Radioligand therapy extends progression-free survival with manageable safety profile in advanced prostate cancer

New data on prolonged prostate-specific antigen (PSA) progression and adverse events grouped by safety topic of interest from the PSMAfore study underscore the statistically significant and clinically meaningful radiographic progression-free survival (rPFS) benefit of [¹⁷⁷Lu]Lu-PSMA-617 radioligand therapy for patients with taxane-naive metastatic castration-resistant prostate cancer (mCRPC).

This study was presented at the Society of Nuclear Medicine and Molecular Imaging (SNMMI) 2024 Annual Meeting and was honored as the meeting’s Abstract of the Year.

Each year, SNMMI chooses an abstract that best exemplifies the most promising advances in the field of nuclear medicine and molecular imaging. This year, the SNMMI Henry N. Wagner, Jr., Abstract of the Year was chosen from more than 1,500 abstracts submitted to the meeting and voted on by reviewers and the society leadership.

“Findings from the pivotal Phase 3 VISION trial led to the U.S. Food and Drug Administration (FDA) approval of [¹⁷⁷Lu]Lu-PSMA-617 for PSMA-positive mCRPC patients previously treated with both an androgen receptor pathway inhibitor (ARPI) and taxane-based chemotherapy,” said Ken Herrmann, MD, chair of the Department of Nuclear Medicine at University Hospital Essen in Essen, Germany.

“The current PSMAfore study aims to assess the benefit of [¹⁷⁷Lu]Lu-PSMA-617 in patients with mCRPC who have never received taxane-based chemotherapy with the hope of making this promising therapy available to more patients earlier in the course of their treatment journey.”

The study included 468 taxane-naive mCRPC patients who were prostate-specific membrane antigen (PSMA)-positive on [⁶⁸Ga]Ga-PSMA-11 PET/CT imaging and candidates for an ARPI change after one progression on prior ARPI therapy. Patients were randomly assigned to one of two treatments: [¹⁷⁷Lu]Lu-PSMA-617 or a change in ARPI (to abiraterone or enzalutamide). Researchers assessed rPFS (primary endpoint) and overall survival (key secondary endpoint), as well as PSA decline of 50% or more from baseline (PSA50), health-related quality of life, and safety.

In the PSMAfore study, [¹⁷⁷Lu]Lu-PSMA-617 was well tolerated with a manageable safety profile consistent with the established safety profile and good tolerability observed in the VISION trial that assessed patients with mCRPC treated with ARPI and taxane-based chemotherapy. Time to PSA progression and objective response rate were also evaluated. Researchers analyzed data for patients in both the [¹⁷⁷Lu]Lu-PSMA-617 and ARPI change groups at 7.3 months (primary analysis) and again at 15.9 months (second interim analysis).

At primary analysis, the median rPFS was 9.30 months for the [¹⁷⁷Lu]Lu-PSMA-617 group and 5.55 months for ARPI change group (HR 0.41, 95% CI 0.29-0.56); results were similar at the second interim analysis. Data collected at the second interim analysis also show that for [¹⁷⁷Lu]Lu-PSMA-617 versus ARPI change, median time to worsening in FACT-P total score was longer (7.46 months versus 4.27 months), objective response rate was higher (50.7% versus 14.9%), PSA50 response was higher (57.6% versus 20.4%), and median time to PSA progression was longer (10.55 months versus 4.24 months).

Incidence of grade >3 adverse events in the second interim analysis were fewer for the [¹⁷⁷Lu]Lu-PSMA-617 group than for the ARPI change group. In the [¹⁷⁷Lu]Lu-PSMA-617 group, the most common groups of any-grade treatment-emergent adverse events according to safety topics of interest were dry mouth and myelosuppression—a condition in which bone marrow activity is decreased, resulting in fewer red blood cells (anemia), white blood cells (thrombocytopenia), and platelets (neutropenia).

Updated overall survival results from the third interim analysis will be presented in an oral presentation this afternoon. Adding to the extensive knowledge on the efficacy and tolerability of [¹⁷⁷Lu]Lu-PSMA-617, these latest findings highlight the potential of [¹⁷⁷Lu]Lu-PSMA-617 as a treatment option for patients in the earlier lines of advanced prostate cancer.

“Patients with advanced prostate cancer face an unmet need for treatments that offer clinically meaningful benefits while minimizing impact of severe adverse events. Results from the PSMAfore study suggest that [¹⁷⁷Lu]Lu-PSMA-617 may have the potential to change the treatment paradigm for patients with advanced prostate cancer in the pre-taxane setting,” noted Oliver Sartor, MD, Director of Radiopharmaceutical Trials at the Mayo Clinic in Rochester, Minnesota and presenter of today’s oral abstract.

Plans are underway to submit an application to the FDA for a label expansion for [¹⁷⁷Lu]Lu-PSMA-617 in the pre-taxane setting for the second half of 2024, according to Novartis, the trial sponsor. If approved, these data will be incorporated into the updated product prescribing information, providing earlier access to this therapy.

Provided by
Society of Nuclear Medicine and Molecular Imaging