Evidence map›Paper›PMID 35880942›Full record

ReviewCancer journal (Sudbury, Mass.)

Adoptive Cellular Therapy for Pediatric Solid Tumors: Beyond Chimeric Antigen Receptor-T Cell Therapy.

Jonathan Hensel, Jonathan Metts, Ajay Gupta, Brian H Ladle, Shari Pilon-Thomas, John Mullinax

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Cancer journal (Sudbury, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05968768 (To Evaluate the Efficacy and Safety of Naxitamab in Patients With Refractory Ewing's Sarcoma), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 37% 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.

NCT05968768 phase2recruitingnot on this map

To Evaluate the Efficacy and Safety of Naxitamab in Patients With Refractory Ewing's Sarcoma

TypeinterventionalSponsorAnna RaciborskaRan2023 to 2028Enrolled24ConditionsEwing SarcomaArmsNaxitamab
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 4 institutions in 1 country.

Jonathan HenselFrom the Sarcoma, Immunology, Cutaneous Oncology, Moffitt Cancer Center, Tampa.
Jonathan MettsCancer and Blood Disorders Institute, Johns Hopkins All Children's Hospital, St Petersburg, FL.
Ajay GuptaDivision of Pediatric Oncology, Roswell Park Comprehensive Cancer Center, Department of Pediatrics, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, NY.
Brian H LadleSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD.
Shari Pilon-ThomasFrom the Sarcoma, Immunology, Cutaneous Oncology, Moffitt Cancer Center, Tampa.
John MullinaxFrom the Sarcoma, Immunology, Cutaneous Oncology, Moffitt Cancer Center, Tampa.
Moffitt Cancer Center · USJohns Hopkins All Children's Hospital · USJohns Hopkins University · USRoswell Park Comprehensive Cancer Center · US

Funding

Imaging Acidosis and Immune Therapy in PDACR01CA239219 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI IBRAHIM HASHIM, ARIG A, PILON-THOMAS, SHARI · 2020 to 2024
$3.4M
Predict radiation-induced shifts in patient-specific tumor immune ecosystem composition to harness immunological consequences of radiotherapyU01CA244100 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ENDERLING, HEIKO, PILON-THOMAS, SHARI · 2020 to 2025
$2.6M
Mathematical Model-Guided Adoptive Immunotherapy in Bladder CancerR01CA259387 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI PILON-THOMAS, SHARI, REJNIAK, KATARZYNA ANNA · 2021 to 2025
$2.3M
Leveraging the Lymphocytic Infiltration of Soft Tissue Sarcoma for Autologous Cellular ImmunotherapyK08CA252642 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI MULLINAX, JOHN · 2020 to 2024
$1.2M
A low-cost topical immunotherapy formulation suitable for treating cervical cancer in low and middle income countries and low-resource settings in the U.S.R43CA257552 · NCI · MORPHOGENESIS, INC. · PI SHAMBLOTT, MICHAEL J · 2021 to 2021
$400k
NCI NIH HHS K08 CA252642NCI NIH HHS R01 CA239219NCI NIH HHS R01 CA259387NCI NIH HHS R43 CA257552NCI NIH HHS U01 CA244100
6 · The paper itself

Abstract

abstractChildren and adolescents with high-risk (metastatic and relapsed) solid tumors have poor outcomes despite intensive multimodal therapy, and there is a pressing need for novel therapeutic strategies. Adoptive cellular therapy (ACT) has demonstrated activity in multiple adult cancer types, and opportunity exists to expand the use of this therapy in children. Employment of immunotherapy in the pediatric population has realized only modest overall clinical trial results, with success thus far restricted mainly to antibody-based therapies and chimeric antigen receptor T-cell therapies for lymphoid malignancy. As we improve our understanding of the orchestrated cellular and molecular mechanisms involved in ACT, this will provide biologic insight and improved ACT strategies for pediatric malignancies. This review focuses on ACT strategies outside of chimeric antigen receptor T-cell therapy, including completed and ongoing clinical trials, and highlights promising preclinical data in tumor-infiltrating lymphocytes that enhance the clinical efficacy of ACT for high-risk pediatric solid tumors.

Indexed as

NeoplasmsReceptors, Chimeric AntigenAdolescentCell- and Tissue-Based TherapyChildHumansImmunotherapy, AdoptiveLymphocytes, Tumor-InfiltratingReceptors, Antigen, T-CellReceptors, Antigen, T-CellReceptors, Chimeric Antigen

Identifiers

PMID35880942
PMCPMC9847472
OpenAlexW4288046715

What OpenQuestion holds

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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.