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Emmanuel Gomez Jennifer Dao Phan Gaëlle Datchoua UEI2 Scientific communication Workshop February 11 & 12, 2010 
Safe Harbor ,[object Object],[object Object]
[object Object],Laboratory:  Dendreon Indication:  asymptomatic metastatic Androgen Independent Prostate Cancer  Agent:  autologous dendritic cells Launch on market:  expected for mid-2010
A short review of advanced prostate cancer ,[object Object],[object Object],[object Object]
Summary for Prostate Cancer epidemiology Jemal et al.  CA Cancer J Clin. 2009;225-249. Commun Oncol 2007;4:447–452  15% Metastatic disease Prostate cancer Initial diagnosis 85 % localized early disease 60-70% Localized disease 30-40% Relapse disease ~ 18-36 months
Diagnosis of advanced prostate cancer Gleason’s score PSA doubling time Residual testosteronemia > 50 ng/mL Digital Rectal Examination+Biopsy Blood test Research of  metastases
Histological grading of Prostate Cancer http://www.stjohn.org/InnerPage.aspx?PageID=1446 ,[object Object],[object Object],[object Object],1. Small, uniform  glands 2. More stroma between glands 3. Distincly infiltrate  margins 4. Irregular masses  of neoplastic glands 5. Only occasional  gland formation Gleason’s grade 2-4 Well differenciated 5-7 Intermediate 8-10 Poorly differentiated Gleason’s score
Prostatic Specific Antigen doubling time (PSA DT)  ,[object Object],[object Object],[object Object],[object Object],Adaptated from:J Clin Oncol 23;2005:4975–9
Gleason’s Score + PSA DT = predictive for PCa outcome Freedland SJ, Humphreys EB, Mangold LA, et al. Risk of prostate cancer-specific mortality following biochemical recurrence after radical prostatectomy.  JAMA . 2005;294:433-439.  Pound CR, Partin AW, Eisenberger MA, et al. Natural history of progression after PSA elevation following radical prostatectomy.  JAMA . 1999;281:1591-1597.
Asymptomatic metastatic PCa : no approved therapies in European guidelines A gap for brand new treatment strategies? Asymptomatic metastatic PCa: a medical unmet need Adaptated from : Nature Reviews Cancer  2 , 389-396 (May 2002)   Progrès en Urologie (2008), Suppl. 7, S343–S348   Commun Oncol 2007;4:447–452
Focus on Provenge® (APC-8015, Sipuleucel-T) ,[object Object],[object Object]
What is Provenge® and how does it work ? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Main protagonists ,[object Object],[object Object],[object Object],[object Object]
Provenge®, the lead A.C.I. candidate of Dendreon ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Animation available on Dendreon website
How do APCs and antigen-specific T cells find each other? ,[object Object],[object Object],[object Object],BLC SLC ELC T zone stromal cell (producing CCL21)
Antigen Presentation to T Cells (BARAS, LICHTMAN, Cellular and Molecular Immunology, Saunders ed., 5e ed., 2003) Secondary lymphoid organs Peripheral tissues Th1/Th2 pathway Macrophage/ B cell activation Cytotoxic effect against targeted cells
How to break the tolerance CD 4 – CD8 LFA - 3 ICAM – 1(=CD54) CD 40 B7 (CD80 and CD86) LFA - 1 CD 2 CD 40 L -S–S - CD 28 T-Cell Antigen Presenting Cells MHC peptide Complexe, I or II -S– S - TCR - CD 3 Peptide
Flow Chart ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Patient management  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
APCs and fusion protein ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Quality control of final product ,[object Object],[object Object],[object Object],[object Object],[object Object],- Swain, S. L., M. Croft, C. Dubey, L. Haynes, P. Rogers, X. Zhang, L. M. Bradley. 1996.  From naive to memory T cells .  Immunol. Rev.   150 : 143 - The Journal of Immunology , 2000, 164: 1705-1712.  Functional Maturation of Adult Mouse Resting Microglia into an APC Is Promoted by Granulocyte-Macrophage Colony-Stimulating Factor and Interaction with Th1 Cells  Francesca Aloisi et al
Clinical Trials and Publications
Clinical development program of Sipuleucel-T
Randomized Placebo Controlled Trial Overall Survival  D9901
APC Activation Correlates with Survival D9901 and D9902
