Evidence map›Paper›PMID 32221013›Full record

Trial reportJournal for immunotherapy of cancer2020

Longitudinal NK cell kinetics and cytotoxicity in children with neuroblastoma enrolled in a clinical phase II trial.

Rosa Nguyen, Natasha Sahr, April Sykes, Mary Beth McCarville, Sara M Federico, Amanda Sooter, David Cullins, Barbara Rooney, William E Janssen, Aimee C Talleur and 6 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01857934 (Neuroblastoma Protocol 2012), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 16% 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.

NCT01857934 phase2completednot on this map

Neuroblastoma Protocol 2012: Therapy for Children With Advanced Stage High-Risk Neuroblastoma

TypeinterventionalSponsorSt. Jude Children's Research HospitalRan2013 to 2025Enrolled153ConditionsNeuroblastomaArmscyclophosphamide, topotecan, hu14.18K322A, peripheral blood stem cell harvest, surgical resection
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Targeted therapies in pediatric oncology: A start.Molecular therapy. Oncology · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. Neuroblastoma: an ongoing cold front for cancer immunotherapy.Journal for immunotherapy of cancer · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. 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 at 2 institutions in 2 countries.

Rosa NguyenOncology Department, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID 0000-0001-5143-2055
Natasha SahrDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
April SykesDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Mary Beth McCarvilleDepartment of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Sara M FedericoOncology Department, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Amanda SooterDepartment of Bone Marrow Transplantation & Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
David CullinsDepartment of Bone Marrow Transplantation & Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Barbara RooneyDepartment of Bone Marrow Transplantation & Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
William E JanssenDepartment of Bone Marrow Transplantation & Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Aimee C TalleurDepartment of Bone Marrow Transplantation & Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Brandon M TriplettDepartment of Bone Marrow Transplantation & Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Gwendolyn AnthonyOncology Department, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Michael A DyerDevelopmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Alberto S PappoOncology Department, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Wing H LeungDepartment of Bone Marrow Transplantation & Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Wayne L FurmanOncology Department, St. Jude Children's Research Hospital, Memphis, Tennessee, USA Wayne.furman@stjude.org.
St. Jude Children's Research Hospital · USNational Institutes of Health · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

backgroundNatural killer (NK) cells are one of the main effector populations of immunotherapy with monoclonal antibody and cytokines, used in combination with chemotherapy to treat children with high-risk neuroblastoma on this phase II trial. However, the impact of chemoimmunotherapy on NK cell kinetics, phenotype, and function is understudied.

methodsWe prospectively examined NK cell properties from 63 children with newly diagnosed neuroblastoma enrolled in a phase II trial (NCT01857934) and correlated our findings with tumor volume reduction after 2 courses of chemoimmunotherapy. NK cell studies were conducted longitudinally during chemoimmunotherapy and autologous hematopoietic cell transplantation (autoHCT) with optional haploidentical NK cell infusion and additional immunotherapy.

resultsChemoimmunotherapy led to significant NK cytopenia, but complete NK cell recovery reliably occurred by day 21 of each therapy course as well as after autoHCT. Haploidentical NK cell infusion elevated the NK cell count transiently during autoHCT. NK cell cytotoxicity increased significantly during treatment compared with diagnosis. In addition, NK cells maintained their ability to respond to cytokine stimulation in culture longitudinally. Unsupervised cluster analysis of CD56

conclusionAfter profound NK cytopenia due to chemoimmunotherapy, endogenously reconstituted NK cells exhibit enhanced NK cytotoxicity compared with pretherapy measurements. Our data suggest a relationship between CD56 TRIAL REGISTRATION NUMBER: NCT01857934.

Indexed as

AdolescentChildChild, PreschoolFemaleHumansImmunotherapyInfantInfant, NewbornKiller Cells, NaturalKineticsMaleNeuroblastomaProspective Studiesimmunologyoncologypaediatric

Identifiers

PMID32221013
PMCPMC7206969
OpenAlexW3013578867

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.