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Molecular Assays to Determine Optimal Duration of Adjuvant Endocrine Therapy in Breast Cancer.
Anandan, Apoorva; Sharifi, Marina; O'Regan, Ruth.
Afiliação
  • Anandan A; Department of Medicine, University of Wisconsin Hospitals and Clinics, Madison, WI, 53705, USA. aanandan@uwhealth.org.
  • Sharifi M; Division of Hematology, Medical Oncology and Palliative Care, University of Wisconsin Carbone Cancer Center, Madison, WI, USA.
  • O'Regan R; Division of Hematology, Medical Oncology and Palliative Care, University of Wisconsin Carbone Cancer Center, Madison, WI, USA.
Curr Treat Options Oncol ; 21(10): 84, 2020 08 15.
Article em En | MEDLINE | ID: mdl-32803324
OPINION STATEMENT: Hormone receptor (HR) positive breast cancer has a high propensity for late recurrences that might be prevented with longer durations of endocrine therapy (ET). However, trials evaluating extended adjuvant ET have produced somewhat conflicting results. Additionally, ET is associated with not only day to day side effects that can impact quality of life, but more detrimental effects that can cause significant morbidity. Although patients with higher stage disease are at greater risk of late recurrences, even patients with stage 1 disease have a significant risk of recurrence after 5 years. Current guidelines recommend extending therapy for patients with node-positive disease, but recommendations for patients with node-negative disease are less clear. This has led to the development of various genomic tests to aid oncologists in further individualizing their approach when it comes to deciding which subpopulation of patients with HR-positive breast cancer may benefit from extending their endocrine therapy beyond 5 years. There are several assays that are prognostic of recurrences years 6 to 10 following diagnosis. Additionally, the breast cancer index has been shown to be predictive of extended ET in patients who have completed 5 years of tamoxifen. None of the available assays are, to date, predictive of recurrence after 10 years. Genomic testing is not appropriate for all patients, especially if the results will not predict the choice of further treatment. Ultimately, genomic testing should help facilitate shared decision making between the patient and oncologist.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptores de Progesterona / Receptores de Estrogênio / Biomarcadores Tumorais / Quimioterapia Adjuvante / Antineoplásicos Hormonais / Recidiva Local de Neoplasia Tipo de estudo: Guideline / Prognostic_studies Aspecto: Patient_preference Limite: Female / Humans Idioma: En Revista: Curr Treat Options Oncol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptores de Progesterona / Receptores de Estrogênio / Biomarcadores Tumorais / Quimioterapia Adjuvante / Antineoplásicos Hormonais / Recidiva Local de Neoplasia Tipo de estudo: Guideline / Prognostic_studies Aspecto: Patient_preference Limite: Female / Humans Idioma: En Revista: Curr Treat Options Oncol Ano de publicação: 2020 Tipo de documento: Article