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Intracavitary cisplatin-fibrin followed by irradiation improved tumor control compared to the single treatments in a mesothelioma rat modelCentral MessagePerspective

Authors :
Michaela B. Kirschner, PhD
Mayura Meerang, PhD
Vanessa Orlowski
Katarzyna Furrer, MD
Fabienne Tschanz, PhD
Ivo Grgic, PhD
Virginia Cecconi, PhD
Maries van den Broek, PhD
Matthias Guckenberger, MD
Martin Pruschy, MD
Olivia Lauk, MD
Isabelle Opitz, MD
Source :
JTCVS Open, Vol 22, Iss , Pp 491-503 (2024)
Publication Year :
2024
Publisher :
Elsevier, 2024.

Abstract

Objective: To test the safety and efficacy of combination treatment for pleural mesothelioma (PM) with intracavitary cisplatin-fibrin (cis-fib) plus hemithoracic irradiation (IR) applied after lung-sparing surgery in an orthotopic immunocompetent rat model. Methods: We randomized male F344 rats into 5 groups: cis-fib (n = 9), 10 Gy IR (n = 6), 20 Gy IR (n = 9), cis-fib+10 Gy IR (n = 6), and cis-fib+20 Gy IR (n = 9). Subpleural tumor implantation was performed on day 0 with 1 million syngeneic rat mesothelioma cells (IL45-luciferase). Tumors were resected on day 9, followed by treatment with intracavitary cis-fib or vehicle control (NaCl-fib). On day 12, computed tomography–guided local irradiation in a single high dose of the former tumor region was applied. Results: We observed only short-term side effects related to 20 Gy radiotherapy. Compared to 20 Gy, 10 Gy IR did not show an impact on tumor growth. At 3 days after treatment with 20 Gy IR (day 15 of the experiment), we detected significantly smaller tumors in the cis-fib+IR group compared to IR alone (mean tumor growth, 252% vs 539%; P = .04). On day 21, there was a significant difference in tumor growth between cis-fib–treated and cis-fib+IR– treated tumors (mean tumor growth, 2295% vs 660%; P = .01). Conclusions: Localized treatment after tumor resection in PM aims to improve local tumor control. Irradiation applied in combination with intracavitary cis-fib in rats is safe up to a dosage of 20 Gy and shows an additive effect on tumor growth delay compared to the single treatments.

Details

Language :
English
ISSN :
26662736
Volume :
22
Issue :
491-503
Database :
Directory of Open Access Journals
Journal :
JTCVS Open
Publication Type :
Academic Journal
Accession number :
edsdoj.4c0a86ac0a6347b3b502279894e7c307
Document Type :
article
Full Text :
https://doi.org/10.1016/j.xjon.2024.07.024