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April 12, 2026Cancer Imaging1 citationsOpen Access

¹⁸FPSMA-1007 and ¹⁸FFDG PET/CT in patients with metastatic triple-negative breast cancer: a prospective head-to-head comparison and assessment of PSMA-targeted radioligand therapy applicability

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TLTatiana Nikolaevna LazutinaAKAleksandr Igorevich KhalimonSUSoslan Rolanovich Urtaev

Key Points

  • This research aims to compare the efficacy of [¹⁸F]PSMA-1007 and [¹⁸F]FDG PET/CT in detecting lesions in metastatic triple-negative breast cancer.
  • Conducted a prospective study with 20 patients
  • All patients underwent both [¹⁸F]PSMA-1007 and [¹⁸F]FDG PET/CT
  • Performed qualitative and quantitative image analysis
  • Assessed applicability of PSMA-targeted radioligand therapy for patients
  • Identified a total of 229 lesions with both tracers
  • [¹⁸F]FDG demonstrated higher uptake in TNBC lesions overall
  • [¹⁸F]PSMA-1007 revealed more discordant lesions
  • Diagnostic CT revealed additional TNBC lesions not seen by PET
  • No patients met the criteria for potential PSMA-targeted therapy based on uptake levels

Abstract

Triple-negative breast cancer (TNBC) is an aggressive molecular subtype of breast cancer with limited treatment approaches. Prostate-specific membrane antigen, widely applied as a target for molecular imaging and radioligand therapy of prostate cancer, demonstrates the highest expression in TNBC across all molecular subtypes of breast cancer, and represents a promising target for imaging and treatment of TNBC patients. This prospective study included 20 patients with metastatic TNBC who underwent both ¹⁸FPSMA-1007 and ¹⁸FFDG PET/CT. Qualitative and quantitative image analysis was performed to determine the uptake predominance of one of the tracers and the added value of the diagnostic CT, as well as to assess the potential applicability of PSMA-RLT. A total of 229 lesions were identified using both ¹⁸FPSMA-1007 and ¹⁸FFDG PET/CT. Concordant and discordant lesions were observed for both tracers, with a greater number of discordant lesions identified by ¹⁸FPSMA-1007. ¹⁸FFDG demonstrated higher uptake in TNBC lesions. An exception was observed in lung lesions, where no significant difference was found between tracers. The application of diagnostic CT revealed additional TNBC lesions that were not identified by PET, for each tracer. None of the patients demonstrated a ¹⁸FPSMA-1007 uptake level sufficient for potential PSMA-RLT application when a lesional SUV-based threshold was used. Despite detectable ¹⁸FPSMA-1007 uptake in TNBC lesions, ¹⁸FFDG uptake was generally higher. Furthermore, the diagnostic CT can identify additional PET-negative lesions. Although PSMA expression is confirmed in TNBC, it may be insufficient to provide potential benefit from PSMA-RLT for this patient group.

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Cite This Study

Lazutina et al. (2026) studied this question.

synapsesocial.com/papers/69db37df4fe01fead37c5e84https://doi.org/10.1186/s40644-026-01028-6
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