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Management of Early-Stage Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer

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JCO ONCOLOGY PRACTICE
卷 17, 期 6, 页码 320-+

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1200/OP.21.00020

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The addition of trastuzumab to chemotherapy has significantly improved the prognosis of early-stage HER2-positive breast cancer, but disease recurrence still remains a challenge. Advances in understanding tumor biology have led to the development of optimized anti-HER2 drugs and strategies to further enhance survival outcomes. Recurrences in the brain, biological heterogeneity within HER2-positive disease, and the need to personalize treatment strategies based on biomarkers are key considerations in the management of early-stage, HER2-positive breast cancer.
The addition of trastuzumab to chemotherapy dramatically improved the prognosis of early-stage human epidermal growth factor receptor 2 (HER2)-positive breast cancer. However, 15%-31% of patients still develop disease recurrence, on the basis of long-term follow-up of adjuvant pivotal trials. A better understanding of tumor biology has led to the development of optimized anti-HER2 drugs and add-on strategies to further improve survival outcomes. In the neoadjuvant setting, dual HER2 blockade with trastuzumab and pertuzumab plus chemotherapy has increased the rate of pathologic complete response, a surrogate marker of improved long-term outcome; yet, in the adjuvant setting, it has led to small benefits in invasive disease-free survival. Extended adjuvant therapy with the irreversible pan-HER2 inhibitor neratinib is an option for selected patients with HER2-positive and estrogen receptor-positive disease who have received neoadjuvant or adjuvant chemotherapy plus trastuzumab. Additionally, the use of the antibody-drug conjugate trastuzumab-emtansine has led to a significant improvement in invasive disease-free survival for patients with residual disease following neoadjuvant therapy and has taught us the importance of using preoperative therapy to adapt adjuvant treatment. Nevertheless, recurrences in the brain remain an important caveat, and not all patients benefit to the same extent from anti-HER2 therapies. Biologic heterogeneity within HER2-positive disease may modulate treatment response and prognosis. De-escalating treatment strategies to avoid unnecessary treatments and toxicities, without compromising outcomes, have become a crucial focus of research. To stratify patient risks and optimize treatment selection, other biomarkers including intrinsic subtype, level of HER2, and tumor-infiltrating lymphocytes should be further evaluated. We discuss the latest evidence on the current approach of early-stage, HER2-positive breast cancer and present future perspectives on its management.

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