This study is a prospective non-interventional real-world study enrolling patients with advanced breast cancer who are ER+/HER2- and have ESR1- gene mutations, collecting information on patients' complaints, physical examination, laboratory tests, imaging tests and adverse events to observe the safety of elacestrant treatment.
Study Type
OBSERVATIONAL
Enrollment
350
345 mg/day once daily oral dosing
Hainan Hospital of Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine (Boao Research Hospital, Hainan)
Qionghai, Hainan, China
RECRUITINGAdverse event rate
Percentage of occurrences of adverse events
Time frame: 6 months
Serious adverse event rate
Percentage of occurrences of serious adverse events
Time frame: 6 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.