Effect of Celecoxib vs Placebo Added to Standard Adjuvant Therapy on Disease-Free Survival Among Patients With Stage III Colon Cancer: The CALGB/SWOG 80702 (Alliance) Randomized Clinical Trial.
Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Celecoxib
/ adverse effects
Chemotherapy, Adjuvant
Colonic Neoplasms
/ drug therapy
Cyclooxygenase 2 Inhibitors
/ adverse effects
Disease-Free Survival
Female
Humans
Male
Middle Aged
Neoplasm Recurrence, Local
/ epidemiology
Neoplasm Staging
Patient Compliance
Proportional Hazards Models
Secondary Prevention
Survival Rate
Treatment Failure
Young Adult
Journal
JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160
Informations de publication
Date de publication:
06 04 2021
06 04 2021
Historique:
entrez:
6
4
2021
pubmed:
7
4
2021
medline:
22
4
2021
Statut:
ppublish
Résumé
Aspirin and cyclooxygenase 2 (COX-2) inhibitors have been associated with a reduced risk of colorectal polyps and cancer in observational and randomized studies. The effect of celecoxib, a COX-2 inhibitor, as treatment for nonmetastatic colon cancer is unknown. To determine if the addition of celecoxib to adjuvant chemotherapy with fluorouracil, leucovorin, and oxaliplatin (FOLFOX) improves disease-free survival in patients with stage III colon cancer. Cancer and Leukemia Group B (Alliance)/Southwest Oncology Group 80702 was a 2 × 2 factorial design, phase 3 trial conducted at 654 community and academic centers throughout the United States and Canada. A total of 2526 patients with stage III colon cancer were enrolled between June 2010 and November 2015 and were followed up through August 10, 2020. Patients were randomized to receive adjuvant FOLFOX (every 2 weeks) for 3 vs 6 months with or without 3 years of celecoxib (400 mg orally daily; n = 1263) vs placebo (n = 1261). This report focuses on the results of the celecoxib randomization. The primary end point was disease-free survival, measured from the time of randomization until documented recurrence or death from any cause. Secondary end points included overall survival, adverse events, and cardiovascular-specific events. Of the 2526 patients who were randomized (mean [SD] age, 61.0 years [11 years]; 1134 women [44.9%]), 2524 were included in the primary analysis. Adherence with protocol treatment, defined as receiving celecoxib or placebo for more than 2.75 years or continuing treatment until recurrence, death, or unacceptable adverse events, was 70.8% for patients treated with celecoxib and 69.9% for patients treated with placebo. A total of 337 patients randomized to celecoxib and 363 to placebo experienced disease recurrence or died, and with 6 years' median follow-up, the 3-year disease-free survival was 76.3% for celecoxib-treated patients vs 73.4% for placebo-treated patients (hazard ratio [HR] for disease recurrence or death, 0.89; 95% CI, 0.76-1.03; P = .12). The effect of celecoxib treatment on disease-free survival did not vary significantly according to assigned duration of adjuvant chemotherapy (P for interaction = .61). Five-year overall survival was 84.3% for celecoxib vs 81.6% for placebo (HR for death, 0.86; 95% CI, 0.72-1.04; P = .13). Hypertension (any grade) occurred while treated with FOLFOX in 14.6% of patients in the celecoxib group vs 10.9% of patients in the placebo group, and a grade 2 or higher increase in creatinine levels occurred after completion of FOLFOX in 1.7% vs 0.5% of patients, respectively. Among patients with stage III colon cancer, the addition of celecoxib for 3 years, compared with placebo, to standard adjuvant chemotherapy did not significantly improve disease-free survival. ClinicalTrials.gov Identifier: NCT01150045.
Identifiants
pubmed: 33821899
pii: 2778113
doi: 10.1001/jama.2021.2454
pmc: PMC8025124
doi:
Substances chimiques
Cyclooxygenase 2 Inhibitors
0
Celecoxib
JCX84Q7J1L
Banques de données
ClinicalTrials.gov
['NCT01150045']
Types de publication
Clinical Trial, Phase III
Comparative Study
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1277-1286Subventions
Organisme : NCI NIH HHS
ID : U10 CA180868
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233320
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189954
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233196
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180794
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180888
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233339
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180821
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233337
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180863
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233180
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180820
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180882
Pays : United States
Commentaires et corrections
Type : CommentIn
Références
Lancet Gastroenterol Hepatol. 2019 Nov;4(11):854-862
pubmed: 31477558
N Engl J Med. 2007 Jul 26;357(4):360-9
pubmed: 17652651
J Clin Oncol. 2010 Oct 20;28(30):4575-80
pubmed: 20837956
Nat Rev Cancer. 2016 Mar;16(3):173-86
pubmed: 26868177
N Engl J Med. 2018 Mar 29;378(13):1177-1188
pubmed: 29590544
Am J Public Health. 1996 May;86(5):726-8
pubmed: 8629727
J Natl Cancer Inst. 2014 Nov 27;107(1):345
pubmed: 25432409
N Engl J Med. 2003 Mar 6;348(10):883-90
pubmed: 12621132
BMC Cancer. 2018 Dec 4;18(1):1210
pubmed: 30514262
Cancer Prev Res (Phila). 2012 Feb;5(2):164-78
pubmed: 22084361
Recent Results Cancer Res. 2007;174:73-8
pubmed: 17302187
Dig Liver Dis. 2018 Mar;50(3):305-307
pubmed: 29402752
Cancer Causes Control. 2003 Jun;14(5):413-8
pubmed: 12946035
N Engl J Med. 2012 Oct 25;367(17):1596-606
pubmed: 23094721
JAMA. 2009 Aug 12;302(6):649-58
pubmed: 19671906
Gut. 2015 Sep;64(9):1419-25
pubmed: 25239119
Anticancer Res. 2014 Dec;34(12):7407-14
pubmed: 25503181
J Clin Oncol. 2011 Apr 10;29(11):1465-71
pubmed: 21383294
J Clin Oncol. 2013 Dec 1;31(34):4297-305
pubmed: 24062397
Gut. 2010 Dec;59(12):1670-9
pubmed: 20844293
Ann Oncol. 2020 Apr;31(4):480-486
pubmed: 32085892
Gut. 2011 Apr;60(4):491-8
pubmed: 21051449
CA Cancer J Clin. 2021 Feb 4;:
pubmed: 33538338
JAMA. 2013 Jun 26;309(24):2563-71
pubmed: 23800934
Pharmacogenomics J. 2008 Aug;8(4):237-47
pubmed: 18195728
JAMA. 1990 Sep 19;264(11):1444-50
pubmed: 2202842
Lancet Oncol. 2012 May;13(5):518-27
pubmed: 22440112
Trials. 2011 Dec 14;12:261
pubmed: 22168568
Biometrics. 1983 Jun;39(2):499-503
pubmed: 6354290
N Engl J Med. 2000 Jun 29;342(26):1960-8
pubmed: 10874065
CA Cancer J Clin. 2021 Jan;71(1):7-33
pubmed: 33433946
JAMA Intern Med. 2014 May;174(5):732-9
pubmed: 24687028
N Engl J Med. 2004 Jun 3;350(23):2343-51
pubmed: 15175436