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A phase II study of weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin as first-line chemotherapy in patients with locally advanced or metastatic gastric cancer
Background: Docetaxel plus cisplatin and 5-fluorouracil has become a new standard for treating advanced gastric cancer. However, high rates of severe neutropenia limit its application. Modification of the regimen could be the solution to get similar activity but less myelosuppression. Methods: Patie...
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Published in: | British journal of cancer 2010-10, Vol.103 (9), p.1343-1348 |
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container_title | British journal of cancer |
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creator | Li, C-P Chen, J-S Chen, L-T Yen, C-J Lee, K-D Su, W-P Lin, P-C Lu, C-H Tsai, H-J Chao, Y |
description | Background:
Docetaxel plus cisplatin and 5-fluorouracil has become a new standard for treating advanced gastric cancer. However, high rates of severe neutropenia limit its application. Modification of the regimen could be the solution to get similar activity but less myelosuppression.
Methods:
Patients with histologically confirmed, locally advanced, or recurrent/metastatic gastric adenocarcinoma without previous chemotherapy were enrolled. This regimen consisted of docetaxel (Tyxan, TTY, Taipei, Taiwan) 30-min infusion at a dose of 36 mg m
−2
, followed by cisplatin 30 mg m
−2
infusion over 1 h on days 1 and 8, and oral tegafur/uracil 300 mg m
−2
per day plus leucovorin 90 mg per day on days 1–14, every 3 weeks. Tumour response was evaluated after every 2 cycles of treatment.
Results:
From August 2007 to March 2009, 45 patients were enrolled. The median age was 56 years (range: 22–75). Among the 40 patients evaluable for tumour response, one achieved a complete response, 22 had partial responses and 11 had stable disease. The overall response rates of the evaluable and intent-to-treat (ITT) populations were 58% (95% CI: 41–74%) and 53% (95% CI: 38–68%), respectively. The disease control rates in these populations were 85% (95% CI: 70–94%) and 82% (95% CI: 68–92%), respectively. In the ITT analysis, the median time to progression and overall survival were 6.8 and 13.9 months, respectively. Major grade 3–4 toxicities were neutropenia (51%), anaemia (22%), diarrhoea (16%), and infections (20%). No patient died of treatment-related toxicities.
Conclusion:
Concurrent weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin are effective and well tolerated in the treatment of advanced gastric cancer. |
doi_str_mv | 10.1038/sj.bjc.6605928 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2990611</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2173287531</sourcerecordid><originalsourceid>FETCH-LOGICAL-c486t-d4f2acc5dffbeef644a9a698166d2aa690af54999ff04275ab70a6452641b443</originalsourceid><addsrcrecordid>eNp1kk1v3CAQhq2qVbNNe-2xQpVy9C7YGNuXSlHUj5Ui9ZI7GmNYs2WNC3iT_V_9gZntbpP20BMD8_C-wwxZ9p7RJaNls4rbZbdVSyFo1RbNi2zBqrLIWVPUL7MFpbTOaVvQi-xNjFvctrSpX2cXBR7ysm4W2a9rMg0QNVmvSUxzfyDekHutf7gD6b3SCR60IzD2RNk4OUh2JJObI_EBHEl6A2YOqzmAsifM6Vn5vQ_IQSTGhphyZ0dN1KB3Pg06wHQgRxXU0mOK5N6mgTivwKEn9HsYle5Rn-zQPSbEFNlgEHBVx2R4m70y4KJ-d14vs7svn-9uvuW337-ub65vc8UbkfKemwKUqnpjOq2N4BxaEG3DhOgLwIiCqXjbtsZQXtQVdDUFwatCcNZxXl5mn06y09ztdK-wWny0nILdQThID1b-mxntIDd-L4u2pYIxFPh4Fgj-56xjkls_hxFLlrWglFHRHF2WJ0gFH2PQ5smAUXmcsYxbiTOW5xnjhQ9_l_WE_xkqAldnACJ21QRsmo3PXFnhR_jtvDpxEVPjRofn8v5j_QjkoMW6</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>760010684</pqid></control><display><type>article</type><title>A phase II study of weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin as first-line chemotherapy in patients with locally advanced or metastatic gastric cancer</title><source>PubMed (Medline)</source><creator>Li, C-P ; Chen, J-S ; Chen, L-T ; Yen, C-J ; Lee, K-D ; Su, W-P ; Lin, P-C ; Lu, C-H ; Tsai, H-J ; Chao, Y</creator><creatorcontrib>Li, C-P ; Chen, J-S ; Chen, L-T ; Yen, C-J ; Lee, K-D ; Su, W-P ; Lin, P-C ; Lu, C-H ; Tsai, H-J ; Chao, Y</creatorcontrib><description>Background:
Docetaxel plus cisplatin and 5-fluorouracil has become a new standard for treating advanced gastric cancer. However, high rates of severe neutropenia limit its application. Modification of the regimen could be the solution to get similar activity but less myelosuppression.
