Evidence map›Paper›PMID 37176035›Full record

ReviewInternational journal of molecular sciences2023

Prospects and Advances in Adoptive Natural Killer Cell Therapy for Unmet Therapeutic Needs in Pediatric Bone Sarcomas.

Halin Bareke, Adrián Ibáñez-Navarro, Pilar Guerra-García, Carlos González Pérez, Pedro Rubio-Aparicio, Diego Plaza López de Sabando, Ana Sastre-Urgelles, Eduardo José Ortiz-Cruz, Antonio Pérez-Martínez

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Halin BarekeTranslational Research Group in Pediatric Oncology, Haematopoietic Transplantation and Cell Therapy, Hospital La Paz Institute for Health Research, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0003-4577-3325
Adrián Ibáñez-NavarroTranslational Research Group in Pediatric Oncology, Haematopoietic Transplantation and Cell Therapy, Hospital La Paz Institute for Health Research, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Pilar Guerra-GarcíaDepartment of Pediatric Hemato-Oncology, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0002-7740-0614
Carlos González PérezDepartment of Pediatric Hemato-Oncology, La Paz University Hospital, 28046 Madrid, Spain.
Pedro Rubio-AparicioDepartment of Pediatric Hemato-Oncology, La Paz University Hospital, 28046 Madrid, Spain.
Diego Plaza López de SabandoDepartment of Pediatric Hemato-Oncology, La Paz University Hospital, 28046 Madrid, Spain.
Ana Sastre-UrgellesDepartment of Pediatric Hemato-Oncology, La Paz University Hospital, 28046 Madrid, Spain.
Eduardo José Ortiz-CruzDepartment of Orthopedic Surgery and Traumatology, La Paz University Hospital, 28046 Madrid, Spain.
Antonio Pérez-MartínezTranslational Research Group in Pediatric Oncology, Haematopoietic Transplantation and Cell Therapy, Hospital La Paz Institute for Health Research, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0002-6436-9195
Hospital Universitario La Paz · ESHospital La Paz Institute for Health Research · ES

Funding

The CRIS Cancer Foundation, Fundación Mari Paz Jiménez Casado and Fundación La Sonrisa de Alex Perez Martinez-FMPJC and FSA
6 · The paper itself

Abstract

Malignant bone tumors are aggressive tumors, with a high tendency to metastasize, that are observed most frequently in adolescents during rapid growth spurts. Pediatric patients with malignant bone sarcomas, Ewing sarcoma and osteosarcoma, who present with progressive disease have dire survival rates despite aggressive therapy. These therapies can have long-term effects on bone growth, such as decreased bone mineral density and reduced longitudinal growth. New therapeutic approaches are therefore urgently needed for targeting pediatric malignant bone tumors. Harnessing the power of the immune system against cancer has improved the survival rates dramatically in certain cancer types. Natural killer (NK) cells are a heterogeneous group of innate effector cells that possess numerous antitumor effects, such as cytolysis and cytokine production. Pediatric sarcoma cells have been shown to be especially susceptible to NK-cell-mediated killing. NK-cell adoptive therapy confers numerous advantages over T-cell adoptive therapy, including a good safety profile and a lack of major histocompatibility complex restriction. NK-cell immunotherapy has the potential to be a new therapy for pediatric malignant bone tumors. In this manuscript, we review the general characteristics of osteosarcoma and Ewing sarcoma, discuss the long-term effects of sarcoma treatment on bones, and the barriers to effective immunotherapy in bone sarcomas. We then present the laboratory and clinical studies on NK-cell immunotherapy for pediatric malignant bone tumors. We discuss the various donor sources and NK-cell types, the engineering of NK cells and combinatorial treatment approaches that are being studied to overcome the current challenges in adoptive NK-cell therapy, while suggesting approaches for future studies on NK-cell immunotherapy in pediatric bone tumors.

Indexed as

Bone NeoplasmsNeoplasmsOsteosarcomaSarcomaSarcoma, EwingAdolescentCell- and Tissue-Based TherapyChildHumansImmunotherapyImmunotherapy, AdoptiveKiller Cells, Naturaladoptive cell therapyEwing sarcomaimmune evasionimmunotherapyNK cellsosteosarcomapediatric bone sarcomatumor microenvironment

Identifiers

PMID37176035
PMCPMC10178897
OpenAlexW4375862942

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.