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Regional Chemotherapy in Locally Advanced Pancreatic Cancer: RECLAP Trial

2019年11月4日 更新者：Udo Rudloff, M.D.、National Cancer Institute (NCI)

Background:

- Pancreatic cancer is difficult to treat because by the time most cases are diagnosed, the tumors are too large to be removed surgically. Standard intravenous chemotherapy may shrink some of the tumor, but even with chemotherapy only about 25 percent of patients will live for 1 year following diagnosis. Several preliminary studies have shown that it is safe to give chemotherapy directly into the pancreas in the area of the tumor, and that giving gemcitabine over a longer period increases the amount of drug that is available to the tumor. Researchers are interested in studying whether giving the approved pancreatic cancer chemotherapy drug gemcitabine directly into the pancreas in the area of the cancer and at a slow rate of infusion is a safe and effective treatment.

Objectives:

- To test the safety and effectiveness of administering gemcitabine directly to a pancreatic tumor at a slow rate of infusion.

Eligibility:

- Individuals at least 18 years of age who have been diagnosed with pancreatic cancer that is currently too large to be removed surgically but has not yet spread to other organs.

Design:

  • Participants will be screened with a full medical history and physical examination, blood and urine tests, and imaging studies.
  • Participants will undergo pancreatic angiography and embolization, during which a catheter will be threaded into the blood vessels near the pancreas and a contrast dye will be used to show the blood vessels supplying the tumor. These blood vessels will then be surgically closed off.
  • After the embolization, gemcitabine will be given as an infusion into the area around the tumor over 24 hours.
  • Participants will return to the clinical center every 2 weeks after the first infusion for additional infusions of gemcitabine, using the same procedures as above. Participants will be monitored with frequent blood tests and imaging studies.
  • Two weeks after the fourth treatment (course 1), participants will have more imaging studies, a physical examination, and blood tests. If the tumor is shrinking, participants will have two more courses of treatment (eight more infusions of gemcitabine).
  • Participants will have followup visits every 3 months for 2 years following the last treatment and then every 6 months.

研究概览

地位

完全的

条件

干预/治疗

详细说明

Background:

  • Pancreatic cancer is the fourth leading cause of cancer death in the United States.
  • Surgery offers the only chance at cure; however, less than 20% of patients are considered resectable at initial presentation.
  • A common reason for being classified as unresectable is loco-regional advanced disease.
  • Several phase I studies of regional administration of chemotherapy have proven safe.
  • The main advantage of pancreatic cancer targeted arterial perfusion of Gemcitabine is achievement of higher local bio-available active drug levels at the tumor bed.
  • The Regional Chemotherapy in Locally Advanced Pancreatic Cancer (RECLAP) trial is a phase I trial offering highly selective 24-hour intra-arterial administration of Gemcitabine via a subcutaneous port for patients with unresectable locally-advanced pancreatic cancer.

Objectives:

Primary Objective:

  • To evaluate feasibility and toxicity of intra-arterial gemcitabine therapy (dose limiting toxicity (DLT)).
  • To establish the maximum tolerated dose (MTD)

Secondary Objectives:

  • To evaluate response rate using Response Evaluation Criteria in Solid Tumors (RECIST), positron emission tomography (PET), magnetic resonance imaging (MRI) and computed tomography (CT) perfusion criteria (European Association for the Study of the Liver (EASL))
  • To determine progression free and overall survival.
  • To evaluate the conversion rate from unresectable or borderline resectable to potentially resectable pancreatic cancer.
  • To determine progression-free and overall survival.
  • To analyze potential selection criteria to be used in future studies for patients who present with marginally unresectable or unresectable locally-advanced pancreatic cancer that might benefit from this approach.

Eligibility:

  • Unresectable locally-advanced pancreatic cancer.
  • 18 years old or greater with an Eastern Cooperative Oncology Group (ECOG) 0-2
  • Laboratory and physical examination parameters within acceptable limits by standard of practice guidelines prior to surgery or chemotherapy.
  • No extra-pancreatic disease except regional lymph nodes.

Design:

  • This is a dose escalation phase-I study.
  • Patients considered unresectable due to locally-advanced pancreatic cancer will receive selective arterial perfusion of gemcitabine over 24 hours via a subcutaneous indwelling port.
  • Treatment will be given on Days 1 and 14. One cycle = 4 weeks for up to six cycles.
  • Three to six patients will be enrolled per dose cohort.
  • 18 to 36 patients in 7 cohorts will be accrued plus 6 more patients at the maximum tolerated dose (MTD over 36 months. Patients will be evaluated every 2 cycles (8 weeks). Upon progression patients will be taken off study. If no progressive disease (PD), patients will continue up to 6 cycles.
  • Chemotherapy na(SqrRoot) ve patients and patients who received previously chemotherapy including gemcitabine will be allowed, as this mode of administration has better bioavailability, offer potential for better biological effect and less systemic toxicity profiles.

