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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06335290
Other study ID # IEO 725
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 22, 2018
Est. completion date December 31, 2024

Study information

Verified date March 2024
Source European Institute of Oncology
Contact Barbara Alicja Jereczek
Phone +39 02 57489326
Email barbara.jereczek@ieo.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluation of clinical and dosimetric aspects, tolerance, and effectiveness of thoracic radiotherapy treatments in patients undergoing radiotherapy for primary or secondary neoplasms localized in the thoracic anatomical region.


Description:

Approximately 60% of patients with neoplasms receive radiotherapy as part of their oncological treatment. Various primary tumors as well as metastases of various origins can be localized in the thoracic anatomical region. Patients with such neoplastic localizations will therefore receive radiotherapy treatment possibly associated with other systemic or surgical treatments. Treatment choice is usually established following multidisciplinary discussions, based on disease characteristics and stage, concurrent pathologies and pharmacological treatments, patient preferences, and functional aspects. The collection of data related to radiotherapy plays a crucial role in understanding various clinical aspects of the treatment itself. The availability of data from an increasing number of patients will allow the identification of clinical situations or technical parameters of radiotherapy correlated with treatment tolerance and effectiveness, aiming to identify the best treatment for these oncological pathologies. This project aims to collect data related to radiotherapy treatments for primary or secondary neoplasms of the thoracic region for scientific dissemination with the goal of establishing the basis for evaluating achieved results over time, and deriving from these elements useful for guiding the most effective treatment strategies and appropriate operational protocols.


Recruitment information / eligibility

Status Recruiting
Enrollment 13200
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patients treated with radiotherapy for curative, palliative, neo-adjuvant, and adjuvant purposes in the thoracic region include those with: - Primary bone tumors, - Primary soft tissue tumors, - Primary tumors of the cardio-circulatory system, - Primary tumors of the lymphatic system, - Primary tumors of the nervous system and skin, - Secondary metastases from various origins localized in the thoracic region. 2. Signed informed consent Exclusion Criteria: 1. Radiotherapy in districts other than the thoracic region.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy European Institute of Oncology Milan

Sponsors (1)

Lead Sponsor Collaborator
European Institute of Oncology

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival Number of patients death 5 years
Primary Disease free survival Number of oncological event (local recurrence, distant metastasis, other primary tumor) 5 years
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