Evidence map›Paper›PMID 29616857›Full record

ArticleLeukemia & lymphoma2018

Pilot trial of K562/GM-CSF whole-cell vaccination in MDS patients.

Tara M Robinson, Gabrielle T Prince, Chris Thoburn, Erica Warlick, Anna Ferguson, Yvette L Kasamon, Ivan M Borrello, Allan Hess, B Douglas Smith

Registry-linked trialAbstract read
In one paragraph

Article in Leukemia & lymphoma, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00361296 (K562/GM-CSF Vaccination in Patients With Myelodysplastic Syndrome), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 30% 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.

NCT00361296 early_phase1terminatednot on this map

K562/GM-CSF Vaccination in Patients With Myelodysplastic Syndrome

TypeinterventionalSponsorSidney Kimmel Comprehensive Cancer Center at Johns HopkinsRan2007 to 2010Enrolled9ConditionsMyelodysplastic SyndromesArmsK562/GM-CSF cell vaccine
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Vaccines: a promising therapy for myelodysplastic syndrome.Journal of hematology & oncology · 2024
    Review
  5. Electrically regulated cell-based intervention for viral infections.Bioengineering & translational medicine · 2023
    Article
  6. Review
  7. Review
  8. Article
  9. 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

9 authors at 3 institutions in 1 country.

Tara M Robinsona Department of Medical Oncology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Gabrielle T Princea Department of Medical Oncology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Chris Thoburnb Department of Pathology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Erica Warlickc Department of Medicine , University of Minnesota Medical Center , St. Paul/Minneapolis , MN , USA.
Anna Fergusona Department of Medical Oncology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Yvette L Kasamona Department of Medical Oncology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Ivan M Borrelloa Department of Medical Oncology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Allan Hessa Department of Medical Oncology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
B Douglas Smitha Department of Medical Oncology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Johns Hopkins Medicine · USJohns Hopkins University · USUniversity of Minnesota Medical Center · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
TUMOR VACCINESP01CA015396 · NCI · JOHNS HOPKINS UNIVERSITY · PI HESS, ALLAN D · 1985 to 2016
$38.1M
NCI NIH HHS P01 CA015396NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA077598
6 · The paper itself

Abstract

Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematopoietic stem cell malignancies. Currently, approved drugs are given with non-curative intent as the only known cure is allogeneic bone marrow transplantation, which relies on the donor's immune system driving an allogeneic effect. Previous efforts to harness the endogenous immune system have been less successful. We present the results of a pilot study of K562/GM-CSF (GVAX) whole-cell vaccination in MDS patients. The primary objective of safety was met as there were no serious adverse events. One patient had a decrease in transfusion requirements and another demonstrated hematologic improvement suggesting a signal for clinical activity. In vitro correlative studies indicated biological effects on immune cells following vaccination. Although only a pilot study, results are encouraging that an immunotherapeutic approach with a whole-cell vaccine may be feasible in MDS patients.

Indexed as

AgedAntigen PresentationBlood TransfusionCancer VaccinesDendritic CellsFemaleHumansImmunotherapyK562 CellsMaleMiddle AgedMyelodysplastic SyndromesPilot ProjectsTreatment OutcomeCancer VaccinesGVAX vaccineCancer vaccineimmunotherapymyelodysplastic syndromephase 1 clinical trial

Identifiers

PMID29616857
PMCPMC6352988
OpenAlexW2796417348

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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.