研究类型

介入性

注册 (实际的)

7

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。

学习地点

  • 美国
    • Maryland
      • Bethesda、Maryland、美国、20892
        • National Institutes of Health Clinical Center, 9000 Rockville Pike

参与标准

研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 99年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

  • INCLUSION CRITERIA:
  • Histologically or cytologically confirmed locally advanced pancreatic adenocarcinoma or clinical and radiographic evidence of pancreatic cancer

Note: Patients with a limited disease burden outside the pancreas, who have undergone systemic chemotherapy for metastatic disease and have achieved a complete response on the metastatic lesions of greater than or equal to 6 months, and have no evidence of disease outside the pancreas at time of enrollment, are eligible.

  • Disease must be evaluable
  • Disease should be deemed unresectable by the MD Anderson criteria
  • Patients may be chemo naive or have received prior chemotherapy (including Gemcitabine) and/or radiation
  • Greater than or equal to 18 years of age
  • Must be able to understand and sign the Informed Consent Document
  • Clinical performance status of Eastern Cooperative Oncology Group (ECOG) less than or equal to 2
  • Life expectancy of greater than three months
  • Patients of both genders must be willing to practice birth control during and for four months after receiving chemotherapy

  • Hematology:

    • Absolute neutrophil count greater than 1300/mm(3) without the support of Filgrastim.
    • Platelet count greater than 75,000/mm(3).
    • Hemoglobin greater than 8.0 g/dl.

  • Chemistry:

    • Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) less or equal to 3 times the upper limit of normal, unless patient carries a biliary stent. For these patients, to account for asymptomatic, transient elevations in transaminases ('transaminitis'), serum ALT/AST may be less than or equal to 5 times the upper limit of normal provided all other eligibility parameters are met.
    • Serum creatinine less than or equal to 1.8 mg/dl unless the measured creatinine clearance is greater than 60 mL/min/1.73 m(2)
    • Total bilirubin less than or equal to 2 mg/dl,
    • Prothrombin time (PT) within 2 seconds of the upper limit of normal or International Normalized Ratio (INR) less than or equal to 1.8
  • No history of prior/other malignancies within the 2 years prior to enrollment with the exception of basal cell carcinoma

EXCLUSION CRITERIA:

  • Metastatic disease including malignant ascites
  • Women of child-bearing potential who are pregnant or breastfeeding because of the potentially dangerous effects of the chemotherapy on the fetus or infant.
  • Active systemic infections, coagulation disorders or other major medical illnesses of the cardiovascular, respiratory or immune system, myocardial infarction, heart failure
  • Childs B or C cirrhosis or with evidence of severe portal hypertension by history, endoscopy, or radiologic studies
  • Weight less than 40 kg
  • Significant ascites, greater than 1000cc in the absence of peritoneal disease
  • Concomitant medical problems that would place the patient at an unacceptable risk for the procedure
  • Need for concurrent chemotherapy
  • Discretion of the principal investigator (PI)

学习计划

本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。

研究是如何设计的？

设计细节

  • 主要用途：治疗
  • 分配：不适用
  • 介入模型：单组作业
  • 屏蔽：无（打开标签）

武器和干预

参与者组/臂
干预/治疗
实验性的：Gemcitabine Dose Escalation
gemcitabine dose escalation
药品：Gemcitabine
Gemcitabine starting dose was 18mg/m(2)/24h via infusion pump on days 1-14. One cycle = 4 weeks for up to six cycles. Three to six patients enrolled per dose cohort. Patients were dosed at successive higher doses until maximum tolerated dose or up to 165 mg/m(2)/24h.
其他名称：
  • 金扎

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
Number of Participants With Dose Limiting Toxicity (DLT )
大体时间：Cycle 1 (4 weeks), for up to 6 cycles
Here is the number of participants with DLT. DLT is defined as follows: All grade 3 or greater toxicities with the exception of Grade 3 constitutional symptoms that persist for less than 72 hours, Grade 3 and 4 myelosuppression (neutrophils and thrombocytopenia) of less than 5 days duration. Grade 3 metabolic/laboratory events that are correctable within 24 hours. Events that are assessed by the principal investigator as clearly unrelated to the agent will not be considered DLTs (e.g., events directly related to catheter insertion, pain related to underlying disease).
Cycle 1 (4 weeks), for up to 6 cycles
MTD (Maximum Tolerated Dose)
大体时间：Cycle 1 (4 weeks), for up to 6 cycles
The MTD is the highest dose that induces dose limiting toxicity (DLT) in no more than 2 patients among a cohort of 6 patients. If 1 or fewer patients experience dose limiting toxicity than the dose level will define the MTD. Only DLT's that occurred during cycle 1 of each dose level were used to determine the MTD.
Cycle 1 (4 weeks), for up to 6 cycles

