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Prostate Cancer: Update Bulletin #2 [April 2018]

March 2018 | | ID: P72607A11A4EN
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Gain new key opinion leader (KOL) insights on the latest events happening in the prostate cancer space. Topics covered include expert opinions on the FDA approval of Johnson & Johnson’s (J&J’s) next-generation androgen receptor inhibitor Erleada (apalutamide) in patients with non-metastatic castration-resistant prostate cancer (CRPC), data published from the PROSPER study for Pfizer/Astellas’ Xtandi (enzalutamide) in the non-metastatic CRPC population and the expanded approval for J&J’s Zytiga (abiraterone acetate) by the FDA in patients with high-risk metastatic hormone-sensitive prostate cancer (mHSPC). Finally, the experts also provide candid insights into their expectations for Pfizer’s PARP inhibitor talazoparib which has entered Phase III development (TALAPRO-2 study) in combination with physician's choice of either Xtandi or Zytiga in patients with metastatic CRPC.

Business Questions
  • What are the experts’ opinions on the FDA approval of J&J’s Erleada in patients with non-metastatic CRPC based on the novel endpoint of metastasis-free survival (MFS)?
  • How do KOLs contrast and compare the efficacy of Erleada and Pfizer/Astellas’ Xtandi in the non-metastatic CRPC setting?
  • In terms of safety, how do KOLs view the data reported for Erleada in the SPARTAN study?
  • Do the KOLs anticipate Erleada and Xtandi to compete head-to-head for market share in the non-metastatic CRPC setting? If so, what will influence their prescribing choices?
  • How do the experts view the expanded approval for J&J’s Zytiga in patients with mHSPC? Will the drug gain significant uptake in this setting going forward?
  • Will Xtandi be able to compete with Zytiga in the mHSPC setting? What data do KOLs expect from the recently completed ENZAMET/ARCHES studies investigating Xtandi?
  • What are KOL expectations for Pfizer’s PARP inhibitor talazoparib in prostate cancer and how can it differentiate itself from the other two PARP inhibitors in Phase III development [AstraZeneca’s Lynparza (olaparib) and Clovis Oncology’s Rubraca (rucaparib)]?
  • In terms of mechanism of action, efficacy and safety, how do the three PARP inhibitors compare so far?
  • Do KOLs think Pfizer’s combination of talazoparib with anti-androgen drugs in the TALAPRO-2 study is a promising strategy?
  • If approved in prostate cancer, how and when will the PARP inhibitors be used?


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