Evidence map›Paper›PMID 24365795›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2014

FLT3L and plerixafor combination increases hematopoietic stem cell mobilization and leads to improved transplantation outcome.

Shun He, Jianhong Chu, Sumithira Vasu, Youcai Deng, Shunzong Yuan, Jianying Zhang, Zhijin Fan, Craig C Hofmeister, Xiaoming He, Henry C Marsh and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% of its field
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. New agents in HSC mobilization.International journal of hematology · 2017
    Review
  9. Review
  10. Article
  11. Article
  12. Review
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

12 authors at 4 institutions in 1 country.

Shun HeDivision of Hematology, Department of Internal Medicine, College of Medicine, Ohio State University, Columbus, Ohio; The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Jianhong ChuThe Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Sumithira VasuDivision of Hematology, Department of Internal Medicine, College of Medicine, Ohio State University, Columbus, Ohio; The Ohio State University Comprehensive Cancer Center, Columbus, Ohio; Blood and Marrow Transplantation Program, The James Cancer Hospital, Ohio State University, Columbus, Ohio.
Youcai DengThe Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Shunzong YuanThe Ohio State University Comprehensive Cancer Center, Columbus, Ohio; Department of Lymphoma, PLA 307 Hospital, Beijing, China.
Jianying ZhangCenter for Biostatistics, Department of Biomedical Informatics, Ohio State University, Columbus, Ohio.
Zhijin FanThe Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Craig C HofmeisterDivision of Hematology, Department of Internal Medicine, College of Medicine, Ohio State University, Columbus, Ohio; The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Xiaoming HeThe Ohio State University Comprehensive Cancer Center, Columbus, Ohio; Department of Biomedical Engineering, Ohio State University, Columbus, Ohio.
Henry C MarshCelldex Therapeutics, Inc., Needham, Massachusetts.
Steven M DevineDivision of Hematology, Department of Internal Medicine, College of Medicine, Ohio State University, Columbus, Ohio; The Ohio State University Comprehensive Cancer Center, Columbus, Ohio; Blood and Marrow Transplantation Program, The James Cancer Hospital, Ohio State University, Columbus, Ohio.
Jianhua YuDivision of Hematology, Department of Internal Medicine, College of Medicine, Ohio State University, Columbus, Ohio; The Ohio State University Comprehensive Cancer Center, Columbus, Ohio; Blood and Marrow Transplantation Program, The James Cancer Hospital, Ohio State University, Columbus, Ohio. Electronic address: Jianhua.yu@osumc.edu.
The Ohio State University · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USCelldex Therapeutics (United States) · USOhio State University Hospital · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI WANCAI YANG · 1985 to 2026
$132.3M
Elucidate and Modulate TGF-b Signaling in NK Cells for Glioma TreatmentR01CA155521 · NCI · OHIO STATE UNIVERSITY · PI YU, JIANHUA · 2012 to 2014
$921k
CDX-301 and Plerixafor Combination in Stem Cell Mobilization for TransplantationR41OD018403 · OD · CELLDEX THERAPEUTICS, INC. · PI MARSH, HENRY, YU, JIANHUA · 2013 to 2013
$111k
NCI NIH HHS CA155521NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA155521NIH HHS OD018403NIH HHS R41 OD018403
6 · The paper itself

Abstract

Hematopoietic stem cell (HSC) transplantation has curative potential for patients with hematological malignancies. Clinically, HSCs derived from mobilized peripheral blood are used more frequently than bone marrow. However, current standard mobilizing agents yield grafts that may not contain sufficient HSCs. Here, using murine models, we discovered that FLT3L synergized with plerixafor to mobilize phenotypically defined HSCs and their combination (FP) was superior to granulocyte colony-stimulating factor (G-CSF) alone or in combination with plerixafor (GP). Additionally, FP mobilized more regulatory T cells, natural killer cells, and plasmacytoid dendritic cells compared with G-CSF alone or GP. Both syngeneic and allogeneic grafts mobilized by FP led to long-term survival in transplanted mice. Collectively, FP represents a promising novel and potent mobilization regimen with potential clinical application in both the autologous and allogeneic transplantation settings.

Indexed as

AnimalsBenzylaminesCyclamsDendritic CellsDrug CombinationsDrug SynergismGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem Cell TransplantationHeterocyclic CompoundsHumansInjections, IntraperitonealKiller Cells, NaturalMembrane ProteinsMiceMice, Inbred BALB CBenzylaminesCyclamsDrug Combinationsflt3 ligand proteinGranulocyte Colony-Stimulating FactorHeterocyclic CompoundsMembrane ProteinsplerixaforRecombinant ProteinsCell mobilizationFLT3LPlerixaforTransplantation

Identifiers

PMID24365795
PMCPMC3943635
OpenAlexW1975766472

What OpenQuestion holds

Textmetadata
LicenceTDM
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.