Patterns of Recurrence After Resection of Pancreatic Ductal Adenocarcinoma: A Secondary Analysis of the ESPAC-4 Randomized Adjuvant Chemotherapy Trial.
Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Capecitabine
/ administration & dosage
Carcinoma, Pancreatic Ductal
/ drug therapy
Chemotherapy, Adjuvant
Deoxycytidine
/ administration & dosage
Disease-Free Survival
Female
Humans
Male
Middle Aged
Neoplasm Recurrence, Local
/ drug therapy
Pancreatic Neoplasms
/ drug therapy
Prospective Studies
Treatment Outcome
Gemcitabine
Journal
JAMA surgery
ISSN: 2168-6262
Titre abrégé: JAMA Surg
Pays: United States
ID NLM: 101589553
Informations de publication
Date de publication:
01 11 2019
01 11 2019
Historique:
pubmed:
5
9
2019
medline:
14
7
2020
entrez:
5
9
2019
Statut:
ppublish
Résumé
The patterns of disease recurrence after resection of pancreatic ductal adenocarcinoma with adjuvant chemotherapy remain unclear. To define patterns of recurrence after adjuvant chemotherapy and the association with survival. Prospectively collected data from the phase 3 European Study Group for Pancreatic Cancer 4 adjuvant clinical trial, an international multicenter study. The study included 730 patients who had resection and adjuvant chemotherapy for pancreatic cancer. Data were analyzed between July 2017 and May 2019. Randomization to adjuvant gemcitabine or gemcitabine plus capecitabine. Overall survival, recurrence, and sites of recurrence. Of the 730 patients, median age was 65 years (range 37-81 years), 414 were men (57%), and 316 were women (43%). The median follow-up time from randomization was 43.2 months (95% CI, 39.7-45.5 months), with overall survival from time of surgery of 27.9 months (95% CI, 24.8-29.9 months) with gemcitabine and 30.2 months (95% CI, 25.8-33.5 months) with the combination (HR, 0.81; 95% CI, 0.68-0.98; P = .03). The 5-year survival estimates were 17.1% (95% CI, 11.6%-23.5%) and 28.0% (22.0%-34.3%), respectively. Recurrence occurred in 479 patients (65.6%); another 78 patients (10.7%) died without recurrence. Local recurrence occurred at a median of 11.63 months (95% CI, 10.05-12.19 months), significantly different from those with distant recurrence with a median of 9.49 months (95% CI, 8.44-10.71 months) (HR, 1.21; 95% CI, 1.01-1.45; P = .04). Following recurrence, the median survival was 9.36 months (95% CI, 8.08-10.48 months) for local recurrence and 8.94 months (95% CI, 7.82-11.17 months) with distant recurrence (HR, 0.89; 95% CI, 0.73-1.09; P = .27). The median overall survival of patients with distant-only recurrence (23.03 months; 95% CI, 19.55-25.85 months) or local with distant recurrence (23.82 months; 95% CI, 17.48-28.32 months) was not significantly different from those with only local recurrence (24.83 months; 95% CI, 22.96-27.63 months) (P = .85 and P = .35, respectively). Gemcitabine plus capecitabine had a 21% reduction of death following recurrence compared with monotherapy (HR, 0.79; 95% CI, 0.64-0.98; P = .03). There were no significant differences between the time to recurrence and subsequent and overall survival between local and distant recurrence. Pancreatic cancer behaves as a systemic disease requiring effective systemic therapy after resection. ClinicalTrials.gov identifier: NCT00058201, EudraCT 2007-004299-38, and ISRCTN 96397434.
Identifiants
pubmed: 31483448
pii: 2749409
doi: 10.1001/jamasurg.2019.3337
pmc: PMC6727687
doi:
Substances chimiques
Deoxycytidine
0W860991D6
Capecitabine
6804DJ8Z9U
Gemcitabine
0
Banques de données
ClinicalTrials.gov
['NCT00058201']
EudraCT
['2007-004299-38']
ISRCTN
['ISRCTN96397434']
Types de publication
Clinical Trial, Phase III
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1038-1048Subventions
Organisme : Department of Health
ID : 08/29/02
Pays : United Kingdom
Organisme : Cancer Research UK
ID : 11883
Pays : United Kingdom
Organisme : Cancer Research UK
ID : 8968
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C245/A8968/A20830
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
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