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Organ Sparing for Locally Advanced Rectal Cancer after Neoadjuvant Treatment Followed by Electrochemotherapy

Authors :
Guglielmo Nasti
Ugo Pace
Vincenza Granata
Carmela Romano
Paolo Delrio
Gerardo Botti
Massimiliano Di Marzo
Antonio Avallone
C. Sassaroli
Daniela Rega
Piera Maiolino
Biagio Pecori
Carmela Cervone
Fabiana Tatangelo
Roberta Fusco
Valeria D’Alessio
Antonella Petrillo
Source :
Cancers, Cancers, Vol 13, Iss 3199, p 3199 (2021)
Publication Year :
2021
Publisher :
MDPI, 2021.

Abstract

Simple Summary This is a Phase II randomized controlled trial conducted with the aim of investigating whether the use of Electrochemotherapy after neoadjuvant therapy (ECT) and before surgery in patients with major clinical response allows for a more conservative surgical approach in patients with Locally Advanced Rectal Cancer (LARC) in comparison with the control group that will not receive ECT. The treatment response, in both the control arm and in the treatment arm, will be assessed using the histopathological tumor regression grade on tissue specimens after local excision. Abstract Background: Currently, 45–55% of rectal cancer patients receive preoperative chemo- radio-therapy for Locally Advanced Rectal Cancer (LARC). The idea of our study is to use Electrochemotherapy (ECT) before surgery, in patients with major clinical response after neoadjuvant therapy, to allow for a more conservative surgical approach. Objective: To evaluate the increase of the complete response rate after neoadjuvant treatment in LARC and to spare organ function due to total mesorectal excision (TME). Patients and Methods: This is a Phase II randomized controlled trial enrolling 70 patients that will be developed in two stages. In the first step, 28 patients will be enrolled: 14 of these will receive ECT for four weeks after neo-adjuvant treatment and then local excision (treatment group) and 14 patients will receive neo-adjuvant treatment and then local excision (control group). If an increase of response rate is observed in the first stage, and/or feasibility/safety is demonstrated, the second stage of the trial will be performed, enrolling an additional 42 patients. The treatment response. in both the control arm and the treatment arm, will be assessed using the histopathological tumor regression grade on tissue specimens after local excision.

Details

Language :
English
ISSN :
20726694
Volume :
13
Issue :
13
Database :
OpenAIRE
Journal :
Cancers
Accession number :
edsair.doi.dedup.....5e7057ef6259018f74285d76d45c4957