Phase 1 radioimmunotherapy study with lutetium 177-labeled anti-carbonic anhydrase IX monoclonal antibody girentuximab in patients with advanced renal cell carcinoma

Eur Urol. 2013 Sep;64(3):478-85. doi: 10.1016/j.eururo.2012.08.024. Epub 2012 Aug 21.

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 ((177)Lu)-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 (177)Lu-cG250.

Intervention: Groups of three patients received (177)Lu-cG250, starting at a dose level of 1110 MBq/m(2)(177)Lu-cG250, with dose increments of 370 MBq/m(2) 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/m(2) 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: (177)Lu-cG250 radioimmunotherapy in metastatic ccRCC patients is well tolerated at an activity dose level as high as 2405 MBq/m(2) (MTD). Radioimmunotherapy with (177)Lu-cG250 may stabilize previously progressive metastatic ccRCC.

Trial registration: ClinicalTrials.gov NCT00142415.

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

Publication types

  • Clinical Trial, Phase I
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal / adverse effects
  • Antibodies, Monoclonal / metabolism
  • Antibodies, Monoclonal / therapeutic use*
  • Antigens, Neoplasm / immunology*
  • Carbonic Anhydrase IX
  • Carbonic Anhydrases / immunology*
  • Carcinoma, Renal Cell / diagnostic imaging
  • Carcinoma, Renal Cell / enzymology
  • Carcinoma, Renal Cell / immunology
  • Carcinoma, Renal Cell / radiotherapy*
  • Carcinoma, Renal Cell / secondary
  • Disease Progression
  • Dose-Response Relationship, Radiation
  • Female
  • Humans
  • Immunoconjugates / adverse effects
  • Immunoconjugates / metabolism
  • Immunoconjugates / therapeutic use*
  • Kidney Neoplasms / diagnostic imaging
  • Kidney Neoplasms / enzymology
  • Kidney Neoplasms / immunology
  • Kidney Neoplasms / pathology
  • Kidney Neoplasms / radiotherapy*
  • Lutetium / adverse effects
  • Lutetium / metabolism
  • Lutetium / therapeutic use*
  • Male
  • Maximum Tolerated Dose
  • Middle Aged
  • Netherlands
  • Radioimmunotherapy* / adverse effects
  • Radionuclide Imaging
  • Radiopharmaceuticals / adverse effects
  • Radiopharmaceuticals / metabolism
  • Radiopharmaceuticals / therapeutic use*
  • Time Factors
  • Tissue Distribution
  • Treatment Outcome
  • Tumor Burden
  • Whole Body Imaging

Substances

  • Antibodies, Monoclonal
  • Antigens, Neoplasm
  • G250 monoclonal antibody
  • Immunoconjugates
  • Radiopharmaceuticals
  • Lutetium
  • CA9 protein, human
  • Carbonic Anhydrase IX
  • Carbonic Anhydrases

Associated data

  • ClinicalTrials.gov/NCT00142415