Evidence map›Paper›PMID 39371123›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Access to Allogeneic Cell Transplantation Based on Donor Search Prognosis: An Interventional Trial.

Jason G Dehn, Brent Logan, Bronwen E Shaw, Steven Devine, Stefan O Ciurea, Mary Horowitz, Naya He, Iskra Pusic, Samer A Srour, Sally Arai and 18 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. 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

5 · Who and what money

Authors and funding

28 authors.

Jason G DehnNMDP, Minneapolis, USA.
Brent LoganCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, USA.
Bronwen E ShawCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, USA.
Steven DevineNMDP, Minneapolis, USA.
Stefan O CiureaUniversity of California-Irvine, Irvine, USA.
Mary HorowitzCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, USA.
Naya HeCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, USA.
Iskra PusicWashington University Barnes Jewish Hospital, St Louis, USA.
Samer A SrourThe University of Texas MD Anderson Cancer Center, Houston, USA.
Sally AraiStanford University, Stanford, USA.
Mark JuckettUniversity of Minnesota, Minneapolis, USA.
Joseph UbertiKarmanos Cancer Institute Wayne State University, Detroit, USA.
LaQuisa HillBaylor College of Medicine, Houston, USA.
Sumithira VasuThe Ohio State University James Comprehensive Cancer Center, Columbus, USA.
William J HoganMayo Clinic, Rochester, USA.ORCID 0000-0002-5841-4105
Brandon Hayes-LattinOregon Health Sciences University Knight Cancer Institute, Portland, USA.
Peter WesterveltMaineHealth Cancer Care, Scarborough, USA.
Asad BasheyNorthside Hospital, Atlanta, USA.
Nosha FarhadfarUniversity of Florida Shands Healthcare, Jacksonville, USA.
Michael R GrunwaldLevine Cancer Institute Atrium Health, Charlotte, USA.
Eric LeiferNational Heart, Lung and Blood Institute, Bethesda, USA.
Heather SymonsJohns Hopkins University, Baltimore, USA.
Ayman SaadKing Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Jenny VogelCenter for International Blood and Marrow Transplant Research, NMDP, Minneapolis, USA.
Connor EricksonCenter for International Blood and Marrow Transplant Research, NMDP, Minneapolis, USA.
Kelly BuckNMDP, Minneapolis, USA.
Stephanie J LeeFred Hutchinson Cancer Center, Seattle, USA.
Joseph PidalaH. Lee Moffitt Cancer Center, Tampa, USA.

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Blood and Marrow Transplant Clinical Trials Network DCC- The Medical College of Wisconsin, Inc.U24HL138660 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI Steven M. DeVine, Mehdi Hussain Hamadani · 2017 to 2026
$71.4M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
Core Clinical Centers for the Blood and Marrow Transplant Clinical Trials Network (UG1)UG1HL108987 · NHLBI · H. LEE MOFFITT CANCER CTR & RES INST · PI Joseph A Pidala · 2017 to 2026
$2.1M
BMT CTN Core - University of MinnesotaUG1HL069290 · NHLBI · UNIVERSITY OF MINNESOTA · PI Mark Juckett, Margaret L MacMillan · 2017 to 2026
$1.9M
NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294NHLBI NIH HHS U24 HL138660NHLBI NIH HHS UG1 HL069290NHLBI NIH HHS UG1 HL108987
6 · The paper itself

Abstract

Importance: Patients requiring allogeneic hematopoietic cell transplantation have variable likelihoods of identifying an 8/8 HLA-matched unrelated donor. A Search Prognosis calculator can estimate the likelihood. Objective: To determine if using a search algorithm based on donor search prognosis can result in similar incidence of transplant between patients Very Likely (>90%) vs Very Unlikely (<10%) to have a matched unrelated donor. Design: This interventional trial utilized a Search Prognosis-based biologic assignment algorithm to guide donor selection. Trial enrollment from June 13, 2019-May 13, 2022; analysis of data as of September 7, 2023 with median follow-up post-evaluability of 14.5 months. Settings: National multi-center Blood and Marrow Transplantation Clinical Trials Network 1702 study of US participating transplant centers. Participants: Acute myeloid and lymphoid leukemias, myelodysplastic syndrome, Hodgkin's and non-Hodgkin's lymphomas, severe aplastic anemia, and sickle cell disease patients referred to participating transplant centers were invited to participate. 2225 patients were enrolled and 1751 were declared evaluable for this study. Patients were declared evaluable once it was determined no suitable HLA-matched related donor was available. Intervention: Patients assigned to the Very Likely arm were to proceed with matched unrelated donor, while Very Unlikely were to utilize alternative donors. A third stratum, Less Likely (~25%) to find a matched unrelated donor, were observed under standard center practices, but were not part of the primary objective. Main Outcome: Cumulative incidence of transplantation by Search Prognosis arm. Results: Evaluable patients included 1751 of which 413 (24%) were from racial/ethnic minorities. Search prognosis was 958 (55%) Very Likely, 517 (30%) Less Likely and 276 (16%) Very Unlikely. 1171 (67%) received HCT, 384 (22%) died without HCT, and 196 (11%) remained alive without HCT. Among the 1,234 patients, the adjusted cumulative incidence (95% CI) of HCT at 6-months was 59.8% (56.7-62.8) in the Very Likely group versus 52.3% (46.1-58.5) in the Very Unlikely (P=0.113). Conclusions: A prospective Search Prognosis-based algorithm can be effectively implemented in a national multicenter clinical trial. This approach resulted in rapid alternative donor identification and comparable rates of HCT in patients Very Likely and Very Unlikely to find a matched unrelated donor.

Identifiers

PMID39371123
PMCPMC11451755

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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.