Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:British journal of cancer 2010-10, Vol.103 (9), p.1343-1348
Main Authors: 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
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c486t-d4f2acc5dffbeef644a9a698166d2aa690af54999ff04275ab70a6452641b443
cites cdi_FETCH-LOGICAL-c486t-d4f2acc5dffbeef644a9a698166d2aa690af54999ff04275ab70a6452641b443
container_end_page 1348
container_issue 9
container_start_page 1343
container_title British journal of cancer
container_volume 103
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 &amp; dosage ; Clinical Study ; Drug Administration Schedule ; Drug Resistance ; Epidemiology ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Leucovorin - administration &amp; 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 &amp; dosage ; Tegafur - administration &amp; 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&amp;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 &amp; 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 &amp; 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 &amp; dosage</subject><subject>Tegafur - administration &amp; 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 &amp; 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 &amp; 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 &amp; dosage</topic><topic>Tegafur - administration &amp; 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 &amp; Allied Health Database (ProQuest)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Nursing &amp; 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>
fulltext fulltext
identifier ISSN: 0007-0920
ispartof British journal of cancer, 2010-10, Vol.103 (9), p.1343-1348
issn 0007-0920
1532-1827
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2990611
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T22%3A50%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20phase%20II%20study%20of%20weekly%20docetaxel%20and%20cisplatin%20plus%20oral%20tegafur/uracil%20and%20leucovorin%20as%20first-line%20chemotherapy%20in%20patients%20with%20locally%20advanced%20or%20metastatic%20gastric%20cancer&rft.jtitle=British%20journal%20of%20cancer&rft.au=Li,%20C-P&rft.date=2010-10-26&rft.volume=103&rft.issue=9&rft.spage=1343&rft.epage=1348&rft.pages=1343-1348&rft.issn=0007-0920&rft.eissn=1532-1827&rft.coden=BJCAAI&rft_id=info:doi/10.1038/sj.bjc.6605928&rft_dat=%3Cproquest_pubme%3E2173287531%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c486t-d4f2acc5dffbeef644a9a698166d2aa690af54999ff04275ab70a6452641b443%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=760010684&rft_id=info:pmid/20924378&rfr_iscdi=true