Systemic chemotherapy for gastric cancer with early recurrence after adjuvant S-1 monotherapy: a multicenter retrospective study
Background S-1 monotherapy is one of the standard adjuvant treatments for patients with stage II and III gastric cancers. Early recurrence after S-1 adjuvant therapy has a poor prognosis. This study aimed to clarify the treatment outcomes of systemic chemotherapy and explore encouraging regimens. Me...
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Veröffentlicht in: | International journal of clinical oncology 2019-10, Vol.24 (10), p.1197-1203 |
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creator | Mitani, Seiichiro Kadowaki, Shigenori Hasegawa, Hiroko Wakatsuki, Takeru Hara, Hiroki Tajika, Masahiro Nishikawa, Kazuhiro Hirao, Motohiro Takahari, Daisuke Chin, Keisho Muro, Kei |
description | Background
S-1 monotherapy is one of the standard adjuvant treatments for patients with stage II and III gastric cancers. Early recurrence after S-1 adjuvant therapy has a poor prognosis. This study aimed to clarify the treatment outcomes of systemic chemotherapy and explore encouraging regimens.
Methods
This was a multicenter retrospective study. Among gastric cancer patients who underwent curative gastrectomy followed by adjuvant S-1 monotherapy, patients who experienced a recurrence while receiving adjuvant therapy or within 6 months after completion and started systemic chemotherapy at four institutions between 2005 and 2015 were eligible.
Results
A total of 112 patients were included. The main treatment regimens were weekly paclitaxel (
n
= 38, 34%), irinotecan plus cisplatin (
n
= 31, 28%), capecitabine plus cisplatin (
n
= 7, 6%), and irinotecan monotherapy (
n
= 6, 5%). For all patients, median progression-free survival and overall survival were 3.7 and 11.4 months, respectively. Among 77 patients with measurable lesions, the overall response and disease control rates were 24.7% and 62.3%, respectively. Multivariate analyses for overall survival showed that Eastern Cooperative Oncology Group performance status 2 [hazard ratio (HR) 3.71; 95% confidence interval (CI) 1.78–7.73] and undifferentiated histological type (HR 2.04; 95% CI 1.35–3.44) were independent prognostic factors, and treatment regimens were not prognostic. Exploratory comparisons did not show statistically significant differences between treatment regimens.
Conclusions
This study of the largest number of patients with early recurrence after S-1 adjuvant monotherapy demonstrated that the prognosis for patients treated by all regimens was similar and poor. |
doi_str_mv | 10.1007/s10147-019-01477-z |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2233849720</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2232987222</sourcerecordid><originalsourceid>FETCH-LOGICAL-c399t-bcfb13fd2e936d2ab644f689560af228c2b873ce1d202996e4146e8378967b2a3</originalsourceid><addsrcrecordid>eNp9kU1v1DAQhi0E6se2f4ADssSFi8EeZ-2YG6qgIFXqoe3ZcpxJN6t8LLZTlJ746XW6LZU49DSjeZ957dFLyHvBPwvO9ZcouCg048KwpdHs_g05EoXUTGsNb3MvC8GMgvUhOY5xy7nQag0H5FAKsQYJ8oj8vZpjwr711G-wH9MGg9vNtBkDvXUxhUVwg8dA_7RpQ9GFbqYB_RQC5jF1Tcqaq7fTnRsSvWKC9uPw7POVOtpPXWo9DgsXMIUx7tCn9g5pTFM9n5B3jesinj7VFbn58f367Ce7uDz_dfbtgnlpTGKVbyohmxrQSFWDq1RRNKo0a8VdA1B6qEotPYoaOBijsBCFwlLq0ihdgZMr8mnvuwvj7wljsn0bPXadG3CcogWQsiyMBp7Rj_-h23EKQ_7dQoEpNeS6IrCnfD4pBmzsLrS9C7MV3C752H0-NudjH_Ox93npw5P1VPVY_1t5DiQDcg_ELA23GF7efsX2AbjbnZs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2232987222</pqid></control><display><type>article</type><title>Systemic chemotherapy for gastric cancer with early recurrence after adjuvant S-1 monotherapy: a multicenter retrospective study</title><source>SpringerLink Journals - AutoHoldings</source><creator>Mitani, Seiichiro ; Kadowaki, Shigenori ; Hasegawa, Hiroko ; Wakatsuki, Takeru ; Hara, Hiroki ; Tajika, Masahiro ; Nishikawa, Kazuhiro ; Hirao, Motohiro ; Takahari, Daisuke ; Chin, Keisho ; Muro, Kei</creator><creatorcontrib>Mitani, Seiichiro ; Kadowaki, Shigenori ; Hasegawa, Hiroko ; Wakatsuki, Takeru ; Hara, Hiroki ; Tajika, Masahiro ; Nishikawa, Kazuhiro ; Hirao, Motohiro ; Takahari, Daisuke ; Chin, Keisho ; Muro, Kei</creatorcontrib><description>Background
S-1 monotherapy is one of the standard adjuvant treatments for patients with stage II and III gastric cancers. Early recurrence after S-1 adjuvant therapy has a poor prognosis. This study aimed to clarify the treatment outcomes of systemic chemotherapy and explore encouraging regimens.
