Biweekly S-1 plus oxaliplatin (SOX) reintroduction in previously treated metastatic colorectal cancer patients (ORION 2 study): a phase II study to evaluate the efficacy and safety
Background The reintroduction of oxaliplatin as a third-or-later-line regimen has been a promising option for patients with metastatic colorectal cancer (mCRC) who previously received chemotherapy including oxaliplatin. In this single-arm phase II study, we evaluated the efficacy of biweekly SOX, wh...
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Veröffentlicht in: | International journal of clinical oncology 2019-07, Vol.24 (7), p.836-841 |
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creator | Tanioka, Hiroaki Honda, Michitaka Tanaka, Chihiro Morita, Yoshitaka Ishibashi, Keiichiro Kato, Takeshi Matsuda, Chu Kataoka, Masato Satake, Hironaga Munemoto, Yoshinori Kobayashi, Kenji Takahashi, Masazumi Nakata, Ken Sakamoto, Junichi Oba, Koji Mishima, Hideyuki |
description | Background
The reintroduction of oxaliplatin as a third-or-later-line regimen has been a promising option for patients with metastatic colorectal cancer (mCRC) who previously received chemotherapy including oxaliplatin. In this single-arm phase II study, we evaluated the efficacy of biweekly SOX, which is the combination of oxaliplatin reintroduction and S-1, as a third-or-later-line treatment.
Methods
Patients with mCRC who had previously received prior chemotherapy including oxaliplatin and irinotecan and were planned to receive the reintroduction of oxaliplatin were enrolled. Oxaliplatin (85 mg/m
2
) with/without bevacizumab (5 mg/kg) was given intravenously on day 1. Oral S-1 was administered on day 2–8 at a dose of 40–60 mg (calculated according to the body surface area) twice a day. Cycles were repeated every 2 weeks. The primary endpoint was the progression-free survival (PFS); our hypothesis was that the median PFS would be 3.5 months with a minimum threshold above 2.0 months. The secondary endpoints included the adverse events (AEs), response rate and overall survival (OS).
Results
A total of 41 patients from 12 institutes were enrolled. The median PFS and OS survival were 3.3 months (95% confidence interval [CI] 2.7–4.2) and 10.1 months (8.3–14.6), and response rate and disease control rate were 10.0% and 65.0%, respectively. Grade 3 AEs included thrombocytopenia (5.0%), anorexia (5.0%), pneumonia (5.0%) and fatigue (5.0%). There were no cases of grade 4 AEs or treatment-related death.
Conclusion
Biweekly SOX regimen with reintroduction of oxaliplatin could be exploitable as the third- and/or later-line treatments for patients with mCRC. |
doi_str_mv | 10.1007/s10147-019-01414-0 |
format | Article |
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The reintroduction of oxaliplatin as a third-or-later-line regimen has been a promising option for patients with metastatic colorectal cancer (mCRC) who previously received chemotherapy including oxaliplatin. In this single-arm phase II study, we evaluated the efficacy of biweekly SOX, which is the combination of oxaliplatin reintroduction and S-1, as a third-or-later-line treatment.
Methods
Patients with mCRC who had previously received prior chemotherapy including oxaliplatin and irinotecan and were planned to receive the reintroduction of oxaliplatin were enrolled. Oxaliplatin (85 mg/m
2
) with/without bevacizumab (5 mg/kg) was given intravenously on day 1. Oral S-1 was administered on day 2–8 at a dose of 40–60 mg (calculated according to the body surface area) twice a day. Cycles were repeated every 2 weeks. The primary endpoint was the progression-free survival (PFS); our hypothesis was that the median PFS would be 3.5 months with a minimum threshold above 2.0 months. The secondary endpoints included the adverse events (AEs), response rate and overall survival (OS).
Results
A total of 41 patients from 12 institutes were enrolled. The median PFS and OS survival were 3.3 months (95% confidence interval [CI] 2.7–4.2) and 10.1 months (8.3–14.6), and response rate and disease control rate were 10.0% and 65.0%, respectively. Grade 3 AEs included thrombocytopenia (5.0%), anorexia (5.0%), pneumonia (5.0%) and fatigue (5.0%). There were no cases of grade 4 AEs or treatment-related death.
