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The ELECLA trial: A multicentre randomised control trial on outcomes of neoadjuvant treatment on locally advanced colon cancer.
Arredondo, Jorge; Almeida, Ana; Castañón, Carmen; Sánchez, Carlos; Villafañe, Amaya; Tejedor, Patricia; Simó, Vicente; Baixauli, Jorge; Rodríguez, Javier; Pastor, Carlos.
Afiliação
  • Arredondo J; Department of General Surgery, Clínica Universidad de Navarra, University of Navarra, Pamplona, Spain.
  • Almeida A; Institute of Health Research of Navarra (IdisNA), Pamplona, Spain.
  • Castañón C; Department of General Surgery, Clínica Universidad de Navarra, University of Navarra, Pamplona, Spain.
  • Sánchez C; Department of Oncology, University Hospital of León, Leon, Spain.
  • Villafañe A; Department of General Surgery, Clínica Universidad de Navarra, University of Navarra, Pamplona, Spain.
  • Tejedor P; Institute of Health Research of Navarra (IdisNA), Pamplona, Spain.
  • Simó V; Department of General Surgery, University Hospital of León, Leon, Spain.
  • Baixauli J; Department of General Surgery, University Hospital Gregorio Marañón, Madrid, Spain.
  • Rodríguez J; Department of General Surgery, University Hospital Río Hortega, Valladolid, Spain.
  • Pastor C; Department of General Surgery, Clínica Universidad de Navarra, University of Navarra, Pamplona, Spain.
Colorectal Dis ; 26(4): 745-753, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38362850
ABSTRACT

BACKGROUND:

Colon cancer (CC) is a public health concern with increasing incidence in younger populations. Treatment for locally advanced CC (LACC) involves oncological surgery and adjuvant chemotherapy (AC) to reduce recurrence and improve overall survival (OS). Neoadjuvant chemotherapy (NAC) is a novel approach for the treatment of LACC, and research is underway to explore its potential benefit in terms of survival. This trial will assess the efficacy of NAC in LACC.

METHODS:

This is a multicentre randomised, parallel-group, open label controlled clinical trial. Participants will be selected based on homogenous inclusion criteria and randomly assigned to two treatment groups NAC, surgery, and AC or surgery followed by AC. The primary aim of this study is to evaluate the 2-year progression-free survival (PFS), with secondary outcomes including 5-year PFS, 2- and 5-year OS, toxicity, radiological and pathological response, morbidity, and mortality.

DISCUSSION:

The results of this study will determine whether NAC induces a clinical and histological tumour response in patients with CCLA and if this treatment sequence improves survival without increasing morbidity and mortality. REGISTRATION NUMBER NCT04188158.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Terapia Neoadjuvante Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Terapia Neoadjuvante Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article