To Observe the Efficacy and Safety of Pyrotinib Maleate in Patients With HER2-positive Advanced Colorectal Cancer
This study is an investigator-initiated, open-label, two-cohort phase II trial, assessing the objective response rate (ORR) of pyrotinib monotherapy (Cohort 1) or in combination with trastuzumab (Cohort 2), in HER2-positive advanced colorectal cancer. HER2 positivity is centrally established by immunohistochemistry (IHC) and silver in situ hybridization (SISH). To be HER2 eligible the original tumor, or the biopsied metastasis (whichever is last available), must be IHC 3+ or 2+ in more than 50% of cells, confirmed by SISH or fluorescence in situ hybridization (FISH) with a HER2:CEP17 ratio ≥ 2.0. For IHC a positive staining (3+) is defined as an intense membrane staining which can be circumferential, basolateral, or lateral of the tumor cells.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Pyrotinib as interventions were used in patients with HER2-positive advanced colorectal cancer
Pyrotinib in combination with trastuzumab as interventions were used in patients with HER2-positive advanced colorectal cancer
The Second Affiliated hospital of Zhejiang University School of Medical
Hangzhou, Zhejiang, China
RECRUITINGObjective Response Rate
The proportion of patients with complete response or partial response according to RECIST v1.1.
Time frame: Approximately 24 months
Disease Control Rate
The proportion of patients with complete response, partial response or stable disease according to RECIST v1.1.
Time frame: Approximately 24 months
Progression-Free Survival
Time from the initiation of treatment to disease progression or any-cause death.
Time frame: Up to 2 years
Overall Survival
Time from the initiation of treatment to any-cause death.
Time frame: Up to 2 years
Duration of Response
Time from complete response or partial response to disease progression or any-cause death.
Time frame: Approximately 24 months
The Incidence of Adverse Events
Adverse Events and Serious Adverse Events were graded according to the NCI-CTCAE V5.0.
Time frame: From the first drug administration to within 28 days for the last treatment
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