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

NCT06035016 | Recruiting

• 1 other identifier: aPC-BC
• Study Type: observational
• Target: 300
• Locations: 1 country
• Sites: 1

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

Outcome Measures

Primary Outcomes (1)

• 3-year IDFS

  The 3-year IDFS (invasive disease-free survival) is defined as the time from the date of enrollment to the first occurrence of recurrent diseases. Recurrent diseases include ipsilateral or contralateral recurrent breast cancer, local or regional recurrence, remote recurrence and death caused by any reason. The observation period is from enrollment to 3 years after enrollment.

  3 Year

Secondary Outcomes (2)

• AEs and SAEs

  3 Year

• QoL

  3 Year

Study Arms (2)

cohort A

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

Drug: pyrotinib combined with Capecitabine

cohort B

treatment of physician's choice

Drug: treatment of physician's choice

Interventions

pyrotinib combined with Capecitabine DRUG

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

cohort A

treatment of physician's choice DRUG

Treatment of physician's choice

cohort B

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

HER2 positive early-stage breast cancer patients expected to receive adjuvant treatment

You may qualify if:

• Female patients ≥ 18 years and ≤ 75 years old;
• Primary invasive breast cancer confirmed by histology;
• 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;
• 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;
• With known ER/PR status of breast cancer;
• ECOG score 0-1;
• The patient's major organ functions meet all of the following requirements for blood tests:
• Neutrophil count (ANC) ≥ 1,500/mm3 (1.5×109/L);
• Platelet count (PLT) ≥ 75,000/mm3 (75×109/L);
• Hemoglobin (Hb) ≥ 8 g/dL (80 g/L);
• Serum creatinine (SCr) ≤ 1.5 times the upper limit of normal (ULN) or creatinine clearance ≥ 60 mL/min;
• Total bilirubin (TBIL) ≤ 1.5 times the upper limit of normal (ULN);
• 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.
• \. The participant voluntarily joins the study, signs the informed consent form, has good compliance, and cooperates with follow-ups.

You may not qualify if:

• Breast cancer recurs before enrollment, or local recurrence/ metastasis confirmed by radiology;
• The subject has participated in other clinical trials within 4 weeks or 5 half-lives (whichever is longer) before enrollment;
• The patient has previously received treatment including tyrosine kinase inhibitors targeting HER2 (e.g., lapatinib, neratinib, and pyrotinib);
• 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;
• The patient is receiving anti-tumor therapies from other clinical trials;
• Inability to swallow, chronic diarrhea, or intestinal obstruction, with multiple factors affecting drug administration and absorption;
• 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;
• 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;
• Pregnant and lactating patients, patients of fertility unwilling to take effective contraceptive measures throughout the trial;
• 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;
• 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.;
• With a history of neurological or mental disorders, including but not restricted to epilepsy or dementia;
• The patient is using CYP3A4 inhibitors or inducers, or any other drugs that potentially prolong the QT interval;
• Any other circumstances in which the researcher believes that the patient is not suitable to participate in this study.

Sponsors & Collaborators

• Peking Union Medical College Hospital: lead

Study Sites (1)

Peking Union Medical College Hospital

Beijing, Beijing Municipality, 100032, China

RECRUITING

MeSH Terms

Conditions

Breast Neoplasms

Interventions

Capecitabine

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Breast Diseases; Skin Diseases; Skin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

Deoxycytidine; Cytidine; Pyrimidine Nucleosides; Pyrimidines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Fluorouracil; Uracil; Pyrimidinones; Deoxyribonucleosides; Nucleosides; Nucleic Acids, Nucleotides, and Nucleosides

Central Study Contacts

Xuefei Wang

CONTACT

861069158720; 1210548954@qq.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: September 6, 2023
• First Posted: September 13, 2023
• Study Start: June 1, 2023
• Primary Completion (Estimated): June 1, 2027
• Study Completion (Estimated): June 1, 2027
• Last Updated: September 13, 2023

Record last verified: 2023-09

Locations

CN (1)