Gemcitabine-based combination therapy compared with gemcitabine alone for advanced pancreatic cancer: a meta-analysis of nine randomized controlled trials
BACKGROUND: Pancreatic cancer is one of the most aggressive malignancies and chemotherapy is an effective strategy for advanced pancreatic cancer. Gemcitabine (GEM) is one of first-line agents. However, GEM-based combination therapy has shown promising efficacy in patients with advanced pancreatic c...
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Veröffentlicht in: | Hepatobiliary & pancreatic diseases international 2017-06, Vol.16 (3), p.236-244 |
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description | BACKGROUND: Pancreatic cancer is one of the most aggressive malignancies and chemotherapy is an effective strategy for advanced pancreatic cancer. Gemcitabine (GEM) is one of first-line agents. However, GEM-based combination therapy has shown promising efficacy in patients with advanced pancreatic cancer. This meta-analysis aimed to compare the efficacy and safety of GEM-based combination therapy versus GEM alone in the treatment of advanced pancreatic cancer.DATA SOURCES: A comprehensive search of literature was performed using PubMed, EMBASE, Web of Science and Cochrane Central Register of Controlled Trials. A quantitative meta-analysis was performed based on the inclusion criteria from all eligible randomized controlled trials. The outcome indicators included overall survival (OS), 6-month survival, 1-year survival, progression-free survival/time-to-progression (PFS/TTP), and toxicities. RESULTS: A total of nine randomized controlled trials involving 1661 patients were included in this meta-analysis. There was significant improvement in the GEM-based combination therapy with regard to the OS (HR=0.85, 95% CI: 0.76-0.95, P=0.003), PFS (HR=0.76, 95% CI: 0.65-0.90, P-0.002), 6-month survival (RR=1.09, 95% CI: 1.01-1.17, P=0.03), and the overall toxicity (RR=l.68, 95% CI: 1.52-1.86, P〈0.01). However, there was no significant difference in the 1-year survival.CONCLUSIONS: GEM-based combination chemotherapy might improve the OS, 6-month survival, and PFS in advanced pancreatic cancer. However, combined therapy also added toxicity. |
doi_str_mv | 10.1016/S1499-3872(17)60022-5 |
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Gemcitabine (GEM) is one of first-line agents. However, GEM-based combination therapy has shown promising efficacy in patients with advanced pancreatic cancer. This meta-analysis aimed to compare the efficacy and safety of GEM-based combination therapy versus GEM alone in the treatment of advanced pancreatic cancer.DATA SOURCES: A comprehensive search of literature was performed using PubMed, EMBASE, Web of Science and Cochrane Central Register of Controlled Trials. A quantitative meta-analysis was performed based on the inclusion criteria from all eligible randomized controlled trials. The outcome indicators included overall survival (OS), 6-month survival, 1-year survival, progression-free survival/time-to-progression (PFS/TTP), and toxicities. RESULTS: A total of nine randomized controlled trials involving 1661 patients were included in this meta-analysis. There was significant improvement in the GEM-based combination therapy with regard to the OS (HR=0.85, 95% CI: 0.76-0.95, P=0.003), PFS (HR=0.76, 95% CI: 0.65-0.90, P-0.002), 6-month survival (RR=1.09, 95% CI: 1.01-1.17, P=0.03), and the overall toxicity (RR=l.68, 95% CI: 1.52-1.86, P〈0.01). However, there was no significant difference in the 1-year survival.CONCLUSIONS: GEM-based combination chemotherapy might improve the OS, 6-month survival, and PFS in advanced pancreatic cancer. However, combined therapy also added toxicity.</description><identifier>ISSN: 1499-3872</identifier><identifier>DOI: 10.1016/S1499-3872(17)60022-5</identifier><identifier>PMID: 28603091</identifier><language>eng</language><publisher>Singapore: Elsevier B.V</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antimetabolites, Antineoplastic - adverse effects ; Antimetabolites, Antineoplastic - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; chemotherapy ; Chi-Square Distribution ; cisplatin ; Deoxycytidine - adverse effects ; Deoxycytidine - analogs & derivatives ; Deoxycytidine - therapeutic use ; Disease Progression ; Disease-Free Survival ; Endocrinology & Metabolism ; Female ; Gastroenterology and Hepatology ; gemcitabine ; Humans ; Male ; meta-analysis ; Middle Aged ; Odds Ratio ; pancreatic cancer ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - mortality ; Pancreatic Neoplasms - pathology ; Randomized Controlled Trials as Topic ; Risk Factors ; S-1 ; Time Factors ; Treatment Outcome</subject><ispartof>Hepatobiliary & pancreatic diseases