A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer

Background: The treatment options for patients with therapy refractory metastatic colorectal cancer (mCRC) are sparse. TAS-102 (FTD/TPI) is a new oral anti-tumour agent composed of a nucleoside analogue, trifluridine, and a thymidine phosphorylase inhibitor, tipiracil, indicated for patients with mC...

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Veröffentlicht in:Acta oncologica 2019-08, Vol.58 (8), p.1149-1157
Hauptverfasser: Andersen, Stig E., Andersen, Ida B., Jensen, Benny V., Pfeiffer, Per, Ota, Takayo, Larsen, Jim S.
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container_end_page 1157
container_issue 8
container_start_page 1149
container_title Acta oncologica
container_volume 58
creator Andersen, Stig E.
Andersen, Ida B.
Jensen, Benny V.
Pfeiffer, Per
Ota, Takayo
Larsen, Jim S.
description Background: The treatment options for patients with therapy refractory metastatic colorectal cancer (mCRC) are sparse. TAS-102 (FTD/TPI) is a new oral anti-tumour agent composed of a nucleoside analogue, trifluridine, and a thymidine phosphorylase inhibitor, tipiracil, indicated for patients with mCRC who are refractory to standard therapies. This study summarizes published and unpublished experience with FTD/TPI in clinical practice settings. Patients and methods: The Medline/PubMed, Embase and Cochrane Library databases were searched to identify observational studies on FTD/TPI monotherapy for mCRC. Papers describing use of FTD/TPI monotherapy outside clinical trials in series of patients evaluable for effectiveness were eligible. The outcomes of interest were median progression free survival (mPFS), median overall survival (mOS) as well as mean PFS time restricted to six months (PFS 6m ) and mean OS time restricted to one year (OS 1y ). Results of the pooled analyses of observational studies were compared to the results of the Japanese phase II trial and the two phase III trials, RECOURSE and TERRA. Results: Seven published and two unpublished studies with 1008 patients from 64 centres were included for analysis. The pooled mPFS was 2.2 months (95% CI 2.1 to 2.3 months), and the pooled mOS was 6.6 months (95% CI 6.1 to 7.1 months). PFS 6m was 2.9 months (95% CI 2.6 to 3.1 months) and OS 1y was 6.8 (95% CI 6.0 to 7.5) months. While these results all reflect RECOURSE, the pooled mOS is lower than in the phase II trial and the OS 1y is inferior to both the phase II trial and TERRA. Conclusion: This systematic review and a meta-analysis indicates that in real life settings, the survival benefit of FTD/TPI monotherapy in patients with therapy refractory mCRC reflects the outcomes in RECOURSE but is inferior to outcomes in the two Asian efficacy trials. What is already known TAS 102 (Lonsurf) is an oral fixed dose combination of trifluridine (FTD) and tipiracil (TPI) indicated as salvage-line treatment in patients with therapy refractory metastatic colorectal cancer (mCRC). A Japanese phase II trial and two phase III trials, RECOURSE and TERRA, demonstrated that FTD/TPI prolonged overall survival. What this study adds This systematic review and meta-analysis of real life data from 64 sites indicates that the effectiveness in daily clinical practice settings of FTD/TPI monotherapy in late stage mCRC reflects the outcomes in RECOURCE but is inferior to the outc
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TAS-102 (FTD/TPI) is a new oral anti-tumour agent composed of a nucleoside analogue, trifluridine, and a thymidine phosphorylase inhibitor, tipiracil, indicated for patients with mCRC who are refractory to standard therapies. This study summarizes published and unpublished experience with FTD/TPI in clinical practice settings. Patients and methods: The Medline/PubMed, Embase and Cochrane Library databases were searched to identify observational studies on FTD/TPI monotherapy for mCRC. Papers describing use of FTD/TPI monotherapy outside clinical trials in series of patients evaluable for effectiveness were eligible. The outcomes of interest were median progression free survival (mPFS), median overall survival (mOS) as well as mean PFS time restricted to six months (PFS 6m ) and mean OS time restricted to one year (OS 1y ). Results of the pooled analyses of observational studies were compared to the results of the Japanese phase II trial and the two phase III trials, RECOURSE and TERRA. Results: Seven published and two unpublished studies with 1008 patients from 64 centres were included for analysis. The pooled mPFS was 2.2 months (95% CI 2.1 to 2.3 months), and the pooled mOS was 6.6 months (95% CI 6.1 to 7.1 months). PFS 6m was 2.9 months (95% CI 2.6 to 3.1 months) and OS 1y was 6.8 (95% CI 6.0 to 7.5) months. While these results all reflect RECOURSE, the pooled mOS is lower than in the phase II trial and the OS 1y is inferior to both the phase II trial and TERRA. Conclusion: This systematic review and a meta-analysis indicates that in real life settings, the survival benefit of FTD/TPI monotherapy in patients with therapy refractory mCRC reflects the outcomes in RECOURSE but is inferior to outcomes in the two Asian efficacy trials. What is already known TAS 102 (Lonsurf) is an oral fixed dose combination of trifluridine (FTD) and tipiracil (TPI) indicated as salvage-line treatment in patients with therapy refractory metastatic colorectal cancer (mCRC). A Japanese phase II trial and two phase III trials, RECOURSE and TERRA, demonstrated that FTD/TPI prolonged overall survival. 