2016
DOI: 10.1007/s10120-016-0666-5
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Impact of progression type on overall survival in patients with advanced gastric cancer based on randomized phase III study of S-1 plus oxaliplatin versus S-1 plus cisplatin

Abstract: Background The association between progression type and survival has been reported in breast cancer, but remains unclear in advanced gastric cancer (AGC). Here, this association was assessed using data obtained from an earlier randomized phase III study demonstrating the non-inferiority of S-1 plus oxaliplatin (SOX) to S-1 plus cisplatin (CS) on progression-free survival and overall survival (OS) in the first-line treatment of AGC. Methods A Cox regression model including two time-dependent covariates, progres… Show more

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Cited by 3 publications
(4 citation statements)
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“…nausea, vomiting and renal toxicity), but was associated with a significantly higher rate of peripheral polyneuropathy (22). In a recent phase III study comparing S-1/oxaliplatin (SOX regimen) and Cis/S-1 in Japanese OAC patients, similar results were obtained with respect to the safety issues, whereas no significant difference in terms of progression-free survival (PFS) and OS were observed between the two regimens (24,25). Haematological toxicity is reversible, nausea and vomiting are preventable, whereas renal toxicity can be monitored.…”
Section: Discussionmentioning
confidence: 75%
“…nausea, vomiting and renal toxicity), but was associated with a significantly higher rate of peripheral polyneuropathy (22). In a recent phase III study comparing S-1/oxaliplatin (SOX regimen) and Cis/S-1 in Japanese OAC patients, similar results were obtained with respect to the safety issues, whereas no significant difference in terms of progression-free survival (PFS) and OS were observed between the two regimens (24,25). Haematological toxicity is reversible, nausea and vomiting are preventable, whereas renal toxicity can be monitored.…”
Section: Discussionmentioning
confidence: 75%
“…Therefore, debate continues about the clinical significance of the anatomic sites of new lesions. However, in view of previous reports that the number of metastatic sites is a prognostic factor [ 33 ] and that progression accompanied by new lesions has a strong negative impact on the prognosis of AGC [ 27 ], not including new lesions in the sum of tumor diameters may lead to underestimation of tumor burden. New lesions especially in an organ different from that involved before initiation of nivolumab could be included in the calculation of TGR and HPD in patients with AGC.…”
Section: Discussionmentioning
confidence: 99%
“…However, peritoneal metastasis is not included in the original definition of HPD because it is not a measurable lesion. Moreover, there has also been a report suggesting that disease progression accompanied by new lesions has a strong negative impact on the prognosis in patients with AGC [ 27 ]. Given the lack of difference in the biological mechanism of ICI-induced rapid progression between measurable lesions and non-measurable/new lesions, exclusion of peritoneal metastasis and new lesions from the definition of HPD may lead to underestimation of accelerated tumor growth during treatment with ICI in patients with AGC.…”
Section: Introductionmentioning
confidence: 99%
“…According to the Japanese guidelines for gastric cancer, S-1 plus cisplatin is the recommended systemic treatment as first-line chemotherapy for patients with HER2-negative disease (2,15,16). S-1 plus oxaliplatin is also recommended chemotherapy regimen for unresectable advanced gastric cancer and was proven to be effective in pivotal trials (17)(18)(19)(20). Recent developments in second-line and further treatments, such as ramucirumab, nivolumab, and trifluridine/tipiracil, for metastatic gastric cancer have improved overall survival and quality of life (21)(22)(23).…”
Section: Discussionmentioning
confidence: 99%