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Articles

Folate-targeted intraoperative fluorescence, OTL38, in robotic-assisted laparoscopic partial nephrectomy

, , , , , , , & show all
Pages 331-336 | Received 24 Jun 2020, Accepted 17 May 2021, Published online: 07 Jun 2021
 

Abstract

Objective

To investigate the safety and efficacy of OTL38, a folate-targeted, intraoperative fluorescence agent, in patients undergoing robotic-assisted laparoscopic partial nephrectomy.

Methods

Patients with proven or suspected localized renal cell carcinoma at a single academic institution were selected from 2016 to 2018. Patients received one dose of OTL38 at 0.025 mg/kg prior to robotic-assisted laparoscopic partial nephrectomy. The da Vinci Fluorescence Imaging Vision System was used to identify the tumor and inspect for residual disease after resection. Immunohistochemistry was performed to quantify folate receptor alpha in both the tumor and surrounding normal parenchyma. Patient follow-up was 1 month. Outcome data included descriptive statistics of the patient cohort and surgeon and pathologist surveys.

Results

Ten cases were performed. Mean patient age was 62.9 years (range = 50–70). Mean tumor size was 2.45 cm. Pathologic tumor stages ranged from T1a–T3a. Histologic tumor types included clear cell, chromophobe, type 1 papillary renal cell carcinoma and oncocytoma. The tumors did not fluoresce, while the surrounding normal parenchyma did show fluorescence. No adverse reactions were seen. Staining for folate receptor alpha was localized to the proximal renal tubules. Average staining in normal surrounding renal parenchyma was significantly greater than staining observed in tumor tissue (0.2086 vs 0.0467; p = 0.002). The mean difference in staining between tumor tissue and surrounding normal renal parenchyma was 0.1619 (95% CI = 0.0796–0.2442).

Conclusions

Based on our initial experience, OTL38 shows potential as a safe, effective and easy to use tool to improve visualization and resection of renal tumors.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This project was funded in part by the Indiana Clinical and Translational Sciences Institute, in part by National Institutes of Health Grant UL1TR001108, and in part by a National Institutes of Health Clinical and Translational Sciences Award. OTL38 was provided by On Target Laboratories, LLC.

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