Conclusion
Biweekly SOX regimen with reintroduction of oxaliplatin could be exploitable as the third- and/or later-line treatments for patients with mCRC.</description><identifier>ISSN: 1341-9625</identifier><identifier>EISSN: 1437-7772</identifier><identifier>DOI: 10.1007/s10147-019-01414-0</identifier><identifier>PMID: 30778794</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>Anorexia ; Bevacizumab ; Cancer Research ; Chemotherapy ; Colorectal cancer ; Colorectal carcinoma ; Disease control ; Fatigue ; Irinotecan ; Medicine ; Medicine & Public Health ; Metastases ; Metastasis ; Monoclonal antibodies ; Oncology ; Original Article ; Oxaliplatin ; Patients ; Reintroduction ; Response rates ; Surgical Oncology ; Survival ; Targeted cancer therapy ; Thrombocytopenia</subject><ispartof>International journal of clinical oncology, 2019-07, Vol.24 (7), p.836-841</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-aae51386a43394b681f5dc11fc05c027fa344c8932ebcfff011684bd1182828a3</citedby><cites>FETCH-LOGICAL-c399t-aae51386a43394b681f5dc11fc05c027fa344c8932ebcfff011684bd1182828a3</cites><orcidid>0000-0003-3492-9881</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/s10147-019-01414-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10147-019-01414-0$$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/30778794$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tanioka, Hiroaki</creatorcontrib><creatorcontrib>Honda, Michitaka</creatorcontrib><creatorcontrib>Tanaka, Chihiro</creatorcontrib><creatorcontrib>Morita, Yoshitaka</creatorcontrib><creatorcontrib>Ishibashi, Keiichiro</creatorcontrib><creatorcontrib>Kato, Takeshi</creatorcontrib><creatorcontrib>Matsuda, Chu</creatorcontrib><creatorcontrib>Kataoka, Masato</creatorcontrib><creatorcontrib>Satake, Hironaga</creatorcontrib><creatorcontrib>Munemoto, Yoshinori</creatorcontrib><creatorcontrib>Kobayashi, Kenji</creatorcontrib><creatorcontrib>Takahashi, Masazumi</creatorcontrib><creatorcontrib>Nakata, Ken</creatorcontrib><creatorcontrib>Sakamoto, Junichi</creatorcontrib><creatorcontrib>Oba, Koji</creatorcontrib><creatorcontrib>Mishima, Hideyuki</creatorcontrib><title>Biweekly S-1 plus oxaliplatin (SOX) reintroduction in previously treated metastatic colorectal cancer patients (ORION 2 study): a phase II study to evaluate the efficacy and safety</title><title>International journal of clinical oncology</title><addtitle>Int J Clin Oncol</addtitle><addtitle>Int J Clin Oncol</addtitle><description>Background
The reintroduction of oxaliplatin as a third-or-later-line regimen has been a promising option for patients with metastatic colorectal cancer (mCRC) who previously received chemotherapy including oxaliplatin. In this single-arm phase II study, we evaluated the efficacy of biweekly SOX, which is the combination of oxaliplatin reintroduction and S-1, as a third-or-later-line treatment.
Methods
Patients with mCRC who had previously received prior chemotherapy including oxaliplatin and irinotecan and were planned to receive the reintroduction of oxaliplatin were enrolled. Oxaliplatin (85 mg/m
2
) with/without bevacizumab (5 mg/kg) was given intravenously on day 1. Oral S-1 was administered on day 2–8 at a dose of 40–60 mg (calculated according to the body surface area) twice a day. Cycles were repeated every 2 weeks. The primary endpoint was the progression-free survival (PFS); our hypothesis was that the median PFS would be 3.5 months with a minimum threshold above 2.0 months. The secondary endpoints included the adverse events (AEs), response rate and overall survival (OS).
Results
A total of 41 patients from 12 institutes were enrolled. The median PFS and OS survival were 3.3 months (95% confidence interval [CI] 2.7–4.2) and 10.1 months (8.3–14.6), and response rate and disease control rate were 10.0% and 65.0%, respectively. Grade 3 AEs included thrombocytopenia (5.0%), anorexia (5.0%), pneumonia (5.0%) and fatigue (5.0%). There were no cases of grade 4 AEs or treatment-related death.
