The Impact of Radiotherapy on Oligometastatic Cancer

NCT05933876 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2024-11-18

No results posted yet for this study

Summary

Metastases represent the most threatening challenge in cancer. One of the management strategies for patients with Oligometastatic Cancer (OC) is Stereotactic ABlative Radiotherapy (SABR). However, there are few studies, and there is no defined clinical standard, nor are the radiobiological mechanisms that contribute to treatment response well understood. The focus should be on generating evidence to guide the personalization of radiotherapy beyond solely technological and anatomical precision. This could be achieved by recollecting clinical and biological data from patients that undergo this treatment and analyzing them to ultimately predict, with the help of artificial intelligence, which patients will be the most beneficiary and improve their survival rate.

Conditions

Interventions

DIAGNOSTIC_TEST

To propose a diagnostic test to determine the viability of Stereotactic ABlative Radiotherapy (SABR).

Analyze clinical data, medical images and molecular circulating features to propose which variables serve to select the patients that will achieve complete response after SABR.

DIAGNOSTIC_TEST

To propose a diagnostic test to determine the effectiveness of SABR.

Collect blood samples at five different time points before and after treatment and analyze circulating tumoral DNA, medical images, and metabolites to monitor the effect of SABR and its effectiveness.

DIAGNOSTIC_TEST

To propose a diagnostic test for Oligometastatic Cancer (OC).

Analyze circulating tumoral DNA and metabolites from blood samples in search of the profile of OC.

Sponsors & Collaborators

  • Hospital Ruber Internacional

    collaborator OTHER
  • Hospital Universitario Rey Juan Carlos

    collaborator OTHER
  • Quirón Madrid University Hospital

    collaborator OTHER
  • Hospital de La Luz

    collaborator OTHER
  • Institut Català d'Oncologia

    collaborator OTHER
  • Hospital Arnau de Vilanova

    collaborator OTHER
  • Hospital Universitari Sant Joan de Reus

    collaborator OTHER
  • Hospital Universitario Virgen Macarena

    collaborator OTHER
  • Hospital Universitario Reina Sofia de Cordoba

    collaborator OTHER_GOV
  • Hospital General Universitario de Valencia

    collaborator OTHER
  • Hospital Clínico Universitario de Valencia

    collaborator OTHER
  • Complejo Hospitalario Universitario de Albacete

    collaborator OTHER
  • Hospital de Terrassa

    collaborator OTHER
  • Hospital Universitario Ramon y Cajal

    collaborator OTHER
  • Hospital del Mar

    collaborator OTHER
  • Hospital Provincial de Castellon

    collaborator OTHER
  • Hospital de la Santa creu i Sant Pau - Barcelona

    collaborator OTHER
  • HM Sanchinarro University Hospital

    collaborator OTHER
  • Hospital Miguel Servet

    collaborator OTHER
  • University Hospital Virgen de las Nieves

    collaborator OTHER
  • Hospital Vall d'Hebron

    collaborator OTHER
  • Institut Investigacio Sanitaria Pere Virgili

    lead OTHER

Principal Investigators

  • Meritxell Arenas, PhD. · Universitat Rovira i Virgili, Hospital Universitari Sant Joan de Reus

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-01
Primary Completion
2037-12-31
Completion
2037-12-31

Countries

  • Spain

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05933876 on ClinicalTrials.gov