Evidence map›Paper›PMID 25807290›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2015

[(18)F]FHBG PET/CT Imaging of CD34-TK75 Transduced Donor T Cells in Relapsed Allogeneic Stem Cell Transplant Patients: Safety and Feasibility.

Linda G Eissenberg, Michael P Rettig, Julie K Ritchey, Julie L Prior, Sally W Schwarz, Jennifer Frye, Brian S White, Robert S Fulton, Armin Ghobadi, Matthew L Cooper and 6 more

Abstract readClinical Trial, Phase I
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Stem cells therapy molecular tracking - the special focus on nuclear medicine.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2026
    Review
  2. Enrichment strategies to enhance genome editing.Journal of biomedical science · 2023
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Detection limit ofEJNMMI research · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Imaging Biomarkers in Immunotherapy.Biomarkers in cancer · 2016
    Review
  14. 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

16 authors.

Linda G EissenbergDivision of Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.
Michael P RettigDivision of Oncology, Washington University School of Medicine, St. Louis, Missouri, USA; Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, USA.
Julie K RitcheyDivision of Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.
Julie L PriorEdward Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri, USA.
Sally W SchwarzDepartment of Radiology Cyclotron Facility, Washington University School of Medicine, St. Louis, Missouri, USA.
Jennifer FryeEdward Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri, USA; Division of Nuclear Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Brian S WhiteDivision of Oncology, Washington University School of Medicine, St. Louis, Missouri, USA; The Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA.
Robert S FultonThe Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA.
Armin GhobadiDivision of Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.
Matthew L CooperDivision of Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.
Daniel R CourielDepartment of Medicine, University of Michigan, Ann Arbor, MI, USA.
Muhammad Esa SeegulamDepartment of Biology, Culver-Stockton College, Canton, Missouri, USA.
David Piwnica-WormsEdward Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri, USA; Department of Radiology Cyclotron Facility, Washington University School of Medicine, St. Louis, Missouri, USA; Department of Cancer Systems Imaging and MD Anderson Cancer Center, Houston, Texas, USA.
Farrokh DehdashtiEdward Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri, USA; Division of Nuclear Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Kenneth CornettaDepartment of Medical and Molecular Genetics, Indiana University, and the Indiana University Viral Production Facility (IU VPF), Indianapolis, Indiana, USA.
John F DiPersioDivision of Oncology, Washington University School of Medicine, St. Louis, Missouri, USA; Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, USA. Electronic address: jdipersi@dom.wustl.edu.

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
Targeting the Bone Marrow Microenvironment In Acute Lymphocytic LeukemiaP50CA171963 · NCI · WASHINGTON UNIVERSITY · PI Daniel C Link · 2013 to 2026
$31.6M
WU-MDACC Inter-Institutional Molecular Imaging CenterP50CA094056 · NCI · WASHINGTON UNIVERSITY · PI PIWNICA-WORMS, DAVID · 2002 to 2016
$26.3M
Genetic Manipulation of T Cells--PreClinical ModelsR01CA083845 · NCI · WASHINGTON UNIVERSITY · PI DIPERSIO, JOHN F · 2001 to 2005
$1.6M
DLI using genetically modified T cells: Phase 1 trialR21CA110489 · NCI · WASHINGTON UNIVERSITY · PI DIPERSIO, JOHN F · 2004 to 2005
$627k
NCI NIH HHS P30 CA091842NCI NIH HHS P50 CA094056NCI NIH HHS P50 CA094056-09NCI NIH HHS P50 CA171963NCI NIH HHS R01 CA083845NCI NIH HHS R01 CA110489NCI NIH HHS R01 CA83845NCI NIH HHS R21 CA110489
6 · The paper itself

Abstract

Described herein is a first-in-man attempt to both genetically modify T cells with an imagable suicide gene and track these transduced donor T cells in allogeneic stem cell transplantation recipients using noninvasive positron emission tomography/computerized tomography (PET/CT) imaging. A suicide gene encoding a human CD34-Herpes Simplex Virus-1-thymidine kinase (CD34-TK75) fusion enabled enrichment of retrovirally transduced T cells (TdT), control of graft-versus-host disease and imaging of TdT migration and expansion in vivo in mice and man. Analysis confirmed that CD34-TK75-enriched TdT contained no replication competent γ-retrovirus, were sensitive to ganciclovir, and displayed characteristic retroviral insertion sites (by targeted sequencing). Affinity-purified CD34-TK75(+)-selected donor T cells (1.0-13 × 10(5))/kg were infused into eight patients who relapsed after allogeneic stem cell transplantation. Six patients also were administered 9-[4-((18)F)fluoro-3-hydroxymethyl-butyl]guanine ([(18)F]FHBG) to specifically track the genetically modified donor T cells by PET/CT at several time points after infusion. All patients were assessed for graft-versus-host disease, response to ganciclovir, circulating TdT cells (using both quantitative polymerase chain reaction and [(18)F]FHBG PET/CT imaging), TdT cell clonal expansion, and immune response to the TdT. This phase 1 trial demonstrated that genetically modified T cells and [(18)F]FHBG can be safely infused in patients with relapsed hematologic malignancies after allogeneic stem cell transplantation.

Indexed as

Transduction, GeneticAnimalsAntigens, CD34Cell Line, TumorFeasibility StudiesFlow CytometryGanciclovirGraft vs Host DiseaseGuanineHerpesvirus 1, HumanHumansLeukocytes, MononuclearMiceNIH 3T3 CellsPilot ProjectsPositron-Emission Tomography9-(4-fluoro-3-hydroxymethylbutyl)guanineAntigens, CD34GanciclovirGuanineThymidine Kinase

Identifiers

PMID25807290
PMCPMC4817759

What OpenQuestion holds

Textmetadata
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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.