Improving the Success Rate for Thoracic Radiotherapy Through Specific Cardiac Substructure Dosimetry: Location Matters. (LOCATION MATTERS)

Locally Advanced Lung Non-Small Cell Carcinoma Clinical Trial

— LM  

Official title:

"Improving the Success Rate for Thoracic Radiotherapy Through Specific Cardiac Substructure Dosimetry: Location Matters - a Prospective Study"

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06361784
• Other study ID #: INT216-23
• Secondary ID: MFAG27480
• Status: Recruiting
• Start date: March 29, 2024
• Est. completion date: March 29, 2029

Study information

• Verified date: November 2023
• Source: Fondazione IRCCS Istituto Nazionale dei Tumori, Milano
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The prospective study LOCATION MATTERS aims to investigate the radiation-induced damage to the heart and the cardiovascular system in patients treated with thoracic radiotherapy. Patients enrolled in the study will complete a set of extensive measures at the baseline, end of RT, and 9 months after treatment. Ultrasound exams, CT scans, pulmonary tests and wearable devices will assess functional and morphological parameters and the association with their variation and the dose delivered to the heart substructures and to the normal lung.

Description:

A cohort of locally advanced lung cancer patients treated with RT will be enrolled at Fondazione IRCCS Istituto dei Tumori. Comorbidities and cardiovascular risk factors will be recorded for all the patients. Heart substructures will be automatically contoured on each patient to provide details on the dose distribution. The investigators will plan an extensive set of cardiac tests before, at the end of RT and 8 months after treatment (to assess cardiac remodelling and pt recovery). It will include an electrocardiogram, echo cardio, spirometry, blood circulating biomarkers (Troponin and Natriuretic peptide tests) and cardiac calcium score from CT. In addition, the researchers will include a set of measures by the use of a vascular ultrasound machine. This machine will allow the investigation of subclinical vascular organ damage indicators, including carotid distention and intima-media thickness (descriptor of the carotid inflammatory state), through a simultaneous and automatic procedure from raw imaging data. This guarantees the extraction of highly reproducible and operator-independent features. Finally, the project will provide smartwatch devices to the patients aiming to get longitudinal information on heart rate, breathe per minute, stress level, Pulse Ox and recovery time after customised exercises. The study's aim is to associate the most "radiosensitive" functional parameters or biomarkers (i.e. the more prone to vary after RT) with the dose delivered to the HSs. First, researchers will analyze the variations of the parameters in patients with doses above and below the identified constraints from the literature. Second, investigators will test whether a dose relationship model can continuously describe the changes for the parameters with statistically significant differences. The primary focus will be the comprehension of the dose response for morphological and functional parameters that are altered chronically, i.e. with more compromised values at the 1-year measurement. For this study, the investigators estimate to enrol 150 lung cancer patients in 3 years. Information on the OS and MACEs will be registered during the clinical standard FU. Researchers expect to fulfil an FU rate of 90% two years after RT completion. Registering MACEs during the FU time will allow to perform a first direct comparison of the competing part of Task 1.3.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 150
• Est. completion date: March 29, 2029
• Est. primary completion date: March 29, 2029
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Patients with NSCLC
• Patients with locally advanced disease (Stage 3)
• Patients treated with RT at Fondazione IRCCS Istituto Nazionale dei Tumori

Exclusion Criteria:

• Previous thoracic radiotherapy
• Previous heart surgery

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Locally Advanced Lung Non-Small Cell Carcinoma

Locations

Country	Name	City	State
Italy	Fondazione IRCCS Istituto Nazionale dei Tumori	Milan

Sponsors (2)

Lead Sponsor	Collaborator
Fondazione IRCCS Istituto Nazionale dei Tumori, Milano	Politecnico di Milano

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Longitudinal variation of cardiopulmonary functional parameters	A set of parameters will be assessed through the use of a smartwatch device. Variation with time will be compared to identify risk factors associated to patterns in time evolution.	Daily evaluations from baseline to 9 months of FU
Other	Texture variation in the heart substructures	Quantitative image analysis will be performed on protocol CT scans to assess morphology and tissue composition	Baseline - End RT - 9 months after RT completion
Primary	Variation in eco-cardio and eco-vascular parameters after thoracic radiotherapy	A set of ultrasound parameters will be normalised to the individual patient value at the baseline. We will evaluate an acute reaction (end of RT) and a late reaction/recovery assessment at 9 months after RT	Baseline - End RT - 9 months after RT completion
Secondary	Major adverse cardiac events post-RT	MACEs will be evaluated and recorded during patient FU as a no/yes variable	Baseline - End RT - 9 months after RT completion
Secondary	Increase in cardiac calcification after RT	Calcification will be assessed through automatic software able to detect calcifications in the heart based on CT scans. Values will be compared with the baseline	Baseline - End RT - 9 months after RT completion