Abstract

At present, little is known about the molecular imaging-based response assessment of prostate-specific membrane antigen (PSMA)-targeted radioligand therapy with 177Lutetium (177Lu-PSMA-617 RLT) in metastatic castration-resistant prostate cancer (mCRPC). Our study evaluated the response to RLT using both molecular imaging and biochemical response assessments, and their potential prediction of progression-free survival (PFS). Fifty-one consecutive patients given two cycles of RLT at 6-week intervals were analyzed retrospectively. 68Ga-PSMA-11 PET/CT was obtained about 2 weeks prior to the first and 4–6 weeks after the second cycle. Molecular imaging-based response using SUVpeak and tumor-to-liver ratio (TLR) was determined by modified PERCIST criteria. ∆TLR and ∆SUV were significantly correlated with ∆PSA (p < 0.001, each). After a median follow-up of 49 months, the median PFS (95% CI) was 8.0 (5.9–10.1) months. In univariate analysis, responders showing partial remission (PRPSA and PRTLR) had significantly (p < 0.001, each) longer PFS (median: 10.5 and 9.3 months) than non-responders showing either stable or progressive disease (median: 4.0 and 3.5 months). Response assessment using SUVpeak failed to predict survival. In multivariable analysis, response assessment using TLR was independently associated with PFS (p < 0.001), as was good performance status (p = 0.002). Molecular imaging-based response assessment with 68Ga-PSMA-11 PET/CT using normalization of the total lesion PSMA over healthy liver tissue uptake (TLR) could be an appropriate biomarker to monitor RLT in mCRPC patients and to predict progression-free survival (PFS) of this treatment modality.

Highlights

  • Many life-prolonging therapy options, such as chemotherapy, androgen receptor targeting agents, and 223 Ra therapy have been approved for the treatment of men with metastatic castration-resistant prostate carcinoma (mCRPC) [2,3,4,5,6]

  • The assessment of response to these treatments still relies on biochemical parameters, such as prostate specific antigen (PSA) and conventional imaging modalities, including computed tomography (CT), magnetic resonance tomography (MRI), and bone scintigraphy [11]

  • A total of 322 tumor lesions on screening 68 GaPSMA-positron emission tomography/computed tomography (PET/CT) in 51 patients were identified as target lesions in the defined five-organ system and evaluated in this study

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Summary

Introduction

Despite advances in early detection and therapy, a significant fraction of patients with prostate cancer develops lethal metastatic castration-resistant prostate carcinoma (mCRPC) [1]. Biomolecules 2021, 11, 1099 prostate specific membrane antigen (PSMA) ligands such as PSMA-617, called 177 Lu-PSMA radioligand therapy (RLT), have shown encouraging results in these patients [7,8,9,10]. The assessment of response to these treatments still relies on biochemical parameters, such as prostate specific antigen (PSA) and conventional imaging modalities, including computed tomography (CT), magnetic resonance tomography (MRI), and bone scintigraphy [11]

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