Status:
UNKNOWN
Pyrotinib in Combination With Letrozole in Patients With HER2-Positive, ER-Positive Metastatic Breast Cancer
Lead Sponsor:
Hunan Cancer Hospital
Collaborating Sponsors:
Jiangsu HengRui Medicine Co., Ltd.
Conditions:
Metastatic Breast Cancer
Eligibility:
All Genders
18-70 years
Phase:
PHASE2
Brief Summary
This is a prospective, single-arm, multi-center clinical study of pyrotinib in combination With letrozole in patients With HER2-Positive, ER-Positive metastatic breast cancer. Our aim was to explore t...
Detailed Description
ER+/HER2+ metastatic breast cancer is a special subtype of HER2+ breast cancer. General guidelines recommend chemotherapy combined with HER2-targeted therapy for this subtype of patients. However, for...
Eligibility Criteria
Inclusion
- Patients with HER2+/ER+ recurrent or metastatic breast cancer confirmed by histopathology;
- HER2 positive: HER2 IHC 3+, or HER2 IHC 2+ and ISH positive
- ER positive: the percentage of cells positive for ER expression ≥ 10%
- Premenopausal, perimenopausal or postmenopausal patients (with OFS, if pre- or perimenopausal);
- If the patient is bilateral breast cancer, metastasis lesions must be HER2 and ER positive;
- 18-70 years old;
- ECOG PS 0～1;
- Life expectancy is not less than 12 weeks;
- At least one measurable lesion according to RECIST 1.1;
- Prior (neo) adjuvant trastuzumab, pertuzumab or chemotherapy were eligible, and the disease free interval must be greater than 12 months from completion of (neo) adjuvant trastuzumab and pertuzumab to metastatic diagnosis;
- Prior (neo) adjuvant hormone therapy was allowed, if received adjuvant AI, the disease free interval must be greater than 12 months from the completion of treatment;
- Disease-free Survival after surgery (DFS) ≥12 months;
- Patients with adequate organ function before enrollment: ANC ≥ 1.5×109/L, PLT ≥ 75×109/L, Hb ≥ 100 g/L; TBIL≤1.0ULN；ALT and AST≤3×ULN (ALT and AST≤5×ULN if liver metastasis); BUN and Cr≤1.5×ULN and CCr≥50 mL/min; LVEF ≥ 50% and QTc \< 480 ms;
- Signed informed consent.
Exclusion
- Central nervous system metastasis;
- patients with Visceral crisis;
- Unable to swallow, chronic diarrhea and intestinal obstruction, there are many factors affecting drug use and absorption;
- received radiotherapy, hormone therapy, chemotherapy, surgery (excluding local puncture) or molecular targeted therapy for advanced or metastatic disease;
- received radiotherapy, chemotherapy, surgery (excluding local puncture) or molecular targeted therapy within 4 weeks prior to randomization;
- Received hormone therapy within 2 weeks prior to randomization;
- Participated in other clinical trial within 4 weeks prior to randomization;
- Previous or ongoing use of HER2-targeted tyrosine kinase inhibitors (lapatinib, neratinib or pyrotinib);
- Other malignancies within 5 years, except for cured skin basal cell carcinoma,carcinoma in-situ of uterine cervix and squamous-cell carcinoma;
- Receive other anti-tumour therapy at the same time;
- History of immunodeficiency, including HIV positive, HCV, active hepatitis B, or other acquired, congenital immunodeficiency disorders, or organ transplantation, is known;
- History of any kind of Heart disease;
- All female patients in pregnancy or breastfeeding period, fertile women with positive baseline pregnancy tests;
- Evidence of significant medical illness that will substantially increase the risk on the participation or completion of the study in the investigator's judgment. Examples included, but not limited to, hypertension, severe diabetes, etc;
- History of neurological or psychiatric disorders, including epilepsy or dementia;
- Patients not eligible for this study judged by the investigator.
Key Trial Info
Start Date :
November 6 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 31 2023
Estimated Enrollment :
86 Patients enrolled
Trial Details
Trial ID
NCT04407988
Start Date
November 6 2019
End Date
March 31 2023
Last Update
October 13 2021
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Hunan Cancer Hospital
Changsha, Hunan, China, 410006