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Combination versus single-agent as palliative chemotherapy for gastric cancer
DC Field | Value | Language |
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dc.contributor.author | Choi, JH | - |
dc.contributor.author | Choi, YW | - |
dc.contributor.author | Kang, SY | - |
dc.contributor.author | Jeong, GS | - |
dc.contributor.author | Lee, HW | - |
dc.contributor.author | Jeong, SH | - |
dc.contributor.author | Park, JS | - |
dc.contributor.author | Ahn, MS | - |
dc.contributor.author | Sheen, SS | - |
dc.date.accessioned | 2022-11-29T01:43:16Z | - |
dc.date.available | 2022-11-29T01:43:16Z | - |
dc.date.issued | 2020 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/22949 | - |
dc.description.abstract | BACKGROUND: Although combination chemotherapy (CC) is generally recommended in recurrent or primary metastatic gastric cancer (RPMGC), the results of randomized trials are conflicting. METHODS: A retrospective review was conducted on 687 RPMGC patients who received palliative chemotherapy. We compared the overall survival (OS) between CC and single-agent chemotherapy (SC) among these patients, and we analyzed the clinicopathological characteristics affecting outcome including neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR). RESULTS: Although 521 patients (75.8%) underwent CC, SC was more frequently performed in elderly patients (57.6%) and ECOG performance status (PS) 2 or 3 (65.8%) patients (p < 0.0001, in each case). The median OS of patients who received CC was significantly longer than that of patients who received SC (11 vs. 8 months, p < 0.0001). No difference in OS between CC and SC was observed in elderly patients (p = 0.583), poor PS (p = 0.810), signet ring cell (p = 0.347), palliative surgical resection (p = 0.307), and high PLR (p = 0.120), with a significant interaction between age and type of regimen (p = 0.012). Moreover, there was no difference in OS between CC and SC after propensity score matching (p = 0.322). Multivariate analysis revealed that palliative resection and >/= second-line chemotherapy were independently associated with favorable OS (p < 0.0001, in each case), whereas poor PS (p = 0.004), signet ring cell (p < 0.0001), peritoneal metastasis (p = 0.04), high NLR (p = 0.001), and high PLR (p = 0.033) were independent prognostic factors of poor OS. CONCLUSIONS: Although CC is the standard of care in RPMGC, SC can be considered a reasonable option in certain subgroups, such as elderly patients. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Antineoplastic Agents | - |
dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Lymphocyte Count | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neutrophils | - |
dc.subject.MESH | Palliative Care | - |
dc.subject.MESH | Platelet Count | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Stomach Neoplasms | - |
dc.subject.MESH | Survival Analysis | - |
dc.subject.MESH | Young Adult | - |
dc.title | Combination versus single-agent as palliative chemotherapy for gastric cancer | - |
dc.type | Article | - |
dc.identifier.pmid | 32122320 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052983 | - |
dc.subject.keyword | Gastric cancer | - |
dc.subject.keyword | Palliative chemotherapy | - |
dc.subject.keyword | Single | - |
dc.subject.keyword | Combination | - |
dc.subject.keyword | Platelet-to-lymphocyte ratio | - |
dc.subject.keyword | Age | - |
dc.contributor.affiliatedAuthor | Choi, JH | - |
dc.contributor.affiliatedAuthor | Choi, YW | - |
dc.contributor.affiliatedAuthor | Kang, SY | - |
dc.contributor.affiliatedAuthor | Lee, HW | - |
dc.contributor.affiliatedAuthor | Jeong, SH | - |
dc.contributor.affiliatedAuthor | Park, JS | - |
dc.contributor.affiliatedAuthor | Ahn, MS | - |
dc.contributor.affiliatedAuthor | Sheen, SS | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1186/s12885-020-6666-1 | - |
dc.citation.title | BMC cancer | - |
dc.citation.volume | 20 | - |
dc.citation.number | 1 | - |
dc.citation.date | 2020 | - |
dc.citation.startPage | 167 | - |
dc.citation.endPage | 167 | - |
dc.identifier.bibliographicCitation | BMC cancer, 20(1). : 167-167, 2020 | - |
dc.identifier.eissn | 1471-2407 | - |
dc.relation.journalid | J014712407 | - |
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