Ovarian Cancer Clinical Trial

Intraoperative Imagery of Renal Nodules With Folate-fluorescein Conjugate(EC17)

Summary

According to the National Cancer Institute, an estimated 64,770 men and women will be diagnosed with kidney cancer in 2012. Of this number, an estimated 13,570 will die of this disease. Surgery remains one of the best options for patients presenting with operable Stage II or III cancers, however the five year survival rate for these candidates remains at a dismal 63.7% for Stage II and 11% for Stage III. The high rates of recurrence suggest that surgeons are unable to completely detect and remove primary tumor nodules in a satisfactory manner as well as lingering metastases in sentinel lymph nodes. By ensuring a negative margin through imaging during surgery it would be possible for the investigators to improve the rates of recurrence free patients and thus overall survival.

Renal cell malignancies are the ideal disease to investigate intra-operative imaging. 70% of kidney malignancies express folate receptor alpha (FRA). It is important to note that FRA is expressed only in the proximal tubules of the kidneys, activated macrophages, and in the choroidal plexus. Thus, the false positive detection rate is expected to be extremely low. A group well known to us in the Netherlands has completed a pilot study utilizing a folate-FITC conjugate in 12 patients with ovarian cancer. Another group of investigators in Mayo have subsequently performed this study on 20 more patients without any serious adverse events (personal communication). They report excellent sensitivity and specificity with this technique with only grade 1 side effects (allergic reaction). All side effects reversed when the injection was halted. Patients with a history of allergic reactions to insect bites should not participate (fluorescein is derived from the firefly insect, folate is an essential vitamin).

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Eligibility Criteria

Inclusion Criteria:

Adult patients 18 years of age or older
Patients presenting with a renal cell nodule or mass that are scheduled for open or laparoscopic resection based on clinical criteria
Good operative candidate
Subject capable of giving informed consent and participating in the process of consent.

Exclusion Criteria:

Pregnant women as determined by urinary or serum beta human chorionic gonadotropin (hCG) test within 72 hours of surgery
Patients with a history of anaphylactic reactions to Folate-FITC or insects

At-risk patient populations

People who would be easily lost to follow-up (ex: People who are homeless or alcohol dependent)
Children and neonates
Patients unable to participate in the consent process

Study is for people with:

Ovarian Cancer

Phase:

Early Phase 1

Estimated Enrollment:

10

Study ID:

NCT01778933

Recruitment Status:

Completed

Sponsor:

University of Pennsylvania

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There is 1 Location for this study

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Hospital of the University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States

How clear is this clinincal trial information?

Study is for people with:

Ovarian Cancer

Phase:

Early Phase 1

Estimated Enrollment:

10

Study ID:

NCT01778933

Recruitment Status:

Completed

Sponsor:


University of Pennsylvania

How clear is this clinincal trial information?

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