RECRUITING

Hyperthermia Treatment Added to Chemotherapy Standard of Care for Pancreatic Tumors

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

In this study, tumors of the pancreas are treated with a device placed around the abdomen that creates an electromagnetic field that generates heat in the tumor. Heating the tumor improves blood flow and the delivery of chemotherapy to the tumor as has been shown in numerous studies for various cancers with potential clinical benefits. Subjects will receive the thermal treatment on the same day and prior to receiving standard of care chemotherapy for a total of 4 treatments. This study is an early feasibility study that aims to demonstrate the safety and the performance of the device.

Official Title

Early Feasibility Study to Evaluate the Initial Safety and Device Functionality of VectRx Thermal Therapy Added to Chemotherapy Treatment of Pancreatic Tumors

Quick Facts

Study Start:2023-08-15

Study Completion:2024-04-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05959395

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Provide signed and dated informed consent form * Subjects who are \> 18 years old * Histologically or cytologically proven adenocarcinoma of the pancreas * Subjects who enrolled prior to- or during initial course of planned chemotherapy. * Subjects with other histology that would typically receive these regimens are included (i.e. adenosquamous) * BR and UR Pancreatic Cancer based on modified NCCN guideline will be used as a guide for radiographic findings (94), or high risk resectable pancreatic cancer recommended by a multi-disciplinary team for chemotherapy based on NCCN recommendations (NCCN version 2.2021). * Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST v1.1) on imaging studies CT * Eastern Cooperative Oncology Group (ECOG) performance of 0-1 (Appendix D) * Estimated life expectancy \> 9 months * If female patient is of child-bearing potential, she must have a negative serum pregnancy test (βhCG) documented at screening * Subjects who meet the following baseline organ function parameters: * Absolute neutrophil count \>/= 1,500cells/mm3 * Platelets \>100,000cells/mm3 * Total Bilirubin ≤1.5X normal institutional limits OR \< 2.0 ULN if stenting occurred * AST(SGOT)/ALT(SGPT) \<2.5X institutional upper limit of normal * Creatinine \< 1.5mg/dl OR Cr clearance \>60 mL/min/1.73 m2 * Subjects with inactive/asymptomatic carrier, chronic, or active HBV infection must meet the following criteria: HBV deoxyribonucleic acid (DNA) \< 500 IU/mL (or 2500 copies/mL) at screening. Subjects with cured hepatitis C virus (HCV) infection at screening can be enrolled but should have HBV DNA levels checked periodically while on study to monitor for reactivation.	* Subjects with any part of the body between the hips and shoulders \>46 inch circumference, with an anterior posterior depth of \~10.5" in a supine position (fit may vary with body shape) * Subjects unable to tolerate magnetic resonance imaging * Subjects receiving treatment with other radiofrequency medical devices * Subject has pacemaker, electrocardiograph, implanted defibrillator, infusion pumps, insulin pumps, cardiac monitoring electrodes and devices, deep brain stimulators, cochlear implants, radiofrequency identification devices attached to devices, or any implanted active electronic device or monitoring system, adhesive skin patches including conductive metal * Metal biliary stents (plastic stents are allowed) * Non-removable implanted designated MR unsafe and/or RF incompatible ferromagnetic metallic devices such as metal joint replacements * Subjects who have ferromagnetic or electrically conductive, metal, or foreign objects in or on or attached to their body * Severe pulmonary disease with a forced expiratory volume (FEV) \<50% * Unstable angina pectoris (under medication) with imminent threat of an infarction * Myocardial infarction \<6 months ago * Cardiac decompensation or arrhythmia necessitating medication * Systolic blood pressure \>180 mmHg and/or \<90 mmHg, while using medication * Diastolic blood pressure \>100 mmHg and/or \<50 mmHg, while using medication * Open skin wounds on the torso * Severe cerebrovascular disease: multiple cerebrovascular accidents (CVA) or a CVA \<6 months before treatment * Subjects having received prior pancreatic surgery, radiation therapy, for pancreatic cancer of any histology * Subjects with tumors extending to or invading the duodenum * Subjects with recurrent/relapsed pancreatic cancer * Progressive disease on pre-protocol enrollment studies for patients already on systemic therapy * Subjects with pancreatitis * Subjects in their reproductive age who are breast feeding or have a positive pregnancy test * Any co-morbid condition such as but not limited to congestive heart failure, cardiac arrhythmia, or psychiatric illness of sufficient severity to limit full compliance with the protocol per assessment by the individual treating physician * Concurrent active infection * Prior malignancies other than cervical cancer in situ, adequately treated basal cell or squamous cell carcinoma of skin or treated low risk prostate cancer within the past 3 years * Patient with known historical or active infection with HIV * Subjects with inactive/asymptomatic carrier, chronic, or active HBV infection with HBV deoxyribonucleic acid (DNA) \> 500 IU/mL (or 2500 copies/mL) at screening * Patient who has undergone recent major surgery, other than diagnostic surgical procedure within 4 weeks prior to screening * Subjects with a history of interstitial lung disease, history of slowly progressive dyspnea and unproductive cough, sarcoidosis, silicosis, interstitial pulmonary fibrosis, pulmonary hypersensitivity pneumonitis or multiple allergies * Subjects with greater than grade 2 peripheral neuropathy * History of any psychiatric condition that might impair the patient's ability to understand or comply with the requirement of the study or to provide consent * Inability or unwillingness to provide informed consent * Currently enrolled in another investigational drug or device trial that clinically interferes with this study.

