive cells, has been strongly associated with relapse risk and serves as a surrogate marker for loss of CAR T-cell persistence. However, clinical use of BCR is hindered by variability in monitoring practices, including inconsistent definitions, timing, and measurement across institutions. To address this gap, we convened an international working group of pediatric cellular therapy experts to establish a consensus definition for BCR. Our collaborative effort outlines standardized criteria for BCR assessment aimed at improving comparability across studies and guiding post-CAR T-cell surveillance strategies.

Identifiers

PMID41367923
PMCPMC12683365

What OpenQuestion holds

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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.