Investigating the Chemokine Receptor 4 as Potential Theranostic Target in Adrenocortical Cancer Patients

Clin Nucl Med. 2017 Jan;42(1):e29-e34. doi: 10.1097/RLU.0000000000001435.

Abstract

Purpose: Adrenocortical carcinoma (ACC) is a rare but aggressive endocrine tumor with limited treatment options. Preclinical studies confirmed overexpression of the chemokine receptor 4 (CXCR4) in this cancer type. This study aimed to analyze the role of CXCR4 imaging using Ga-pentixafor for ACC staging and selection of patients for CXCR4-directed endoradiotherapy.

Methods: Thirty patients with histologically proven advanced, metastasized ACC underwent F-FDG PET/CT and Ga-pentixafor PET/CT within a time interval of 3 ± 4 days to evaluate suitability for CXCR4-directed endoradiotherapy. Scans were analyzed retrospectively for visual extent of ACC and SUVmax/mean of the tumor lesions. Ga-pentixafor PET was compared with F-FDG PET, the reference imaging standard. All patients were rated for suitability of CXCR4-directed endoradiotherapy considering patient's history, previous treatment, and CXCR4 expression of FDG-positive lesions compared with background activity within the same organ.

Results: All patients had lesions that were positive for both F-FDG and Ga-pentixafor PET and were rated as positive for disease. In 2 patients (7%), Ga-pentixafor PET identified more lesions compared with F-FDG PET. In 5 patients (17%) and 10 patients (33%), complementary and comparable information, respectively, was provided by dual-tracer imaging. In 13 patients (43%), more tumor lesions were identified by F-FDG PET compared with Ga-pentixafor PET. The F-FDG uptake of the malignant lesions was significantly higher (P < 0.01) than the SUVmax/mean for Ga-pentixafor. Overall, 70% of the patients were rated as suitable or potentially suitable for CXCR4-directed treatment.

Conclusions: Ga-pentixafor allows in vivo imaging of CXCR4 expression in patients with advanced ACC and may serve as companion diagnostic tool in selecting patients for potential CXCR4-directed endoradiotherapy. Seventy percent of the patients with advanced, metastasized ACC may be suitable for a CXCR4-directed treatment after failure of standard treatment options.

MeSH terms

  • Adrenal Cortex Neoplasms / diagnostic imaging*
  • Adrenal Cortex Neoplasms / metabolism
  • Adrenal Cortex Neoplasms / radiotherapy
  • Adrenocortical Carcinoma / diagnostic imaging*
  • Adrenocortical Carcinoma / metabolism
  • Adrenocortical Carcinoma / radiotherapy
  • Adult
  • Aged
  • Coordination Complexes
  • Female
  • Gallium Radioisotopes
  • Humans
  • Lutetium / therapeutic use
  • Male
  • Middle Aged
  • Patient Selection
  • Peptides / therapeutic use
  • Peptides, Cyclic
  • Positron Emission Tomography Computed Tomography
  • Radioisotopes / therapeutic use
  • Radionuclide Imaging
  • Radiotherapy
  • Receptors, CXCR4 / metabolism*
  • Yttrium Radioisotopes / therapeutic use

Substances

  • 177Lu-pentixather
  • 68Ga-pentixafor
  • 90Y-pentixather
  • CXCR4 protein, human
  • Coordination Complexes
  • Gallium Radioisotopes
  • Peptides
  • Peptides, Cyclic
  • Radioisotopes
  • Receptors, CXCR4
  • Yttrium Radioisotopes
  • Lutetium