All research
2026-06-30 PubMed

18F-Fluciclovine PET/CT more likely to change prostate cancer salvage radiotherapy field than 68Ga-PSMA-11.

18F-Fluciclovine or 68Ga-PSMA-11 PET/CT-guided Salvage Radiotherapy Changes in Postprostatectomy Biochemical Recurrence: Secondary Analysis of the EMPIRE-2 Trial.

Background

For men experiencing postprostatectomy biochemical recurrence (BCR) of prostate cancer, accurately identifying the location of recurrence is critical for effective salvage radiation therapy (sRT) planning. Conventional imaging often falls short in localizing subtle disease. Positron emission tomography/computed tomography (PET/CT) using agents like 68Ga-PSMA-11 (targeting prostate-specific membrane antigen) and 18F-fluciclovine (targeting amino acid transport) has emerged as a superior tool to guide sRT, but their comparative impact on treatment decisions needed further assessment.

Study Design

This secondary analysis of the prospective randomized EMPIRE-2 trial included 140 men (age range, 47-83 years) with detectable prostate-specific antigen (PSA) levels after prostatectomy. Participants were randomized 1:1 to undergo either 18F-fluciclovine PET/CT (arm A, 65 participants) or 68Ga-PSMA-11 PET/CT (arm B, 69 participants). The study compared changes in sRT decisions—specifically, whether to offer radiation therapy and to which field (with or without boost)—between pre- and post-PET time points in each arm, and between the two imaging agents. The Clopper-Pearson binomial method was used for statistical evaluation.

Results

Overall sRT decision changes occurred in 19 of 65 participants (29%) in the 18F-fluciclovine arm (P < .001) and 29 of 69 participants (42%) in the 68Ga-PSMA-11 arm (P < .001). However, there was no statistically significant difference in overall sRT decision changes between the two arms (P = .12). Among participants for whom the final decision was to offer sRT, changes in the specific treatment field (and/or boost) were substantial.

18F-fluciclovine PET/CT led to treatment field changes in 43 of 60 participants (72%) (P < .001), while 68Ga-PSMA-11 PET/CT resulted in changes for 33 of 61 participants (54%) (P < .001). Crucially, 18F-fluciclovine PET/CT was significantly more likely to induce changes in the treatment field or boost compared to 68Ga-PSMA-11 PET/CT (P = .046).

Key Findings

  • Overall sRT decision changes occurred in 29% of 18F-fluciclovine patients and 42% of 68Ga-PSMA-11 patients (both p<.001).
  • No significant difference in overall sRT decision changes between 18F-fluciclovine and 68Ga-PSMA-11 arms (p=0.12).
  • Treatment field/boost changes occurred in 72% of 18F-fluciclovine patients receiving sRT (p<.001).
  • Treatment field/boost changes occurred in 54% of 68Ga-PSMA-11 patients receiving sRT (p<.001).
  • 18F-fluciclovine PET/CT was significantly more likely to change treatment field/boost than 68Ga-PSMA-11 PET/CT (p=0.046).

Why It Matters

This study provides crucial evidence for optimizing salvage radiation therapy (sRT) protocols in postprostatectomy biochemical recurrence. Choosing 18F-fluciclovine PET/CT for sRT planning may lead to more precise targeting of recurrent prostate cancer, potentially allowing for more focused radiation delivery and minimizing exposure to healthy tissues. This could translate to improved efficacy and reduced side effects for patients. While both agents significantly alter treatment decisions, the higher rate of field/boost changes with 18F-fluciclovine suggests it offers a distinct advantage in refining the spatial aspects of radiation planning, potentially impacting long-term outcomes. Clinicians should consider these differences when selecting imaging modalities for sRT guidance.


prostate-cancer biochemical-recurrence salvage-radiotherapy 18f-fluciclovine 68ga-psma-11 pet-ct
Source: pubmed:42377125 · Ingested 2026-06-30 · Digest: gemini-2.5-flash