Methods
This was a multicenter retrospective study. Among gastric cancer patients who underwent curative gastrectomy followed by adjuvant S-1 monotherapy, patients who experienced a recurrence while receiving adjuvant therapy or within 6 months after completion and started systemic chemotherapy at four institutions between 2005 and 2015 were eligible.
Results
A total of 112 patients were included. The main treatment regimens were weekly paclitaxel (
n
= 38, 34%), irinotecan plus cisplatin (
n
= 31, 28%), capecitabine plus cisplatin (
n
= 7, 6%), and irinotecan monotherapy (
n
= 6, 5%). For all patients, median progression-free survival and overall survival were 3.7 and 11.4 months, respectively. Among 77 patients with measurable lesions, the overall response and disease control rates were 24.7% and 62.3%, respectively. Multivariate analyses for overall survival showed that Eastern Cooperative Oncology Group performance status 2 [hazard ratio (HR) 3.71; 95% confidence interval (CI) 1.78–7.73] and undifferentiated histological type (HR 2.04; 95% CI 1.35–3.44) were independent prognostic factors, and treatment regimens were not prognostic. Exploratory comparisons did not show statistically significant differences between treatment regimens.
Conclusions
This study of the largest number of patients with early recurrence after S-1 adjuvant monotherapy demonstrated that the prognosis for patients treated by all regimens was similar and poor.</description><identifier>ISSN: 1341-9625</identifier><identifier>EISSN: 1437-7772</identifier><identifier>DOI: 10.1007/s10147-019-01477-z</identifier><identifier>PMID: 31152323</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>Cancer Research ; Chemotherapy ; Cisplatin ; Disease control ; Gastrectomy ; Gastric cancer ; Health risk assessment ; Irinotecan ; Medical prognosis ; Medicine ; Medicine & Public Health ; Oncology ; Original Article ; Paclitaxel ; Prognosis ; Statistical analysis ; Surgical Oncology ; Survival</subject><ispartof>International journal of clinical oncology, 2019-10, Vol.24 (10), p.1197-1203</ispartof><rights>Japan Society of Clinical Oncology 2019</rights><rights>International Journal of Clinical Oncology is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-bcfb13fd2e936d2ab644f689560af228c2b873ce1d202996e4146e8378967b2a3</citedby><cites>FETCH-LOGICAL-c399t-bcfb13fd2e936d2ab644f689560af228c2b873ce1d202996e4146e8378967b2a3</cites><orcidid>0000-0001-9923-5309</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10147-019-01477-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10147-019-01477-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31152323$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitani, Seiichiro</creatorcontrib><creatorcontrib>Kadowaki, Shigenori</creatorcontrib><creatorcontrib>Hasegawa, Hiroko</creatorcontrib><creatorcontrib>Wakatsuki, Takeru</creatorcontrib><creatorcontrib>Hara, Hiroki</creatorcontrib><creatorcontrib>Tajika, Masahiro</creatorcontrib><creatorcontrib>Nishikawa, Kazuhiro</creatorcontrib><creatorcontrib>Hirao, Motohiro</creatorcontrib><creatorcontrib>Takahari, Daisuke</creatorcontrib><creatorcontrib>Chin, Keisho</creatorcontrib><creatorcontrib>Muro, Kei</creatorcontrib><title>Systemic chemotherapy for gastric cancer with early recurrence after adjuvant S-1 monotherapy: a multicenter retrospective study</title><title>International journal of clinical oncology</title><addtitle>Int J Clin Oncol</addtitle><addtitle>Int J Clin Oncol</addtitle><description>Background
S-1 monotherapy is one of the standard adjuvant treatments for patients with stage II and III gastric cancers. Early recurrence after S-1 adjuvant therapy has a poor prognosis. This study aimed to clarify the treatment outcomes of systemic chemotherapy and explore encouraging regimens.