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TAS-102 (FTD/TPI) is a new oral anti-tumour agent composed of a nucleoside analogue, trifluridine, and a thymidine phosphorylase inhibitor, tipiracil, indicated for patients with mCRC who are refractory to standard therapies. This study summarizes published and unpublished experience with FTD/TPI in clinical practice settings. Patients and methods: The Medline/PubMed, Embase and Cochrane Library databases were searched to identify observational studies on FTD/TPI monotherapy for mCRC. Papers describing use of FTD/TPI monotherapy outside clinical trials in series of patients evaluable for effectiveness were eligible. The outcomes of interest were median progression free survival (mPFS), median overall survival (mOS) as well as mean PFS time restricted to six months (PFS 6m ) and mean OS time restricted to one year (OS 1y ). Results of the pooled analyses of observational studies were compared to the results of the Japanese phase II trial and the two phase III trials, RECOURSE and TERRA. Results: Seven published and two unpublished studies with 1008 patients from 64 centres were included for analysis. The pooled mPFS was 2.2 months (95% CI 2.1 to 2.3 months), and the pooled mOS was 6.6 months (95% CI 6.1 to 7.1 months). PFS 6m was 2.9 months (95% CI 2.6 to 3.1 months) and OS 1y was 6.8 (95% CI 6.0 to 7.5) months. While these results all reflect RECOURSE, the pooled mOS is lower than in the phase II trial and the OS 1y is inferior to both the phase II trial and TERRA. Conclusion: This systematic review and a meta-analysis indicates that in real life settings, the survival benefit of FTD/TPI monotherapy in patients with therapy refractory mCRC reflects the outcomes in RECOURSE but is inferior to outcomes in the two Asian efficacy trials. What is already known TAS 102 (Lonsurf) is an oral fixed dose combination of trifluridine (FTD) and tipiracil (TPI) indicated as salvage-line treatment in patients with therapy refractory metastatic colorectal cancer (mCRC). A Japanese phase II trial and two phase III trials, RECOURSE and TERRA, demonstrated that FTD/TPI prolonged overall survival. What this study adds This systematic review and meta-analysis of real life data from 64 sites indicates that the effectiveness in daily clinical practice settings of FTD/TPI monotherapy in late stage mCRC reflects the outcomes in RECOURCE but is inferior to the outcomes in the Japanese phase II trial and TERRA.</description><subject>Administration, Oral</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - mortality</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Drug Combinations</subject><subject>Drug Resistance, Neoplasm</subject><subject>Humans</subject><subject>Observational Studies as Topic</subject><subject>Progression-Free Survival</subject><subject>Pyrrolidines - therapeutic use</subject><subject>Trifluridine - therapeutic use</subject><subject>Uracil - analogs &amp; derivatives</subject><subject>Uracil - therapeutic use</subject><issn>0284-186X</issn><issn>1651-226X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFO3DAQhq2qVVloH6EoRzhk8dix17l1hWhBQuJQKnGzHGcsuUrixXZA-_Z1ugvHnmY0880_0kfIN6BroIpeUaYaUPJpzSi0a5BUQMs-kBVIATVj8ukjWS1MvUAn5DSlP5RSxjfiMznhUFpK1Yo8b6u0TxlHk72tIr54fK2Cq0KXML6UYZjMUKU89x7TssjRu2GOvvcTXmW_89FYP1QXj9tfNVB2WbkQqxGzSflfpA1DiGhzSbFmshi_kE_ODAm_HusZ-f3j5vH6tr5_-Hl3vb2vbQM81y2z3WajgDe8E7I1hnOmBDipQLGub7HvW9ZSvmHGKexUI5noFqgzDafK8TNyccjdxfA8Y8p69MniMJgJw5w0YwCtYELKgooDamNIKaLTu-hHE_caqF5s6zfberGtj7bL3fnxxdyN2L9fvektwPcD4KeiZTSvIQ69zmZfnLhYdPi0wP_78RdfGI8D</recordid><startdate>20190803</startdate><enddate>20190803</enddate><creator>Andersen, Stig E.</creator><creator>Andersen, Ida B.</creator><creator>Jensen, Benny V.</creator><creator>Pfeiffer, Per</creator><creator>Ota, Takayo</creator><creator>Larsen, Jim S.