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.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
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

1277-1286

Subventions

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

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Auteurs

Jeffrey A Meyerhardt (JA)

Department of Medical Oncology, Dana-Farber/Partners CancerCare, Boston, Massachusetts.

Qian Shi (Q)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota.

Charles S Fuchs (CS)

Yale Cancer Center, Yale School of Medicine, Smilow Cancer Hospital, New Haven, Connecticut.

Jeffrey Meyer (J)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota.

Donna Niedzwiecki (D)

Department of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, North Carolina.

Tyler Zemla (T)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota.

Priya Kumthekar (P)

Feinberg School of Medicine, Northwestern Medicine, Chicago, Illinois.

Katherine A Guthrie (KA)

SWOG Statistics and Data Management Center, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Felix Couture (F)

Hôtel-Dieu de Québec, Quebec, Canada.

Philip Kuebler (P)

Columbus NCI Community Oncology Research Program, Columbus, Ohio.

Johanna C Bendell (JC)

Sarah Cannon Research Institute/Tennessee Oncology, Nashville.

Pankaj Kumar (P)

Illinois CancerCare PC, Peoria, Illinois.

Dequincy Lewis (D)

Cone Health Medical Group, Asheboro, North Carolina.

Benjamin Tan (B)

Siteman Cancer Center, Washington University School of Medicine in St Louis, St Louis, Missouri.

Monica Bertagnolli (M)

Office of the Alliance Group Chair, Brigham and Women's Hospital, Boston, Massachusetts.

Axel Grothey (A)

West Cancer Center & Research Institute, Germantown, Tennessee.

Howard S Hochster (HS)

Rutgers Cancer Institute, New Brunswick, New Jersey.

Richard M Goldberg (RM)

West Virginia University Cancer Institute, Morgantown.

Alan Venook (A)

University of California, San Francisco.

Charles Blanke (C)

SWOG Cancer Research Network Group Chair's Office, Oregon Health and Science University Knight Cancer Institute.

Eileen M O'Reilly (EM)

Memorial Sloan Kettering Cancer Center, Weill Cornell Medical Center, New York, New York.

Anthony F Shields (AF)

Department of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, Michigan.

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