Biomarkers for Adjuvant Endocrine and Chemotherapy in Early-Stage Breast Cancer: ASCO Guideline Update

Author:

Andre Fabrice1ORCID,Ismaila Nofisat2ORCID,Allison Kimberly H.3,Barlow William E.4ORCID,Collyar Deborah E.5ORCID,Damodaran Senthil6ORCID,Henry N. Lynn7ORCID,Jhaveri Komal89,Kalinsky Kevin10,Kuderer Nicole M.11ORCID,Litvak Anya12,Mayer Erica L.13ORCID,Pusztai Lajos14ORCID,Raab Rachel15ORCID,Wolff Antonio C.16ORCID,Stearns Vered16ORCID

Affiliation:

1. Institute Gustave Roussy, Paris, France

2. American Society of Clinical Oncology, Alexandria, VA

3. Stanford University Medical Center, Stanford, CA

4. Cancer Research and Biostatistics, Seattle, WA

5. Patient Advocates in Research (PAIR), Danville, CA

6. MD Anderson Cancer Center, Houston, TX

7. University of Michigan Rogel Cancer Center, Ann Arbor, MI

8. Memorial Sloan Kettering Cancer Center, New York, NY

9. Weill Cornell Medical College, New York, NY

10. Winship Cancer Institute at Emory University, Atlanta, GA

11. Advanced Cancer Research Group, Kirkland, WA

12. Cancer Center at Saint Barnabas Medical Center, Livingston, NJ

13. Dana-Farber Cancer Institute, Boston, MA

14. Yale Cancer Center, New Haven, CT

15. Messino Cancer Centers-A Division of American Oncology Partners, Asheville, NC

16. Johns Hopkins University, Baltimore, MD

Abstract

PURPOSE To update recommendations on appropriate use of breast cancer biomarker assay results to guide adjuvant endocrine and chemotherapy decisions in early-stage breast cancer. METHODS An updated literature search identified randomized clinical trials and prospective-retrospective studies published from January 2016 to October 2021. Outcomes of interest included overall survival and disease-free or recurrence-free survival. Expert Panel members used informal consensus to develop evidence-based recommendations. RESULTS The search identified 24 studies informing the evidence base. RECOMMENDATIONS Clinicians may use Onco type DX, MammaPrint, Breast Cancer Index (BCI), and EndoPredict to guide adjuvant endocrine and chemotherapy in patients who are postmenopausal or age > 50 years with early-stage estrogen receptor (ER)–positive, human epidermal growth factor receptor 2 (HER2)–negative (ER+ and HER2–) breast cancer that is node-negative or with 1-3 positive nodes. Prosigna and BCI may be used in postmenopausal patients with node-negative ER+ and HER2– breast cancer. In premenopausal patients, clinicians may use Onco type in patients with node-negative ER+ and HER2– breast cancer. Current data suggest that premenopausal patients with 1-3 positive nodes benefit from chemotherapy regardless of genomic assay result. There are no data on use of genomic tests to guide adjuvant chemotherapy in patients with ≥ 4 positive nodes. Ki67 combined with other parameters or immunohistochemistry 4 score may be used in postmenopausal patients without access to genomic tests to guide adjuvant therapy decisions. BCI may be offered to patients with 0-3 positive nodes who received 5 years of endocrine therapy without evidence of recurrence to guide decisions about extended endocrine therapy. None of the assays are recommended for treatment guidance in individuals with HER2-positive or triple-negative breast cancer. Treatment decisions should also consider disease stage, comorbidities, and patient preferences. Additional information is available at www.asco.org/breast-cancer-guidelines .

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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