HER2-positive Breast Cancer Clinical Trial
Official title:
Trastuzumab Combined With Pyrotinib and Chemotherapy for Locally Advanced, Inflammatory, or Early HER2-positive Mammary glandsCancer: One Arm, Open, Phase II Clinical Study
This study is a one-arm, open, phase II clinical study, and the study subjects are locally advanced and inflammatoryPatients with sexual or early HER2-positive breast cancer entered the trial period after signing informed consentTo evaluate trastuzumab combined with pyrrolitinib and chemotherapy regimen (TCbH+Py) for HER2 positive breastPathologic complete response rate (pCR) for adenocarcinoma.
This study is a single-arm, open, phase II clinical study. The subjects are patients with
locally advanced, inflammatory, or early HER2-positive breast cancer. The patients enter the
trial period after signing informed consent. This study aims to evaluate trastuzumab The
pathological complete response rate (pCR) of anti-combined pyrrotinib and chemotherapy
(TCbH+Py) in the treatment of HER2-positive breast cancer.
The subjects began to take continuous medication after joining the group, and the total
duration of medication was 6 cycles. Three to four weeks after the end of treatment, the
surgeon will choose radical mastectomy, modified radical mastectomy or breast-sparing surgery
according to the individual conditions of the patient. Regardless of whether the pCR is
achieved, the adjuvant trastuzumab therapy or trastuzumab plus pertuzumab therapy is
continued after the operation, and the total course of anti-HER2 therapy is up to 1 year
(about 18 treatment cycles). According to the clinical stage and molecular classification of
the tumor, it is necessary to decide whether adjuvant radiotherapy, chemotherapy and
endocrine therapy are needed.
After the subject finishes all treatments, the subjects who are out of the group for non-PD
and non-death causes need to receive the validity Follow-up until PD, start receiving other
anti-tumor drug treatment or death (whichever comes first).
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