Treatment of Patients With Cancer With Genetically Modified Salmonella Typhimurium Bacteria

March 3, 2008 updated by: National Cancer Institute (NCI)

A Phase I Trial of a Live, Genetically Modified Salmonella Typhimurium (VNP20009) for the Treatment of Cancer by Intravenous Administration

This study will examine the safety and toxicities of intravenously administering a genetically modified type of Salmonella bacteria (VNP20009) and its impact on tumor growth in advanced or metastatic cancer (cancer that has spread from the primary site). The first patients in the study will be given the smallest dose of VNP20009, and those who enter later will receive increasingly larger doses. This will be done to determine the maximum dose that can be given without serious side effects.

Normally, Salmonella bacteria ingested in food or water can cause diarrhea or more severe illness. The bacteria in this study are altered genetically so they can be injected through a vein and circulate in the blood with less likelihood of causing side effects. It is believed that the bacteria will travel in the blood to the tumor and infect it. In studies of mice, tumor growth slowed in animals whose tumors were infected with VNP0009.

Patients with advanced or metastatic cancer 18 years of age or older whose disease is not responding to standard treatment, or for which there is no treatment, may be eligible for this study. Candidates will undergo a medical history and physical examination, including blood tests, scans, X-rays, electrocardiogram, and urine, stool and blood cultures.

Study participants will be admitted to the hospital for 2 to 4 days. On day 1, they will receive the first dose of VNP0009, infused over a 30-minute period through an intravenous catheter (a small plastic tube inserted into a vein). Blood will be drawn every day to determine if the bacteria are still in the body. After discharge, patients will return to the hospital on days after approximately 1-2 weeks and again after 4-5 weeks for additional blood tests to measure levels of the bacteria and for collection of blood, urine and stool samples. Patients whose tumors are on or just beneath the skin may be asked to have one or two tumors removed surgically.

Patients will have tests after approximately 4-5 weeks, including CTs and X-rays, to determine the size and extent of the tumor. Patients whose tumor remained the same size or smaller than before starting treatment, and whose side effects were acceptable will be offered a second treatment cycle. Those whose tumor grew during treatment will be taken off the study. Patients remaining in the study will begin the second cycle on approximately day 36. Tumor growth will be evaluated again between days 64 and 70, and a third cycle will be offered to patients whose tumors have remained stable or have shrunk. Patients may have up to 12 treatment cycles as long as evaluations continue to show the tumor is stable or shrinking. Completing all 12 cycles takes about 13 months. Patients will continue to be evaluated after treatment ends, if they agree to continued follow-up.

Patients must follow health precautions to prevent infecting others with Salmonella bacteria as long as they, themselves, remain infected. These include, for example, stringent hand washing practices and avoiding contact with people with weakened immune systems. All the precautions will be explained to the study participants.

Patients who leave the study must take antibiotic therapy to rid the body of any remaining bacteria. They will return for urine, stool and blood cultures 30 days after the start of antibiotics, and may undergo three types of scans to look for sites of infection. Treatment will be given as needed.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Patients with metastatic cancer will receive the intravenous injection of live genetically modified Salmonella typhimurium. This bacteria has been genetically modified to alter its pathogenicity and to attempt to increase its localization to sites of growing cancer. Cohorts of patients will receive increasing doses of the bacteria to establish the maximum tolerated dose.

Study Type

Interventional

Enrollment

45

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Maryland
      • Bethesda, Maryland, United States, 20892
        • National Cancer Institute (NCI)

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.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

INCLUSION CRITERIA:

Only patients must have advanced and/or metastatic, histologically documented solid tumors will be included.

Patients must have a solid tumor which is no longer considered responsive to available conventional modalities or treatments (failed any known standard curative or palliative therapy for that disease), or a previously untreated tumor for which no effective standard treatment is available. Patients must have measurable or evaluable metastatic disease.

All patients must have at least one tumor mass suitable and easily accessible for excisional biopsy or fine needle aspiration. The procedure must be able to be performed with minimum morbidity and discomfort to the patient.

ECOG performance status of 0 or 1.

Patients must be 18 years of age or older.

