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NCT05674422

GEMCAD-REVEAL STUDY - Circulating Tumor DNA as a Predictor of Relapse in Patients With Locally Advanced Rectal Cancer.

Sponsor: Grupo Espanol Multidisciplinario del Cancer Digestivo

View on ClinicalTrials.gov

Summary

The evaluation of the tumor response to chemoradiotherapy/total neoadjuvant therapy (CRT/TNT) remains a challenge. The integration of a blood-based biomarker such as ctDNA with clinico-radiological tools could offer the potential advantage of improving accuracy of assessment of tumor response to neoadjuvant therapy. Furthermore, data on functional outcomes and quality of life after total mesorectal excision (TME) and especially after " Watch And Wait" (WW) is scarce. REVEAL is a prospective, multicenter study in which the response to TNT in correlation with liquid biopsy (LB) of patients with rectal cancer in Spain will be evaluated. It is planned to include 120 patients. All patients will be aged 18 years or older, with histologically confirmed rectal adenocarcinoma, located in the mid or distal third (with the inferior margin within 12cm from the anal verge), clinically staged II and III (cT3-T4 and/or any TN+), scheduled to undergo TNT will be eligible. All cases and treatment decisions will be discussed by local Multidisciplinary Boards. Patients will be included consecutively when visiting the corresponding health centers for outpatient visits or hospitalization. The objective of the present study is to evaluate the role of ctDNA in the prediction of relapse in patients diagnosed with locally advanced rectal cancer (LARC) treated with TNT followed by WW or TME based on a clinical assessment of the local response

Official title: Circulating Tumor DNA as a Predictor of Relapse in Patients With Locally Advanced Rectal Cancer Treated With Total Neoadjuvant Therapy Followed by Watch and Wait or Total Mesorectal Excision Based on Clinical Assessment of Response

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

120

Start Date

2023-05-26

Completion Date

2026-07

Last Updated

2024-10-31

Healthy Volunteers

No

Interventions

DRUG

total neoadjuvant therapy

All patients will be aged 18 years or older, with histologically confirmed rectal adenocarcinoma, located in the mid or distal third (with the inferior margin within 12cm from the anal verge), clinically staged II and III (cT3-T4 and/or any TN+), scheduled to undergo TNT will be eligible. All cases and treatment decisions will be discussed by local Multidisciplinary Boards

Locations (15)

Hospital Germans Trias i Pujol - ICO Badalona

Badalona, Barcelona, Spain

Hospital Universitari Mutua de Terrassa

Terrassa, Barcelona, Spain

Hospital Universitario 12 de Octubre

Madrid, Madrid, Spain

H. de la Santa Creu i Sant Pau

Barcelona, Spain

H.U. Vall d'Hebron

Barcelona, Spain

Hospital Clínic, Universitat de Barcelona

Barcelona, Spain

Hospital Del Mar, Barcelona

Barcelona, Spain

Hospital Sant Joan Despí - Moisés Broggi.

Barcelona, Spain

ICO-Hospitalet

Barcelona, Spain

ICO Girona

Girona, Spain

H. Univeristario La Paz

Madrid, Spain

Hospital Quirón Salud Valencia

Valencia, Spain

Hospital Universitari i Politècnic La Fe

Valencia, Spain

Hospital Clínico Universitario Lozano Blesa

Zaragoza, Spain

Hospital Universitario Miguel Servet

Zaragoza, Spain