A Phase I/II Study of Nintedanib and Capecitabine in Refractory Metastatic Colorectal Cancer
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 42
- 试验地点
- 2
- 主要终点
- To Examine the DLT
研究概览
简要总结
This phase I/II trial studies the side effects and best dose of nintedanib when given together with capecitabine and to see how well they work in treating patients with colorectal cancer that has not responded to previous treatment (refractory) and has spread to other places in the body (metastatic). Nintedanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It may also block the growth of new blood vessels necessary for tumor growth. Drugs used in chemotherapy, such as capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving nintedanib with capecitabine may be a better treatment for colorectal cancer.
详细描述
PRIMARY OBJECTIVES:
- I. To estimate the maximum tolerated dose (MTD) and examine the dose-limiting toxicities of nintedanib when administered with capecitabine within the study population and, establish the recommended phase II dose (RP2D). (Phase I)
- II. To assess progression free survival at 18 weeks. (Phase II)
SECONDARY OBJECTIVES:
- I. To assess median progression free survival. (Phase II)
- II. To assess median overall survival from the date of enrollment to the time of death will be documented. (Phase II)
- III. To assess the objective response rate as measured by Response Evaluation Criteria in Solid Tumors (RECIST) version (v) 1.1. (Phase II)
- IV. To assess the toxicity of dose regimen using the Cancer Therapy Evaluation Program (CTEP) National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE version 4.0). (Phase II)
TERTIARY OBJECTIVES:
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
- •Hemoglobin >= 9 g/dL
- •Absolute neutrophil count >= 1500/mm^3
- •Platelet count >= 100,000/mm^3
- •Creatinine =< 1.5 upper limit of normal (ULN) AND creatinine clearance (CrCl) > 50 mL/min by Cockcroft-Gault equation
- •Males = (140 -age (yrs) (body weight (kg)/(72) (serum creatinine) (mg/dL)
- •Females = 0.85 * (140-age (yrs) (body weight (kg)/(72)(serum creatinine (mg/dL)
- •Bilirubin < ULN
- •Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) =< 1.5 ULN if without liver metastases
- •AST/ALT =< 2.5 x ULN if with liver metastases
- •Coagulation parameters: international normalized ratio (INR) =< 2, prothrombin time (PT) and partial thromboplastin time (PTT) < 1.5 X institutional ULN
- •Have measurable disease per RECIST 1.1 criteria
- •Histologically or cytologically proven adenocarcinoma of the colon or rectum
- •Prior progression following a fluoropyrimidine-based therapy and progression following or intolerance to irinotecan and oxaliplatin, as well as anti-epidermal growth factor receptor (EGFR) therapy (e.g., panitumumab or cetuximab) for rat sarcoma viral oncogene homolog (RAS) wild-type patients
- •Ability to swallow and retain oral medication
- •Participants of child-bearing potential must agree to use adequate contraceptive methods (e.g., hormonal or barrier method of birth control; abstinence) prior to study entry and for three months following completion of therapy; should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately
- •Participant or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure
排除标准
- •Prior treatment with nintedanib
- •Prior treatment with regorafenib
- •Major injuries or surgery within the 4 weeks prior to initiation of therapy with incomplete wound healing or planned surgery during the on-study treatment period
- •Uncontrolled hypertension: systolic blood pressure >= 160, diastolic blood pressure >= 90
- •Urine protein/creatinine ratio >= 1.0
- •History of clinically significant hemorrhagic or thrombotic event within the past 6 months, not including uncomplicated catheter-associated venous thrombosis; patients on anti-coagulation are not permitted to be on any oral formulations (warfarin, rivaroxaban, dabigatran, etc.) due to concern for drug-drug interaction
