Oral SERD, a Novel Endocrine Therapy for Estrogen Receptor-Positive Breast Cancer

Author:

Neupane Niraj1,Bawek Sawyer2,Gurusinghe Sayuri2,Ghaffary Elham Moases3,Mirmosayyeb Omid3ORCID,Thapa Sangharsha4,Falkson Carla5,O’Regan Ruth5,Dhakal Ajay5

Affiliation:

1. Department of Internal Medicine, Rochester General Hospital, Rochester, NY 14621, USA

2. Department of Internal Medicine, University at Buffalo, Buffalo, NY 14203, USA

3. Isfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan 8174673461, Iran

4. Westchester Medical Center, New York Medical College, Valhalla, NY 10595, USA

5. Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA

Abstract

Breast cancer is the most common cancer among women worldwide, and estrogen receptor-positive (ER+) breast cancer accounts for a significant proportion of cases. While various treatments are available, endocrine therapies are often the first-line treatment for this type of breast cancer. However, the development of drug resistance poses a significant challenge in managing this disease. ESR1 mutations have been identified as a common mechanism of endocrine therapy resistance in ER+ breast cancer. The first-generation selective estrogen receptor degrader (SERD) fulvestrant has shown some activity against ESR1 mutant tumors. However, due to its poor bioavailability and need for intramuscular injection, it may not be the optimal therapy for patients. Second-generation SERDs were developed to overcome these limitations. These newer drugs have improved oral bioavailability and pharmacokinetics, making them more convenient and effective for patients. Several oral SERDs are now in phase III trials for early and advanced ER+ breast cancer. This review summarizes the background of oral SERD development, the current status, and future perspectives.

Publisher

MDPI AG

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