Adjuvant trastuzumab regimen for HER2-positive early-stage breast cancer: a systematic review and meta-analysis

Objective: Breast cancer remains to be the globally leading female cancer. About 15% to 20% of breast cancers have human epidermal growth factor receptor 2 (HER2)-positive tumors – a more aggressive breast cancer subtype with shortened survival. In the light of new and updated trial data on trastuzumab therapy for HER2-positive early-stage breast cancer (EBC), we conducted a systematic review and meta-analysis to update the pooling of its relative treatment effects. Methods: Systematic search was performed through Pubmed and Scopus to identify studies comparing survival outcomes and risks of heart toxicity effects of adjuvant trastuzumab with chemotherapy versus chemotherapy alone for HER2-positive EBC patients. Results: Based on the eight included studies in the review, combining trastuzumab with chemotherapy continues to show lowered death and relapse risks by one-third. The decision to initiate trastuzumab, however, needs to be prudently deliberated as two to three times more cardiotoxicity risk was shown to be associated with its use. Conclusion: Administering adjuvant trastuzumab in a weekly cycle concurrently with anthracycline-taxane chemotherapy regimen appears to be a preferable option to optimize its favorable effect in improving DFS and to prevent significantly higher risk for cardiotoxic effects.

Tags
Data and Resources
To access the resources you must log in

This item has no data

Identity

Description: The Identity category includes attributes that support the identification of the resource.

Field Value
PID https://www.doi.org/10.1080/17512433.2019.1637252
PID https://www.doi.org/10.6084/m9.figshare.8845679
PID pmc:PMC6816496
PID pmid:31287333
PID https://www.doi.org/10.6084/m9.figshare.8845679.v1
URL https://www.tandfonline.com/doi/pdf/10.1080/17512433.2019.1637252?needAccess=true
URL http://dx.doi.org/10.1080/17512433.2019.1637252
URL https://pesquisa.bvsalud.org/portal/resource/pt/mdl-31287333
URL https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816496
URL http://dx.doi.org/10.6084/m9.figshare.8845679
URL http://dx.doi.org/10.6084/m9.figshare.8845679.v1
URL https://tandfonline.com/doi/pdf/10.1080/17512433.2019.1637252
URL http://europepmc.org/articles/PMC6816496
URL https://academic.microsoft.com/#/detail/2957213237
URL https://www.tandfonline.com/doi/pdf/10.1080/17512433.2019.1637252
URL https://www.tandfonline.com/doi/full/10.1080/17512433.2019.1637252
Access Modality

Description: The Access Modality category includes attributes that report the modality of exploitation of the resource.

Field Value
Access Right Open Access
Attribution

Description: Authorships and contributors

Field Value
Author Ong The Due , 0000-0001-5787-4145
Publishing

Description: Attributes about the publishing venue (e.g. journal) and deposit location (e.g. repository)

Field Value
Collected From PubMed Central; ORCID; UnpayWall; Datacite; figshare; Crossref; Microsoft Academic Graph
Hosted By Europe PubMed Central; figshare; Expert Review of Clinical Pharmacology
Journal Expert Review of Clinical Pharmacology, 12, null
Publication Date 2019-07-09
Publisher Informa UK Limited
Additional Info
Field Value
Language Undetermined
Resource Type Other literature type; Article
keyword keywords.General Pharmacology, Toxicology and Pharmaceutics
keyword FOS: Computer and information sciences
system:type publication
Management Info
Field Value
Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::d8b1e9889d255f49d6d9463ee4d9723c
Author jsonws_user
Last Updated 27 December 2020, 02:03 (CET)
Created 27 December 2020, 02:03 (CET)