Modified FOLFIRINOX and Pentamidine in Advanced and Metastatic Pancreatic Cancer (FALCON)
Modified FOLFIRINOX and Pentamidine as First-line Treatment in Advanced and Metastatic Pancreatic Ductal Adenocarcinoma
研究概览
详细说明
The patients will undergo testing, exams, and procedures per the Protocol. On study, patients will be randomized into one of the two arms. In Arm A (up to 15 patients) will be treated with modified FOLFIRINOX every two weeks, delivered as follows:
- Oxaliplatin 85mg/m2 IV over 2 hours on Day 1, followed by,
- Irinotecan 150mg/m2 IV over 90 minutes on Day 1, followed by
- Leucovorin 400mg/m2 IV over 2 hours on Day 1, followed by
- 5FU 2400mg/m2 IV over 46-48 hours on Days 1-3
In arm B patients (up to 15), the same modified FOLFIRINOX regimen will be used, as above, plus 300 mg pentamidine will be administered IV over a one-hour infusion on Day 1 of each cycle.
In both arms, patients will be treated over eight two-week cycles, and the entire treatment is expected to last approximately 4 months.
After eight cycles, patients will undergo another EUS core biopsy. At the same time as the biopsy, an additional blood draw (for translational endpoints) will be done.
After the biopsy, patients will continue treatment per physician's discretion for an additional 2 months (or 4 cycles) for a total of 12 cycles (or 6 months of treatment) until disease progression or appearance of unacceptable toxicity.
研究类型
注册 (估计的)
阶段
- 阶段1
联系人和位置
学习联系方式
- 姓名:Marisha Williams
- 电话号码:572-244-0111
- 邮箱:SCC-IIT-Office@ouhsc.edu
研究联系人备份
- 姓名:Lead Nurse
- 电话号码:572-244-0111
- 邮箱:SCC-IIT-Office@ouhsc.edu
学习地点
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Oklahoma
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Oklahoma City、Oklahoma、美国、73104
- University of Oklahoma Health Campus
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接触:
- Susanna Ulahannan, MD
- 电话号码:572-244-0111
- 邮箱:Susanna-Ulahannan@ou.edu
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-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Written informed consent signed and dated by the patient
- At least 18 years-of-age at the time of signature of the informed consent form (ICF)
- Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1
- Patients with a confirmed diagnosis of locally advanced, unresectable and/or metastatic pancreatic cancer
- Patients must have at least one measurable disease per RECIST v1.1,
- Patients must have at least 1 tumor lesion amenable to biopsy and must be willing to undergo a biopsy prior to first treatment and after receiving 8th cycle of therapy.
- Adequate bone marrow function defined as ANC> 1000/μL and platelets>75,000/μL
- Adequate liver function defined as total bilirubin<1.5g/L
- Adequate renal function defined as creatinine <1.5ULN or creatinine clearance greater than 30 ml/m2.
- AST and ALT <2.5x ULN or AST and ALT<5xULN if liver function abnormalities are due to liver metastases
- Male or female patients. Male patients with female partners of childbearing potential and female patients of childbearing potential are required to use two forms of acceptable contraception, including one barrier method, during their participation in the study and for 30 days following the last dose. Male patients must also refrain from donating sperm during their participation in the study.
- Life expectancy ≥ 3 months according to the Investigator's judgment.
Exclusion Criteria:
- Any systemic anti-cancer chemotherapy, small molecule, biologic, or from a previous treatment regimen or clinical study in a metastatic setting before the first dose of study drug.
- Active bacterial infection
- Women who are pregnant, nursing, or who plan to become pregnant while in the study and for at least 6 months after the last administration of study treatment
- Men who plan to father a child while in the study and for at least 6 months after the last administration of study treatment
Any of the following cardiac criteria currently or within the last 6 months:
- Mean resting corrected QT interval (QTc) >480 msec
- Any clinically important abnormalities (as assessed by the Investigator) in rhythm, conduction, or morphology of resting electrocardiograms (ECGs), e.g., complete left bundle branch block, third degree heart block
- Congestive heart failure (New York Heart Association ≥ Grade 2
- Any factors that increase the risk of QTc prolongation or risk of arrhythmic events such as heart failure, hypokalemia, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death under 40 years-of-age, or any concomitant medication known to prolong the QT interval
- Incidences of chronic hypokalemia that cannot be corrected.
