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Wie ich mit Prostatakrebs umgehe Stephen B. Strum, MD, FACP Medical Oncologist

Wie ich mit Prostatakrebs umgehe Stephen B. Strum, MD, FACP Medical Oncologist. Stuttgart, Germany 11.05.2009. Active Objectified Surveillance & Other Strategies. Active Objectified Surveillance. Patients with “insignificant” PC based on set clinical & pathological criteria

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Wie ich mit Prostatakrebs umgehe Stephen B. Strum, MD, FACP Medical Oncologist

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  1. Wie ich mit Prostatakrebs umgehe • Stephen B. Strum, MD, FACP • Medical Oncologist Stuttgart, Germany 11.05.2009

  2. Active Objectified Surveillance & Other Strategies

  3. Active Objectified Surveillance • Patients with “insignificant” PC based on set clinical & pathological criteria • Patients with significant age & co-morbidity factors • Patients able to be monitored over time • Determine thresholds relating to treatment intervention • Patients who are reclassified as higher risk can be treated with cure • Reduce psychological stress of living with untreated cancer

  4. “Insignificant” Prostate Cancer • Gleason score 6 or less • PSA 10 or less • Clinical stage T2a or less • Free to total PSA percent > 15% • Less than 3 cores involved • 50% or less of any one core with PC • PSA doubling time > 3 years

  5. AOS (active objectified surveillance): Key Role of Status

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  7. Importance of Milieu in PC Behavior A Key Ingredient in any Active Surveillance Strategy

  8. Klotz L: Active surveillance with selective delayed intervention is the way to manage 'good-risk' prostate cancer. Nat Clin Pract Urol 2:136-42; 2005. Key Findings • Study begun in 1995 involving 299 patients • Median PSADT 7 yrs with 42% having DT > 10 yrs • At 8 yrs, overall actuarial survival 85% with PC-specific survival of 99%

  9. Optimal ADT (androgen deprivation therapy)

  10. Block androgen access to the PC cell Ensure significant lowering of Testosterone Measure testosterone using accurate lab assay Use US-PSA as biologic endpoint for ADT Use measures that down-regulate (dR) sensitivity of the androgen receptor (AR) Block bone-derived growth factors that are released due to excessive osteoclast activity (induced by androgen deprivation) 6 Ways to Optimize ADT

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  13. Are We Using the Optima Dose of Dutasteride ? Dr. Mostaghel's group looked for gene changes in 75 men with localized PC. Twenty-five had RP alone, 26 were given neoadjuvant dutasteride at 0.5 mg, and the remaining 24 received dutasteride, 3.5 mg orally per day for 4 months prior to RP.

  14. Testosterone assays inaccurate at low T levels: need to use LC/MS/MS based assays. ADT is about Androgen Availability Huggins won Nobel Prize 43 years ago showing PC dependence on Androgens. PC growth is mediated by androgens. We call it Androgen Dependent PC (ADPC) or Androgen Independent PC (AIPC) or Castration Resistant PC (CRPC) but PC growth is androgen related. PC mets even synthesize their own androgens. Testosterone level (T) is a key Biological End Point. T not measured in 95% of men with PC. “Castration” threshold should be < 20 ng/dl. Further lowering of T may enhance response.

  15. Lowest T level with impact on survival was 32 ng/dl. • Mean survival, free of developing AIPC, in men with breakthrough increases in T > 32 ng/dl was 88 months (CI 55-121 mos). • Mean survival in men with T < 20 ng/dl and no breakthrough increases > 32 ng/dl was 137 mos (CI 104-170). • In men with breakthrough increases > 50 ng/dl, those men with maximal ADT had a significantly longer survival free of AIPC. <20 20-50 > 50

  16. Importance of US-PSA (ultra-sensitive) to Monitor ADT • PSA nadir > 0.05 highly correlated with shorter time to progressive PC & prostate cancer-specific survival.

  17. The achievement of a PSA nadir of 0.05 or less was the most significant endpoint insofar as time to progressive PC and PC mortality.

  18. Androgen Receptor (AR) Related Dysfunction • (1) Reduce AR sensitivity • Prolactin Inhibitors • 5AR inhibitors • EGCG • HSP inhibitors • PPAR-G ligands • DIM & POMx • Silymarin • Melatonin • (2) Avoid Drugs Stimulating “Promiscuous” AR • Avoid or use cautiously standard glucocorticoids such as prednisone & dexamethasone • Use triamcinolone instead e.g. HDK with triamcinolone instead of Hydrocortisone (HC)

  19. Androgen Receptor (AR) Related Dysfunction • (3) Evaluate for ARM (androgen receptor mutation)– see http://www.prostate-cancer.org/education/andeprv/Strum_IADT.html • Withdraw anti-androgen, progestin, estrogen to see if PSA or other marker is reduced. • If possible ARM due to Casodex need 6 weeks to eliminate Casodex (bicalutamide) from body. • (4) Avoid agents that stimulate ARM • Steroidal anti-androgens such as CPA (cyproterone acetate) • Progestins, in certain contexts.

  20. Androgen Deprivation Therapy (ADT) immediately induces bone resorption Orchiectomy LHRH agonists (Lupron, Zoladex) LHRH antagonists (Plenaxis) Anti-androgens, Ketoconazole, Estrogens Androgen Receptor Antagonists Clarke NW, McClure J, & George NJR: The effects of orchidectomy on skeletal metabolism in metastatic prostate cancer. Scand J Urol Nephrol 27: 475-483, 1993.

  21. Lowering of Testosterone removes an osteoclast inhibitor. ADT (androgen deprivation therapy) lowers Testosterone. Increased osteoclast function leads to net bone loss due to excessive resorption. Testosterone Inhibits Osteoclast Formation Chen Q, Kaji H, Sugimoto T, et al: Testosterone inhibits osteoclast formation stimulated by parathyroid hormone through androgen receptor. FEBS Lett 491:91-3, 2001. Graphic per Strum, A Primer on PC

  22. All of Biology is a Two Edged Sword • Part of optimizing ADT is recognition of the above statement. • We need to start therapies to minimize the down-sides of any treatment we use, including ADT. • A key focus should be to prevent osteoclast activation with release of bone-derived growth factors. • Agents like bisphoshonates & Denosumab should be used early in the treatment of men with PC.

  23. Monoclonal antibody to Receptor Activator of Nuclear Kappa Ligand (RANKL) Stops Bone Resorption & Decreases Skeletal-Related Events Better then Aredia or Zometa.

  24. When we decrease the side-effects of any treatment, we improve the therapeutic index (TI) Treatment Benefits Treatment Side Effects = TI http://www.prostate-cancer.org/resource/pdf/Is2-1.pdf

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