Conclusion
Biweekly SOX regimen with reintroduction of oxaliplatin could be exploitable as the third- and/or later-line treatments for patients with mCRC.</description><subject>Anorexia</subject><subject>Bevacizumab</subject><subject>Cancer Research</subject><subject>Chemotherapy</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Disease control</subject><subject>Fatigue</subject><subject>Irinotecan</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Monoclonal antibodies</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Oxaliplatin</subject><subject>Patients</subject><subject>Reintroduction</subject><subject>Response rates</subject><subject>Surgical Oncology</subject><subject>Survival</subject><subject>Targeted cancer therapy</subject><subject>Thrombocytopenia</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>eNp9kcFu1DAURSMEoqXwAyzQk9hMFwE_24kTdlBRGKliJAoSu8jjPNMUT5zaTiH_xQfWZQpILJBl2bo-99rWLYqnyF4gY-plRIZSlQzbPCXKkt0rDlEKVSql-P28FxLLtubVQfEoxkvGUNUVf1gcCKZUo1p5WPx8M3wn-uYWOC8RJjdH8D-0Gyan0zDC6nzz5RgCDWMKvp9NGvwIWZ8CXQ9-jtmXAulEPewo6Ziyy4DxzgcySTswejQUYMo6jSnCavNxvfkAHGKa--X4FWiYLnQkWK_3EiQPdK3dnEMhXRCQtYPRZgE99hC1pbQ8Lh5Y7SI9uVuPis-nbz-dvC_PNu_WJ6_PSiPaNpVaU4WiqbUUopXbukFb9QbRGlYZxpXVQkrTtILT1lhrGWLdyG2P2PA8tDgqVvvcKfirmWLqdkM05JweKX--49iIWmLVqIw-_we99HMY8-tuKd7W2DaYKb6nTPAxBrLdFIadDkuHrLvttNt32uVOu1-ddiybnt1Fz9sd9X8sv0vMgNgDMR-NXyn8vfs_sTdBmq2T</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Tanioka, Hiroaki</creator><creator>Honda, Michitaka</creator><creator>Tanaka, Chihiro</creator><creator>Morita, Yoshitaka</creator><creator>Ishibashi, Keiichiro</creator><creator>Kato, Takeshi</creator><creator>Matsuda, Chu</creator><creator>Kataoka, Masato</creator><creator>Satake, Hironaga</creator><creator>Munemoto, Yoshinori</creator><creator>Kobayashi, Kenji</creator><creator>Takahashi, Masazumi</creator><creator>Nakata, Ken</creator><creator>Sakamoto, Junichi</creator><creator>Oba, Koji</creator><creator>Mishima, Hideyuki</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/0000-0003-3492-9881</orcidid></search><sort><creationdate>20190701</creationdate><title>Biweekly S-1 plus oxaliplatin (SOX) reintroduction in previously treated metastatic colorectal cancer patients (ORION 2 study): a phase II study to evaluate the efficacy and safety</title><author>Tanioka, Hiroaki ; Honda, Michitaka ; Tanaka, Chihiro ; Morita, Yoshitaka ; Ishibashi, Keiichiro ; Kato, Takeshi ; Matsuda, Chu ; Kataoka, Masato ; Satake, Hironaga ; Munemoto, Yoshinori ; Kobayashi, Kenji ; Takahashi, Masazumi ; Nakata, Ken ; Sakamoto, Junichi ; Oba, Koji ; Mishima, Hideyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-aae51386a43394b681f5dc11fc05c027fa344c8932ebcfff011684bd1182828a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anorexia</topic><topic>Bevacizumab</topic><topic>Cancer Research</topic><topic>Chemotherapy</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Disease control</topic><topic>Fatigue</topic><topic>Irinotecan</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Monoclonal antibodies</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Oxaliplatin</topic><topic>Patients</topic><topic>Reintroduction</topic><topic>Response rates</topic><topic>Surgical Oncology</topic><topic>Survival</topic><topic>Targeted cancer therapy</topic><topic>Thrombocytopenia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tanioka, Hiroaki</creatorcontrib><creatorcontrib>Honda, Michitaka</creatorcontrib><creatorcontrib>Tanaka, Chihiro</creatorcontrib><creatorcontrib>Morita, Yoshitaka</creatorcontrib><creatorcontrib>Ishibashi, Keiichiro</creatorcontrib><creatorcontrib>Kato, Takeshi</creatorcontrib><creatorcontrib>Matsuda, Chu</creatorcontrib><creatorcontrib>Kataoka, Masato</creatorcontrib><creatorcontrib>Satake, Hironaga</creatorcontrib><creatorcontrib>Munemoto, Yoshinori</creatorcontrib><creatorcontrib>Kobayashi, Kenji</creatorcontrib><creatorcontrib>Takahashi, Masazumi</creatorcontrib><creatorcontrib>Nakata, Ken</creatorcontrib><creatorcontrib>Sakamoto, Junichi</creatorcontrib><creatorcontrib>Oba, Koji</creatorcontrib><creatorcontrib>Mishima, Hideyuki</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 