Methods
This was a multicenter retrospective study. Among gastric cancer patients who underwent curative gastrectomy followed by adjuvant S-1 monotherapy, patients who experienced a recurrence while receiving adjuvant therapy or within 6 months after completion and started systemic chemotherapy at four institutions between 2005 and 2015 were eligible.
Results
A total of 112 patients were included. The main treatment regimens were weekly paclitaxel (
n
= 38, 34%), irinotecan plus cisplatin (
n
= 31, 28%), capecitabine plus cisplatin (
n
= 7, 6%), and irinotecan monotherapy (
n
= 6, 5%). For all patients, median progression-free survival and overall survival were 3.7 and 11.4 months, respectively. Among 77 patients with measurable lesions, the overall response and disease control rates were 24.7% and 62.3%, respectively. Multivariate analyses for overall survival showed that Eastern Cooperative Oncology Group performance status 2 [hazard ratio (HR) 3.71; 95% confidence interval (CI) 1.78–7.73] and undifferentiated histological type (HR 2.04; 95% CI 1.35–3.44) were independent prognostic factors, and treatment regimens were not prognostic. Exploratory comparisons did not show statistically significant differences between treatment regimens.
Conclusions
This study of the largest number of patients with early recurrence after S-1 adjuvant monotherapy demonstrated that the prognosis for patients treated by all regimens was similar and poor.</description><subject>Cancer Research</subject><subject>Chemotherapy</subject><subject>Cisplatin</subject><subject>Disease control</subject><subject>Gastrectomy</subject><subject>Gastric cancer</subject><subject>Health risk assessment</subject><subject>Irinotecan</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Paclitaxel</subject><subject>Prognosis</subject><subject>Statistical analysis</subject><subject>Surgical Oncology</subject><subject>Survival</subject><issn>1341-9625</issn><issn>1437-7772</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kU1v1DAQhi0E6se2f4ADssSFi8EeZ-2YG6qgIFXqoe3ZcpxJN6t8LLZTlJ746XW6LZU49DSjeZ957dFLyHvBPwvO9ZcouCg048KwpdHs_g05EoXUTGsNb3MvC8GMgvUhOY5xy7nQag0H5FAKsQYJ8oj8vZpjwr711G-wH9MGg9vNtBkDvXUxhUVwg8dA_7RpQ9GFbqYB_RQC5jF1Tcqaq7fTnRsSvWKC9uPw7POVOtpPXWo9DgsXMIUx7tCn9g5pTFM9n5B3jesinj7VFbn58f367Ce7uDz_dfbtgnlpTGKVbyohmxrQSFWDq1RRNKo0a8VdA1B6qEotPYoaOBijsBCFwlLq0ihdgZMr8mnvuwvj7wljsn0bPXadG3CcogWQsiyMBp7Rj_-h23EKQ_7dQoEpNeS6IrCnfD4pBmzsLrS9C7MV3C752H0-NudjH_Ox93npw5P1VPVY_1t5DiQDcg_ELA23GF7efsX2AbjbnZs</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Mitani, Seiichiro</creator><creator>Kadowaki, Shigenori</creator><creator>Hasegawa, Hiroko</creator><creator>Wakatsuki, Takeru</creator><creator>Hara, Hiroki</creator><creator>Tajika, Masahiro</creator><creator>Nishikawa, Kazuhiro</creator><creator>Hirao, Motohiro</creator><creator>Takahari, Daisuke</creator><creator>Chin, Keisho</creator><creator>Muro, Kei</creator><general>Springer Singapore</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9923-5309</orcidid></search><sort><creationdate>20191001</creationdate><title>Systemic chemotherapy for gastric cancer with early recurrence after adjuvant S-1 monotherapy: a multicenter retrospective study</title><author>Mitani, Seiichiro ; Kadowaki, Shigenori ; Hasegawa, Hiroko ; Wakatsuki, Takeru ; Hara, Hiroki ; Tajika, Masahiro ; Nishikawa, Kazuhiro ; Hirao, Motohiro ; Takahari, Daisuke ; Chin, Keisho ; Muro, Kei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-bcfb13fd2e936d2ab644f689560af228c2b873ce1d202996e4146e8378967b2a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Cancer Research</topic><topic>Chemotherapy</topic><topic>Cisplatin</topic><topic>Disease control</topic><topic>Gastrectomy</topic><topic>Gastric cancer</topic><topic>Health risk assessment</topic><topic>Irinotecan</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Paclitaxel</topic><topic>Prognosis</topic><topic>Statistical