TY - JOUR
T1 - Rectal Sparing Approach After Neoadjuvant Therapy in Patients with Rectal Cancer: The Preliminary Results of the ReSARCh Trial
AU - Marchegiani, Francesco
AU - Palatucci, Valeria
AU - Capelli, Giulia
AU - Capelli, Giovanni
AU - Guerrieri, Mario
AU - Guerrieri, Maria Chiara
AU - Belluco, Claudio
AU - Rega, Daniela
AU - Morpurgo, Emilio
AU - Coco, Claudio
AU - Restivo, Angelo
AU - Restivo, Attilio
AU - De Franciscis, Silvia
AU - Aschele, Carlo
AU - Perin, Alessandro
AU - Bonomo, Michele
AU - Muratore, Andrea
AU - Spinelli, Antonino
AU - Ramuscello, Salvatore
AU - Bergamo, Francesca
AU - Montesi, Giampaolo
AU - Spolverato, Gaya
AU - Del Bianco, Paola
AU - Gambacorta, Maria Antonietta
AU - Delrio, Paolo
AU - Pucciarelli, Salvatore
PY - 2022
Y1 - 2022
N2 - Background: Rectum-preservation for locally advanced rectal cancer has been proposed as an alternative to total mesorectal excision (TME) in patients with major (mCR) or complete clinical response (cCR) after neoadjuvant therapy. The purpose of this study was to report on the short-term outcomes of ReSARCh (Rectal Sparing Approach after preoperative Radio- and/or Chemotherapy) trial, which is a prospective, multicenter, observational trial that investigated the role of transanal local excision (LE) and watch-and-wait (WW) as integrated approaches after neoadjuvant therapy for rectal cancer. Methods: Patients with mid-low rectal cancer who achieved mCR or cCR after neoadjuvant therapy and were fit for major surgery were enrolled. Clinical response was evaluated at 8 and 12 weeks after completion of chemoradiotherapy. Treatment approach, incidence, and reasons for subsequent TME were recorded. Results: From 2016 to 2019, 160 patients were enrolled; mCR or cCR at 12 weeks was achieved in 64 and 96 of patients, respectively. Overall, 98 patients were managed with LE and 62 with WW. In the LE group, Clavien–Dindo 3+ complications occurred in three patients. The rate of cCR increased from 8- to 12-week restaging. Thirty-three (94.3%) of 35 patients with cCR had ypT0–1 tumor. At a median 24 months follow-up, a tumor regrowth was found in 15 (24.2%) patients undergoing WW. Conclusions: LE for patients achieving cCR or mCR is safe. A 12-week interval from chemoradiotherapy completion to LE is correlated with an increased cCR rate. The risk of ypT > is reduced when LE is performed after cCR.
AB - Background: Rectum-preservation for locally advanced rectal cancer has been proposed as an alternative to total mesorectal excision (TME) in patients with major (mCR) or complete clinical response (cCR) after neoadjuvant therapy. The purpose of this study was to report on the short-term outcomes of ReSARCh (Rectal Sparing Approach after preoperative Radio- and/or Chemotherapy) trial, which is a prospective, multicenter, observational trial that investigated the role of transanal local excision (LE) and watch-and-wait (WW) as integrated approaches after neoadjuvant therapy for rectal cancer. Methods: Patients with mid-low rectal cancer who achieved mCR or cCR after neoadjuvant therapy and were fit for major surgery were enrolled. Clinical response was evaluated at 8 and 12 weeks after completion of chemoradiotherapy. Treatment approach, incidence, and reasons for subsequent TME were recorded. Results: From 2016 to 2019, 160 patients were enrolled; mCR or cCR at 12 weeks was achieved in 64 and 96 of patients, respectively. Overall, 98 patients were managed with LE and 62 with WW. In the LE group, Clavien–Dindo 3+ complications occurred in three patients. The rate of cCR increased from 8- to 12-week restaging. Thirty-three (94.3%) of 35 patients with cCR had ypT0–1 tumor. At a median 24 months follow-up, a tumor regrowth was found in 15 (24.2%) patients undergoing WW. Conclusions: LE for patients achieving cCR or mCR is safe. A 12-week interval from chemoradiotherapy completion to LE is correlated with an increased cCR rate. The risk of ypT > is reduced when LE is performed after cCR.
KW - Rectal Cancer
KW - Rectal Cancer
UR - http://hdl.handle.net/10807/298238
U2 - 10.1245/s10434-021-11121-8
DO - 10.1245/s10434-021-11121-8
M3 - Article
SN - 1068-9265
VL - 29
SP - 1880
EP - 1889
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
ER -