2008
DOI: 10.1200/jco.2008.26.15_suppl.lba4504
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CONKO-001: Final results of the randomized, prospective, multicenter phase III trial of adjuvant chemotherapy with gemcitabine versus observation in patients with resected pancreatic cancer (PC)

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Cited by 127 publications
(87 citation statements)
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“…1503 /cmaj .121368 / -/ DC1) and meta-analyses. Either gemcitabine or 5 -fluorouracil (5-FU) prolongs median survival by 3 months (95% CI 0.3-5.7), [28][29][30][31]49 …”
mentioning
confidence: 99%
See 1 more Smart Citation
“…1503 /cmaj .121368 / -/ DC1) and meta-analyses. Either gemcitabine or 5 -fluorouracil (5-FU) prolongs median survival by 3 months (95% CI 0.3-5.7), [28][29][30][31]49 …”
mentioning
confidence: 99%
“…[26][27][28][29][30][31][32][33][34][35][36][37][38][39] Twenty percent of cases are candidates for surgery and have CT evidence of no distant metastases, with the primary tumour free from the hepatic portal and superior…”
mentioning
confidence: 99%
“…Tani et al have reported that adjuvant chemotherapy was an independent factor affecting long-term survival in patients with locally advanced pancreatic cancer who had undergone surgery (10). Oettle et al have shown that adjuvant chemotherapy with GEM for pancreatic cancer patients was significantly effective for prolonging disease-free survival (7), and their subsequent study revealed that it was also capable of prolonging OAS (9). In their study, Ueno et al have shown that GEM prolonged diseasefree survival in patients who had undergone macroscopically curative resection of pancreatic cancer (8).…”
Section: Discussionmentioning
confidence: 95%
“…The available data from randomized phase III trials (ESPAC-1 and CONKO-001) indicate that adjuvant chemotherapy may substantially prolong DFS and cause a moderate increase of overall survival (18)(19)(20)(21). However, an optimal chemotherapy regimen remains to be defined.…”
Section: Discussionmentioning
confidence: 99%
“…However, an optimal chemotherapy regimen remains to be defined. Notably, in Italy as well as in Germany (4), gemcitabine chemotherapy [according to the CONKO-001 trial (20,21)] was the preferred schema, while aCT according to the Ê»Mayo regimenʼ [bolus 5-FU plus folinic acid, ESPAC-1 study (19)] was selected by few physicians. A reduction in toxicity was cited as the explanation, based on the ESPAC-3 trial, whereas gemcitabine was not superior to the Mayo regimen with respect to the primary end-point of overall survival, although the authors reported a 50% reduction of treatment-associated serious adverse events using gemcitabine (22).…”
Section: Discussionmentioning
confidence: 99%