international, 2017-06, Vol.16 (3), p.236-244</ispartof><rights>The Editorial Board of Hepatobiliary & Pancreatic Diseases International</rights><rights>2017 The Editorial Board of Hepatobiliary & Pancreatic Diseases International</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-eba4a140914d65d01749495b9a4b4843bac9e8b705be8ae3c02cd2ae11af181c3</citedby><cites>FETCH-LOGICAL-c447t-eba4a140914d65d01749495b9a4b4843bac9e8b705be8ae3c02cd2ae11af181c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/89801X/89801X.jpg</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1499387217600225$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28603091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jin, Shui-Fang</creatorcontrib><creatorcontrib>Fan, Zhao-Kun</creatorcontrib><creatorcontrib>Pan, Lei</creatorcontrib><creatorcontrib>Jin, Li-Ming</creatorcontrib><title>Gemcitabine-based combination therapy compared with gemcitabine alone for advanced pancreatic cancer: a meta-analysis of nine randomized controlled trials</title><title>Hepatobiliary & pancreatic diseases international</title><addtitle>Hepatobiliary & Pancreatic Diseases International</addtitle><description>BACKGROUND: Pancreatic cancer is one of the most aggressive malignancies and chemotherapy is an effective strategy for advanced pancreatic cancer. Gemcitabine (GEM) is one of first-line agents. However, GEM-based combination therapy has shown promising efficacy in patients with advanced pancreatic cancer. This meta-analysis aimed to compare the efficacy and safety of GEM-based combination therapy versus GEM alone in the treatment of advanced pancreatic cancer.DATA SOURCES: A comprehensive search of literature was performed using PubMed, EMBASE, Web of Science and Cochrane Central Register of Controlled Trials. A quantitative meta-analysis was performed based on the inclusion criteria from all eligible randomized controlled trials. The outcome indicators included overall survival (OS), 6-month survival, 1-year survival, progression-free survival/time-to-progression (PFS/TTP), and toxicities. RESULTS: A total of nine randomized controlled trials involving 1661 patients were included in this meta-analysis. There was significant improvement in the GEM-based combination therapy with regard to the OS (HR=0.85, 95% CI: 0.76-0.95, P=0.003), PFS (HR=0.76, 95% CI: 0.65-0.90, P-0.002), 6-month survival (RR=1.09, 95% CI: 1.01-1.17, P=0.03), and the overall toxicity (RR=l.68, 95% CI: 1.52-1.86, P〈0.01). However, there was no significant difference in the 1-year survival.CONCLUSIONS: GEM-based combination chemotherapy might improve the OS, 6-month survival, and PFS in advanced pancreatic cancer. However, combined therapy also added toxicity.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antimetabolites, Antineoplastic - adverse effects</subject><subject>Antimetabolites, Antineoplastic - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>chemotherapy</subject><subject>Chi-Square Distribution</subject><subject>cisplatin</subject><subject>Deoxycytidine - adverse effects</subject><subject>Deoxycytidine - analogs & derivatives</subject><subject>Deoxycytidine - therapeutic use</subject><subject>Disease Progression</subject><subject>Disease-Free Survival</subject><subject>Endocrinology & Metabolism</subject><subject>Female</subject><subject>Gastroenterology and Hepatology</subject><subject>gemcitabine</subject><subject>Humans</subject><subject>Male</subject><subject>meta-analysis</subject><subject>Middle Aged</subject><subject>Odds Ratio</subject><subject>pancreatic cancer</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - mortality</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Risk Factors</subject><subject>S-1</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>1499-3872</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUcFu1DAQzQFES-ETQBancgjYiRPbF1BVQUGqxAE4WxNnsuuS2KntLVo-BfEp_BO_gLO7LBIXLpn4-b03njdF8YTRF4yy9uVHxpUqaymqcyaet5RWVdncK06P8EnxMMabjEvZtA-Kk0q2tKaKnRY_rnAyNkFnHZYdROyJ8VM-QbLekbTGAPN2wWYI-fKrTWuy-qshMPr8HXwg0N-BM5kz5xIwGxhiFiT8-vmdAJkwQQkOxm20kfiBuEUfwPV-st92jV0KfhzzbwoWxviouD_kgo8P9az4_PbNp8t35fWHq_eXF9el4VykEjvgwHieh_dt01MmuOKq6RTwjkted2AUyk7QpkMJWBtamb4CZAwGJpmpz4rzve8c_O0GY9KTjQbHERz6TdRMUSmU5IJmarOnmuBjDDjoOdgJwlYzqpdl6N0y9JK6ZkLvlqGbrHt6aLHpJuyPqj-byITXewLmQe8sBh2NxSVPG9Ak3Xv73xav_nEwo3XWwPgFtxhv_Cbk8PM0Olaa7k0WDyZ2DovBs8Nsa-9Wt9atjs9sRVXlJFVd_watfsDZ</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Jin, Shui-Fang</creator><creator>Fan, Zhao-Kun</creator><creator>Pan, Lei</creator><creator>Jin, Li-Ming</creator><general>Elsevier B.V</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20170601</creationdate><title>Gemcitabine-based combination therapy compared with gemcitabine