500mg Fulvestrant Versus Everolimus Plus Exemestane in MBC Patients Refractory to Previous AI
NCT ID: NCT03695341
Last Updated: 2019-06-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
130 participants
OBSERVATIONAL
2018-05-14
2019-05-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Fulvestrant
Fulvestrant 500mg per month (D1, D28, q28d), with a loading dose 500mg of first dose at D15
No interventions assigned to this group
Everolimus plus Exemestane
Everolimys 10 mg or 5 mg daily; Exemestane 25mg per day
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Patients who were refractory to previous Aromatase Inhibitors
3. Patients treated with Fulvestrant or Everolimus plus Exemestane in any line in metastatic setting in Fudan University Shanghai Cancer Center，starting from 2013.06.01-2016.06.01
4. Available medical history
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
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Fudan University
OTHER
Responsible Party
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Biyun Wang, MD
Professor
Principal Investigators
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Biyun Wang, Professor
Role: PRINCIPAL_INVESTIGATOR
Fudan University
Locations
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Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, China
Countries
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References
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Li Y, Xie Y, Gong C, Zhao Y, Zhang J, Zhang S, Wang L, Chen S, Hu X, Wang B. Comparative Treatment Patterns and Outcomes of Fulvestrant versus Everolimus Plus Exemestane for Postmenopausal Metastatic Breast Cancer Resistant to Aromatase Inhibitors in Real-World Experience. Ther Clin Risk Manag. 2020 Jun 30;16:607-615. doi: 10.2147/TCRM.S255365. eCollection 2020.
Other Identifiers
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YOUNGBC-3
Identifier Type: -
Identifier Source: org_study_id
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