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European Urology

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Phase 1 Radioimmunotherapy Study with Lutetium 177–labeled Anti-Carbonic Anhydrase IX Monoclonal Antibody Girentuximab in Patients with Advanced Renal Cell Carcinoma

Alexander B. Stillebroer, Otto C. Boerman, Ingrid M.E. Desar, Marije J. Boers-Sonderen, Carla M.L. van Herpen, Johannes F. Langenhuijsen, Peter M. Smith-Jones, Egbert Oosterwijk, Wim J.G. Oyen and Peter F.A. Mulders

Accepted 13 August 2012, Published online 22 August 2012


Abstract

Background

Patients with metastatic clear cell renal cell carcinoma (ccRCC) have a dismal prognosis. Therefore, new and less toxic treatments are needed.

Objective

We determined the maximum tolerated dose (MTD) and potential therapeutic efficacy of multiple infusions of lutetium 177 (177Lu)-girentuximab (cG250) on various dose levels in a phase 1 trial in patients with progressive metastasized ccRCC.

Design, setting, and participants

In this uncontrolled case series in 23 patients with progressive ccRCC metastases, cG250 accumulation was verified by diagnostic indium 111-cG250 imaging. Patients then received a high-activity dose of 177Lu-cG250.

Intervention

Groups of three patients received 177Lu-cG250, starting at a dose level of 1110 MBq/m2177Lu-cG250, with dose increments of 370 MBq/m2 per group. In the absence of persistent toxicity, progressive disease, and accelerated blood clearance, patients were eligible for retreatment after 3 mo with 75% of the previous activity dose. Patients could receive a total of three treatment cycles.

Outcome measurements and statistical analysis

Determination of the MTD was the primary and therapeutic efficacy was the secondary outcome measurement of the study.

Results and limitations

The MTD was 2405 MBq/m2 because higher doses resulted in dose-limiting myelotoxicity. Some patients received second (13 of 23 [56%]) and third (4 of 23 [17%]) treatment cycles. Most patients (17 of 23 [74%]) demonstrated stable disease 3 mo after the first treatment, and one patient showed a partial response that lasted for 9 mo. Mean growth of target tumor lesions was reduced from 40.4% (95% confidence interval [CI], ±17.0) during the last 3 mo before study entry to 5.5% (95% CI, ±5.3; p < 0.001) at 3 mo after the first treatment cycle. No major nonhematologic side effects were observed.

Conclusions

177Lu-cG250 radioimmunotherapy in metastatic ccRCC patients is well tolerated at an activity dose level as high as 2405 MBq/m2 (MTD). Radioimmunotherapy with 177Lu-cG250 may stabilize previously progressive metastatic ccRCC.

Take Home Message

Radioimmunotherapy with 177lutetium-girentuximab for metastatic clear cell renal cell carcinoma (ccRCC) is well tolerated and could stabilize previously progressive metastatic ccRCC. Because the side effects of tyrosine kinase inhibitors are common and often severe, radioimmunotherapy may be an alternative treatment.

Keywords: Renal cell carcinoma, Radioimmunotherapy, cG250, Lutetium.


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