ASCO adds Oncotype DX to marker guideline

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 16 No 11
Volume 16
Issue 11

ASCO has added the Oncotype DX gene expression assay to its updated guideline for the use of tumor markers in breast cancer

ALEXANDRIA, Virginia—ASCO has added the Oncotype DX gene expression assay to its updated guideline for the use of tumor markers in breast cancer (J Clin Oncol November 20, 2007). ASCO evaluated but did not recommend four other new markers for breast cancer: cyclin E, proteomic analysis, bone marrow micrometastases, and circulating tumor cells. Previously recommended tests include CA 15-3, CA 27.29, CEA, ER/PR, and HER2.

The Oncotype DX tumor marker test is recommended for patients with newly diagnosed node-negative breast cancer that is ER-positive and/or PR-positive. The test measures multiple genes at once to estimate the risk of breast cancer recurrence. Patients with a low recurrence score may be able to receive only hormone therapy and avoid chemotherapy. Other gene assays under investigation but not yet recommended include MammaPrint, the Rotterdam Signature, and the Breast Cancer Gene Expression Ratio.

Also newly recommended for estimating a node-negative patient's prognosis are urokinase plasminogen activator (uPA) and plasminogen activator inhibitor (PAI-1). Patients with tumors that do not have uPA and PAI-1 have a good prognosis and may not need chemotherapy. However, the test is not currently commercially available in the US.

Related Videos
Sara M. Tolaney, MD, MPH, an expert on breast cancer
Sara M. Tolaney, MD, MPH, an expert on breast cancer
The August CancerNetwork Snap Recap takes a look back at key FDA news updates, as well as expert perspectives on the chemotherapy shortage.
Ann H. Partridge, MD, MPH, talks about how fertility preservation can positively impact the psychosocial health in patients with breast cancer.
Daniel G. Stover, MD, describes how findings from the phase 3 NATALEE trial may support expanding the portion of patients who receive CDK 4/6 inhibitors as a treatment for hormone receptor–positive, HER2-negative breast cancer.
Daniel G. Stover, MD, suggests that stromal tumor infiltrating lymphocytes may serve as a biomarker of immune activation and can potentially help optimize therapy with microtubule-targeting agents for patients with metastatic breast cancer.
Sara M. Tolaney, MD, MPH, discusses how, compared with antibody-drug conjugates, chemotherapy produces low response rates and disease control in the treatment of those with hormone receptor–positive, HER2-negative metastatic breast cancer.
Hope Rugo, MD, speaks to the importance of identifying patients with aromatase inhibitor–resistant, hormone receptor–positive, HER2-negative advanced breast cancer who are undergoing treatment with capivasertib/fulvestrant who may be at a high risk of developing diabetes or hyperglycemia.
Sara M. Tolaney, MD, MPH, describes the benefit of sacituzumab govitecan for patients with HER2-low metastatic breast cancer seen in the final overall survival analysis of the phase 3 TROPiCS-02 study.
An expert from Dana-Farber Cancer Institute describes which patients hormone receptor-positive,  HER2-negative breast cancer will benefit most from treatment with sacituzumab govitecan.
Related Content