- •Unstable angina, symptomatic congestive heart failure or cardiac arrhythmia requiring anti-arrhythmic therapy (beta-blockers, calcium channel blockers and digoxin are allowed)
- •History of cerebrovascular or myocardial ischemia within 6 months of initiation
- •Known inherited predisposition to bleeding or thrombosis
- •Known active or chronic hepatitis B or C or human immunodeficiency virus (HIV)
- •Untreated brain metastases
- •History of second primary malignancy diagnosed within 3 years prior to enrollment, excluding:
- •In-situ cervical carcinoma
- •Superficial bladder cancer
- •Non-melanoma skin cancer
- •Stage I breast cancer
- •Low grade (Gleason =< 6) localized prostate cancer
- •Any additional malignancy which has been in clinical remission for at least 1 year
- •Pregnant or nursing female participants
- •Unwilling or unable to follow protocol requirements
- •Any condition which in the Investigator's opinion deems the participant an unsuitable candidate to receive study drug
- •Received an investigational agent within 4 weeks prior to enrollment
- •PHASE I: History of intolerance to capecitabine at doses =< 1000 mg/m^2 BID, as defined by documented >= grade 3 hand-foot syndrome, documented severe diarrhea requiring hospitalization, or other documented severe adverse events (AEs) attributable to capecitabine
- •PHASE II: History of intolerance to capecitabine at doses below 1000 mg/m^2 BID, as defined by documented >= grade 3 hand-foot syndrome; documented severe diarrhea requiring hospitalization; or other documented severe AEs attributable to capecitabine
研究组 & 干预措施
Treatment (capecitabine, nintedanib)
Patients received capecitabine PO BID (every 12 hours) on days 1-14 and nintedanib PO BID (every 12 hours) on days 1-21. Courses repeated every 21 days in the absence of disease progression or unacceptable toxicity.
干预措施: Laboratory Biomarker Analysis (Other)
Treatment (capecitabine , nintendanib)
Patients receive the highest safe dose of the combination of nintedanib and capcitabine.
干预措施: Nintedanib (Drug)
Treatment (capecitabine, nintedanib)
Patients received capecitabine PO BID (every 12 hours) on days 1-14 and nintedanib PO BID (every 12 hours) on days 1-21. Courses repeated every 21 days in the absence of disease progression or unacceptable toxicity.
干预措施: Capecitabine (Drug)
Treatment (capecitabine, nintedanib)
Patients received capecitabine PO BID (every 12 hours) on days 1-14 and nintedanib PO BID (every 12 hours) on days 1-21. Courses repeated every 21 days in the absence of disease progression or unacceptable toxicity.
干预措施: Nintedanib (Drug)
Treatment (capecitabine, nintedanib)
Patients received capecitabine PO BID (every 12 hours) on days 1-14 and nintedanib PO BID (every 12 hours) on days 1-21. Courses repeated every 21 days in the absence of disease progression or unacceptable toxicity.
干预措施: Pharmacological Study (Other)
结局指标
主要结局
To Examine the DLT
时间窗: At least 21 days.
The recommended Phase II dose is of the Nintedanib and Capecitabine combination is defined as the dose level that causes dose limiting toxicities (DLTs) in ≤ 1 out of 6 patients at highest dose level below the maximally administered dose. Capecitabine is fixed dose at 2000 mg/m2; while Nintedanib is evaluated at 150mg (dose level 1) and 200 mg (dose level 2).
Progression Free Survival (PFS) Rate, Defined as the Proportion of Patients Who Survive Without Disease Progression Via the RECIST Version 1.1 (Phase II)
时间窗: At 18 weeks
Progressive disease is defined as at least a 20% increase in the sum of diameters of target lesions (the sum must also demonstrate an absolute increase of at least 5 mm) or the appearance of new lesions. Will be summarized using standard Kaplan-Meier methods.
次要结局
- Median PFS (Phase II)(Up to 2 years)
- Median OS (Phase II)(From the date of enrollment to the time of death, assessed up to 2 years)
- Objective Response Rate(After every 3 cycles (9 weeks) of therapy.)
- Aggregate Rates of Adverse Events Measured by CTCAE Version 4.0 (Phase II)(Up to 30 days after the last dose of study drug)