The Innate Immune System also engaged ,[object Object],[object Object],[object Object],[object Object],[object Object]
T-cell Mediated Immune Response Week 0 to Week 8, Study D9901
Cytokine Signature of Activated T cells observed in Sipuleucel-T after first priming dose ,[object Object],[object Object],[object Object],pg/nL
Randomized Phase 3 IMPACT Trial (9902B) (Immunotherapy Prostate AdenoCarcinoma Treatment) Primary endpoint: Overall survival Secondary endpoint: Time to objective disease progression
Consistency Across Phase 3 Studies *Unadjusted Cox model & log rank  **Cox model adjusted for PSA and LDH
Keep an eye on … Group Sipuleucel-T n / N (%) Placebo n / N (%) Odds Ratio (95% CI) p-value  All Subjects All CVA’s 18 /461 (3.9%) 6/231 (2.6%) 1.52 (0.596, 3.892) 0.510 Deaths attributed to CVAs 7 / 461 (1.5%)  2 / 231 (0.9%) 1.76 (0.364, 8.566)  0.725  AIPC (Proposed Indication) All CVA’s 17 / 345 (4.9%) 3 / 172 (1.7%) 2.92 (0.84, 10) 0.092 Deaths attributed to CVAs 7 / 345 (2.0%) 2 / 172 (1.2%) 1.76 (0.36, 8.6) 0.724 ADPC (P-11) All CVA’s 1 / 116 (0.9%) 3 / 59 (5.1%) 0.16 (0.016, 1.596) 0.112 Deaths attributed to CVAs 0 0 --- ---
PROTECT (P11): PROVENGE Treatment and Early Cancer Treatment.  Ongoing Phase 3 trial with enrollment completed
Open Trials (Phase II) - AIPC  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Open Trials (Phase II & IIIB) – ADPC ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Challenges for Provenge® ,[object Object],[object Object]
Sipuleucel-T (Provenge ® )   production and delivery PROVENGE® (sipuleucel-T) Cellular, Tissue, and Gene Therapies  Advisory Committee Meeting March 29, 2007 The Mattson Jack Group, Cancer Metric Database 2009 COMPLETE COURSE OF THERAPY: 3 CYCLES 100 000 patients in USA with metastatic AIPC in 2010 100 000 X 3 = 300 000 doses to prepare and to deliver on time How will Dendreon make it? Day 1  Leukapheresis Apheresis Center Day 2-3 Manufacturing Dendreon’s facility Day 3-4 Infusion Doctor’s Office
Advance Planning System (APS) ,[object Object],[object Object],[object Object],[object Object]
Track patients sample through process using barcode ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Exemple of a workstation to manufacture Provenge
Transportation ,[object Object],[object Object],[object Object],[object Object]
Manufacturing sites location SDI, PCa Patient Population 2006
Product Follow-Up
Regulatory aspects
Patents ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Regulatory Strategy in US ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
FDA Decision on Provenge: Who’s who, who’s connected ? www.caretolive.com/research
Regulatory framework in Europe (1) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Regulatory framework in Europe (2) Pr JH Trouvin
Regulation 1394/2007: Consequences ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Pr JH Trouvin
Best option for Dendreon in Europe ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Dendreon ,[object Object],[object Object],[object Object]
Targeting cancer, transforming lives™
Dendreon Corporation ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Dendreon’s pipeline (1) Dendreon website Sipuleucel- T  (PROVENGE) Mature autologous DCs obtained via leukapheresis procedure Treatment of metastatic androgen- independent prostate cancer (AIPC).   Phase 3 Lapuleucel-T (NEUVENGE) Targets the  HER2/neu  Ag. Same process as sipuleucel-T. The treatment of breast, ovarian and colorectal solid tumors Phase 2 Preclinical Program: CA-9 and CEA ,[object Object],[object Object],[object Object],[object Object],Preclinic
Dendreon’s pipeline (2)
Sales and income 2009 THOMSON REUTERS When and How will they make Money ? Millions US$
Financial analysis (stock price)
Wholesale  price of Provenge® ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
US sales projection (2011-2019)
EU sales projection (2011-2019)
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
What’s next for Dendreon ? ,[object Object],[object Object]
Best option for Dendreon in Europe ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Any idea?… ,[object Object],[object Object],[object Object]
Thanks for your attention! Any question?
