Evaluation of Safety and Efficacy of Electrochemotherapy in the Treatment of Pancreatic Adenocarcinoma
Completed · Phase 1
Conditions studied: Pancreatic Adenocarcinoma
In brief
The purpose of this study is to see how well electrochemotherapy works at treating people with Stage III pancreatic adenocarcinoma. Electrochemotherapy is a treatment that combines electroporation and chemotherapy administration. Electroporation uses an electric current to produce holes in pancreatic tumor, which causes the tumor cells to die or take up a higher concentration of administered chemotherapy agent. This study will test the safety and look at the effect of electrochemotherapy in the treatment of stage III pancreatic adenocarcinoma. This study will also help to find the safest and most effective amount of electroporation voltage to apply to this type of tumor.
Key facts
- Study ID
- NCT02514421
- Run by
- The University of Texas Health Science Center, Houston
- People needed
- 6
- Starts
- 2015-07-01
- Expected to finish
- 2017-04-18
- Last updated by the study team
- 2019-04-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histologically or cytologically proven pancreatic carcinoma which is safely accessible by percutaneous methods;
- Locally advanced un-resectable pancreatic adenocarcinoma;
- At least one measurable lesion according to Response Evaluation Criteria In Solid Tumors (RECIST) criteria (longest diameter >=20 mm using conventional techniques or >=10 mm with spiral CT or MRI scan);
- WHO performance status (PS) < 2 or Eastern Cooperative Oncology Group < 2;
- Age >18;
- Life expectancy > 3 months;
- No history of gastric or esophageal varices;
- No active, uncontrolled infection;
- All patients must have adequate physiologic (hematologic, renal and hepatic) reserves as evidenced by: neutrophil count >1500/mL; platelet count >100,000/mL; serum creatinine <1.5x the upper limit of normal (ULN) value; serum glutamic-pyruvic transaminase (SGPT) <2.5 x ULN and bilirubin <1.5 x ULN functions
- Pain and biliary obstruction controlled before the start of the study
- Absence of psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule;
- Women of childbearing potential (defined as sexually mature woman who 1) has not undergone hysterectomy [the surgical removal of the uterus] or bilateral oophorectomy [the surgical removal of both ovaries] or 2) has not been naturally post-menopausal for at last 24 consecutive months) must have a negative pregnancy test prior to starting therapy. Men and women of childbearing potential must be willing to use effective contraceptive while on treatment and for a reasonable period thereafter.
You may not qualify if…
- Prior chemotherapy with gemcitabine and nab-paclitaxel;
- Prior history of pancreatic electroporation;
- Untreatable contrast allergy;
- History of allergy or hypersensitivity to gemcitabine, nab-paclitaxel, or any of the excipients;
- Presence of metal biliary stent;
- Psychosis or seizures;
- Evidence of serious gastrointestinal bleeding or bowel obstruction;
- Pregnant or lactating women;
- Women of childbearing potential who are not using adequate protection;
- Inability to tolerate MRI imaging
Where it is running
- The University of Texas Health Science Center at Houston — Houston, Texas, United States
Full record on ClinicalTrials.gov
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