Evidence map›Paper›PMID 41451373›Full record

ArticleFrontiers in pharmacology2025

Real-world patient outcomes with Blinatumomab and Inotuzumab in adult relapsed/refractory B-cell acute lymphoblastic leukemia: a retrospective analysis from two Romanian oncology centers.

Ion Antohe, Amalia Titieanu, Vlad Andrei Cianga, Cosmin Minciună, Cătălin Dănăilă, Alina Daniela Tănase, Iuliu Ivanov, Loredana Dragoş, Mihaela Zlei, Mihaela Mențel and 4 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Ion Antohe *Grigore T. Popa University of Medicine and Pharmacy, Iaşi, Romania.
Amalia Titieanu *Hematology Department, Regional Oncology Institute, Iaşi, Romania.
Vlad Andrei CiangaGrigore T. Popa University of Medicine and Pharmacy, Iaşi, Romania.
Cosmin MinciunăGrigore T. Popa University of Medicine and Pharmacy, Iaşi, Romania.
Cătălin DănăilăGrigore T. Popa University of Medicine and Pharmacy, Iaşi, Romania.
Alina Daniela TănaseBone Marrow Transplant Department, Fundeni Clinical Institute, Bucharest, Romania.
Iuliu IvanovMolecular Diagnostic Department, Regional Oncology Institute, Iaşi, Romania.
Loredana DragoşMolecular Diagnostic Department, Regional Oncology Institute, Iaşi, Romania.
Mihaela ZleiFlow Cytometry Department, Regional Oncology Institute, Iaşi, Romania.
Mihaela MențelFlow Cytometry Department, Regional Oncology Institute, Iaşi, Romania.
Ciprian TomuleasaDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research - Department of Hematology, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Anamaria BancosDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research - Department of Hematology, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Manuela CiocoiuPhysiopathology Department, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, Iaşi, Romania.
Angela DăscălescuGrigore T. Popa University of Medicine and Pharmacy, Iaşi, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The management of adult relapsed/refractory B-cell acute lymphoblastic leukemia (R/R B-ALL) remains a significant challenge, with patients presenting particularly poor historical outcomes. Novel immunotherapies, such as Blinatumomab and Inotuzumab, have revived the therapeutic landscape of R/R B-ALL, but their optimal sequencing, toxicity management, and post-transplant integration remain unclear, particularly in real-world, resource-limited settings. Methods: We conducted a retrospective analysis of 33 adult patients with R/R B-ALL treated between 2019 and 2023 at two major oncology centers in Romania. Results: Blinatumomab and Inotuzumab achieved complete remission rates of 47.6% and 90%, respectively, with measurable residual disease negativity in over 60% of responders. Inotuzumab was more effective in early relapses and cases with high disease burden, while Blinatumomab showed benefit in later relapses and post-transplant settings. Eleven patients were successfully bridged to allogeneic stem cell transplant, and four were treated for post-transplant relapse, demonstrating the feasibility of immunotherapy in both contexts. Sequential monoclonal antibody use yielded poor survival unless used as a bridge to curative therapy. Conclusion: Our findings emphasize the need for individualized treatment selection, rational immunotherapy sequencing, and the development of predictive biomarkers to optimize outcomes and minimize toxicity. Further studies are needed to refine therapeutic algorithms and define such prognostic biomarkers, particularly in underfunded healthcare systems.

Indexed as

B-cell acute lymphoblastic leukemiaBlinatumomabCAR-T cellsimmunotherapyInotuzumab

Identifiers

PMID41451373
PMCPMC12728000

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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.