Oxaliplatin, fluorouracil, and leucovorin versus fluorouracil and leucovorin as adjuvant chemotherapy for locally advanced rectal cancer after preoperative chemoradiotherapy (ADORE): an open-label, multicentre, phase 2, randomised controlled trial

2014 ◽  
Vol 15 (11) ◽  
pp. 1245-1253 ◽  
Author(s):  
Yong Sang Hong ◽  
Byung-Ho Nam ◽  
Kyu-pyo Kim ◽  
Jeong Eun Kim ◽  
Seong Joon Park ◽  
...  
2015 ◽  
Vol 16 (8) ◽  
pp. 957-966 ◽  
Author(s):  
Julio Garcia-Aguilar ◽  
Oliver S Chow ◽  
David D Smith ◽  
Jorge E Marcet ◽  
Peter A Cataldo ◽  
...  

2016 ◽  
Vol 34 (27) ◽  
pp. 3300-3307 ◽  
Author(s):  
Yanhong Deng ◽  
Pan Chi ◽  
Ping Lan ◽  
Lei Wang ◽  
Weiqing Chen ◽  
...  

Purpose Total mesorectal excision with fluorouracil-based preoperative chemoradiotherapy and postoperative chemotherapy is a standard treatment of locally advanced rectal cancer. This study investigated the addition of oxaliplatin with and without preoperative radiotherapy. Methods In this multicenter, open-label, phase III trial, we randomly assigned (1:1:1) Chinese adults (age 18 to 75 years) with locally advanced stage II/III rectal cancer to three treatments: five 2-week cycles of infusional fluorouracil (leucovorin 400 mg/m2, fluorouracil 400 mg/m2, and fluorouracil 2.4 g/m2 over 48 h) plus radiotherapy (46.0 to 50.4 Gy delivered in 23 to 25 fractions during cycles 2 through 4) followed by surgery and seven cycles of infusional fluorouracil, the same treatment plus intravenous oxaliplatin 85 mg/m2 on day 1 of each cycle (modified FOLFOX6 [mFOLFOX6]), or four to six cycles of mFOLFOX6 followed by surgery and six to eight cycles of mFOLFOX6. Random assignment was performed by using computer-generated block randomization codes. The primary end point was 3-year disease-free survival. Secondary end points of histopathologic response and toxicity are reported. Results A total of 495 patients were enrolled from June 2010 to February 2015; 475 were evaluable (fluorouracil-radiotherapy, n = 155; mFOLFOX6-radiotherapy, n = 157; mFOLFOX6, n = 163). In the fluorouracil-radiotherapy, mFOLFOX6-radiotherapy, and mFOLFOX6 groups, the rate of pathologic complete response (pCR) was 14.0%, 27.5%, and 6.6%, and downstaging (ypStage 0 to 1) was achieved by 37.1%, 56.4%, and 35.5% of patients, respectively. Higher toxicity and more postoperative complications were observed in patients who received radiotherapy. Conclusion mFOLFOX6-based preoperative chemoradiotherapy results in a higher pCR rate than fluorouracil-based treatment. Perioperative mFOLFOX6 alone had inferior results and a lower pCR rate than chemoradiotherapy but led to a similar downstaging rate as fluorouracil-radiotherapy, with less toxicity and fewer postoperative complications.


2019 ◽  
Vol 133 ◽  
pp. S191 ◽  
Author(s):  
A. Couwenberg ◽  
H.M. Verkooijen ◽  
M. Berbee ◽  
J.P.M. Burbach ◽  
S. Hoendervangers ◽  
...  

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