Methods:
Patients with histologically confirmed, locally advanced, or recurrent/metastatic gastric adenocarcinoma without previous chemotherapy were enrolled. This regimen consisted of docetaxel (Tyxan, TTY, Taipei, Taiwan) 30-min infusion at a dose of 36 mg m
−2
, followed by cisplatin 30 mg m
−2
infusion over 1 h on days 1 and 8, and oral tegafur/uracil 300 mg m
−2
per day plus leucovorin 90 mg per day on days 1–14, every 3 weeks. Tumour response was evaluated after every 2 cycles of treatment.
Results:
From August 2007 to March 2009, 45 patients were enrolled. The median age was 56 years (range: 22–75). Among the 40 patients evaluable for tumour response, one achieved a complete response, 22 had partial responses and 11 had stable disease. The overall response rates of the evaluable and intent-to-treat (ITT) populations were 58% (95% CI: 41–74%) and 53% (95% CI: 38–68%), respectively. The disease control rates in these populations were 85% (95% CI: 70–94%) and 82% (95% CI: 68–92%), respectively. In the ITT analysis, the median time to progression and overall survival were 6.8 and 13.9 months, respectively. Major grade 3–4 toxicities were neutropenia (51%), anaemia (22%), diarrhoea (16%), and infections (20%). No patient died of treatment-related toxicities.
Conclusion:
Concurrent weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin are effective and well tolerated in the treatment of advanced gastric cancer.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/sj.bjc.6605928</identifier><identifier>PMID: 20924378</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/154/436/108 ; 692/699/67/1504/1829 ; 692/700/565/1436/1437 ; Administration, Oral ; Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Cisplatin - administration & dosage ; Clinical Study ; Drug Administration Schedule ; Drug Resistance ; Epidemiology ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Leucovorin - administration & dosage ; Medical sciences ; Middle Aged ; Molecular Medicine ; Neoplasm Metastasis ; Oncology ; Stomach Neoplasms - drug therapy ; Stomach Neoplasms - pathology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Taxoids - administration & dosage ; Tegafur - administration & dosage ; Tumors ; Uracil - therapeutic use</subject><ispartof>British journal of cancer, 2010-10, Vol.103 (9), p.1343-1348</ispartof><rights>The Author(s) 2010</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Oct 26, 2010</rights><rights>Copyright © 2010 Cancer Research UK 2010 Cancer Research UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-d4f2acc5dffbeef644a9a698166d2aa690af54999ff04275ab70a6452641b443</citedby><cites>FETCH-LOGICAL-c486t-d4f2acc5dffbeef644a9a698166d2aa690af54999ff04275ab70a6452641b443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990611/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990611/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23500984$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20924378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, C-P</creatorcontrib><creatorcontrib>Chen, J-S</creatorcontrib><creatorcontrib>Chen, L-T</creatorcontrib><creatorcontrib>Yen, C-J</creatorcontrib><creatorcontrib>Lee, K-D</creatorcontrib><creatorcontrib>Su, W-P</creatorcontrib><creatorcontrib>Lin, P-C</creatorcontrib><creatorcontrib>Lu, C-H</creatorcontrib><creatorcontrib>Tsai, H-J</creatorcontrib><creatorcontrib>Chao, Y</creatorcontrib><title>A phase II study of weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin as first-line chemotherapy in patients with locally advanced or metastatic gastric cancer</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>Background:
Docetaxel plus cisplatin and 5-fluorouracil has become a new standard for treating advanced gastric cancer. However, high rates of severe neutropenia limit its application. Modification of the regimen could be the solution to get similar activity but less myelosuppression.