alone for advanced pancreatic cancer: a meta-analysis of nine randomized controlled trials</title><author>Jin, Shui-Fang ; Fan, Zhao-Kun ; Pan, Lei ; Jin, Li-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-eba4a140914d65d01749495b9a4b4843bac9e8b705be8ae3c02cd2ae11af181c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antimetabolites, Antineoplastic - adverse effects</topic><topic>Antimetabolites, Antineoplastic - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>chemotherapy</topic><topic>Chi-Square Distribution</topic><topic>cisplatin</topic><topic>Deoxycytidine - adverse effects</topic><topic>Deoxycytidine - analogs & derivatives</topic><topic>Deoxycytidine - therapeutic use</topic><topic>Disease Progression</topic><topic>Disease-Free Survival</topic><topic>Endocrinology & Metabolism</topic><topic>Female</topic><topic>Gastroenterology and Hepatology</topic><topic>gemcitabine</topic><topic>Humans</topic><topic>Male</topic><topic>meta-analysis</topic><topic>Middle Aged</topic><topic>Odds Ratio</topic><topic>pancreatic cancer</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - mortality</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Risk Factors</topic><topic>S-1</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jin, Shui-Fang</creatorcontrib><creatorcontrib>Fan, Zhao-Kun</creatorcontrib><creatorcontrib>Pan, Lei</creatorcontrib><creatorcontrib>Jin, Li-Ming</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Hepatobiliary & pancreatic diseases international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jin, Shui-Fang</au><au>Fan, Zhao-Kun</au><au>Pan, Lei</au><au>Jin, Li-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gemcitabine-based combination therapy compared with gemcitabine alone for advanced pancreatic cancer: a meta-analysis of nine randomized controlled trials</atitle><jtitle>Hepatobiliary & pancreatic diseases international</jtitle><addtitle>Hepatobiliary & Pancreatic Diseases International</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>16</volume><issue>3</issue><spage>236</spage><epage>244</epage><pages>236-244</pages><issn>1499-3872</issn><abstract>BACKGROUND: Pancreatic cancer is one of the most aggressive malignancies and chemotherapy is an effective strategy for advanced pancreatic cancer. Gemcitabine (GEM) is one of first-line agents. However, GEM-based combination therapy has shown promising efficacy in patients with advanced pancreatic cancer. This meta-analysis aimed to compare the efficacy and safety of GEM-based combination therapy versus GEM alone in the treatment of advanced pancreatic cancer.DATA SOURCES: A comprehensive search of literature was performed using PubMed, EMBASE, Web of Science and Cochrane Central Register of Controlled Trials. A quantitative meta-analysis was performed based on the inclusion criteria from all eligible randomized controlled trials. The outcome indicators included overall survival (OS), 6-month survival, 1-year survival, progression-free survival/time-to-progression (PFS/TTP), and toxicities. RESULTS: A total of nine randomized controlled trials involving 1661 patients were included in this meta-analysis. There was significant improvement in the GEM-based combination therapy with regard to the OS (HR=0.85, 95% CI: 0.76-0.95, P=0.003), PFS (HR=0.76, 95% CI: 0.65-0.90, P-0.002), 6-month survival (RR=1.09, 95% CI: 1.01-1.17, P=0.03), and the overall toxicity (RR=l.68, 95% CI: 1.52-1.86, P〈0.01). However, there was no significant difference in the 1-year survival.CONCLUSIONS: GEM-based combination chemotherapy might improve the OS, 6-month survival, and PFS in advanced pancreatic cancer. However, combined therapy also added toxicity.</abstract><cop>Singapore</cop><pub>Elsevier B.V</pub><pmid>28603091</pmid><doi>10.1016/S1499-3872(17)60022-5</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antimetabolites, Antineoplastic - adverse effects Antimetabolites, Antineoplastic - therapeutic use Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use chemotherapy Chi-Square Distribution cisplatin Deoxycytidine - adverse effects Deoxycytidine - analogs & derivatives Deoxycytidine - therapeutic use Disease Progression Disease-Free Survival Endocrinology & Metabolism Female Gastroenterology and Hepatology gemcitabine Humans Male meta-analysis Middle Aged Odds Ratio pancreatic cancer Pancreatic Neoplasms - drug therapy Pancreatic Neoplasms - mortality Pancreatic Neoplasms - pathology Randomized Controlled Trials as Topic Risk Factors S-1 Time Factors Treatment Outcome |
title | Gemcitabine-based combination therapy compared with gemcitabine alone for advanced pancreatic cancer: a meta-analysis of nine randomized controlled trials |
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