Updates in Imaging of Advanced Prostate Cancer



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Updates in Imaging of Advanced Prostate Cancer H. Alberto Vargas Director, Genitourinary Radiology Hedvig Hricak Chair, Department of Radiology New York, 16 July 2015

Nothing to disclose

Outline MRI, PET/CT what is the difference? Which PET tracers? Basis for uptake in Prostate Cancer (PCa)? Potential clinical uses Beyond cancer detection and staging Focus on non-invasive assessment of tumor biology

Prostate MRI: the beginning Initial focus on zonal anatomy

Prostate MRI in 2015: The role of MRI has evolved! Zonal Anatomy is still immensely important

Prostate MRI in 2015: The role of MRI has evolved! Prostate MRI staging only It s about providing meaningful information relevant to patient management in specific clinical contexts Move away from the one size fits all approach to prostate MRI and towards a wearing the right hat for the right outfit approach

Clinically Low-risk Prostate Cancer The critical question: does the MR fit with the biopsy result? Patient 1: Gleason 6, PSA 5, ct2a Axial T2WI Coronal T2WI Repeat bx: Gleason 6, 1 core +, 5% tumor Patient 2: Gleason 6, PSA 5, ct2a Axial T2WI Coronal T2WI Repeat bx: Gleason 4+3 4 cores + 50-70% tumor Vargas,,Hricak. Journal of Urology 2012

Clinically Low-risk Prostate Cancer What is the problem with random prostate biopsies? Gleason 4+4=8 Gross ECE Gleason 3+3=6 1/12 cores positive 10% involvement

Prostate Cancer Clinical States Clinically Localized Disease Rising PSA Clinical Metastases: Non-Castrate Clinical Metastases: Castrate Rising PSA: Castrate Scher HI et al. Urology 2000

Prostate Cancer Clinical States Clinically Localized Disease Rising PSA Clinical Metastases: Non-Castrate Clinical Metastases: Castrate Rising PSA: Castrate MRI Scher HI et al. Urology 2000

Prostate Cancer Clinical States Clinically Localized Disease Rising PSA Clinical Metastases: Non-Castrate Clinical Metastases: Castrate Rising PSA: Castrate PET Scher HI et al. Urology 2000

PET Radiotracers Isotope F C11 N13 O15 Zr89 Ga68 Pharmaceutical compound Fluorodeoxyglucose (FDG) Choline Aminoacids Sodium Fluoride Receptors: FDHT, PSMA, Bombesin

PET has revolutionized cancer imaging! F-FDG Fluorodeoxyglucose GLUT X Cancer cell HK F-FDG F-FDG-6P G6-PI X

FDG and Prostate Cancer For the initial diagnosis and staging of prostate cancer, FDG PET is considered limited Patterns of GLUT expression in PCa is variable Affected by dedifferentiation, aggressiveness, androgen sensitivity, hypoxia Overlap in tracer uptake in normal and abnormal prostate tissue (including inflammation!)

PET tracers used in Prostate Cancer Cell Metabolism Bone Matrix Receptors and Membrane Proteins

PET tracers used in Prostate Cancer Cell Metabolism Glucose Choline Acetate Amino Acids F-FDG 11 C-choline F-choline 11 C-acetate F-acetate F-FACBC

Choline Precursor for phospholipid synthesis Major components of the cellular membrane Enters the cell through choline transporters Can be labeled with 11 C or F FDA approval evaluation of recurrence

Choline Pooled sensitivity and specificity of 86% and 93% for detecting PCa Performance correlated to PSA levels Recent study compared Choline PET and MRI: Choline better for lymph nodes MRI better for prostate bed Both good for bone metastases Evangelista L et al. Clin Nuc Med 2013 Giovacchini et al. J Urol. 2010 Kitajima K et al. J Nuc Med. 2014

PET tracers used in Prostate Cancer Cell Metabolism Glucose Choline Acetate Amino Acids F-FDG 11 C-choline F-choline 11 C-acetate F-acetate F-FACBC

Acetate Major sources of acetate consumption: Krebs cycle Production of phospholipids in cellular membranes Upregulation of fatty acid synthetase basis of PCa uptake

Acetate PET Uptake appears unaffected by androgens (in contrast to FDG and choline) Study comparing 11 C-Acetate PET and MRI Sensitivity/specificity (tumors >5 mm): 62%/80% for PET/CT and 82%/95% for MRI >9 mm, comparable accuracy for PET and MRI Emonds KM et al. EJNMMI research. 2013 Mohsen B et al. BJU Int 2013 Mena E et al. JNM. 2012

PET tracers used in Prostate Cancer Cell Metabolism Glucose Choline Acetate Amino Acids F-FDG 11 C-choline F-choline 11 C-acetate F-acetate F-FACBC

Aminoacids (AA): Leucine Basis for uptake in Pca: AA transport + protein synthesis F-FACBC tumor uptake comparable to FDG; but bladder excretion 20-fold; cancer/inflammation uptake ratios SUVmax tumor than in normal prostate Sensitivity/specifity for tumor detection slightly for MRI (73/79%) than FACBC (67/66%) Recurrence: Sensitivity/specificity 90/40% for prostatic fossa vs 55/97% in distant disease (n=93) Oka S et al. JNM 2007 Turkbey B et al. Radiology. 2014 Schuster DM et al. J Urol 2013

PET tracers used in Prostate Cancer Bone Matrix F-NaF

Sodium Fluoride (NaF) Developed in 1962; FDA approved 1972 Uptake mechanism similar to bone scan blood clearance, bone/background ratio, interval from administration to imaging Similar pitfalls to bone scan accumulates in bone matrix; not cancer cells no uptake in non-bone metastases Uptake in degenerative bone disease Flare phenomenon

T2w-MRI T1w-MRI 99m Tc-MDP Gleason 8. PSA 22. Metastases? Anything outside of the pelvis?

