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

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer. / Andersen, Stig E.; Andersen, Ida B; Jensen, Benny V; Pfeiffer, Per; Ota, Takayo; Larsen, Jim S.

I: Acta Oncologica, Bind 58, Nr. 8, 2019, s. 1149-1157.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Andersen, SE, Andersen, IB, Jensen, BV, Pfeiffer, P, Ota, T & Larsen, JS 2019, 'A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer', Acta Oncologica, bind 58, nr. 8, s. 1149-1157. https://doi.org/10.1080/0284186X.2019.1605192

APA

Andersen, S. E., Andersen, I. B., Jensen, B. V., Pfeiffer, P., Ota, T., & Larsen, J. S. (2019). A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer. Acta Oncologica, 58(8), 1149-1157. https://doi.org/10.1080/0284186X.2019.1605192

Vancouver

Andersen SE, Andersen IB, Jensen BV, Pfeiffer P, Ota T, Larsen JS. A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer. Acta Oncologica. 2019;58(8):1149-1157. https://doi.org/10.1080/0284186X.2019.1605192

Author

Andersen, Stig E. ; Andersen, Ida B ; Jensen, Benny V ; Pfeiffer, Per ; Ota, Takayo ; Larsen, Jim S. / A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer. I: Acta Oncologica. 2019 ; Bind 58, Nr. 8. s. 1149-1157.

Bibtex

@article{36625483df6d4614a91257b09ad1659a,
title = "A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer",
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 This study summarizes published and unpublished experience with FTD/TPI in clinical practice settings.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 (PFS6m) and mean OS time restricted to one year (OS1y). 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). PFS6m was 2.9 months (95% CI 2.6 to 3.1 months) and OS1y 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 OS1y 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.",
keywords = "Administration, Oral, Antineoplastic Agents/therapeutic use, Colorectal Neoplasms/drug therapy, Drug Combinations, Drug Resistance, Neoplasm, Humans, Observational Studies as Topic, Progression-Free Survival, Pyrrolidines/therapeutic use, Trifluridine/therapeutic use, Uracil/analogs & derivatives",
author = "Andersen, {Stig E.} and Andersen, {Ida B} and Jensen, {Benny V} and Per Pfeiffer and Takayo Ota and Larsen, {Jim S.}",
year = "2019",
doi = "10.1080/0284186X.2019.1605192",
language = "English",
volume = "58",
pages = "1149--1157",
journal = "Acta Oncologica",
issn = "1100-1704",
publisher = "Taylor & Francis",
number = "8",

}

RIS

TY - JOUR

T1 - A systematic review of observational studies of trifluridine/tipiracil (TAS-102) for metastatic colorectal cancer

AU - Andersen, Stig E.

AU - Andersen, Ida B

AU - Jensen, Benny V

AU - Pfeiffer, Per

AU - Ota, Takayo

AU - Larsen, Jim S.

PY - 2019

Y1 - 2019

N2 - 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 (PFS6m) and mean OS time restricted to one year (OS1y). 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). PFS6m was 2.9 months (95% CI 2.6 to 3.1 months) and OS1y 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 OS1y 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.

AB - 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 (PFS6m) and mean OS time restricted to one year (OS1y). 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). PFS6m was 2.9 months (95% CI 2.6 to 3.1 months) and OS1y 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 OS1y 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.

KW - Administration, Oral

KW - Antineoplastic Agents/therapeutic use

KW - Colorectal Neoplasms/drug therapy

KW - Drug Combinations

KW - Drug Resistance, Neoplasm

KW - Humans

KW - Observational Studies as Topic

KW - Progression-Free Survival

KW - Pyrrolidines/therapeutic use

KW - Trifluridine/therapeutic use

KW - Uracil/analogs & derivatives

U2 - 10.1080/0284186X.2019.1605192

DO - 10.1080/0284186X.2019.1605192

M3 - Review

C2 - 31002008

VL - 58

SP - 1149

EP - 1157

JO - Acta Oncologica

JF - Acta Oncologica

SN - 1100-1704

IS - 8

ER -

ID: 235406741