Pyrotinib Combined With Capecitabine Metronomic Therapy in HER2-postitive Advanced Breast Cancer

  • STATUS
    Recruiting
  • days left to enroll
    78
  • participants needed
    35
  • sponsor
    Chinese Academy of Medical Sciences
Updated on 23 January 2021
measurable disease
metastasis
capecitabine
advanced breast cancer
HER2
trastuzumab
erbb2

Summary

Overexpression of the HER2 gene accounts for 20% to 30% of breast cancer. Although trastuzumab combined with chemotherapy has become the basic treatment for patients with HER2-positive advanced breast cancer, For patients who have progressed or relapsed after trastuzumab treatment, There are still many issues to explore on the choice of program of retargeted therapy. In HER2-positive advanced breast cancer, the results of Phase I and Phase I/II trials of pyrotinib or pyrotinib combined with capecitabine show that the anti-tumor effect is rapid, efficient and sustainable, and the patient is safe and well tolerated. Capecitabine is an oral cytotoxic drug that has high selectivity and specificity against tumors. Many patients need to adjust the dose due to adverse reactions, especially for patients after multi-line treatment. Previous studies have shown that sustained low-dose capecitabine reduces the adverse effects of the drug while ensuring efficacy. Based on the above, this study is to conduct a single-center, one-arm phase II clinical trial to explore the efficacy and safety of pyrotinib and capecitabine in the treatment of HER2-positive advanced breast cancer.

Details
Condition Breast Cancer, Breast Cancer Diagnosis, breast carcinoma, cancer, breast
Treatment Capecitabine, Pyrotinib
Clinical Study IdentifierNCT03923166
SponsorChinese Academy of Medical Sciences
Last Modified on23 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Age18~75 years
Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
A life expectancy of more than 12 weeks
patients have at least one measurable lesion exists according to Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 criteria and progresses after the last anti-tumor treatment or during treatment
Pathologically confirmed HER2-expressing patients with locally advanced or metastatic breast cancer: HER2 IHC 3+, or HER2 IHC 2+ and FISH detection gene amplification
Progression after treatment with trastuzumab (receiving at least 6 weeks of trastuzumab treatment)
Have not received capecitabine for the past, or Previously received capecitabine and PFS for more than 6 months
echocardiography indicates that LVEF 50%
The laboratory tests confirmed that the bone marrow function and liver and kidney function of the patient met the following requirements before the first dose
ANC1.510^9/L
PLT10010^9/L
Hb100 g/L
serum creatinine(Scr) less than 1.5 times the upper limit of normal value or the creatinine clearance rate calculated greater than 60 mL/min
total bilirubin less than 1.5 times the upper limit of normal value
aspartate aminotransferase (AST), or alanine aminotransferase (ALT) less than 2.5 times the upper limit of normal value, less than 5 times the upper limit of normal value in patients with liver metastases
urine routine test with urinary protein more than ++, or 24 hour urinary protein more than 1.0 g
Females of childbearing potential must be a pregnancy test in 7 days before participating ( including serum or urine), and the results were negative, and they are willing to take effective contraceptive methods during the trial
The patient volunteered to join the study and signed an informed consent form

Exclusion Criteria

Patients who have been treated with capecitabine for a period of 6 months and whose disease progresses
Previously treated with pyrotinib or neratinib
Patients with high blood pressure who are not well controlled by antihypertensive medication (systolic blood pressure >140 mmHg, diastolic blood pressure >90 mmHg); have uncontrolled or severe cardiovascular disease, such as within 6 months before screening Refractory angina pectoris, congestive heart failure occurred; myocardial infarction occurred within 12 months before screening; any clinically significant ventricular arrhythmia history, QT interval prolongation; history of cerebrovascular accident, symptomatic and need Medically treated coronary heart disease
having significant clinical dysfunction of the digestive tract may affect the intake, transport or absorption of oral medications (eg, inability to swallow, chronic diarrhea, intestinal obstruction, etc.)
Refractory, 2 degrees and above persistent diarrhea
exiting unstable brain metastasis and / or meningeal metastasis
Have undergone major surgery or severe traumatic injury, fracture, or healed wound within 4 weeks
Allergic to pyrotinib, capecitabine and/or its excipients has been confirmed
Female patients during pregnancy or lactation, female patients with fertility and positive pregnancy test, or women of childbearing age who are unwilling to take effective contraceptive measures during the whole trial period
The patient has a severe concomitant disease, or any other condition that the investigator believes is not suitable for the study
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