Stereotactic Ablative Radiation Therapy in 3 Fractions Induces a Favorable Systemic Immune Cell Profiling in Prostate Cancer Patients.

Immunomonitoring combined therapies immunotherapy peripheral immune cells prostate cancer radiotherapy stereotactic body radiation therapy

Journal

Oncoimmunology
ISSN: 2162-402X
Titre abrégé: Oncoimmunology
Pays: United States
ID NLM: 101570526

Informations de publication

Date de publication:
2023
Historique:
entrez: 17 2 2023
pubmed: 18 2 2023
medline: 22 2 2023
Statut: epublish

Résumé

The impact of radiotherapy (RT) on immune cell status in prostate cancer (PCa) is only partially determined. The aim of this study was to assess the effect of different RT strategies on peripheral B, T, and Natural killer (NK) lymphocytes at precise longitudinal time-points in PCa. 18 patients treated with stereotactic body radiation therapy (SBRT) (40 Gy/3FRX), definitive moderate-hypofractionation (62 Gy/20FRX), or post-operative conventional-fractionation RT (66-69 Gy/30FRX) were prospectively evaluated for the immune cell profile in terms of immune cell composition, differentiation stage, cytokine production and inhibitory receptor (IR) expression. The immune-monitoring of the 18 patients revealed that RT affects the balance of systemic immune cells, with the main differences observed between SBRT and conventionally fractionated RT. SBRT favorably impacts immune response in term of increased B cells, central-memory and effector-memory CD8

Identifiants

pubmed: 36798427
doi: 10.1080/2162402X.2023.2174721
pii: 2174721
pmc: PMC9928462
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2174721

Informations de copyright

© 2023 The Author(s). Published with license by Taylor & Francis Group, LLC.

Déclaration de conflit d'intérêts

The authors report there are no competing interests to declare

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Auteurs

Belinda Palermo (B)

Unit Tumor Immunology and Immunotherapy, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Marta Bottero (M)

Radiation Oncology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Mariangela Panetta (M)

Unit Tumor Immunology and Immunotherapy, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Adriana Faiella (A)

Radiation Oncology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Isabella Sperduti (I)

Biostatistical Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Serena Masi (S)

Clinical Pathology and Cancer Biobank, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Giuseppe Frisullo (G)

Unit Tumor Immunology and Immunotherapy, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Maria Laura Foddai (ML)

Transfusion Medicine, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Iole Cordone (I)

Clinical Pathology and Cancer Biobank, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Paola Nisticò (P)

Unit Tumor Immunology and Immunotherapy, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Giuseppe Sanguineti (G)

Radiation Oncology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

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