Evidence map›Paper›PMID 41922739›Full record

ArticleBone marrow transplantation2026

Twelve-year utilization and outcomes of haploidentical hematopoietic stem cell transplantation (HSCT) in the Eastern Mediterranean (EM) region: A multicenter EMBMT registry analysis.

Jean El Cheikh, Ali Tarhini, Ali Bazarbachi, Ibrahim Muhsen, Rawad Rihani, Hasan Hashem, Amr Hanbali, Muhammad Ayaz Younus Mir, Khadija Bano, Riad Youniss and 8 more

Abstract readMulticenter Study
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In one paragraph

Article in Bone marrow transplantation, 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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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

18 authors.

Jean El CheikhBone Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon. je46@aub.edu.lb.ORCID 0000-0003-2846-9428
Ali TarhiniDivision of Hematology/Oncology, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.ORCID 0009-0003-6477-5286
Ali BazarbachiBone Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Ibrahim MuhsenDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0002-7156-2532
Rawad RihaniKing Hussein Cancer Centre, Department of Pediatrics, Pediatric BMT Program, Amman, Jordan.ORCID 0009-0007-4610-6272
Hasan HashemDivision of Pediatric Hematology Oncology and BMT, King Hussein Cancer Center, Amman, Jordan.ORCID 0000-0002-4681-4726
Amr HanbaliKing Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Muhammad Ayaz Younus MirDivision of Pediatric Hematology Oncology and BMT, King Hussein Cancer Center, Amman, Jordan.ORCID 0000-0003-3287-9016
Khadija BanoBone Marrow & Stem Cell Transplant Shifa International Hospital, Islamabad, Pakistan.
Riad YounissKing Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Maryam GharachehChildren Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Mansour AlfayezKing Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Ahmad IbrahimDepartment of Hematology, Makassed Hospital and Middle East Institute of Health Lebanese University-University of Balamand, Beirut, Lebanon.
Mohammed MareiAdult Hematology & Bone Marrow Transplant Department, Comprehensive Cancer Center at King Fahad Medical City, Riyadh, Saudi Arabia.
Salem AlshemmariKuwait Cancer Center, Kuwait, Kuwait.ORCID 0000-0002-5597-5839
Tariq GhafoorArmed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.ORCID 0000-0003-1279-7160
Riad El FakihKing Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.ORCID 0000-0003-4498-3865
Mahmoud AljurfKing Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. maljurf@kfshrc.edu.sa.ORCID 0000-0003-3942-7370

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Haploidentical hematopoietic stem cell transplant (Haplo-HSCT) has emerged as an alternative for patients lacking matched human leukocyte antigen (HLA) donors. The scarcity of stem cell donor registries and cord banks across the Eastern Mediterranean (EM) region has led to increased need of Haplo-HSCT as a mean to overcome this limitation. In this study, we aimed to assess trends in Haplo-HSCT utilization within the Eastern Mediterranean Blood and Marrow Transplantation (EMBMT) registry from 2012 to 2024, and describe key clinical and transplant-related factors associated with patient outcomes. We conducted a retrospective, multicenter registry-based analysis of patients who had their first un-manipulated Haplo-HSCT in ten EMBMT centers across six countries, who responded and accepted to participate in the study. Due to the variability in time-to-event reporting across different centers, survival and relapse-related outcomes were analyzed descriptively. Continuous variables were summarized using medians and ranges, and categorical variables were described by counts and percentages. The association between individual baseline variables and patient survival, was conducted using a univariate analysis utilizing the chi-square test. Categorical variables such as patient and transplant characteristics were compared against survival status at last follow-up. All variables were further evaluated in the multivariate analysis. Overall survival (OS) and progression-free survival (PFS) were estimated using Kaplan-Meier survival analysis. Between 2012 and 2024, a total of 673 patients received haplo-HSCT across ten centers, in six EMBMT-registered countries. Median age was 25 years, and the predominant indication for haplo-HSCT was leukemia (64.3%). Transplant was done using stem cells collected from peripheral blood in majority of cases (65.7%), and Total Body Irradiation (TBI) was utilized in 37.6% of all patient. 76.5% had malignant hematological disorders, while 23.5% had non-malignant disorders. Relapse was reported in 232 patients (34.5%) and death in 220 patients (32.7%). Of these, 88 deaths (12.8%) were attributed to disease progression. Haplo-HSCT activity increased steadily over the study period, with a marked increase in the last few years, reflecting broader regional adoption. PFS was 66% and 60% at 1- and 2- years after transplantation. Also, the 1-year and 2-year post-transplant OS was 71% and 65%, respectively. Multivariate analysis identified disease type and chronic GVHD as factors associated with improved outcomes. Despite variability across centers, outcomes were consistent with international benchmarks, underscoring the growing feasibility and therapeutic value of haplo-HSCT in the EMRO region. Haplo-HSCT is increasingly adopted across the EMRO region as the primary alternative donor HSCT modality. Our findings confirm its clinical efficacy, with outcomes comparable to international benchmarks. These results underscore the importance of continued regional collaboration and the development of personalized strategies to address challenges such as graft-versus-host disease (GVHD), disease relapse, and disparities in access to transplantation services.

Indexed as

Hematopoietic Stem Cell TransplantationRegistriesTransplantation, HaploidenticalAdolescentAdultChildChild, PreschoolFemaleHumansMaleMediterranean RegionMiddle AgedRetrospective StudiesTreatment OutcomeYoung Adult

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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.