Patients must have expected survival of at least 3 months.

Men and women of child-bearing potential (i.e., women who are premenopausal or not surgically sterile), must use acceptable contraceptive methods (abstinence, intrauterine device (IUD), oral contraceptive or double barrier device), and women must have a negative serum or urine pregnancy test 1 week before beginning treatment on this trial. Nursing patients are also excluded.

Must be able and willing to give written informed consent.

Must be able and willing to execute a durable power of attorney (DPA).

No treatment with cytotoxic agents, or treatment with biologic agents within 3 weeks prior to treatment with VNP20009. Must have fully recovered from toxicities of any prior treatment with cytotoxic drugs, radiotherapy or other anti-cancer modalities.

Patients must have the following clinical laboratory values: (a) Granulocyte count of greater than or equal to 2,000/mm(3); (b) Platelets greater than or equal to 100,000/mm(3); (c) Serum creatinine less than or equal to 1.5 mg/dl; (d) Bilirubin less than or equal to 1.6 mg/dl, ALT, AST less than or equal to 1.5 times the upper limit of normal, alkaline phosphatase less than or equal to 1.5 times the upper limit of normal, (ALT, AST, alkaline phosphatase less than or equal to 3 times the upper limit in presence of liver metastases); (e) Prothrombin Time (PT) and activated partial thromboplastin time (aPTT) less than or equal to 1.5 times the upper limit of normal; (f) Hematocrit greater than or equal to 30% (may be corrected by transfusion); (g) Patients should have daily T max less than or equal to 38.0 degrees C.

EXCLUSION CRITERIA:

Patients with any one of the following criteria will not be eligible for study participation:

Diagnosis of lymphoma or other hematologic malignancy.

An artificial implant that cannot be removed (e.g., heart valves, prosthetic hips or knees, or other devices) which could represent a nidus of infection.

Known history of valvular disease or severe arteriosclerosis. Patients with a significant murmur on physical examination will undergo an echocardiogram to evaluate for valvular disease.

Known clinically significant atherosclerotic disease, peripheral vascular disease, or arterial aneurysm(s) or arterial or venous malformations. Patients in atrial fibrillation will undergo an echocardiogram to rule out presence of thrombus, which would make them ineligible.

An ultrasound will be performed pre-treatment in patients with intact gallbladders. No patients with any evidence of cholelithiasis or obstruction, unless they are able to undergo a simple cholecystectomy with minimal morbidity, in which case they would be eligible once they have fully recovered to their baseline status.

All patients will be screened with an ultrasound of the kidneys. Patients with urolithiasis will be excluded.

Active infection of any kind, including Hepatitis B or chronic viral hepatitis.

Documented Salmonella infections within 6 months.

Currently using antibiotics.

Patients with tumor fever, or fever of unknown origin or cause.

Any known bleeding disorder.

Patients must not have had a splenectomy or documented immunodeficiency such as HIV infection. These patients are excluded because VNP2009 may be more toxic in severely immunocompromised patients.

Patients on steroids, immunosuppressives, or any other medications that can directly or indirectly suppress the immune system.

Presence of any other life-threatening illness, such as unstable angina, severe oxygen dependent chronic obstructive pulmonary disease (COPD), end stage liver or renal disease.

Requirement immediate palliative treatment of any kind including surgery.

Presence of a known brain metastases. Patients with previously treated brain metastases and no evidence of recurrence are eligible.

Unwilling and unable to follow protocol requirements.

Hypersensitivity (history of allergic reactions) to quinolone or cephalosporin antibodies.

Patients who have been vaccinated against Salmonella Typhii within the past 6 months.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

National Cancer Institute (NCI)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 Major Dates

Study Start

March 1, 2000

Study Completion

October 1, 2002

Study Registration Dates

First Submitted

March 18, 2000

First Submitted That Met QC Criteria

March 18, 2000

First Posted (Estimate)

March 20, 2000

Study Record Updates

Last Update Posted (Estimate)

March 4, 2008

Last Update Submitted That Met QC Criteria

March 3, 2008

Last Verified

October 1, 2002

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 000098
  • 00-C-0098

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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