Systematic review with network meta‐analysis: adjuvant therapy for resected biliary tract cancer

Summary Background Major adjuvant therapies for biliary tract cancer (BTC) include fluorouracil, gemcitabine and chemoradiation (CRT), but the optimum regimen remains inconclusive. Aim To compare these therapies in terms of patient survival rates after resection and toxic effects. Methods We searche...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2014-10, Vol.40 (7), p.759-770
Hauptverfasser: Zhu, G.‐Q., Shi, K.‐Q., You, J., Zou, H., Lin, Y.‐Q., Wang, L.‐R., Braddock, M., Chen, Y.‐P., Zheng, M.‐H.
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container_end_page 770
container_issue 7
container_start_page 759
container_title Alimentary pharmacology & therapeutics
container_volume 40
creator Zhu, G.‐Q.
Shi, K.‐Q.
You, J.
Zou, H.
Lin, Y.‐Q.
Wang, L.‐R.
Braddock, M.
Chen, Y.‐P.
Zheng, M.‐H.
description Summary Background Major adjuvant therapies for biliary tract cancer (BTC) include fluorouracil, gemcitabine and chemoradiation (CRT), but the optimum regimen remains inconclusive. Aim To compare these therapies in terms of patient survival rates after resection and toxic effects. Methods We searched PubMed for controlled trials comparing the above three therapies with each other or observation alone until 31 January 2014. We estimated the hazard ratios (HRs) for death and odds ratios (ORs) for toxic effects among different therapies. Subgroup analyses based on positive lymph node or resection margin were also performed. Results Twelve eligible articles were included. Gemcitabine improved 5‐year survival (HR 2.12, 95% CI, confidence interval 1.23–4.02, P = 0.01), whereas fluorouracil (HR 1.61, 95% CI 0.74–3.67) and CRT (HR 1.55, 95% CI 0.82–3.32) provided a poorer survival outcome compared with gemcitabine after 1 year. Similarly, for 5‐year survival rates, although differing, CRT did not provide a significant improvement in survival (HR 0.46, 95% CI 0.20–0.97) compared with gemcitabine. Fluorouracil did not appear to provide benefit over gemcitabine (HR 1.56, 95% CI 0.77–3.35). CRT was ranked highest for toxic effects including haematological (OR 5.45, 95% CI 0.01–483.85) and nonhaematological (OR 5.77, 95% CI 0.01–3807.40). Conclusions Chemotherapy with gemcitabine is the optimum adjuvant treatment with a balanced benefit‐toxicity ratio for resected biliary tract cancer. Chemoradiation was more likely to cause toxic effects.
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Aim To compare these therapies in terms of patient survival rates after resection and toxic effects. Methods We searched PubMed for controlled trials comparing the above three therapies with each other or observation alone until 31 January 2014. We estimated the hazard ratios (HRs) for death and odds ratios (ORs) for toxic effects among different therapies. Subgroup analyses based on positive lymph node or resection margin were also performed. Results Twelve eligible articles were included. Gemcitabine improved 5‐year survival (HR 2.12, 95% CI, confidence interval 1.23–4.02, P = 0.01), whereas fluorouracil (HR 1.61, 95% CI 0.74–3.67) and CRT (HR 1.55, 95% CI 0.82–3.32) provided a poorer survival outcome compared with gemcitabine after 1 year. Similarly, for 5‐year survival rates, although differing, CRT did not provide a significant improvement in survival (HR 0.46, 95% CI 0.20–0.97) compared with gemcitabine. Fluorouracil did not appear to provide benefit over gemcitabine (HR 1.56, 95% CI 0.77–3.35). CRT was ranked highest for toxic effects including haematological (OR 5.45, 95% CI 0.01–483.85) and nonhaematological (OR 5.77, 95% CI 0.01–3807.40). Conclusions Chemotherapy with gemcitabine is the optimum adjuvant treatment with a balanced benefit‐toxicity ratio for resected biliary tract cancer. Chemoradiation was more likely to cause toxic effects.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/apt.12900</identifier><identifier>PMID: 25099956</identifier><language>eng</language><publisher>Oxford: Blackwell</publisher><subject>Antimetabolites, Antineoplastic - therapeutic use ; Biliary Tract Neoplasms - surgery ; Biliary Tract Neoplasms - therapy ; Biological and medical sciences ; Chemoradiotherapy, Adjuvant ; Deoxycytidine - analogs &amp; derivatives ; Deoxycytidine - therapeutic use ; Fluorouracil - therapeutic use ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Medical sciences ; Tumors</subject><ispartof>Alimentary pharmacology &amp; therapeutics, 2014-10, Vol.40 (7), p.759-770</ispartof><rights>2014 John Wiley &amp; Sons Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2014 John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4600-2cefc9a3194c957791876362db66930740321d971761f32295e5f42c1e909f6c3</citedby><cites>FETCH-LOGICAL-c4600-2cefc9a3194c957791876362db66930740321d971761f32295e5f42c1e909f6c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fapt.12900$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fapt.12900$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28776186$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25099956$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, G.‐Q.</creatorcontrib><creatorcontrib>Shi, K.‐Q.</creatorcontrib><creatorcontrib>You, J.</creatorcontrib><creatorcontrib>Zou, H.</creatorcontrib><creatorcontrib>Lin, Y.‐Q.</creatorcontrib><creatorcontrib>Wang, L.‐R.</creatorcontrib><creatorcontrib>Braddock, M.</creatorcontrib><creatorcontrib>Chen, Y.‐P.</creatorcontrib><creatorcontrib>Zheng, M.‐H.