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
Hauptverfasser: 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
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container_end_page 841
container_issue 7
container_start_page 836
container_title International journal of clinical oncology
container_volume 24
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
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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 &amp; 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. 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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 &amp; 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 &amp; 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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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1437-7772
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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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