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Clinical Characteristics Associated with High [68Ga]Ga-PSMA-11 Uptake and Preliminary Therapeutic Outcomes in
Hyunpil Sung1,2, Minseok Suh1, Joonhyung Gil1
1Department of Nuclear Medicine, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul, 03080 Republic of Korea.
Purpose:
Adenoid cystic carcinoma (ACC) is a rare cancer that arises from the salivary glands. Recent studies have shown that prostate-specific membrane antigen (PSMA) expression is high in ACC. We conducted a prospective study to evaluate clinical factors associated with high [68Ga]Ga-PSMA-11 uptake and to report preliminary therapeutic outcomes of 177Lu-PSMA therapy in recurred or metastatic ACC.
Materials And Methods:
Thirty patients were prospectively enrolled. Any focal accumulation of [68Ga]Ga-PSMA-11 not explained by physiological uptake was defined as pathological lesions. Clinicopathological features relevant for high [68Ga]Ga-PSMA-11 uptake in recurred or metastatic ACC were analyzed. Therapeutic outcomes of patients who received 177Lu-PSMA therapy under compassionate use were also reviewed as a secondary component.
Results:
A total of 238 lesions were evaluated, and the SUVmax ranged between 0.9 and 11.0, showing mild to moderate PSMA uptake. Higher SUVmax was observed in lung and bone metastases. The longest tumor diameter (R = 0.190, P = 0.009) and tumor % growth rate (R = 0.220, P = 0.006) were significantly correlated with SUVmax. A longer duration from diagnosis was a relevant factor for high [68Ga]Ga-PSMA-11 uptake. Seven patients received 177Lu-PSMA therapy, but therapeutic outcomes were limited.
Conclusion:
High [68Ga]Ga-PSMA-11 uptake in recurred or metastatic ACC was associated with location of metastases, longer tumor diameter, high tumor % growth rate, and a longer duration from diagnosis. While 177Lu-PSMA therapy was performed in a limited cohort and outcomes were preliminary, these findings provide exploratory insights into potential factors relevant for patient selection and warrant further investigation in larger studies.
Supplementary Information:
The online version contains supplementary material available at 10.1007/s13139-025-00955-9.
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