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Beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review

BACKGROUND: The optimal chemotherapeutic regimen for use beyond the second line for patients with metastatic colorectal cancer (mCRC) remains unclear. MATERIALS AND METHODS: We systematically searched the Cochrane Database of Systematic Reviews, EMBASE and Medline for records published between Janua...

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Autores principales: Arnold, D, Prager, G W, Quintela, A, Stein, A, Moreno Vera, S, Mounedji, N, Taieb, J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913602/
https://www.ncbi.nlm.nih.gov/pubmed/29452346
http://dx.doi.org/10.1093/annonc/mdy038
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author Arnold, D
Prager, G W
Quintela, A
Stein, A
Moreno Vera, S
Mounedji, N
Taieb, J
author_facet Arnold, D
Prager, G W
Quintela, A
Stein, A
Moreno Vera, S
Mounedji, N
Taieb, J
author_sort Arnold, D
collection PubMed
description BACKGROUND: The optimal chemotherapeutic regimen for use beyond the second line for patients with metastatic colorectal cancer (mCRC) remains unclear. MATERIALS AND METHODS: We systematically searched the Cochrane Database of Systematic Reviews, EMBASE and Medline for records published between January 2002 and May 2017, and cancer congress databases for records published between January 2014 and June 2017. Eligible studies evaluated the efficacy, safety and patient-reported outcomes of monotherapies or combination therapies at any dose and number of treatment cycles for use beyond the second line in patients with mCRC. Studies were assessed for design and quality, and a qualitative data synthesis was conducted to understand the impact of treatment on overall survival and other relevant cancer-related outcomes. RESULTS: The search yielded 938 references of which 68 were included for qualitative synthesis. There was limited evidence to support rechallenge with chemotherapy, targeted therapy or both. Compared with placebo, an overall survival benefit for trifluridine/tipiracil (also known as TAS-102) or regorafenib has been shown for patients previously treated with conventional chemotherapy and targeted therapy. There was no evidence to suggest a difference in efficacy between these treatments. Patient choice and quality of life at this stage of treatment should also be considered when choosing an appropriate therapy. CONCLUSIONS: These findings support the introduction of an approved agent such as trifluridine/tipiracil or regorafenib beyond the second line before any rechallenge in patients with mCRC who have failed second-line treatment.
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spelling pubmed-59136022018-04-30 Beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review Arnold, D Prager, G W Quintela, A Stein, A Moreno Vera, S Mounedji, N Taieb, J Ann Oncol Reviews BACKGROUND: The optimal chemotherapeutic regimen for use beyond the second line for patients with metastatic colorectal cancer (mCRC) remains unclear. MATERIALS AND METHODS: We systematically searched the Cochrane Database of Systematic Reviews, EMBASE and Medline for records published between January 2002 and May 2017, and cancer congress databases for records published between January 2014 and June 2017. Eligible studies evaluated the efficacy, safety and patient-reported outcomes of monotherapies or combination therapies at any dose and number of treatment cycles for use beyond the second line in patients with mCRC. Studies were assessed for design and quality, and a qualitative data synthesis was conducted to understand the impact of treatment on overall survival and other relevant cancer-related outcomes. RESULTS: The search yielded 938 references of which 68 were included for qualitative synthesis. There was limited evidence to support rechallenge with chemotherapy, targeted therapy or both. Compared with placebo, an overall survival benefit for trifluridine/tipiracil (also known as TAS-102) or regorafenib has been shown for patients previously treated with conventional chemotherapy and targeted therapy. There was no evidence to suggest a difference in efficacy between these treatments. Patient choice and quality of life at this stage of treatment should also be considered when choosing an appropriate therapy. CONCLUSIONS: These findings support the introduction of an approved agent such as trifluridine/tipiracil or regorafenib beyond the second line before any rechallenge in patients with mCRC who have failed second-line treatment. Oxford University Press 2018-04 2018-02-14 /pmc/articles/PMC5913602/ /pubmed/29452346 http://dx.doi.org/10.1093/annonc/mdy038 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the European Society for Medical Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Reviews
Arnold, D
Prager, G W
Quintela, A
Stein, A
Moreno Vera, S
Mounedji, N
Taieb, J
Beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review
title Beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review
title_full Beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review
title_fullStr Beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review
title_full_unstemmed Beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review
title_short Beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review
title_sort beyond second-line therapy in patients with metastatic colorectal cancer: a systematic review
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913602/
https://www.ncbi.nlm.nih.gov/pubmed/29452346
http://dx.doi.org/10.1093/annonc/mdy038
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