Upfront Surgery Versus NeoAdjuvant Chemotherapy Followed by Surgery for Resectable Advanced Gastric Cancer: SNAC Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSan Luigi Gonzaga Hospital

About this trial

Based on the concerns about the actual low strength of evidence of the efficacy of NAC on survival of proper gastric cancer treated with adequate D2 gastrectomy as compared to the results of optimal upfront surgery (S), and considering the actual difficulties of additional RCTs, the aim of this study is to assess the non-inferiority of upfront surgery alone with optimal D2 dissection compared to NAC regimens followed by surgery. Methods: This is a nationwide Multicenter observational retrospective study with matched comparison of two therapeutic strategies (NAC vs S). We will include patients with cT\>2, every cN M0, or with every T and N+ M0, histologically proven adenocarcinoma of the stomach, submitted either to pre- or peri-operative treatment and D2 gastrectomy or to upfront D2 gastrectomy, between January 2012 and December 2019, followed by adjuvant treatment when recommended.

All patients matching the inclusion/exclusion criteria will be registered into the study and classified into one of the two arms: a, patients who underwent pre- or perioperative treatment and D2 gastrectomy (NAC) or b, patients submitted to upfront D2 gastrectomy (S). Given the results reported in the "FLOT" trial, a 3-years OS of 55% in the control arm (NAC) was assumed. Three-year OS in the experimental arm (S) was assumed to be 47.4% under the null hypothesis of inferiority and 55% under the alternative hypothesis of non-inferiority. A sample size of 684 patients (342 in each arm) achieves 80% power to detect a non-inferiority margin Hazard Ratio of 1.25

Eligibility criteria

Qualifiers

3.1.1. Locally advanced (T>2 any N or N+ any T) histologically proven adenocarcinoma of the stomach without distant metastases (M0) and without infiltration of adjacent structures and organs.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • pre- or perioperative treatment and D2 gastrectomy

Treatment groups

684 Participants
are divided into 2 treatment groups

Sponsors and collaborators

San Luigi Gonzaga Hospital

Lead sponsor

Azienda Ospedaliera Universitaria Senese

Collaborator

IRCCS Ospedale San Raffaele

Collaborator

Federico II University

Collaborator

Azienda Ospedaliero-Universitaria di Parma

Collaborator

Azienda Ospedaliero Universitaria Policlinico Modena

Collaborator

Istituti Tumori Giovanni Paolo II

Collaborator

Fondazione IRCCS Policlinico San Matteo di Pavia

Collaborator

ASST Grande Ospedale Metropolitano Niguarda

Collaborator

Azienda Ospedaliera Sant'Anna

Collaborator

Ospedale di Circolo - Fondazione Macchi

Collaborator

Ospedale San Donato

Collaborator

Government hospital in Forlì, Italy

Collaborator

Istituti Ospitalieri di Cremona

Collaborator

Azienda Ospedaliero-Universitaria Careggi

Collaborator

Azienda ULSS di Verona e Provincia

Collaborator

Azienda Ospedaliera di Perugia

Collaborator

A.O. Ospedale Papa Giovanni XXIII

Collaborator

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

Collaborator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Collaborator

Provincia Autonoma di Trento

Collaborator

University of Florence

Collaborator

Ospedale M. Bufalini Cesena

Collaborator

Azienda Ospedaliera di Padova

Collaborator

Ospedale Guglielmo da Saliceto, Piacenza

Collaborator

Azienda Ospedaliera San Gerardo di Monza

Collaborator

A.O.U. Città della Salute e della Scienza

Collaborator

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Collaborator

Ospedale Santo Stefano

Collaborator

Policlinico Abano Terme

Collaborator

Istituto Europeo di Oncologia

Collaborator

Azienda Ospedaliera OO.RR. S. Giovanni di Dio e Ruggi D'Aragona

Collaborator

Humanitas Hospital, Italy

Collaborator