Inclusion Criteria

Exclusion Criteria

* Provide signed and dated informed consent form
* Subjects who are \> 18 years old
* Histologically or cytologically proven adenocarcinoma of the pancreas
* Subjects who enrolled prior to- or during initial course of planned chemotherapy.
* Subjects with other histology that would typically receive these regimens are included (i.e. adenosquamous)
* BR and UR Pancreatic Cancer based on modified NCCN guideline will be used as a guide for radiographic findings (94), or high risk resectable pancreatic cancer recommended by a multi-disciplinary team for chemotherapy based on NCCN recommendations (NCCN version 2.2021).
* Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST v1.1) on imaging studies CT
* Eastern Cooperative Oncology Group (ECOG) performance of 0-1 (Appendix D)
* Estimated life expectancy \> 9 months
* If female patient is of child-bearing potential, she must have a negative serum pregnancy test (βhCG) documented at screening
* Subjects who meet the following baseline organ function parameters:
* Absolute neutrophil count \>/= 1,500cells/mm3
* Platelets \>100,000cells/mm3
* Total Bilirubin ≤1.5X normal institutional limits OR \< 2.0 ULN if stenting occurred
* AST(SGOT)/ALT(SGPT) \<2.5X institutional upper limit of normal
* Creatinine \< 1.5mg/dl OR Cr clearance \>60 mL/min/1.73 m2
* Subjects with inactive/asymptomatic carrier, chronic, or active HBV infection must meet the following criteria: HBV deoxyribonucleic acid (DNA) \< 500 IU/mL (or 2500 copies/mL) at screening. Subjects with cured hepatitis C virus (HCV) infection at screening can be enrolled but should have HBV DNA levels checked periodically while on study to monitor for reactivation.

* Subjects with any part of the body between the hips and shoulders \>46 inch circumference, with an anterior posterior depth of \~10.5" in a supine position (fit may vary with body shape)
* Subjects unable to tolerate magnetic resonance imaging
* Subjects receiving treatment with other radiofrequency medical devices
* Subject has pacemaker, electrocardiograph, implanted defibrillator, infusion pumps, insulin pumps, cardiac monitoring electrodes and devices, deep brain stimulators, cochlear implants, radiofrequency identification devices attached to devices, or any implanted active electronic device or monitoring system, adhesive skin patches including conductive metal
* Metal biliary stents (plastic stents are allowed)
* Non-removable implanted designated MR unsafe and/or RF incompatible ferromagnetic metallic devices such as metal joint replacements
* Subjects who have ferromagnetic or electrically conductive, metal, or foreign objects in or on or attached to their body
* Severe pulmonary disease with a forced expiratory volume (FEV) \<50%
* Unstable angina pectoris (under medication) with imminent threat of an infarction
* Myocardial infarction \<6 months ago
* Cardiac decompensation or arrhythmia necessitating medication
* Systolic blood pressure \>180 mmHg and/or \<90 mmHg, while using medication
* Diastolic blood pressure \>100 mmHg and/or \<50 mmHg, while using medication
* Open skin wounds on the torso
* Severe cerebrovascular disease: multiple cerebrovascular accidents (CVA) or a CVA \<6 months before treatment
* Subjects having received prior pancreatic surgery, radiation therapy, for pancreatic cancer of any histology
* Subjects with tumors extending to or invading the duodenum
* Subjects with recurrent/relapsed pancreatic cancer
* Progressive disease on pre-protocol enrollment studies for patients already on systemic therapy
* Subjects with pancreatitis
* Subjects in their reproductive age who are breast feeding or have a positive pregnancy test
* Any co-morbid condition such as but not limited to congestive heart failure, cardiac arrhythmia, or psychiatric illness of sufficient severity to limit full compliance with the protocol per assessment by the individual treating physician
* Concurrent active infection
* Prior malignancies other than cervical cancer in situ, adequately treated basal cell or squamous cell carcinoma of skin or treated low risk prostate cancer within the past 3 years
* Patient with known historical or active infection with HIV
* Subjects with inactive/asymptomatic carrier, chronic, or active HBV infection with HBV deoxyribonucleic acid (DNA) \> 500 IU/mL (or 2500 copies/mL) at screening
* Patient who has undergone recent major surgery, other than diagnostic surgical procedure within 4 weeks prior to screening
* Subjects with a history of interstitial lung disease, history of slowly progressive dyspnea and unproductive cough, sarcoidosis, silicosis, interstitial pulmonary fibrosis, pulmonary hypersensitivity pneumonitis or multiple allergies
* Subjects with greater than grade 2 peripheral neuropathy
* History of any psychiatric condition that might impair the patient's ability to understand or comply with the requirement of the study or to provide consent
* Inability or unwillingness to provide informed consent
* Currently enrolled in another investigational drug or device trial that clinically interferes with this study.

Contacts and Locations

Study Contact

Kelly Kitzmiller, MPH

CONTACT

(410) 369-5264

kelly.kitzmiller@umm.edu

Principal Investigator

Pierre Floriano, PhD

STUDY_DIRECTOR

NeoTherma Oncology

Jason Molitoris, MD

PRINCIPAL_INVESTIGATOR

University of Maryland

Study Locations (Sites)

University of Maryland

Baltimore, Maryland, 21201

United States

Collaborators and Investigators

Sponsor: NeoTherma Oncology

Pierre Floriano, PhD, STUDY_DIRECTOR, NeoTherma Oncology
Jason Molitoris, MD, PRINCIPAL_INVESTIGATOR, University of Maryland

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-08-15

Study Completion Date2024-04-30

Study Record Updates

Study Start Date2023-08-15

Study Completion Date2024-04-30

Terms related to this study

Additional Relevant MeSH Terms

Pancreatic Cancer