Phase Ib Study of MEK162 in Combination With Capecitabine in Gemcitabine-pretreated Advanced Biliary Tract Cancer
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 31
- 试验地点
- 1
- 主要终点
- Maximum tolerated dose (MTD)
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically / cytologically verified, non-resectable, recurrent, or metastatic biliary tract carcinoma including intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma and gallbladder carcinoma
- •Patients who have previously treated with gemcitabine-based chemotherapy (Prior treatment regimen up to 2 is allowed)
- •Patients must have measurable or evaluable disease by RECIST 1.1
- •Eastern Eastern Cooperative Oncology Group (ECOG) performance status: 0, 1
- •Age ≥ 20 years
- •Adequate bone marrow function defined as: Hb ≥ 8 g/dl, absolute neutrophil count (ANC) ≥ 1500/microliter (mcL), Platelets ≥ 100 x10^3/mcL
- •Adequate renal function defined as serum creatinine < 1.6 mg/dl and/or measured creatinine clearance from 24-hour urine collection of ≥ 60 ml/min
- •Adequate hepatic function defined as total bilirubin ≤ 2 mg/dl, alanine aminotransferase (ALT)/aspartate aminotransferase (AST) ≤ 5 x upper limit of normal (ULN)
- •Patients with biliary obstruction can join if bilirubin corrects to required limit after adequate biliary drainage
- •Women of childbearing potential must have a negative pregnancy test within 7 days prior to study treatment
- •Men and women of childbearing potential must be willing to consent to using effective contraception while on treatment and for at least 3 months thereafter
- •Ability to understand and the willingness to sign a written informed consent document
排除标准
- •Evidence of another active cancer that may influence patient outcome, except for nonmelanoma skin carcinoma, melanoma in-situ, in-situ carcinoma of the cervix curatively treated, treated superficial bladder cancer, and adenocarcinoma of the prostate that has been surgically treated with a post-treatment prostate surface antigen (PSA) that is non-detectable
- •Known brain metastases or primary central nervous system tumors with seizures that are not well controlled with standard medical therapy
- •Uncontrolled intercurrent illness including, but not limited to psychiatric illness/social situations that would limit compliance with study requirements
- •Known HIV positive patient
- •Significant cardiovascular disease including congestive heart failure (New York Heart Association Class II or higher) or active angina pectoris
- •Uncontrolled diabetes mellitus
- •History of a myocardial infarction within 6 months
- •History of a stroke or transient ischemic attack within 6 months
- •Clinically significant peripheral vascular disease
- •Major surgical procedure within 4 weeks
- •Uncontrolled infection
- •Known or suspected allergy to capecitabine
- •Pregnant (positive pregnancy test)
- •Breast-feeding should be discontinued if a nursing mother is to be treated on clinical trial
- •Any condition that impairs patient's ability to swallow whole pills
- •Malabsorption problem that may limit or inhibit the absorption of MEK162
- •History of any organ or bone marrow transplant
研究组 & 干预措施
Phase 1 part
to assess the maximal tolerated dose (MTD) of MEK162+Capecitabine combination
干预措施: MEK162+capecitabine (Drug)
Expansion part
to assess the efficacy (PFS) of MEK162+Capecitabine combination
干预措施: MEK162+capecitabine (Drug)
结局指标
主要结局
Maximum tolerated dose (MTD)
时间窗: 6 months
MTD in all treated population (Phase 1 part)
Progression-free survival (PFS)
时间窗: 3 months
PFS in all treated population (Expansion part)
次要结局
- Overall survival (OS)(1 year)
- Dose-limiting Toxicity (DLT)(6 months)
- Recommended Phase 2 Dose (RP2D)(6 months)
- Response rate(6 months)