Methods:
Patients with histologically confirmed, locally advanced, or recurrent/metastatic gastric adenocarcinoma without previous chemotherapy were enrolled. This regimen consisted of docetaxel (Tyxan, TTY, Taipei, Taiwan) 30-min infusion at a dose of 36 mg m
−2
, followed by cisplatin 30 mg m
−2
infusion over 1 h on days 1 and 8, and oral tegafur/uracil 300 mg m
−2
per day plus leucovorin 90 mg per day on days 1–14, every 3 weeks. Tumour response was evaluated after every 2 cycles of treatment.
Results:
From August 2007 to March 2009, 45 patients were enrolled. The median age was 56 years (range: 22–75). Among the 40 patients evaluable for tumour response, one achieved a complete response, 22 had partial responses and 11 had stable disease. The overall response rates of the evaluable and intent-to-treat (ITT) populations were 58% (95% CI: 41–74%) and 53% (95% CI: 38–68%), respectively. The disease control rates in these populations were 85% (95% CI: 70–94%) and 82% (95% CI: 68–92%), respectively. In the ITT analysis, the median time to progression and overall survival were 6.8 and 13.9 months, respectively. Major grade 3–4 toxicities were neutropenia (51%), anaemia (22%), diarrhoea (16%), and infections (20%). No patient died of treatment-related toxicities.
Conclusion:
Concurrent weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin are effective and well tolerated in the treatment of advanced gastric cancer.</description><subject>631/154/436/108</subject><subject>692/699/67/1504/1829</subject><subject>692/700/565/1436/1437</subject><subject>Administration, Oral</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Cisplatin - administration & dosage</subject><subject>Clinical Study</subject><subject>Drug Administration Schedule</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Leucovorin - administration & dosage</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Neoplasm Metastasis</subject><subject>Oncology</subject><subject>Stomach Neoplasms - drug therapy</subject><subject>Stomach Neoplasms - pathology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Taxoids - administration & dosage</subject><subject>Tegafur - administration & dosage</subject><subject>Tumors</subject><subject>Uracil - therapeutic use</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp1kk1v3CAQhq2qVbNNe-2xQpVy9C7YGNuXSlHUj5Ui9ZI7GmNYs2WNC3iT_V_9gZntbpP20BMD8_C-wwxZ9p7RJaNls4rbZbdVSyFo1RbNi2zBqrLIWVPUL7MFpbTOaVvQi-xNjFvctrSpX2cXBR7ysm4W2a9rMg0QNVmvSUxzfyDekHutf7gD6b3SCR60IzD2RNk4OUh2JJObI_EBHEl6A2YOqzmAsifM6Vn5vQ_IQSTGhphyZ0dN1KB3Pg06wHQgRxXU0mOK5N6mgTivwKEn9HsYle5Rn-zQPSbEFNlgEHBVx2R4m70y4KJ-d14vs7svn-9uvuW337-ub65vc8UbkfKemwKUqnpjOq2N4BxaEG3DhOgLwIiCqXjbtsZQXtQVdDUFwatCcNZxXl5mn06y09ztdK-wWny0nILdQThID1b-mxntIDd-L4u2pYIxFPh4Fgj-56xjkls_hxFLlrWglFHRHF2WJ0gFH2PQ5smAUXmcsYxbiTOW5xnjhQ9_l_WE_xkqAldnACJ21QRsmo3PXFnhR_jtvDpxEVPjRofn8v5j_QjkoMW6</recordid><startdate>20101026</startdate><enddate>20101026</enddate><creator>Li, C-P</creator><creator>Chen, J-S</creator><creator>Chen, L-T</creator><creator>Yen, C-J</creator><creator>Lee, K-D</creator><creator>Su, W-P</creator><creator>Lin, P-C</creator><creator>Lu, C-H</creator><creator>Tsai, H-J</creator><creator>Chao, Y</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>IQODW</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>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope></search><sort><creationdate>20101026</creationdate><title>A phase II study of weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin as first-line chemotherapy in patients with locally advanced or metastatic gastric cancer</title><author>Li, C-P ; Chen, J-S ; Chen, L-T ; Yen, C-J ; Lee, K-D ; Su, W-P ; Lin, P-C ; Lu, C-H ; Tsai, H-J ; Chao, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-d4f2acc5dffbeef644a9a698166d2aa690af54999ff04275ab70a6452641b443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>631/154/436/108</topic><topic>692/699/67/1504/1829</topic><topic>692/700/565/1436/1437</topic><topic>Administration, Oral</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Cisplatin - administration & dosage</topic><topic>Clinical Study</topic><topic>Drug Administration Schedule</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Leucovorin - administration & dosage</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Medicine</topic><topic>Neoplasm