4.3 Article

Preclinical evaluation of PSMA expression in response to androgen receptor blockade for theranostics in prostate cancer

Journal

EJNMMI RESEARCH
Volume 8, Issue -, Pages -

Publisher

SPRINGEROPEN
DOI: 10.1186/s13550-018-0451-z

Keywords

PSMA; Prostate cancer; Ga-68-PSMA PET; CT; Androgen receptor blockade; Radioligand therapy

Funding

  1. US Department of Energy, Office of Science Award [DE-SC0012353]
  2. UCLA SPORE in Prostate Cancer [P50 CA092131]
  3. Prostate Cancer Foundation [17CHAL02]
  4. Johnson Comprehensive Cancer Center NIH-NCI Cancer Center Support Grant [P30 CA016042]
  5. German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) [807122, 807454]
  6. Deutsche Forschungsgemeinschaft, Bonn, Germany [SFB 824]
  7. Fondation ARC pour la recherche sur le cancer [SAE20160604150]

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BackgroundProstate-specific membrane antigen (PSMA)-directed radioligand therapy (RLT) is a promising yet not curative approach in castration-resistant (CR) prostate cancer (PC). Rational combination therapies may improve treatment efficacy. Here, we explored the effect of androgen receptor blockade (ARB) on PSMA expression visualized by PET and its potential additive effect when combined with Lu-177-PSMA RLT in a mouse model of prostate cancer.MethodsMice bearing human CRPC (C4-2 cells) xenografts were treated with 10mg/kg enzalutamide (ENZ), with 50mg/kg bicalutamide (BIC), or vehicle (control) for 21days. PSMA expression was evaluated by Ga-68-PSMA11 PET/CT and quantified by flow cytometry of tumor fine needle aspirations before treatment and on days 23, 29, 34, and 39 post-therapy induction. For the RLT combination approach, mice bearing C4-2 tumors were treated with 10mg/kg ENZ or vehicle for 21days before receiving either 15MBq (84GBq/mol) Lu-177-PSMA617 or vehicle. DNA damage was assessed as phospho-H2A.X foci in tumor biopsies. Reduction of tumor volume on CT and survival were used as study endpoints.ResultsTumor growth was delayed by ARB while Ga-68-PSMA11 uptake increased up to 2.3-fold over time when compared to controls. ABR-induced upregulation of PSMA expression was confirmed by flow cytometry. Phospho-H2A.X levels increased 1.8- and 3.4-fold at 48h in response to single treatment ENZ or RLT and ENZ+RLT, respectively. Despite significantly greater DNA damage and persistent increase of PSMA expression at the time of RLT, no additional tumor growth retardation was observed in the ENZ+RLT group (vs. RLT only, p=0.372 at day 81). Median survival did not improve significantly when ENZ was combined with RLT.ConclusionARB-mediated increases in PSMA expression in PC xenografts were evident by Ga-68-PSMA11 PET imaging and flow cytometry. Lu-177-PSMA617 effectively decreased C4-2 tumor size. However, while pre-treatment with ARB increased DNA damage significantly, it did not result in synergistic effects when combined with RLT.

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