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Impact of TP53 loss-of-function alterations on the response to PSMA radioligand therapy in metastatic castration-resistant prostate cancer patients.

Authors :
Slootbeek PHJ
Luna-Velez MV
Privé BM
van der Doelen MJ
Kloots ISH
Pamidimarri Naga S
Onstenk HE
Nagarajah J
Westdorp H
van Oort IM
Kroeze LI
Schalken JA
Bloemendal HJ
Mehra N
Source :
Theranostics [Theranostics] 2024 Aug 01; Vol. 14 (12), pp. 4555-4569. Date of Electronic Publication: 2024 Aug 01 (Print Publication: 2024).
Publication Year :
2024

Abstract

Rationale: PSMA-targeting radioligand therapy (PSMA-RLT) has shown promise in metastatic castration-resistant prostate cancer (mCRPC), particularly in PSMA-avid tumours. However, predicting response remains challenging. Preclinical data suggests aberrant p53-signalling as a predictor of poor response. Methods: The patient population of this pre-planned retrospective cohort study consists of 96 patients with mCRPC who underwent treatment with PSMA-RLT and were molecularly profiled by whole-genome sequencing and or targeted next-generation sequencing. Response to PSMA-RLT was assessed per molecular subtype, including TP53 -mutational status. Results: Patients with TP53 loss-of-function alterations had a shorter median progression-free survival (3.7 versus 6.2 months, P <0.001), a lower median PSA change (-55% vs. -75%, P =0.012) and shorter overall survival from initiation of PMSA-RLT (7.6 vs. 13.9 months, P =0.003) compared to TP53 -wildtype patients. Pathogenic alterations in AR , MYC , BRCA1 , or BRCA2 as well as in genes linked to the PI3K or MAPK pathways or genes involved in homologous recombination repair, were not associated with response. Only lactate dehydrogenase was, alongside TP53 -status, significantly associated with response. Transcriptome analysis of 21 patients, identified six p53 signalling genes whose low expression was associated to a shorter progression-free survival ( P <0.05). Conclusion: TP53 loss-of-function may serve as a prognostic factor for PSMA-RLT outcomes in patients with mCRPC.<br />Competing Interests: Competing Interests: Maarten J. van der Doelen: Research support: 'Bayer, Janssen-Cilag'. Travel support: 'Astellas'. James Nagarajah: Research support: 'ABX, Novartis'. Advisory role: 'ITM, POINT biopharma, CURIUM, Novartis, Bayer'. Inge M. van Oort: Advisory role: 'Bayer, Astellas, Janssen, MSD/AstraZeneca'. Research support: 'Astellas, Janssen, Bayer'. Jack. A. Schalken: Speaker honorarium: 'Astellas, Bayer'. Niven Mehra: Advisory role: 'Roche, MSD, BMS, Bayer, Astellas, Janssen'. Research support: 'Astellas, Janssen, Pfizer, Roche and Sanofi' Genzyme'. Travel support: 'Astellas, MSD'. The remaining authors declare no conflict of interest.<br /> (© The author(s).)

Details

Language :
English
ISSN :
1838-7640
Volume :
14
Issue :
12
Database :
MEDLINE
Journal :
Theranostics
Publication Type :
Academic Journal
Accession number :
39239510
Full Text :
https://doi.org/10.7150/thno.96322