次要结果测量

结果测量
措施说明
大体时间
Response Using the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.
大体时间：Every 2 cycles (8 weeks), up to 18 weeks
Complete response is disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. Partial response is at least a 30% decrease in the sum of diameters of target lesions taking as reference the baseline sum diameters. Progression is at least a 20% increase in the sum of diameters of target lesions taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study) or the appearance of one or more new lesions. Stable disease is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD taking as references the smallest sum diameters while on study.
Every 2 cycles (8 weeks), up to 18 weeks
Response Rate Using Positron Emission Tomography (PET)
大体时间：Every 2 cycles (8 weeks), up to 18 weeks
Complete response is disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. Partial response is at least a 30% decrease in the sum of diameters of target lesions taking as reference the baseline sum diameters. Progression is at least a 20% increase in the sum of diameters of target lesions taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study) or the appearance of one or more new lesions. Stable disease is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD taking as references the smallest sum diameters while on study.
Every 2 cycles (8 weeks), up to 18 weeks
Response Rate Using Magnetic Resonance Imaging (MRI)
大体时间：Every 2 cycles (8 weeks), up to 18 weeks
Complete response is disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. Partial response is at least a 30% decrease in the sum of diameters of target lesions taking as reference the baseline sum diameters. Progression is at least a 20% increase in the sum of diameters of target lesions taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study) or the appearance of one or more new lesions. Stable disease is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD taking as references the smallest sum diameters while on study.
Every 2 cycles (8 weeks), up to 18 weeks
Response Using Computed Tomography (CT) Perfusion Criteria European Association for the Study of the Liver (EASL1)
大体时间：Every 2 cycles (8 weeks), up to 18 weeks
Complete response is disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. Partial response is at least a 30% decrease in the sum of diameters of target lesions taking as reference the baseline sum diameters. Progression is at least a 20% increase in the sum of diameters of target lesions taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study) or the appearance of one or more new lesions. Stable disease is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD taking as references the smallest sum diameters while on study.
Every 2 cycles (8 weeks), up to 18 weeks
Median Time to Progression
大体时间：From first day of treatment to the day of progression, assessed up to 221 months
Time to progression is the time between the first day of treatment to the day of disease progression. Progression is defined as at least a 20% increase in the sum of diameters of target lesions taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study) or the appearance of one or more new lesions.
From first day of treatment to the day of progression, assessed up to 221 months
Median Overall Survival (OS)
大体时间：Overall survival was assessed through study completion, an average of 3 years.
Overall survival is defined as the time between the first day of treatment to the day of death.
Overall survival was assessed through study completion, an average of 3 years.
Number of Participants Who Converted From Unresectable or Borderline Resectable To Potentially Resectable Pancreatic Cancer
大体时间：4 months
Resectability is defined by the MD Anderson Resectability criteria: Resectable is no extension; normal fat plane between the tumor and the artery (superior mesenteric artery (SMA)). No extension (celiac axis/hepatic artery). Patent (superior mesenteric vein/portal vein (SMV/PV)). Borderline resectable is tumor abutment ≤180◦ (one half or less) of the circumference of the artery; periarterial stranding and tumor points of contact forming a convexity against the vessel improve chances of resection (SMA). Short-segment encasement/abutment of the common hepatic artery (typically at the gastroduodenal origin) (celiac axis/hepatic artery). Short-segment occlusion with suitable vessel above and below (SMV/PV). Locally advanced is encased (>180◦) (SMA). Encased and no technical option for reconstruction usually because of extension to the celiac axis/splenic/left gastric junction or the celiac origin (celiac axis/hepatic artery). Occluded and no technical option for reconstruction (SMV/PV).
4 months
Number of Potential Selection Criteria to Be Used in Future Studies for Patients With Marginally Unresectable Or Unresectable Locally-Advanced Pancreatic Cancer
大体时间：up to 2.5 years
Number of selection criteria that can be used for unresectable pancreatic cancer.
up to 2.5 years
Number of Participants With Serious and Non-Serious Adverse Events
大体时间：Date treatment consent signed to date off study, approximately 2 years and 2 months and 21 days
Here is the count of participants with serious and non-serious adverse events assessed by the Common Terminology Criteria in Adverse Events (CTCAE v4.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned
Date treatment consent signed to date off study, approximately 2 years and 2 months and 21 days

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

National Cancer Institute (NCI)

调查人员

  • 首席研究员：Udo Rudloff, M.D.、National Cancer Institute (NCI)

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2011年1月26日

初级完成 (实际的)

2014年7月23日

研究完成 (实际的)

2014年7月23日

研究注册日期

首次提交

2011年2月10日

首先提交符合 QC 标准的

2011年2月10日

首次发布 (估计)

2011年2月11日

研究记录更新

最后更新发布 (实际的)

2019年11月13日

上次提交的符合 QC 标准的更新

2019年11月4日

最后验证

2019年11月1日

更多信息

与本研究相关的术语

关键字

其他相关的 MeSH 术语

其他研究编号

  • 110099
  • 11-C-0099
  • P10764 (其他标识符：National Institutes of Health Clinical Center (CC))

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)？

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

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