Biliary Tract Cancer Clinical Trial
Official title:
Phase Ib Study of MEK162 in Combination With Capecitabine in Gemcitabine-pretreated Advanced Biliary Tract Cancer
This study is to test the efficacy of MEK162 plus capecitabine in gemcitabine-pretreated advanced biliary tract cancer, and to explore the predictive biomarkers for future large-scale clinical trials using this combination.
Biliary tract cancer is one of rare cancers, which is relatively more frequent in east Asia.
The frequency of KRAS mutation and/or BRAF mutation is reported at 40 to 60%. The prognosis
is still very poor, with only limited treatment options. The most commonly used 1st-line
chemotherapy is gemcitabine+cisplatin combination. In gemcitabine-pretreated advanced biliary
tract cancer, fluoropyrimidine-based chemotherapy is used. However, the overall survival with
these cytotoxic chemotherapies is still only about 8-10 months, calling for urgent
development of efficient treatment options.
Recently, mitogen-activated extracellular signal regulated kinase kinase (MEK) inhibition was
shown to have antitumor effects in KRAS mutated biliary tract cancers in preclinical model.
In phase II study of MEK inhibitor (selumetinib) in metastatic biliary tract cancers,
selumetinib displayed interesting activity and acceptable tolerability.
MEK162 is an oral, highly selective MEK inhibitor. It was shown to promote apoptosis and in
vivo antitumor activity against human biliary tract cancer cell lines. So far, there has been
no study to test the MEK inhibitor mainly in gemcitabine-pretreated advanced biliary tract
cancer, especially in combination of capecitabine chemotherapy.
The aim of this study is to test the efficacy of MEK162 plus capecitabine in
gemcitabine-pretreated advanced biliary tract cancer, and to explore the predictive
biomarkers for future large-scale clinical trials using this combination.
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