Pyrotinib Plus Capecitabine for Adjuvant Treatment of HER2 Positive Early-stage Breast Cancer

NCT ID: NCT06035016

Last Updated: 2023-09-13

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 300 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-06-01
• Study Completion Date: 2027-06-01

Brief Summary

This is a prospective, multicenter, registry-based cohort study to explore the efficacy and safety of Pyrotinib combined with Capecitabine for adjuvant treatment of HER2 positive early breast cancer compared with treatment of physician's choice. Pyrotinib is a small molecule tyrosine kinase inhibitor which can irreversibly inhibit HER1, HER2, and HER4.

Conditions

HER2-positive Breast Cancer; Early-stage Breast Cancer

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

cohort A

Pyrotinib 400mg, qd, po, day 1-21, q3w, Capecitabine 1000mg/m2, bid po d1-14, q3w

pyrotinib combined with Capecitabine

Intervention Type: DRUG

Pyrotinib 400mg, qd, po, day 1-21, q3w, Capecitabine 1000mg/m2, bid po d1-14, q3w

cohort B

treatment of physician's choice

treatment of physician's choice

Intervention Type: DRUG

Treatment of physician's choice

Interventions

pyrotinib combined with Capecitabine

Pyrotinib 400mg, qd, po, day 1-21, q3w, Capecitabine 1000mg/m2, bid po d1-14, q3w

Intervention Type: DRUG

treatment of physician's choice

Treatment of physician's choice

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Female patients ≥ 18 years and ≤ 75 years old;

2. Primary invasive breast cancer confirmed by histology;

3. HER2 positive breast cancer (IHC 3+, or IHC 2+ and FISH positive); lymph node positive, except for T0; lymph node negative and tumor >1cm, or tumor > 0.5 cm and ≤ 1cm, and accompanied by any of the following high-risk factors: pathological grade 3, ER/PR negative, or < 35 years old;

4. Having received mastectomy or breast conserving surgery, and received sentinel lymph node biopsy or axillary lymph node dissection, and within 90 days from the breast surgery;

5. With known ER/PR status of breast cancer;

6. ECOG score 0-1;

7. The patient's major organ functions meet all of the following requirements for blood tests:

1. Neutrophil count (ANC) ≥ 1,500/mm3 (1.5×109/L);

2. Platelet count (PLT) ≥ 75,000/mm3 (75×109/L);

3. Hemoglobin (Hb) ≥ 8 g/dL (80 g/L);

4. Serum creatinine (SCr) ≤ 1.5 times the upper limit of normal (ULN) or creatinine clearance ≥ 60 mL/min;

5. Total bilirubin (TBIL) ≤ 1.5 times the upper limit of normal (ULN);

6. Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) level ≤ 2.5 times the upper limit of normal (ULN), patients with liver metastases should be ≤ 5×ULN.

9. The participant voluntarily joins the study, signs the informed consent form, has good compliance, and cooperates with follow-ups.

Exclusion Criteria

1. Breast cancer recurs before enrollment, or local recurrence/ metastasis confirmed by radiology;

2. The subject has participated in other clinical trials within 4 weeks or 5 half-lives (whichever is longer) before enrollment;

3. The patient has previously received treatment including tyrosine kinase inhibitors targeting HER2 (e.g., lapatinib, neratinib, and pyrotinib);

4. The patient has been diagnosed with other malignancies within 5 years of enrollment, except for cervical carcinoma in situ, basal cell carcinoma of the skin, or squamous cell carcinoma of the skin which has been cured;

5. The patient is receiving anti-tumor therapies from other clinical trials;

6. Inability to swallow, chronic diarrhea, or intestinal obstruction, with multiple factors affecting drug administration and absorption;

7. The patient has undergone major surgical procedures unrelated to breast cancer within 4 weeks of enrollment, or has not fully recovered from such surgical procedures;

8. With known allergies to any components of the agents to be administered in this study; history of acquired or congenital immunodeficiency diseases, including HIV; history of HCV, active hepatitis B, or history of organ transplantation;

9. Pregnant and lactating patients, patients of fertility unwilling to take effective contraceptive measures throughout the trial;

10. With any heart disease including: (1) arrhythmia requiring medication or clinical attention; (2) myocardial infarction; (3) heart failure; (4) any other heart diseases that are considered unsuitable to the trial;

11. With any comorbidities that are considered to potentially endanger the patient's safety or interfere with the study, including but not restricted to resistant hypertension, severe diabetes, active infection, etc.;

12. With a history of neurological or mental disorders, including but not restricted to epilepsy or dementia;

13. The patient is using CYP3A4 inhibitors or inducers, or any other drugs that potentially prolong the QT interval;

14. Any other circumstances in which the researcher believes that the patient is not suitable to participate in this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Peking Union Medical College Hospital

OTHER

Sponsor Role: lead

Responsible Party

Qiang SUN

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Peking Union Medical College Hospital

Beijing, Beijing Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Xuefei Wang

Role: CONTACT

1210548954@qq.com

861069158720

Facility Contacts

Xuefei Wang, Dr.

Role: primary

1210548954@qq.com

861069158720

Other Identifiers

aPC-BC

Identifier Type: -

Identifier Source: org_study_id