Metastasis</topic><topic>Oncology</topic><topic>Stomach Neoplasms - drug therapy</topic><topic>Stomach Neoplasms - pathology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Taxoids - administration & dosage</topic><topic>Tegafur - administration & dosage</topic><topic>Tumors</topic><topic>Uracil - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, C-P</creatorcontrib><creatorcontrib>Chen, J-S</creatorcontrib><creatorcontrib>Chen, L-T</creatorcontrib><creatorcontrib>Yen, C-J</creatorcontrib><creatorcontrib>Lee, K-D</creatorcontrib><creatorcontrib>Su, W-P</creatorcontrib><creatorcontrib>Lin, P-C</creatorcontrib><creatorcontrib>Lu, C-H</creatorcontrib><creatorcontrib>Tsai, H-J</creatorcontrib><creatorcontrib>Chao, Y</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, C-P</au><au>Chen, J-S</au><au>Chen, L-T</au><au>Yen, C-J</au><au>Lee, K-D</au><au>Su, W-P</au><au>Lin, P-C</au><au>Lu, C-H</au><au>Tsai, H-J</au><au>Chao, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A phase II study of weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin as first-line chemotherapy in patients with locally advanced or metastatic gastric cancer</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><addtitle>Br J Cancer</addtitle><date>2010-10-26</date><risdate>2010</risdate><volume>103</volume><issue>9</issue><spage>1343</spage><epage>1348</epage><pages>1343-1348</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>Background:
Docetaxel plus cisplatin and 5-fluorouracil has become a new standard for treating advanced gastric cancer. However, high rates of severe neutropenia limit its application. Modification of the regimen could be the solution to get similar activity but less myelosuppression.
Methods:
Patients with histologically confirmed, locally advanced, or recurrent/metastatic gastric adenocarcinoma without previous chemotherapy were enrolled. This regimen consisted of docetaxel (Tyxan, TTY, Taipei, Taiwan) 30-min infusion at a dose of 36 mg m
−2
, followed by cisplatin 30 mg m
−2
infusion over 1 h on days 1 and 8, and oral tegafur/uracil 300 mg m
−2
per day plus leucovorin 90 mg per day on days 1–14, every 3 weeks. Tumour response was evaluated after every 2 cycles of treatment.
Results:
From August 2007 to March 2009, 45 patients were enrolled. The median age was 56 years (range: 22–75). Among the 40 patients evaluable for tumour response, one achieved a complete response, 22 had partial responses and 11 had stable disease. The overall response rates of the evaluable and intent-to-treat (ITT) populations were 58% (95% CI: 41–74%) and 53% (95% CI: 38–68%), respectively. The disease control rates in these populations were 85% (95% CI: 70–94%) and 82% (95% CI: 68–92%), respectively. In the ITT analysis, the median time to progression and overall survival were 6.8 and 13.9 months, respectively. Major grade 3–4 toxicities were neutropenia (51%), anaemia (22%), diarrhoea (16%), and infections (20%). No patient died of treatment-related toxicities.
Conclusion:
Concurrent weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin are effective and well tolerated in the treatment of advanced gastric cancer.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>20924378</pmid><doi>10.1038/sj.bjc.6605928</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | PubMed (Medline) |
subjects | 631/154/436/108 692/699/67/1504/1829 692/700/565/1436/1437 Administration, Oral Adult Aged Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Biomedical and Life Sciences Biomedicine Cancer Research Cisplatin - administration & dosage Clinical Study Drug Administration Schedule Drug Resistance Epidemiology Female Gastroenterology. Liver. Pancreas. Abdomen Humans Leucovorin - administration & dosage Medical sciences Middle Aged Molecular Medicine Neoplasm Metastasis Oncology Stomach Neoplasms - drug therapy Stomach Neoplasms - pathology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Taxoids - administration & dosage Tegafur - administration & dosage Tumors Uracil - therapeutic use |
title | A phase II study of weekly docetaxel and cisplatin plus oral tegafur/uracil and leucovorin as first-line chemotherapy in patients with locally advanced or metastatic gastric cancer |
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