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Trastuzumab emtansine for HER2-positive metastatic breast cancer: Outcomes from a whole-of-population Australian cohort.
Daniels, Benjamin; Kiely, Belinda E; Tang, Monica; Houssami, Nehmat; Lord, Sarah J; Pearson, Sallie-Anne.
Afiliação
  • Daniels B; Medicines Policy Research Unit, Centre for Big Data Research in Health, UNSW, Sydney, Australia. Electronic address: b.daniels@unsw.edu.au.
  • Kiely BE; NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
  • Tang M; Medicines Policy Research Unit, Centre for Big Data Research in Health, UNSW, Sydney, Australia.
  • Houssami N; Sydney School of Public Health, Faculty of Medicine & Health, University of Sydney, Sydney, Australia.
  • Lord SJ; NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia; School of Medicine, University of Notre Dame Australia, NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
  • Pearson SA; Medicines Policy Research Unit, Centre for Big Data Research in Health, UNSW, Sydney, Australia.
Breast ; 58: 106-112, 2021 Aug.
Article em En | MEDLINE | ID: mdl-33992964
ABSTRACT

PURPOSE:

We aim to describe the treatment patterns and overall survival (OS) outcomes in patients receiving trastuzumab emtansine (T-DM1) for HER2-positive metastatic breast cancer (HER2+MBC) in routine clinical care.

METHODS:

Retrospective, whole-of-population cohort study of people initiating T-DM1 for HER2+MBC between October 2015 and May 2019 in Australia. We used dispensing claims to estimate time-to-T-DM1 initiation, duration of treatment, and treatments administered prior to and following T-DM1 therapy. We estimated OS from T-DM1 initiation and stratified results based on whether patients received first- or second-line T-DM1 treatment. We benchmarked outcomes to those reported in the pivotal, EMILIA trial.

RESULTS:

345 patients initiated T-DM1 309 as second-line therapy for HER2+MBC and 36 as first-line therapy. 51% of patients had received endocrine therapy and 98% of second-line patients received pertuzumab prior to starting T-DM1. The median age was 57 years (53 in EMILIA); median time-to-T-DM1 initiation from start of HER2-targeted therapy for HER2+MBC was 11.6 months (IQR 7.9-16.6); median duration of T-DM1 treatment was 6.5 months (3.1-13.5; 7.6 months in EMILIA), and median OS was 19.3 months (7.9-29.5; 29.9 months in EMILIA).

CONCLUSIONS:

Our findings highlight differences in patient characteristics (older, more previous pertuzumab therapy) and outcomes (shorter OS) from the T-DM1 pivotal trial and provide real-world estimates that can inform patient, clinician and policy, decisions around the use of HER2-targeted therapies in routine clinical care.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Maitansina Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Maitansina Idioma: En Ano de publicação: 2021 Tipo de documento: Article