analysis</topic><topic>Surgical Oncology</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitani, Seiichiro</creatorcontrib><creatorcontrib>Kadowaki, Shigenori</creatorcontrib><creatorcontrib>Hasegawa, Hiroko</creatorcontrib><creatorcontrib>Wakatsuki, Takeru</creatorcontrib><creatorcontrib>Hara, Hiroki</creatorcontrib><creatorcontrib>Tajika, Masahiro</creatorcontrib><creatorcontrib>Nishikawa, Kazuhiro</creatorcontrib><creatorcontrib>Hirao, Motohiro</creatorcontrib><creatorcontrib>Takahari, Daisuke</creatorcontrib><creatorcontrib>Chin, Keisho</creatorcontrib><creatorcontrib>Muro, Kei</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitani, Seiichiro</au><au>Kadowaki, Shigenori</au><au>Hasegawa, Hiroko</au><au>Wakatsuki, Takeru</au><au>Hara, Hiroki</au><au>Tajika, Masahiro</au><au>Nishikawa, Kazuhiro</au><au>Hirao, Motohiro</au><au>Takahari, Daisuke</au><au>Chin, Keisho</au><au>Muro, Kei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systemic chemotherapy for gastric cancer with early recurrence after adjuvant S-1 monotherapy: a multicenter retrospective study</atitle><jtitle>International journal of clinical oncology</jtitle><stitle>Int J Clin Oncol</stitle><addtitle>Int J Clin Oncol</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>24</volume><issue>10</issue><spage>1197</spage><epage>1203</epage><pages>1197-1203</pages><issn>1341-9625</issn><eissn>1437-7772</eissn><abstract>Background
S-1 monotherapy is one of the standard adjuvant treatments for patients with stage II and III gastric cancers. Early recurrence after S-1 adjuvant therapy has a poor prognosis. This study aimed to clarify the treatment outcomes of systemic chemotherapy and explore encouraging regimens.
Methods
This was a multicenter retrospective study. Among gastric cancer patients who underwent curative gastrectomy followed by adjuvant S-1 monotherapy, patients who experienced a recurrence while receiving adjuvant therapy or within 6 months after completion and started systemic chemotherapy at four institutions between 2005 and 2015 were eligible.
Results
A total of 112 patients were included. The main treatment regimens were weekly paclitaxel (
n
= 38, 34%), irinotecan plus cisplatin (
n
= 31, 28%), capecitabine plus cisplatin (
n
= 7, 6%), and irinotecan monotherapy (
n
= 6, 5%). For all patients, median progression-free survival and overall survival were 3.7 and 11.4 months, respectively. Among 77 patients with measurable lesions, the overall response and disease control rates were 24.7% and 62.3%, respectively. Multivariate analyses for overall survival showed that Eastern Cooperative Oncology Group performance status 2 [hazard ratio (HR) 3.71; 95% confidence interval (CI) 1.78–7.73] and undifferentiated histological type (HR 2.04; 95% CI 1.35–3.44) were independent prognostic factors, and treatment regimens were not prognostic. Exploratory comparisons did not show statistically significant differences between treatment regimens.
Conclusions
This study of the largest number of patients with early recurrence after S-1 adjuvant monotherapy demonstrated that the prognosis for patients treated by all regimens was similar and poor.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>31152323</pmid><doi>10.1007/s10147-019-01477-z</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-9923-5309</orcidid></addata></record> |
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subjects | Cancer Research Chemotherapy Cisplatin Disease control Gastrectomy Gastric cancer Health risk assessment Irinotecan Medical prognosis Medicine Medicine & Public Health Oncology Original Article Paclitaxel Prognosis Statistical analysis Surgical Oncology Survival |
title | Systemic chemotherapy for gastric cancer with early recurrence after adjuvant S-1 monotherapy: a multicenter retrospective study |
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