Association of Treatment Adherence With Oncologic Outcomes for Patients With Rectal Cancer: A Post Hoc Analysis of the CAO/ARO/AIO-04 Phase 3 Randomized Clinical Trial.
Adolescent
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Chemotherapy, Adjuvant
Child
Child, Preschool
Disease-Free Survival
Female
Fluorouracil
/ administration & dosage
Humans
Male
Middle Aged
Neoadjuvant Therapy
/ methods
Neoplasm Recurrence, Local
/ drug therapy
Neoplasm Staging
Oxaliplatin
/ administration & dosage
Proportional Hazards Models
Rectal Neoplasms
/ drug therapy
Treatment Adherence and Compliance
/ psychology
Young Adult
Journal
JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861
Informations de publication
Date de publication:
01 09 2020
01 09 2020
Historique:
pubmed:
10
7
2020
medline:
7
2
2021
entrez:
10
7
2020
Statut:
ppublish
Résumé
Despite numerous published phase 3 trials, the association of treatment adherence with outcomes for patients with rectal cancer remains largely unexplored. To analyze the association of treatment adherence with disease-free survival (DFS) among patients with rectal cancer in the CAO/ARO/AIO-04 trial. This post hoc analysis of a phase 3 randomized clinical trial was conducted from July 25, 2006, to February 26, 2010, among 1232 patients from 80 centers with T3 to T4 or node-positive rectal adenocarcinoma. Statistical analysis was performed from May 5, 2019, to February 2, 2020. A total of 625 patients received neoadjuvant fluorouracil-based chemoradiotherapy (nCRT), and a total of 607 patients received fluorouracil-based nCRT with addition of oxaliplatin. Of the 1126 patients who underwent curative surgery, 439 started fluorouracil-based adjuvant chemotherapy and 419 started fluorouracil-based adjuvant chemotherapy with oxaliplatin. The association of adherence with nCRT and adjuvant chemotherapy with DFS was assessed in both groups in the as-treated population. Among the 625 patients (442 men; mean age, 63.0 years) who received fluorouracil nCRT and the 607 patients (430 men; mean age, 63.0 years) who received fluorouracil-based nCRT with addition of oxaliplatin, after a median follow-up of 50 months (interquartile range, 38-61 months), 3-year DFS in the as-treated population was 71.1% in the fluorouracil group and 75.8% in the fluorouracil-oxaliplatin group (hazard ratio [HR], 0.803; 95% CI, 0.651-0.990; P = .04). Overall, 419 patients in the fluorouracil nCRT group (67.0%) and 434 patients in the fluorouracil-oxaliplatin nCRT group (71.5%) received full doses of preoperative nCRT. Likewise, 253 of 439 patients in the fluorouracil group (57.6%) and 134 of 419 patients in the fluorouracil-oxaliplatin group (32.0%) received full doses of adjuvant chemotherapy. Adherence to nCRT was associated with 3-year DFS in both the fluorouracil group (complete vs near complete: HR, 1.325; 95% CI, 0.959-1.832; P = .09; complete vs reduced: HR, 1.877; 95% CI, 1.147-3.072; P = .01) and the fluorouracil-oxaliplatin group (complete vs near complete: HR, 1.501; 95% CI, 0.980-2.299; P = .06; complete vs reduced: HR, 1.724; 95% CI, 1.144-2.596; P = .009) in multivariable analyses. In contrast, adjuvant chemotherapy was not associated with DFS in both the fluorouracil group (complete vs near complete: HR, 0.900; 95% CI, 0.559-1.448; P = .66; complete vs incomplete: HR, 1.057; 95% CI, 0.807-1.386; P = .69) and the fluorouracil-oxaliplatin group (complete vs near complete: HR, 1.155; 95% CI, 0.716-1.866; P = .56; complete vs incomplete: HR, 1.073; 95% CI, 0.790-1,457; P = .65). To our knowledge, this is the first analysis of a phase 3 trial to assess the association of treatment adherence with some clinical outcomes for patients with rectal cancer. The findings emphasize the need for appropriate trial design with optimized nCRT dose and schedule and supportive strategies to facilitate good adherence and precision delivery, especially for intensified nCRT. ClinicalTrials.gov Identifier: NCT00349076.
Identifiants
pubmed: 32644104
pii: 2768008
doi: 10.1001/jamaoncol.2020.2394
pmc: PMC7349129
doi:
Substances chimiques
Oxaliplatin
04ZR38536J
Fluorouracil
U3P01618RT
Banques de données
ClinicalTrials.gov
['NCT00349076']
Types de publication
Clinical Trial, Phase III
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
1416-1421Commentaires et corrections
Type : CommentIn
Références
Nat Rev Clin Oncol. 2012 Jul 03;9(8):471-8
pubmed: 22751283
Lancet Oncol. 2017 Jun;18(6):e354-e363
pubmed: 28593861
J Clin Oncol. 2019 Dec 1;37(34):3212-3222
pubmed: 31150315
Lancet Oncol. 2015 Aug;16(8):979-89
pubmed: 26189067
J Clin Oncol. 2007 Jan 1;25(1):110-7
pubmed: 17194912
J Natl Cancer Inst. 2019 Sep 1;111(9):887-902
pubmed: 31077329
J Clin Oncol. 2012 Dec 20;30(36):4558-65
pubmed: 23109696
Ann Oncol. 2018 Oct 1;29(Suppl 4):iv263
pubmed: 29741565
J Clin Oncol. 2011 Jul 10;29(20):2773-80
pubmed: 21606427
J Clin Oncol. 2012 Jun 1;30(16):1926-33
pubmed: 22529255
J Clin Oncol. 2019 Dec 1;37(34):3223-3233
pubmed: 31557064
J Natl Cancer Inst. 2015 Sep 14;107(11):
pubmed: 26374429
Chin J Cancer Res. 2015 Dec;27(6):588-96
pubmed: 26752933
J Clin Oncol. 2019 Nov 20;37(33):3111-3123
pubmed: 31593484