BRIDGE -1 TRIAL: BReak Interval Delayed surgery for Gastrointestinal Extraperitoneal rectal cancer, a multicentric phase III randomized trial.

Neoadjuvant chemoradiotherapy Personalized treatment Rectal cancer Surgical Interval

Journal

Clinical and translational radiation oncology
ISSN: 2405-6308
Titre abrégé: Clin Transl Radiat Oncol
Pays: Ireland
ID NLM: 101713416

Informations de publication

Date de publication:
May 2022
Historique:
received: 29 12 2021
revised: 04 03 2022
accepted: 05 03 2022
entrez: 28 3 2022
pubmed: 29 3 2022
medline: 29 3 2022
Statut: epublish

Résumé

Neoadjuvant chemoradiotherapy (nCRT) followed by surgery is the standard of care for locally advanced rectal cancer (LARC).Several studies have shown a correlation between a longer interval between the end of nCRT and surgery (surgical interval - SI) and an increased pathological complete response (pCR) rate, with a maximum obtained between 10 and 13 weeks.The primary endpoint of this multicenter, 2-arm randomised trial is to investigate SI lengthening, evaluating the difference in terms of complete response (CR) and Tumor Regression Grade (TRG)1 rate in the two arms. Secondly, the impact of SI lengthening on survival outcomes and quality of life (QoL) will be investigated. Intermediate-risk LARC patients undergoing nCRT will be prospectively included in the study. nCRT will be administered with a total dose of 55 Gy in 25 fractions on Gross Tumor Volume (GTV) plus the corresponding mesorectum of 45 Gy in 25 fractions on the whole pelvis. Chemotherapy with oral capecitabine will be administered continuously.The patients achieving a clinical major or complete response assessed at clinical-instrumental re-evaluation at 7-8 weeks after treatment completion, will be randomized into two groups, to undergo surgery or local excision at 9-11 weeks (control arm) or at 13-16 weeks (experimental arm). Pathological response will be assessed on the surgical specimen using the AJCC TNM v.7 and the TRG according to Mandard. Patients will be followed up to evaluate toxicity and QoL.The promoter center of the trial will conduct the randomization process through an automated procedure to prevent any possible bias.For sample size calculation, using CR difference of 20% as endpoint, 74 patients per arm will be enrolled. The results of this study may prospectively provide a new time frame for the clinical re-evaluation for complete/major responders patients in order to increase the CR rate to nCRT.

Identifiants

pubmed: 35340685
doi: 10.1016/j.ctro.2022.03.002
pii: S2405-6308(22)00015-5
pmc: PMC8943334
doi:

Banques de données

ClinicalTrials.gov
['NCT03581344']

Types de publication

Journal Article

Langues

eng

Pagination

30-36

Informations de copyright

© 2022 Published by Elsevier B.V. on behalf of European Society for Radiotherapy and Oncology.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Giuditta Chiloiro (G)

Department of Diagnostic Imaging, Radiation Oncology and Haematology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Elisa Meldolesi (E)

Department of Diagnostic Imaging, Radiation Oncology and Haematology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Barbara Corvari (B)

Department of Diagnostic Imaging, Radiation Oncology and Haematology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Angela Romano (A)

Department of Diagnostic Imaging, Radiation Oncology and Haematology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Brunella Barbaro (B)

Department of Diagnostic Imaging, Radiation Oncology and Haematology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Claudio Coco (C)

Department of Surgical Sciences, Catholic University of Rome, Rome, Italy.

Antonio Crucitti (A)

Department of Translational Medicine and Surgery, Università Cattolica del Sacro Cuore, Rome, Italy.

Domenico Genovesi (D)

Department of Radiotherapy, "SS Annunziata" Hospital "G. D'Annunzio" University, Chieti, Italy.

Marco Lupattelli (M)

Radiation Oncology Section, General Hospital, Perugia, Italy.

Giovanna Mantello (G)

Department of Oncology and Radiotherapy, Azienda Ospedaliero Universitaria Ospedali Riuniti, Ancona, Italy.

Roberta Menghi (R)

Gemelli Pancreatic Center, CRMPG (Advanced Pancreatic Research Center) Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Mattia Falchetto Osti (M)

Department of Radiation Oncology, "Sapienza" University, Sant'Andrea Hospital, Rome, Italy.

Roberto Persiani (R)

Department of General Surgery, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome - Università Cattolica del Sacro Cuore, Rome, Italy.

Lucio Petruzziello (L)

Digestive Endoscopy Unit, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Riccardo Ricci (R)

Department of Pathology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Luigi Sofo (L)

Department of Gastroenterological, Endocrino-Metabolic and Nephro-Urological Sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome - Università Cattolica del Sacro Cuore, Rome, Italy.

Chiara Valentini (C)

Klinik für Radioonkologie-OncoRay Universitätsklinikum C.G. Carus an der TU, Dresden, Germany.

Antonino De Paoli (A)

Department of Radiation Oncology, Centro di Riferimento Oncologico, Aviano, Italy.

Vincenzo Valentini (V)

Department of Diagnostic Imaging, Radiation Oncology and Haematology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Maria Antonietta Gambacorta (M)

Department of Diagnostic Imaging, Radiation Oncology and Haematology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.

Classifications MeSH