</creatorcontrib><title>Systematic review with network meta‐analysis: adjuvant therapy for resected biliary tract cancer</title><title>Alimentary pharmacology &amp; therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Summary Background Major adjuvant therapies for biliary tract cancer (BTC) include fluorouracil, gemcitabine and chemoradiation (CRT), but the optimum regimen remains inconclusive. Aim To compare these therapies in terms of patient survival rates after resection and toxic effects. Methods We searched PubMed for controlled trials comparing the above three therapies with each other or observation alone until 31 January 2014. We estimated the hazard ratios (HRs) for death and odds ratios (ORs) for toxic effects among different therapies. Subgroup analyses based on positive lymph node or resection margin were also performed. Results Twelve eligible articles were included. Gemcitabine improved 5‐year survival (HR 2.12, 95% CI, confidence interval 1.23–4.02, P = 0.01), whereas fluorouracil (HR 1.61, 95% CI 0.74–3.67) and CRT (HR 1.55, 95% CI 0.82–3.32) provided a poorer survival outcome compared with gemcitabine after 1 year. Similarly, for 5‐year survival rates, although differing, CRT did not provide a significant improvement in survival (HR 0.46, 95% CI 0.20–0.97) compared with gemcitabine. Fluorouracil did not appear to provide benefit over gemcitabine (HR 1.56, 95% CI 0.77–3.35). CRT was ranked highest for toxic effects including haematological (OR 5.45, 95% CI 0.01–483.85) and nonhaematological (OR 5.77, 95% CI 0.01–3807.40). Conclusions Chemotherapy with gemcitabine is the optimum adjuvant treatment with a balanced benefit‐toxicity ratio for resected biliary tract cancer. Chemoradiation was more likely to cause toxic effects.</description><subject>Antimetabolites, Antineoplastic - therapeutic use</subject><subject>Biliary Tract Neoplasms - surgery</subject><subject>Biliary Tract Neoplasms - therapy</subject><subject>Biological and medical sciences</subject><subject>Chemoradiotherapy, Adjuvant</subject><subject>Deoxycytidine - analogs &amp; derivatives</subject><subject>Deoxycytidine - therapeutic use</subject><subject>Fluorouracil - therapeutic use</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Liver. Biliary tract. Portal circulation. 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Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical sciences</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, G.‐Q.</creatorcontrib><creatorcontrib>Shi, K.‐Q.</creatorcontrib><creatorcontrib>You, J.</creatorcontrib><creatorcontrib>Zou, H.</creatorcontrib><creatorcontrib>Lin, Y.‐Q.</creatorcontrib><creatorcontrib>Wang, L.‐R.</creatorcontrib><creatorcontrib>Braddock, M.</creatorcontrib><creatorcontrib>Chen, Y.‐P.</creatorcontrib><creatorcontrib>Zheng, M.‐H.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, G.‐Q.</au><au>Shi, K.‐Q.</au><au>You, J.</au><au>Zou, H.</au><au>Lin, Y.‐Q.</au><au>Wang, L.‐R.</au><au>Braddock, M.</au><au>Chen, Y.‐P.</au><au>Zheng, M.‐H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systematic review with network meta‐analysis: adjuvant therapy for resected biliary tract cancer</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2014-10</date><risdate>2014</risdate><volume>40</volume><issue>7</issue><spage>759</spage><epage>770</epage><pages>759-770</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>Summary Background Major adjuvant therapies for biliary tract cancer (BTC) include fluorouracil, gemcitabine and chemoradiation (CRT), but the optimum regimen remains inconclusive. Aim To compare these therapies in terms of patient survival rates after resection and toxic effects. Methods We searched PubMed for controlled trials comparing the above three therapies with each other or observation alone until 31 January 2014. We estimated the hazard ratios (HRs) for death and odds ratios (ORs) for toxic effects among different therapies. Subgroup analyses based on positive lymph node or resection margin were also performed. Results Twelve eligible articles were included. Gemcitabine improved 5‐year survival (HR 2.12, 95% CI, confidence interval 1.23–4.02, P = 0.01), whereas fluorouracil (HR 1.61, 95% CI 0.74–3.67) and CRT (HR 1.55, 95% CI 0.82–3.32) provided a poorer survival outcome compared with gemcitabine after 1 year. Similarly, for 5‐year survival rates, although differing, CRT did not provide a significant improvement in survival (HR 0.46, 95% CI 0.20–0.97) compared with gemcitabine. Fluorouracil did not appear to provide benefit over gemcitabine (HR 1.56, 95% CI 0.77–3.35). CRT was ranked highest for toxic effects including haematological (OR 5.45, 95% CI 0.01–483.85) and nonhaematological (OR 5.77, 95% CI 0.01–3807.40). Conclusions Chemotherapy with gemcitabine is the optimum adjuvant treatment with a balanced benefit‐toxicity ratio for resected biliary tract cancer. Chemoradiation was more likely to cause toxic effects.</abstract><cop>Oxford</cop><pub>Blackwell</pub><pmid>25099956</pmid><doi>10.1111/apt.12900</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Antimetabolites, Antineoplastic - therapeutic use
Biliary Tract Neoplasms - surgery
Biliary Tract Neoplasms - therapy
Biological and medical sciences
Chemoradiotherapy, Adjuvant
Deoxycytidine - analogs & derivatives
Deoxycytidine - therapeutic use
Fluorouracil - therapeutic use
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Medical sciences
Tumors
title Systematic review with network meta‐analysis: adjuvant therapy for resected biliary tract cancer
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