- As judged by the Investigator, any evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension, uncontrolled diabetes mellitus, active bleeding diatheses, or active infection requiring treatment including hepatitis B, hepatitis C, and human immunodeficiency virus. Screening for chronic conditions is not required.
- Presence of other active invasive cancers other than the one treated in this study within 2 years prior to screening, except appropriately treated basal cell carcinoma of the skin, or in situ carcinoma of uterine cervix, or other local tumors considered cured by local treatment
- Psychological, familial, sociological, or geographical conditions that do not permit compliance with the protocol and/or follow-up procedures outlined in the protocol.
- Prisoners
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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有源比较器:modified FOLFIRINOX
In Arm A (up to 15 patients) will be treated with modified FOLFIRINOX every two weeks, delivered as follows:
Patients will be treated over eight two-week cycles, and the entire treatment is expected to last approximately 4 months. |
In Arm A (up to 15 patients) will be treated with modified FOLFIRINOX every two weeks, delivered as follows:
|
|
实验性的:modified FOLFIRINOX + Pentamidine
In arm B patients (up to 15), the same modified FOLFIRINOX regimen will be used, as above, plus 300 mg pentamidine will be administered IV over a one-hour infusion on Day 1 of each cycle. Patients will be treated over eight two-week cycles, and the entire treatment is expected to last approximately 4 months. |
In Arm A (up to 15 patients) will be treated with modified FOLFIRINOX every two weeks, delivered as follows:
In arm B patients (up to 15), the same modified FOLFIRINOX regimen will be used, as above, plus 300 mg pentamidine will be administered IV over a one-hour infusion on Day 1 of each cycle.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Number and proportion of patients with Grade 3 and higher adverse events deemed related to pentamidine during trial treatment, using CTCAE v.6.0.
大体时间:3 years
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To evaluate the safety in patients with metastatic or nonresectable locally advanced pancreatic cancer treated with modified FOLFIRINOX (arm A) versus modified FOLFIRINOX plus Pentamidine (arm B)
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3 years
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Evaluation of the objective response rate in modified FOLFIRINOX (arm A) versus modified FOLFIRINOX plus Pentamidine (arm B)
大体时间:3 years
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Proportion of patients with Objective response rate and partial response as measured by RECIST version 1.1 to be evaluated by imaging study and radiology review.
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3 years
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Evaluation of the rate of progression-free survival in both arms
大体时间:3 years
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Proportion of patients with a response rate measurement of Progression-free survival determined by the number of days from the start of study treatment to date of imaging-confirmed tumor progression, death or last time of follow up
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3 years
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Evaluation of the duration of response in both arms
大体时间:3 years
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Proportion of patients with Duration of response determined as the number of days from the onset of the first response to disease progression or death
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3 years
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Evaluation of genetic mutations that predict patient response to modified FOLFIRINOX plus Pentamidine
大体时间:3 years
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Proportion of patients with expression levels of MUC1, SAT1, and other metabolic genes by performing transcriptomic analysis of biopsies.
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3 years
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Evaluation of potential utility of N1-acetylspermidine and nucleotide pools as a biomarker of efficacy of the combination therapy.
大体时间:3 years
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Proportion of patients with circulating N'acetylspermidine1levels, other circulating polyamines levels, tumor tissue uptake of pentamidine by quantitating N1-acetylspermidine levels by liquid chromatography-coupled tandem mass spectrometry, and quantitate nucleotide pools in biopsy tissues by liquid chromatography-coupled tandem mass spectrometry
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3 years
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合作者和调查者
调查人员
- 首席研究员:Susanna Ulahannan, MD、University of Oklahoma
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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