[68Ga]Ga-PSMA-11 PET baseline imaging as a prognostic tool for clinical outcomes to [177Lu]Lu-PSMA-617 in patients with mCRPC: A VISION substudy.

Author:

Kuo Phillip1,Hesterman Jacob2,Rahbar Kambiz3,Kendi Ayse T.4,Wei Xiao X.5,Fang Bruno6,Adra Nabil7,Armstrong Andrew J.8,Garje Rohan9,Michalski Jeff M.10,Ghebremariam Samson11,Brackman Marcia12,Wong Connie13,Benson Taylor14,Vogelzang Nicholas J.15

Affiliation:

1. University of Arizona, Tucson, AZ;

2. Invicro, Needham, MD;

3. Universitätsklinikum Münster, Münster, Germany;

4. Mayo Clinic, Rochester, MN;

5. Dana-Farber Cancer Institute, Boston, MA;

6. Astera Cancer Care, East Brunswick, NJ;

7. Indiana University Simon Comprehensive Cancer Center, Indianapolis, IN;

8. Duke Cancer Institute Center for Prostate and Urologic Cancer, Duke University, Durham, NC;

9. University of Iowa, Iowa City, IA;

10. Washington University in St. Louis, St. Louis, MO;

11. Novartis Pharmaceuticals Corporation, East Hanover, NJ;

12. Novartis Pharmaceuticals Corporation, Indianapolis, IN;

13. Novartis Pharmaceuticals Corporation, Cambridge, United Kingdom;

14. Novartis Pharmaceuticals Corporation, St George, UT;

15. Comprehensive Cancer Centers, Las Vegas, NV;

Abstract

5002 Background: In the phase 3 VISION study, gallium (68Ga) gozetotide (68Ga-PSMA-11) PET/CT imaging was used to determine eligibility for lutetium (177Lu) vipivotide tetraxetan (177Lu-PSMA-617). Given that 177Lu-PSMA-617 targets PSMA, we assessed the association between quantitative PSMA imaging parameters and treatment outcomes. Methods: In VISION, adults with mCRPC with ≥ 1 PSMA-positive (+) and no PSMA-negative lesions meeting the exclusion criteria were enrolled. In this sub-study, the association between imaging data from pre-enrollment 68Ga-PSMA-11 PET/CT scans of pts in the 177Lu-PSMA-617 group and clinical outcomes was assessed. Imaging data meeting quality requirements were analyzed for 548/551 pts. PSMA expression was quantified by 5 PET parameters: PSMA+ lesions by region, mean standardized uptake value (SUVmean), maximum SUV (SUVmax), PSMA+ tumor volume, and tumor load (PSMA+ tumor volume × SUVmean). Parameters were extracted from the whole body and 4 regions. Association between PET parameters and radiographic progression-free survival (rPFS; primary objective), overall survival (OS), objective response rate (ORR), and prostate–specific antigen 50 (PSA50) response was assessed. Results: Most pts (92.7%) had PSMA uptake in bone. In both the whole-body and regional analyses, statistically significant associations of PSMA PET parameters to clinical outcomes were observed (whole-body data shown in Table). Higher whole-body SUVmean was associated with improved clinical outcomes; pts in the highest quartile (SUVmean: rPFS, ≥ 10.2; OS, ≥ 9.9) had a median rPFS and OS of 14.1 and 21.4 months, vs 5.8 and 14.5 months for those in the lowest quartile (< 6.0; < 5.7), respectively. Absence of PSMA+ lesions in bone, liver, and lymph node, and lower PSMA+ tumor load, were indicators of good prognosis. Conclusions: Higher SUVmean is strongly associated with improved outcomes with 177Lu-PSMA-617; clinical efficacy for different SUV levels vs the SoC arm is being assessed. Data support use of 68Ga-PSMA-11 PET/CT scan to identify pts who will benefit from PSMA-targeted radioligand therapy.[Table: see text]

Funder

Advanced Accelerator Applications, a Novartis Company.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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