Evidence map›Paper›PMID 41547399›Full record

ArticleTransplantation and cellular therapy2026

Donor Search and Selection Strategy to Facilitate Comparable Transplant Rates across Donor Search Prognosis Groups: A Report from the BMT CTN 1702 Trial.

Joseph Pidala, Brent Logan, Stephanie J Lee, Bronwen E Shaw, Steven Devine, Stefan O Ciurea, Mary Horowitz, Naya He, Iskra Pusic, Samer A Srour and 18 more

Abstract read
In one paragraph

Article in Transplantation and cellular therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

28 authors.

Joseph PidalaDepartment of Blood and Marrow Transplantation and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida. Electronic address: Joseph.pidala@moffitt.org.
Brent LoganCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Biostatistics, Medical College of Wisconsin, Milwaukee, Wisconsin.
Stephanie J LeeFred Hutchinson Cancer Center, Seattle, Washington.
Bronwen E ShawCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Steven DevineDepartment of Blood and Marrow Transplantation and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida; Center for International Blood and Marrow Transplant Research, National Marrow Donor Program, Minneapolis, Minnesota.
Stefan O CiureaUniversity of California-Irvine, Irvine, California.
Mary HorowitzCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Naya HeCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Iskra PusicWashington University Barnes Jewish Hospital, St Louis, Missouri.
Samer A SrourThe University of Texas MD Anderson Cancer Center, Houston, Texas.
Sally AraiStanford University, Stanford, California.
Mark JuckettUniversity of Minnesota, Minneapolis, Minnesota.
Joseph UbertiKarmanos Cancer Institute Wayne State University, Detroit, Michigan.
LaQuisa HillBaylor College of Medicine, Houston, Texas.
Sumithira VasuThe Ohio State University James Comprehensive Cancer Center, Columbus, Ohio.
William J HoganMayo Clinic, Rochester, Minnesota.
Brandon Hayes-LattinOregon Health Sciences University Knight Cancer Institute, Portland, Oregon.
Peter WesterveltMaine Health Cancer Care, Scarborough, Maine.
Asad BasheyNorthside Hospital, Atlanta, Georgia.
Nosha FarhadfarUniversity of Florida Shands Healthcare, Gainesville, Florida.
Michael R GrunwaldLevine Cancer Institute. Atrium Health, Charlotte, North Carolina.
Eric LeiferNational Heart, Lung and Blood Institute, Bethesda, Maryland.
Heather SymonsJohns Hopkins University, Baltimore, Maryland.
Ayman SaadKing Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Jenny VogelCenter for International Blood and Marrow Transplant Research, National Marrow Donor Program, Minneapolis, Minnesota.
Connor EricksonCenter for International Blood and Marrow Transplant Research, National Marrow Donor Program, Minneapolis, Minnesota.
Kelly BuckNational Marrow Donor Program, Minneapolis, Minnesota.
Jason G DehnNational Marrow Donor Program, Minneapolis, Minnesota.

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
The Ohio State University Blood and Marrow Transplant Research ConsortiumUG1HL109322 · NHLBI · OHIO STATE UNIVERSITY · PI Sumithira Vasu · 2017 to 2026
$2.0M
Phase III, Multicenter, Randomized, Double-Blind Study of Duvelisib as Cytokine Release Syndrome Prophylaxis in Patients with Large Cell or Mantle Cell Lymphoma Undergoing CAR T-Cell TherapiesUG1HL109137 · NHLBI · WASHINGTON UNIVERSITY · PI Iskra Pusic · 2017 to 2026
$1.9M
Translational Research in Blood and Marrow TransplantationUG1HL069310 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI RICHARD J JONES · 2017 to 2026
$1.6M
NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294NHLBI NIH HHS U24 HL138660NHLBI NIH HHS UG1 HL069310NHLBI NIH HHS UG1 HL109137NHLBI NIH HHS UG1 HL109322
6 · The paper itself

Abstract

In a secondary analysis from the BMT CTN 1702 trial, we report on donor search and selection strategies according to baseline recipient search prognosis (SP). A total of 1751 patients in 3 SP groups-very likely, 958; less likely, 517; very unlikely, 276- were analyzed. The target time to HCT was most often 6 to 12 weeks (SP P = nonsignificant) and was associated with acute myelogenous leukemia remission status (P < .01). The baseline preferred alternative donor (across all SP groups was most commonly a haploidentical (haplo) donor (62.2% overall), whereas the use of mismatched unrelated donors (MMUDs) increased over time during the study period. Those in the less/very unlikely groups prioritized more alternative donor types at baseline and had more priority ranking changes (SP P < .01). While a comparable number of donors were typed (all SP: median, 3 donors; median time, 1.1 months), less/very unlikely SP had greater use of alternative donors (SP P < .01). Reasons for nonselection of typed donors varied by SP group. For less/very unlikely SP, the rates of HLA mismatching and donor-specific antibodies were higher, while for very likely SP, the use of other preferred donors was more common. Of 1751, 65% reached HCT: 94% of the very likely had an 8/8 matched unrelated donor (MUD) and 91% of the very unlikely had an alternative donor (haplo, 61%; MMUD, 22%; umbilical cord blood, 8%). HCT occurred within the initial desired timeline in 38% of all subjects. HCT delays occurred in 29%, mostly for disease or patient health overall, and of these 52% reached HCT after delay. In this prospective, multicenter evaluation of donor search and selection practices, we demonstrate that patients with poor likelihood of 8/8 MUD matching can reach HCT at comparable rates and with similar effort (time spent typing, number of donors typed) using an early alternative donor-centered strategy. Uniformly across SP groups, the target time to HCT is not commonly reached and is disrupted mostly by disease/patient health delays and not by donor unavailability.

Indexed as

Bone Marrow TransplantationDonor SelectionHematopoietic Stem Cell TransplantationTissue DonorsAdultFemaleHumansMaleMiddle AgedPrognosisUnrelated DonorsDonor search and selection

Identifiers

PMID41547399
PMCPMC13086071

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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.