</creator><general>Taylor &amp; Francis</general><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>7X8</scope></search><sort><creationdate>20190803</creationdate><title>A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer</title><author>Andersen, Stig E. ; Andersen, Ida B. ; Jensen, Benny V. ; Pfeiffer, Per ; Ota, Takayo ; Larsen, Jim S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-92cb7781343b569aa332851f68182bd9edd9290372af8eb84625ba332ba4308f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Administration, Oral</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Colorectal Neoplasms - drug therapy</topic><topic>Colorectal Neoplasms - mortality</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Drug Combinations</topic><topic>Drug Resistance, Neoplasm</topic><topic>Humans</topic><topic>Observational Studies as Topic</topic><topic>Progression-Free Survival</topic><topic>Pyrrolidines - therapeutic use</topic><topic>Trifluridine - therapeutic use</topic><topic>Uracil - analogs &amp; derivatives</topic><topic>Uracil - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andersen, Stig E.</creatorcontrib><creatorcontrib>Andersen, Ida B.</creatorcontrib><creatorcontrib>Jensen, Benny V.</creatorcontrib><creatorcontrib>Pfeiffer, Per</creatorcontrib><creatorcontrib>Ota, Takayo</creatorcontrib><creatorcontrib>Larsen, Jim S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Acta oncologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andersen, Stig E.</au><au>Andersen, Ida B.</au><au>Jensen, Benny V.</au><au>Pfeiffer, Per</au><au>Ota, Takayo</au><au>Larsen, Jim S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer</atitle><jtitle>Acta oncologica</jtitle><addtitle>Acta Oncol</addtitle><date>2019-08-03</date><risdate>2019</risdate><volume>58</volume><issue>8</issue><spage>1149</spage><epage>1157</epage><pages>1149-1157</pages><issn>0284-186X</issn><eissn>1651-226X</eissn><abstract>Background: The treatment options for patients with therapy refractory metastatic colorectal cancer (mCRC) are sparse. TAS-102 (FTD/TPI) is a new oral anti-tumour agent composed of a nucleoside analogue, trifluridine, and a thymidine phosphorylase inhibitor, tipiracil, indicated for patients with mCRC who are refractory to standard therapies. This study summarizes published and unpublished experience with FTD/TPI in clinical practice settings. Patients and methods: The Medline/PubMed, Embase and Cochrane Library databases were searched to identify observational studies on FTD/TPI monotherapy for mCRC. Papers describing use of FTD/TPI monotherapy outside clinical trials in series of patients evaluable for effectiveness were eligible. The outcomes of interest were median progression free survival (mPFS), median overall survival (mOS) as well as mean PFS time restricted to six months (PFS 6m ) and mean OS time restricted to one year (OS 1y ). Results of the pooled analyses of observational studies were compared to the results of the Japanese phase II trial and the two phase III trials, RECOURSE and TERRA. Results: Seven published and two unpublished studies with 1008 patients from 64 centres were included for analysis. The pooled mPFS was 2.2 months (95% CI 2.1 to 2.3 months), and the pooled mOS was 6.6 months (95% CI 6.1 to 7.1 months). PFS 6m was 2.9 months (95% CI 2.6 to 3.1 months) and OS 1y was 6.8 (95% CI 6.0 to 7.5) months. While these results all reflect RECOURSE, the pooled mOS is lower than in the phase II trial and the OS 1y is inferior to both the phase II trial and TERRA. Conclusion: This systematic review and a meta-analysis indicates that in real life settings, the survival benefit of FTD/TPI monotherapy in patients with therapy refractory mCRC reflects the outcomes in RECOURSE but is inferior to outcomes in the two Asian efficacy trials. What is already known TAS 102 (Lonsurf) is an oral fixed dose combination of trifluridine (FTD) and tipiracil (TPI) indicated as salvage-line treatment in patients with therapy refractory metastatic colorectal cancer (mCRC). A Japanese phase II trial and two phase III trials, RECOURSE and TERRA, demonstrated that FTD/TPI prolonged overall survival. What this study adds This systematic review and meta-analysis of real life data from 64 sites indicates that the effectiveness in daily clinical practice settings of FTD/TPI monotherapy in late stage mCRC reflects the outcomes in RECOURCE but is inferior to the outcomes in the Japanese phase II trial and TERRA.</abstract><cop>England</cop><pub>Taylor &amp; Francis</pub><pmid>31002008</pmid><doi>10.1080/0284186X.2019.1605192</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Taylor & Francis:Master (3349 titles); Alma/SFX Local Collection
subjects Administration, Oral
Antineoplastic Agents - therapeutic use
Colorectal Neoplasms - drug therapy
Colorectal Neoplasms - mortality
Colorectal Neoplasms - pathology
Drug Combinations
Drug Resistance, Neoplasm
Humans
Observational Studies as Topic
Progression-Free Survival
Pyrrolidines - therapeutic use
Trifluridine - therapeutic use
Uracil - analogs & derivatives
Uracil - therapeutic use
title A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer
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