Evidence map›Paper›PMID 30232225›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Activated Natural Killer Cells in Combination with Anti-GD2 Antibody Dinutuximab Improve Survival of Mice after Surgical Resection of Primary Neuroblastoma.

Wesley E Barry, Jeremy R Jackson, Grace E Asuelime, Hong-Wei Wu, Jianping Sun, Zesheng Wan, Jemily Malvar, Michael A Sheard, Larry Wang, Robert C Seeger and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. FOXJ3, a novel tumor suppressor in neuroblastoma.Molecular therapy. Oncology · 2025
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  15. Oncoimmunology · 2022
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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

11 authors at 2 institutions in 1 country.

Wesley E BarryDepartment of Surgery, Keck School of Medicine, University of Southern California, Los Angeles, California.
Jeremy R JacksonDivision of Pediatric Surgery, Children's Hospital Los Angeles, Los Angeles, California.
Grace E AsuelimeDivision of Pediatric Surgery, Children's Hospital Los Angeles, Los Angeles, California.
Hong-Wei WuDivision of Hematology, Oncology, and Blood and Marrow Transplantation, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Jianping SunDivision of Hematology, Oncology, and Blood and Marrow Transplantation, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Zesheng WanDivision of Hematology, Oncology, and Blood and Marrow Transplantation, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Jemily MalvarDivision of Hematology, Oncology, and Blood and Marrow Transplantation, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Michael A SheardDivision of Hematology, Oncology, and Blood and Marrow Transplantation, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Larry WangDepartment of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Robert C SeegerDivision of Hematology, Oncology, and Blood and Marrow Transplantation, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
Eugene S KimDepartment of Surgery, Keck School of Medicine, University of Southern California, Los Angeles, California. eugeneskim@chla.usc.edu.ORCID 0000-0001-7959-5614
Children's Hospital of Los Angeles · USUniversity of Southern California · US

Funding

Tumor microenvironment-dependent therapy resistanceP01CA217959 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI Kimberly Stegmaier · 2017 to 2026
$20.7M
NCI NIH HHS P01 CA217959
6 · The paper itself

Abstract

purposeImmunotherapy of neuroblastoma that remains after myeloablative chemotherapy with anti-GD2 antibody dinutuximab has increased the two-year event-free and overall survival of high-risk neuroblastoma patients; however, 40% of patients develop recurrent disease during or after this treatment. To determine the potential of such antibody-based immunotherapy earlier in treatment, a mouse model was developed in which surgical resection of the primary tumor was followed by therapy of residual disease with dinutuximab combined with EXPERIMENTAL

designThe effect of combining dinutuximab with human aNK cells was determined

results

conclusionsThe combination of dinutuximab and adoptively transferred human aNK cells following surgical resection of primary neuroblastomas significantly improves survival of immunodeficient mice.

Indexed as

AnimalsAntibodies, Anti-IdiotypicAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyCytotoxicity, ImmunologicDisease Models, AnimalHeterograftsHumansImmunotherapyKiller Cells, NaturalMiceN-AcetylgalactosaminyltransferasesNeuroblastomaAntibodies, Anti-IdiotypicAntibodies, MonoclonaldinutuximabN-Acetylgalactosaminyltransferases(N-acetylneuraminyl)-galactosylglucosylceramide N-acetylgalactosaminyltransferase

Identifiers

PMID30232225
PMCPMC6320320
OpenAlexW2892305145

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.