F-NaF PET 3D MIP Anything outside the pelvis?

PET tracers used in Prostate Cancer Receptors and Membrane Proteins Androgen Receptor (AR) Gastrin Releasing Peptide Receptor (GRP-R) Prostate Specific Membrane Antigen (PSMA) F-FDHT F, 68 Ga, 64 Cu, 177 Lu Bombesin analogues Antibodies 111 In, 64 Cu, 89 Zr, 90 Y, 177 Lu Antibody Fragments Minibodies Small molecules 7E11 J591 89 Zr-Df-IAB2M F-DCFBC

Prostate Cancer Clinical States Clinically Localized Disease Rising PSA Clinical Metastases: Non-Castrate Clinical Metastases: Castrate Rising PSA: Castrate Androgen Receptor (AR) gene activation is a hallmark of castration-resistant prostate cancer

The Androgen Receptor (AR) AR ligand-dependent transcription activator involved in cellular proliferation and differentiation Almost all PCa patients initially respond to androgen deprivation, but eventually progress to a castration-resistant clinical state bypassing or sensitizing the AR pathway Novel therapies targeting the AR have shown survival recent FDA/EU approval

-38 patients with castration resistant prostate cancer and discrete bone lesions - All underwent CT, FDG PET and FDHT PET - CT features (including Hounsfield Units), SUVmax from FDG and FDHT PET

1. Bone metastases demonstrate variable appearance on CT Densely sclerotic Groundglass Mixed Lytic

2. CT density is inversely associated with FDG and FDHT PET uptake FDG Reader 1: r = -0.30; P <.001 Reader 2: r = -0.31; P <.001 FDHT Reader 1: r = -0.27; P =.001 Reader 2: = -0.37; P <.001

3. Preliminary associations with clinical outcomes -# lesions on CT, FDG and FDHT PET associated with overall survival (p<0.05) - SUVmax on FDHT, shorter overall survival (P=0.02) - No association between SUVmax on FDG PET and survival (P = 0.38-0.65)

FDHT for documenting pharmacologic targeting - FDHT PET pre- and 4 weeks post enzalutamide - Uptake suppression: drug hits the pharmacologic target (AR) Scher HI. The Lancet 2010

FDHT for measuring dose related targeting efficacy - FDHT PET pre- and 4 weeks post ARN-509 - Uptake suppression: dose dependent Rathkopf D E et al. JCO 2013

Rathkopf D E et al. JCO 2013

Movember GAP 2 Imaging Project: FDHT Multi-institutional study, Co-PIs MSKCC (lead site): Vargas, Morris Royal Marsden London: Chua VUMC Amsterdam: Hoekstra Austin Health Australia: Scott Total funding: $2.8 million

FDHT PET for guiding AR-targeted therapy Is there a target present? Yes Is there a response to the drug? Yes Continue therapy No No Alternative drug Alternative therapy

PET tracers used in Prostate Cancer Receptors and Membrane Proteins Androgen Receptor (AR) Gastrin Releasing Peptide Receptor (GRP-R) Prostate Specific Membrane Antigen (PSMA) F-FDHT F, 68 Ga, 64 Cu, 177 Lu Bombesin analogues Antibodies 111 In, 64 Cu, 89 Zr, 90 Y, 177 Lu Antibody Fragments Minibodies Small molecules 7E11 J591 89 Zr-Df-IAB2M F-DCFBC

Gastrin Releasing Peptide Receptor Bombesin-like peptide family Pca GRP-R overexpression at the mrna and protein levels (low to non-detectable in benign prostate) Can be labeled with 68 Ga generator produced

PET tracers used in Prostate Cancer Receptors and Membrane Proteins Androgen Receptor (AR) Gastrin Releasing Peptide Receptor (GRP-R) Prostate Specific Membrane Antigen (PSMA) F-FDHT F, 68 Ga, 64 Cu, 177 Lu Bombesin analogues Antibodies 111 In, 64 Cu, 89 Zr, 90 Y, 177 Lu Antibody Fragments Minibodies Small molecules 7E11 J591 89 Zr-Df-IAB2M F-DCFBC

Prostate Specific Membrane Antigen (PSMA) Transmembrane protein normally expressed in prostate epithelium, bowel, renal tubular cells and salivary glands PSMA expression imaged with labeled: Monoclonal antibodies (Mab) 7E11: labeled with 111 In (SPECT); 89 Zr (PET) J591 Antibody fragments: Minibodies Small molecules

7E11: What happened to capromab pendetide- ProstaScint? FDA approved in 1996; labeled with 111 In 7E11 binds to the intracellular domain of PSMA only accessible if there is membrane disruption (e.g. dead or dying cells) The number of available targets for binding of the tracer is limited low sensitivity for detecting viable tumor sites In contrast to PET, SPECT remains only semiquantitative in the clinical setting

Humanized monoclonal antibody J591 Targets the extracellular domain of PSMA accessible even if no membrane disruption The number of available targets for binding of the tracer better that 7E11 higher sensitivity for detecting viable tumor sites Labeled with 64 Cu, 89 Zr or 90 Y and 177 Lu for therapy Other mab: 3/A12, 3/E7, 3/F11 and 3C6

Castration resistant PCA. PSA. Recurrence? CT FDG 89 Zr- J591

Use of WB-MRI is increasing: beyond simple detection Blackledge et al. Plos One 2014

Summary PET is being increasingly used for the assessment of prostate cancer FDA approved tracers: FDG, Choline, NaF Tracers to watch: Androgen receptor imaging (FDHT) PSMA imaging Bombesin Whole-body MRI may also have a role More research needed to determine which probe(s) should be used for each clinical scenario