Author:
Volpe Stefania,Zaffaroni Mattia,Piperno Gaia,Vincini Maria Giulia,Zerella Maria Alessia,Mastroleo Federico,Cattani Federica,Fodor Cristiana Iuliana,Bellerba Federica,Bonaldi Tiziana,Bonizzi Giuseppina,Ceci Francesco,Cremonesi Marta,Fusco Nicola,Gandini Sara,Garibaldi Cristina,Torre Davide La,Noberini Roberta,Petralia Giuseppe,Spaggiari Lorenzo,Venetis Konstantinos,Orecchia Roberto,Casiraghi Monica,Jereczek-Fossa Barbara Alicja
Abstract
Abstract
Background
Currently, main treatment strategies for early-stage non-small cell lung cancer (ES-NSCLC) disease are surgery or stereotactic body radiation therapy (SBRT), with successful local control rates for both approaches. However, regional and distant failure remain critical in SBRT, and it is paramount to identify predictive factors of response to identify high-risk patients who may benefit from more aggressive approaches. The main endpoint of the MONDRIAN trial is to identify multi-omic biomarkers of SBRT response integrating information from the individual fields of radiomics, genomics and proteomics.
Methods
MONDRIAN is a prospective observational explorative cohort clinical study, with a data-driven, bottom-up approach. It is expected to enroll 100 ES-NSCLC SBRT candidates treated at an Italian tertiary cancer center with well-recognized expertise in SBRT and thoracic surgery. To identify predictors specific to SBRT, MONDRIAN will include data from 200 patients treated with surgery, in a 1:2 ratio, with comparable clinical characteristics. The project will have an overall expected duration of 60 months, and will be structured into five main tasks: (i) Clinical Study; (ii) Imaging/ Radiomic Study, (iii) Gene Expression Study, (iv) Proteomic Study, (v) Integrative Model Building.
Discussion
Thanks to its multi-disciplinary nature, MONDRIAN is expected to provide the opportunity to characterize ES-NSCLC from a multi-omic perspective, with a Radiation Oncology-oriented focus. Other than contributing to a mechanistic understanding of the disease, the study will assist the identification of high-risk patients in a largely unexplored clinical setting. Ultimately, this would orient further clinical research efforts on the combination of SBRT and systemic treatments, such as immunotherapy, with the perspective of improving oncological outcomes in this subset of patients.
Trial registration
The study was prospectively registered at clinicaltrials.gov (NCT05974475).
Funder
Fondazione AIRC per la ricerca sul cancro ETS
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics,Oncology
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献