Evidence map›Paper›PMID 42115907›Full record

ArticleBMC pediatrics2026

Comparing the impact of blinatumomab therapy versus standard chemotherapy on the progression of relapsed/refractory pediatric B-ALL: a two-center retrospective cohort study.

Aziz Eghbali, Zeynab Nasri Nasrabadi, Mohammad Faranoush, Ali Ghasemi, Kazem Ghaffari

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in BMC pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

5 authors.

Aziz EghbaliClinical Research Development Center of Aliasghar Hospital, Iran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-5118-0094
Zeynab Nasri NasrabadiDepartment of Pediatrics, School of Medicine, Iran University of Medical Sciences, Teharn, Iran.ORCID 0000-0001-9503-3179
Mohammad FaranoushPediatric Growth and Development Research Center, Institute of Endocrinology, Iran Universty of Medical Sciences, Tehran, Iran.ORCID 0000-0002-2775-2347
Ali GhasemiNervous System Stem Cells Research Center, Semnan University of Medical Sciences, Semnan, Iran. a.qasemi2012@yahoo.com.ORCID 0000-0002-4996-7656
Kazem GhaffariDepartment of Hematology and Blood Transfusion Sciences, School of Allied Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran. kg.hematology@gmail.com.ORCID 0000-0002-6077-3123

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite advances in risk-adapted chemotherapy and allogeneic hematopoietic stem cell transplantation (allo-HSCT), relapse remains the leading cause of treatment failure and mortality in pediatric acute lymphoblastic leukemia (ALL). Achieving measurable residual disease (MRD)-negative status prior to allo-HSCT is strongly associated with improved outcomes. This study aimed to compare the effectiveness of blinatumomab versus conventional re-induction chemotherapy in relapsed/refractory pediatric B cell acute lymphoblastic leukemia (B-ALL) patients.

methodThis retrospective, non-randomized cohort study included pediatric patients (1-18 years) diagnosed with relapsed/refractory CD19⁺ B-ALL. Patients received either conventional re-induction chemotherapy followed by consolidation according to institutional protocols or blinatumomab administered as a continuous intravenous infusion in 28-day cycles. Treatment allocation was based on physician decision and drug availability. Primary endpoints included complete remission (CR) and MRD negativity after one treatment cycle. Secondary endpoints included eligibility for allo-HSCT, relapse-free survival, overall survival, and adverse events.

resultsA total of 52 patients were analyzed (blinatumomab, n = 30; chemotherapy, n = 22). MRD negativity after one cycle was significantly higher in the blinatumomab group compared with chemotherapy (83.4% vs. 18.2%, P < 0.001). A greater proportion of patients in the blinatumomab group proceeded to allo-HSCT (68.2% vs. 40%, P = 0.041). Overall survival was significantly improved with blinatumomab (77.3% vs. 30%, P < 0.001). Mortality was primarily associated with FAB type L3 following the first treatment cycle.

conclusionsIn this retrospective cohort of pediatric patients with relapsed/refractory B-ALL, blinatumomab was associated with significantly higher MRD negativity rates, improved transplant eligibility, and superior survival compared with conventional chemotherapy. These findings support the role of blinatumomab as an effective therapeutic option in this high-risk population.

Indexed as

Antibodies, BispecificAntineoplastic AgentsPrecursor B-Cell Lymphoblastic Leukemia-LymphomaAdolescentChildChild, PreschoolDisease ProgressionFemaleHematopoietic Stem Cell TransplantationHumansInfantMaleNeoplasm, ResidualRecurrenceRemission InductionRetrospective StudiesAntibodies, BispecificAntineoplastic AgentsblinatumomabAllogeneic hematopoietic stem cell transplantationBlinatumomabChemotherapyPediatricRelapsed/refractory B cell acute lymphoblastic leukemia

Identifiers

PMID42115907
PMCPMC13335187

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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.