Standard (8 weeks) vs long (12 weeks) timing to minimally-invasive surgery after NeoAdjuvant Chemoradiotherapy for rectal cancer: a multicenter randomized controlled parallel group trial (TiMiSNAR)
Igor Monsellato,
Filippo Alongi,
Elisa Bertocchi,
Stefania Gori,
Giacomo Ruffo,
Elisa Cassinotti,
Ludovica Baldarti,
Luigi Boni,
Graziano Pernazza,
Fabio Pulighe,
Carlo De Nisco,
Roberto Perinotti,
Emilio Morpurgo,
Tania Contardo,
Enzo Mammano,
Ugo Elmore,
Roberto Delpini,
Riccardo Rosati,
Federico Perna,
Andrea Coratti,
Benedetta Menegatti,
Sergio Gentilli,
Paolo Baroffio,
Piero Buccianti,
Riccardo Balestri,
Cristina Ceccarelli,
Valter Torri,
Davide Cavaliere,
Leonardo Solaini,
Giorgio Ercolani,
Elena Traverso,
Vittorio Fusco,
Maura Rossi,
Fabio Priora,
G. Numico,
Paola Franzone,
Sara Orecchia
Affiliations
Igor Monsellato
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo
Filippo Alongi
Ospedale Sacro Cuore Don Calabria
Elisa Bertocchi
Ospedale Sacro Cuore Don Calabria
Stefania Gori
Ospedale Sacro Cuore Don Calabria
Giacomo Ruffo
Ospedale Sacro Cuore Don Calabria
Elisa Cassinotti
Department of Surgery, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan
Ludovica Baldarti
Department of Surgery, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan
Luigi Boni
Department of Surgery, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan
Graziano Pernazza
Azienda Ospedaliera San Giovanni Addolorata
Fabio Pulighe
Ospedale San Francesco
Carlo De Nisco
Ospedale San Francesco
Roberto Perinotti
Ospedale degli Infermi
Emilio Morpurgo
Ospedale Civile Pietro Cosma, Camposampiero/Ospedale Sant’Antonio
Tania Contardo
Ospedale Civile Pietro Cosma
Enzo Mammano
Ospedale Civile Pietro Cosma, Camposampiero/Ospedale Sant’Antonio
Ugo Elmore
Ospedale San raffaele IRCCS
Roberto Delpini
Ospedale San raffaele IRCCS
Riccardo Rosati
Ospedale San raffaele IRCCS
Federico Perna
Azienda Ospedaliero Universitaria Careggi
Andrea Coratti
Azienda Ospedaliero Universitaria Careggi
Benedetta Menegatti
Azienda Ospedaliero Universitaria Careggi
Sergio Gentilli
Azienda Ospedaliero Universitaria Maggiore Della Carità
Paolo Baroffio
Azienda Ospedaliero Universitaria Maggiore Della Carità
Piero Buccianti
Azienda Ospedaliero Universitaria Pisana
Riccardo Balestri
Azienda Ospedaliero Universitaria Pisana
Cristina Ceccarelli
Azienda Ospedaliero Universitaria Pisana
Valter Torri
Istituto di Ricerche Farmacologiche Mario Negri IRCCS
Davide Cavaliere
Ospedale G.B. Morgagni L. Pierantoni
Leonardo Solaini
Ospedale G.B. Morgagni L. Pierantoni
Giorgio Ercolani
Ospedale G.B. Morgagni L. Pierantoni
Elena Traverso
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo
Vittorio Fusco
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo
Maura Rossi
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo
Fabio Priora
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo
G. Numico
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo
Paola Franzone
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo
Sara Orecchia
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo
Abstract Background The optimal timing of surgery in relation to chemoradiation is still controversial. Retrospective analysis has demonstrated in the recent decades that the regression of adenocarcinoma can be slow and not complete until after several months. More recently, increasing pathologic Complete Response rates have been demonstrated to be correlated with longer time interval. The purpose of the trial is to demonstrate if delayed timing of surgery after neoadjuvant chemoradiotherapy actually affects pathologic Complete Response and reflects on disease-free survival and overall survival rather than standard timing. Methods The trial is a multicenter, prospective, randomized controlled, unblinded, parallel-group trial comparing standard and delayed surgery after neoadjuvant chemoradiotherapy for the curative treatment of rectal cancer. Three-hundred and forty patients will be randomized on an equal basis to either robotic-assisted/standard laparoscopic rectal cancer surgery after 8 weeks or robotic-assisted/standard laparoscopic rectal cancer surgery after 12 weeks. Discussion To date, it is well-know that pathologic Complete Response is associated with excellent prognosis and an overall survival of 90%. In the Lyon trial the rate of pCR or near pathologic Complete Response increased from 10.3 to 26% and in retrospective studies the increase rate was about 23–30%. These results may be explained on the relationship between radiation therapy and tumor regression: DNA damage occurs during irradiation, but cellular lysis occurs within the next weeks. Study results, whether confirmed that performing surgery after 12 weeks from neoadjuvant treatment is advantageous from a technical and oncological point of view, may change the current pathway of the treatment in those patient suffering from rectal cancer. Trial registration ClinicalTrials.gov NCT3465982.