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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>Tanioka, Hiroaki</au><au>Honda, Michitaka</au><au>Tanaka, Chihiro</au><au>Morita, Yoshitaka</au><au>Ishibashi, Keiichiro</au><au>Kato, Takeshi</au><au>Matsuda, Chu</au><au>Kataoka, Masato</au><au>Satake, Hironaga</au><au>Munemoto, Yoshinori</au><au>Kobayashi, Kenji</au><au>Takahashi, Masazumi</au><au>Nakata, Ken</au><au>Sakamoto, Junichi</au><au>Oba, Koji</au><au>Mishima, Hideyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biweekly S-1 plus oxaliplatin (SOX) reintroduction in previously treated metastatic colorectal cancer patients (ORION 2 study): a phase II study to evaluate the efficacy and safety</atitle><jtitle>International journal of clinical oncology</jtitle><stitle>Int J Clin Oncol</stitle><addtitle>Int J Clin Oncol</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>24</volume><issue>7</issue><spage>836</spage><epage>841</epage><pages>836-841</pages><issn>1341-9625</issn><eissn>1437-7772</eissn><abstract>Background
The reintroduction of oxaliplatin as a third-or-later-line regimen has been a promising option for patients with metastatic colorectal cancer (mCRC) who previously received chemotherapy including oxaliplatin. In this single-arm phase II study, we evaluated the efficacy of biweekly SOX, which is the combination of oxaliplatin reintroduction and S-1, as a third-or-later-line treatment.
Methods
Patients with mCRC who had previously received prior chemotherapy including oxaliplatin and irinotecan and were planned to receive the reintroduction of oxaliplatin were enrolled. Oxaliplatin (85 mg/m
2
) with/without bevacizumab (5 mg/kg) was given intravenously on day 1. Oral S-1 was administered on day 2–8 at a dose of 40–60 mg (calculated according to the body surface area) twice a day. Cycles were repeated every 2 weeks. The primary endpoint was the progression-free survival (PFS); our hypothesis was that the median PFS would be 3.5 months with a minimum threshold above 2.0 months. The secondary endpoints included the adverse events (AEs), response rate and overall survival (OS).
Results
A total of 41 patients from 12 institutes were enrolled. The median PFS and OS survival were 3.3 months (95% confidence interval [CI] 2.7–4.2) and 10.1 months (8.3–14.6), and response rate and disease control rate were 10.0% and 65.0%, respectively. Grade 3 AEs included thrombocytopenia (5.0%), anorexia (5.0%), pneumonia (5.0%) and fatigue (5.0%). There were no cases of grade 4 AEs or treatment-related death.
Conclusion
Biweekly SOX regimen with reintroduction of oxaliplatin could be exploitable as the third- and/or later-line treatments for patients with mCRC.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>30778794</pmid><doi>10.1007/s10147-019-01414-0</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-3492-9881</orcidid></addata></record> |
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subjects | Anorexia Bevacizumab Cancer Research Chemotherapy Colorectal cancer Colorectal carcinoma Disease control Fatigue Irinotecan Medicine Medicine & Public Health Metastases Metastasis Monoclonal antibodies Oncology Original Article Oxaliplatin Patients Reintroduction Response rates Surgical Oncology Survival Targeted cancer therapy Thrombocytopenia |
title | Biweekly S-1 plus oxaliplatin (SOX) reintroduction in previously treated metastatic colorectal cancer patients (ORION 2 study): a phase II study to evaluate the efficacy and safety |
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