Evidence map›Paper›PMID 39866945›Full record

ArticleEJHaem2025

CD58 expression does not impact response to inotuzumab ozogamicin in patients with B-cell acute lymphoblastic leukemia.

Rafael Madero-Marroquin, Ryan W Hunter, Caner Saygin, Hannah Johnston, Adam S DuVall, Hamed Rahmani Youshanlouei, Clinton Osei, Syed Shah, Wendy Stock, Sandeep Gurbuxani and 1 more

Abstract read
In one paragraph

Article in EJHaem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Rafael Madero-MarroquinDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.ORCID https://orcid.org/0009-0002-9243-2662
Ryan W HunterDepartment of Pathology University of Chicago Chicago Illinois USA.
Caner SayginDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.
Hannah JohnstonDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.
Adam S DuVallDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.
Hamed Rahmani YoushanloueiDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.
Clinton OseiDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.
Syed ShahDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.
Wendy StockDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.
Sandeep GurbuxaniDepartment of Pathology University of Chicago Chicago Illinois USA.
Anand A PatelDepartment of Medicine, Section of Hematology/Oncology University of Chicago Chicago Illinois USA.ORCID https://orcid.org/0000-0002-0296-8686

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: CD58 loss has been described as a mechanism of resistance to blinatumomab and chimeric antigen receptor T-cell therapy, functioning as a modulator of response to T-cell activation. Methods: Using flow cytometry, we evaluated the impact of CD58 mean fluorescence intensity (MFI) on the probability of achieving measurable residual disease (MRD) negativity in patients with B-cell acute lymphoblastic leukemia treated with inotuzumab ozogamicin (InO). Results: The odds ratio of achieving MRD negativity was 1.03 for every 1000 unit increase in CD58 MFI. Conclusion: Our results suggest that MRD negativity rates after InO are high, regardless of the intensity of CD58 expression.

Indexed as

acute leukemiaALLCD58inotuzumab ozogamicin

Identifiers

PMID39866945
PMCPMC11756963

What OpenQuestion holds

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Registered trials

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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.