The efficacy and applicability of chimeric antigen receptor (CAR) T cell-based regimens for primary bone tumors: A comprehensive review of current evidence.

CAR T cell Chimeric Antigen Receptor (CAR) Ewing’s sarcoma (ES) Osteosarcoma (OS) Primary bone tumors (PBT)

Journal

Journal of bone oncology
ISSN: 2212-1366
Titre abrégé: J Bone Oncol
Pays: Netherlands
ID NLM: 101610292

Informations de publication

Date de publication:
Oct 2024
Historique:
received: 21 06 2024
revised: 17 09 2024
accepted: 17 09 2024
medline: 9 10 2024
pubmed: 9 10 2024
entrez: 9 10 2024
Statut: epublish

Résumé

Primary bone tumors (PBT), although rare, could pose significant mortality and morbidity risks due to their high incidence of lung metastasis. Survival rates of patients with PBTs may vary based on the tumor type, therapeutic interventions, and the time of diagnosis. Despite advances in the management of patients with these tumors over the past four decades, the survival rates seem not to have improved significantly, implicating the need for novel therapeutic interventions. Surgical resection with wide margins, radiotherapy, and systemic chemotherapy are the main lines of treatment for PBTs. Neoadjuvant and adjuvant chemotherapy, along with emerging immunotherapeutic approaches such as chimeric antigen receptor (CAR)-T cell therapy, have the potential to improve the treatment outcomes for patients with PBTs. CAR-T cell therapy has been introduced as an option in hematologic malignancies, with FDA approval for several CD19-targeting CAR-T cell products. This review aims to highlight the potential of immunotherapeutic strategies, specifically CAR T cell therapy, in managing PBTs.

Identifiants

pubmed: 39381633
doi: 10.1016/j.jbo.2024.100635
pii: S2212-1374(24)00115-5
pmc: PMC11460493
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

100635

Informations de copyright

© 2024 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Atefeh Barzegari (A)

Cell Science Research Center, Kian Immune Cell Co, Tehran, Iran.

Fateme Salemi (F)

Hematology, Oncology and Stem Cell Transplantation Research Center, Research Institute for Oncology, Hematology and Cell Therapy, Tehran University of Medical Sciences, Tehran, Iran.

Amirhossein Kamyab (A)

Faculty of Medicine, Fasa University of Medical Sciences, Fasa, Iran.

Adarsh Aratikatla (A)

School of Medicine, Royal College of Surgeons in Ireland, Dublin, County Dublin, Ireland.

Negar Nejati (N)

Pediatric Cell and Gene Therapy Research Centre, Gene, Cell & Tissue Research Institute, Tehran University of Medical Sciences, Iran.

Mojgan Valizade (M)

School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

Ehab Eltouny (E)

Department of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.

Alireza Ebrahimi (A)

Department of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.

Classifications MeSH