Evidence map›Paper›PMID 28292947›Full record

Trial reportBlood2017

Mobilization of allogeneic peripheral blood stem cell donors with intravenous plerixafor mobilizes a unique graft.

Mark A Schroeder, Michael P Rettig, Sandra Lopez, Stephanie Christ, Mark Fiala, William Eades, Fazia A Mir, Jin Shao, Kyle McFarland, Kathryn Trinkaus and 10 more

Abstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
–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

47 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Article
  8. Article
  9. Review
  10. Mapping Hematopoietic Fate after Transplantation.Stem cell reviews and reports · 2025
    Review
  11. Article
  12. Graft-Versus-Host Disease Mouse Models: A Clinical-Translational Perspective.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  13. Review
  14. Graft Source Choice.Advances in experimental medicine and biology · 2025
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Mark A SchroederDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Michael P RettigDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Sandra LopezDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Stephanie ChristDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Mark FialaDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
William EadesDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Fazia A MirDivision of Hematology and Medical Oncology, Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO; and.
Jin ShaoDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Kyle McFarlandDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Kathryn TrinkausDivision of Biostatistics and.
William ShannonDivision of Biostatistics and.
Elena DeychDivision of Biostatistics and.
Jinsheng YuDepartment of Genetics, Washington University School of Medicine, St. Louis, MO.
Ravi VijDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Keith Stockerl-GoldsteinDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Amanda F CashenDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Geoffrey L UyDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Camille N AbboudDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Peter WesterveltDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
John F DiPersioDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
TARGETING AML-STROMAL INTERACTIONSR01CA152329 · NCI · WASHINGTON UNIVERSITY · PI DIPERSIO, JOHN F. · 2011 to 2015
$2.5M
BM NICHE DISRUPTION AND IMMUNOTHERAPY IN HEMATOLOGICAL MALIGNANCIESR50CA211466 · NCI · WASHINGTON UNIVERSITY · PI Michael Rettig · 2016 to 2026
$2.3M
TARGETING THE CXCR4-SDF1 AXIS AS THERAPY FOR RELAPSED/REFRACTORY AMLR21CA132269 · NCI · WASHINGTON UNIVERSITY · PI DIPERSIO, JOHN F. · 2009 to 2010
$669k
OPTIMIZING ALLOGENEIC TRANSPLANTATION USING CXCR4 BLOCKADER21CA141523 · NCI · WASHINGTON UNIVERSITY · PI DIPERSIO, JOHN F. · 2009 to 2010
$669k
NCATS NIH HHS UL1 TR000448NCI NIH HHS P30 CA091842NCI NIH HHS R01 CA152329NCI NIH HHS R21 CA132269NCI NIH HHS R21 CA141523NCI NIH HHS R50 CA211466
6 · The paper itself

Abstract

A single subcutaneous (SC) injection of plerixafor results in rapid mobilization of hematopoietic progenitors, but fails to mobilize 33% of normal allogeneic sibling donors in 1 apheresis. We hypothesized that changing the route of administration of plerixafor from SC to IV may overcome the low stem cell yields and allow collection in 1 day. A phase 1 trial followed by a phase 2 efficacy trial was conducted in allogeneic sibling donors. The optimal dose of IV plerixafor was determined to be 0.32 mg/kg. The primary outcome of reducing the failure to collect ≥2 × 10

Indexed as

Administration, IntravenousAdultAgedAntigens, CD34BenzylaminesBlood Component RemovalCyclamsFemaleGraft vs Host DiseaseGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem Cell TransplantationHeterocyclic CompoundsHumansMaleMiddle AgedAntigens, CD34BenzylaminesCyclamsGranulocyte Colony-Stimulating FactorHeterocyclic Compoundsplerixafor

Identifiers

PMID28292947
PMCPMC5428459

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.