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Cellular Therapy in NSCLC: Between Myth and Reality.
Imbimbo, Martina; Wetterwald, Laureline; Friedlaender, Alex; Parikh, Kaushal; Addeo, Alfredo.
Afiliação
  • Imbimbo M; Oncology Department, Centre Hospitalier Universitaire Vaudois (CHUV), Rue du Bugnon 46, Lausanne University Hospital, Lausanne, Switzerland. Martina.imbimbo@chuv.ch.
  • Wetterwald L; Oncology Department, Centre Hospitalier Universitaire Vaudois (CHUV), Rue du Bugnon 46, Lausanne University Hospital, Lausanne, Switzerland.
  • Friedlaender A; Oncology Department, University Hospital Geneva (HUG), 1205, Geneva, Switzerland.
  • Parikh K; Oncology Department, Clinique Générale Beaulieu, 1206, Geneva, Switzerland.
  • Addeo A; Division of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Curr Oncol Rep ; 25(10): 1161-1174, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37646900
ABSTRACT
PURPOSE OF REVIEW In this paper, we review the current state and modalities of adoptive cell therapies (ACT) in non-small cell lung carcinoma (NSCLC). We also discuss the challenges hampering the use of ACT and the approaches to overcome these barriers. RECENT

FINDINGS:

Several trials are ongoing investigating the three main modalities of T cell-based ACT tumor-infiltrating lymphocytes (TILs), genetically engineered T-cell receptors (TCRs), and chimeric antigen receptor (CAR) T cells. The latter, in particular, has revolutionized the treatment of hematologic malignancies. However, the efficacy against solid tumor is still sparse. Major limitations include the following severe toxicities, restricted infiltration and activation within the tumors, antigen escape and heterogeneity, and manufacturing issues. ACT is a promising tool to improve the outcome of metastatic NSCLC, but significant translational and clinical research is needed to improve its application and expand the use in NSCLC.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article