Evidence map›Paper›PMID 40534485›Full record

Trial reportHaematologica2026

Intensified conditioning with high-dose total marrow irradiation and myeloablative chemotherapy reduces risk of relapse without increasing toxicity in allogeneic hematopoietic stem cell transplant for high-risk myeloid malignancies: a phase II study.

Lucas Maahs, Ana Maria Avila, Matthew Koshy, Karen Sweiss, Kang-Hyun Ahn, Zhengjia Chen, Chukwuemeka Uzoka, Carlos Galvez, Matias Sanchez, Paul Rubinstein and 6 more

Registry-linked trialAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Haematologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03121014 (A Phase II Study of Intensity Modulated Total Marrow Irradiation), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT03121014 phase2active not recruitingnot on this map

A Phase II Study of Intensity Modulated Total Marrow Irradiation (IM-TMI) in Addition to Fludarabine/Busulfan Conditioning for Allogeneic Transplantation in High Risk AML and Myelodysplastic Syndromes

TypeinterventionalSponsorUniversity of Illinois at ChicagoRan2017 to 2026Enrolled38ConditionsAcute Myeloid Leukemia, Myelodysplastic SyndromesArmsFludarabine, Busulfan, ATG, Total Marrow Irradiation, Stem Cell Product Infusion
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. 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

16 authors.

Lucas MaahsDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL.
Ana Maria AvilaDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL.
Matthew KoshyDepartment of Radiation Oncology, University of Illinois at Chicago, Chicago, IL, USA; Cancer Center, University of Illinois at Chicago, Chicago, IL.
Karen SweissCancer Center, University of Illinois at Chicago, Chicago, IL, USA; College of Pharmacy, University of Illinois at Chicago, Chicago, IL.
Kang-Hyun AhnCancer Center, University of Illinois at Chicago, Chicago, IL, USA; Division of Epidemiology and Biostatistics, School of Public Health, University of Illinois at Chicago Chicago, IL.
Zhengjia ChenCancer Center, University of Illinois at Chicago, Chicago, IL, USA; Division of Epidemiology and Biostatistics, School of Public Health, University of Illinois at Chicago Chicago, IL.
Chukwuemeka UzokaDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL, USA; Cancer Center, University of Illinois at Chicago, Chicago, IL.
Carlos GalvezDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL, USA; Cancer Center, University of Illinois at Chicago, Chicago, IL.
Matias SanchezDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL, USA; Cancer Center, University of Illinois at Chicago, Chicago, IL.
Paul RubinsteinDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL, USA; Cancer Center, University of Illinois at Chicago, Chicago, IL.
John QuigleyDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL, USA; Cancer Center, University of Illinois at Chicago, Chicago, IL.
Elisa ZucchettiDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL.
Nadim MahmudDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL, USA; Cancer Center, University of Illinois at Chicago, Chicago, IL.
Bulent AydoganDivision of Biological Sciences, University of Chicago Chicago, IL.
Pritesh PatelDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL.
Damiano RondelliDivision of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago; Chicago, IL, USA; Cancer Center, University of Illinois at Chicago, Chicago, IL. drond@uic.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intensity of the conditioning regimen in hematopoietic stem cell transplantation (HSCT) correlates with the risk of relapse, however its potential benefit may be outweighed by the associated risk of toxicity. The addition of total marrow irradiation (TMI) to myeloablative conditioning provides an opportunity to increase intensity with minimal additional toxicity. In this phase II clinical trial, 30 patients with high-risk myeloid malignancies underwent allogeneic HSCT using myeloablative TMI at 9 Gy in combination with standard myeloablative fludarabine/intravenous busulfan (FluBu4) chemotherapy. The study included patients with matched related donors (N=10) receiving TMI/FluBu4 and patients with matched unrelated (N=14) or one-antigen mismatched unrelated (N=6) donors receiving TMI/FluBu4 and rabbit anti-thymocyte globulin. All patients achieved sustained engraftment. Grade 3-4 extramedullary toxicities were mucositis in 59% (N=17), nausea/vomiting in 10% (N=3) and diarrhea in 7% (N=2) of the patients. Acute graft-versus-host disease (GvHD) grade 3 or 4 was seen in four patients (13.3%). Moderate/severe chronic GvHD was observed in 11 patients (36.7%). With a median follow-up of 1,483 days (range, 63-2,260 days) for patients alive, the overall survival and disease-free survival at 1 year were 72.4% and 65.5%, respectively. GvHD-free relapse-free survival at 1 year was 41.4%. Of 30 patients in the study, six relapsed/progressed (20%) and five of them died of the disease (16.7%), whereas six patients (20%) died of transplant-related causes. We conclude that a myeloablative regimen with TMI at 9 Gy and FluBu4 was well tolerated and achieved encouraging results in patients with myeloid malignancies at high risk of relapse (clinicaltrials.gov identifier: NCT03121014).

Indexed as

Hematopoietic Stem Cell TransplantationTransplantation ConditioningWhole-Body IrradiationAdolescentAdultAgedAntineoplastic Combined Chemotherapy ProtocolsBone MarrowBusulfanFemaleGraft vs Host DiseaseHumansMaleMiddle AgedMyeloablative AgonistsRecurrenceBusulfanfludarabineMyeloablative AgonistsVidarabine

Identifiers

PMID40534485
PMCPMC12775750

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Registered trials

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.