Type of « vaccine » in clinical study Trade name What’s that? Company Type of drug Phase Provenge Autologous (reimplanted) dendritic cells complexed with the Prostatic Acid Phosphatase (PAP) antigen and GM-CSF Dendreon Cell therapy Phase 3 DCVax Prostate Whole cells derived from two prostate cancer lines modified to secrete GM-CSF and irradiated to arrest growth. Northwest Biotherapeutics Cellular vaccine Phase 3 GVax . Patients dendritic cells boosted with Prostate Membrane Specific Antigen (PMSA) Cell Genesis  Cellular vaccine Phase 3 Trovax Designed to induce an immune response against the tumor-associated antigen 5T4 using a viral vector, Modified Vaccinia Ankara (MVA). The 5T4 tumor antigen is expressed at high levels in the majority of epithelial-derived cancers such as colorectal, renal, prostate, lung and breast.  Oxford Biomedical  Viral vector Phase 2 PROSTVAC Vaccinia-PSA-TRICOM and Fowl pox-PSA-TRICOM  Bavarian Nordic  Viral vector Phase 2

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Provenge (sipuleucel t)

  • 1. Emmanuel Gomez Jennifer Dao Phan Gaëlle Datchoua UEI2 Scientific communication Workshop February 11 & 12, 2010 
  • 2.
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  • 5. Summary for Prostate Cancer epidemiology Jemal et al. CA Cancer J Clin. 2009;225-249. Commun Oncol 2007;4:447–452 15% Metastatic disease Prostate cancer Initial diagnosis 85 % localized early disease 60-70% Localized disease 30-40% Relapse disease ~ 18-36 months
  • 6. Diagnosis of advanced prostate cancer Gleason’s score PSA doubling time Residual testosteronemia > 50 ng/mL Digital Rectal Examination+Biopsy Blood test Research of metastases
  • 7.
  • 8.
  • 9. Gleason’s Score + PSA DT = predictive for PCa outcome Freedland SJ, Humphreys EB, Mangold LA, et al. Risk of prostate cancer-specific mortality following biochemical recurrence after radical prostatectomy. JAMA . 2005;294:433-439. Pound CR, Partin AW, Eisenberger MA, et al. Natural history of progression after PSA elevation following radical prostatectomy. JAMA . 1999;281:1591-1597.
  • 10. Asymptomatic metastatic PCa : no approved therapies in European guidelines A gap for brand new treatment strategies? Asymptomatic metastatic PCa: a medical unmet need Adaptated from : Nature Reviews Cancer 2 , 389-396 (May 2002) Progrès en Urologie (2008), Suppl. 7, S343–S348 Commun Oncol 2007;4:447–452
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  • 17. Antigen Presentation to T Cells (BARAS, LICHTMAN, Cellular and Molecular Immunology, Saunders ed., 5e ed., 2003) Secondary lymphoid organs Peripheral tissues Th1/Th2 pathway Macrophage/ B cell activation Cytotoxic effect against targeted cells
  • 18. How to break the tolerance CD 4 – CD8 LFA - 3 ICAM – 1(=CD54) CD 40 B7 (CD80 and CD86) LFA - 1 CD 2 CD 40 L -S–S - CD 28 T-Cell Antigen Presenting Cells MHC peptide Complexe, I or II -S– S - TCR - CD 3 Peptide
  • 19.
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  • 21.
  • 22.
  • 23. Clinical Trials and Publications
  • 24. Clinical development program of Sipuleucel-T
  • 25. Randomized Placebo Controlled Trial Overall Survival D9901
  • 26. APC Activation Correlates with Survival D9901 and D9902
  • 27.
  • 28. T-cell Mediated Immune Response Week 0 to Week 8, Study D9901
  • 29.
  • 30. Randomized Phase 3 IMPACT Trial (9902B) (Immunotherapy Prostate AdenoCarcinoma Treatment) Primary endpoint: Overall survival Secondary endpoint: Time to objective disease progression
  • 31. Consistency Across Phase 3 Studies *Unadjusted Cox model & log rank **Cox model adjusted for PSA and LDH
  • 32. Keep an eye on … Group Sipuleucel-T n / N (%) Placebo n / N (%) Odds Ratio (95% CI) p-value All Subjects All CVA’s 18 /461 (3.9%) 6/231 (2.6%) 1.52 (0.596, 3.892) 0.510 Deaths attributed to CVAs 7 / 461 (1.5%) 2 / 231 (0.9%) 1.76 (0.364, 8.566) 0.725 AIPC (Proposed Indication) All CVA’s 17 / 345 (4.9%) 3 / 172 (1.7%) 2.92 (0.84, 10) 0.092 Deaths attributed to CVAs 7 / 345 (2.0%) 2 / 172 (1.2%) 1.76 (0.36, 8.6) 0.724 ADPC (P-11) All CVA’s 1 / 116 (0.9%) 3 / 59 (5.1%) 0.16 (0.016, 1.596) 0.112 Deaths attributed to CVAs 0 0 --- ---
  • 33. PROTECT (P11): PROVENGE Treatment and Early Cancer Treatment. Ongoing Phase 3 trial with enrollment completed
  • 34.
  • 35.
  • 36.
  • 37.
  • 38. Sipuleucel-T (Provenge ® ) production and delivery PROVENGE® (sipuleucel-T) Cellular, Tissue, and Gene Therapies Advisory Committee Meeting March 29, 2007 The Mattson Jack Group, Cancer Metric Database 2009 COMPLETE COURSE OF THERAPY: 3 CYCLES 100 000 patients in USA with metastatic AIPC in 2010 100 000 X 3 = 300 000 doses to prepare and to deliver on time How will Dendreon make it? Day 1 Leukapheresis Apheresis Center Day 2-3 Manufacturing Dendreon’s facility Day 3-4 Infusion Doctor’s Office
  • 39.
  • 40.
  • 41. Exemple of a workstation to manufacture Provenge
  • 42.
  • 43. Manufacturing sites location SDI, PCa Patient Population 2006
  • 46.
  • 47.
  • 48. FDA Decision on Provenge: Who’s who, who’s connected ? www.caretolive.com/research
  • 49.
  • 50. Regulatory framework in Europe (2) Pr JH Trouvin
  • 51.
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  • 58.
  • 59. Sales and income 2009 THOMSON REUTERS When and How will they make Money ? Millions US$
  • 61.
  • 62. US sales projection (2011-2019)
  • 63. EU sales projection (2011-2019)
  • 64.
  • 65.
  • 66.
  • 67.
  • 68.
  • 69. Thanks for your attention! Any question?
  • 70. Type of « vaccine » in clinical study Trade name What’s that? Company Type of drug Phase Provenge Autologous (reimplanted) dendritic cells complexed with the Prostatic Acid Phosphatase (PAP) antigen and GM-CSF Dendreon Cell therapy Phase 3 DCVax Prostate Whole cells derived from two prostate cancer lines modified to secrete GM-CSF and irradiated to arrest growth. Northwest Biotherapeutics Cellular vaccine Phase 3 GVax . Patients dendritic cells boosted with Prostate Membrane Specific Antigen (PMSA) Cell Genesis Cellular vaccine Phase 3 Trovax Designed to induce an immune response against the tumor-associated antigen 5T4 using a viral vector, Modified Vaccinia Ankara (MVA). The 5T4 tumor antigen is expressed at high levels in the majority of epithelial-derived cancers such as colorectal, renal, prostate, lung and breast. Oxford Biomedical Viral vector Phase 2 PROSTVAC Vaccinia-PSA-TRICOM and Fowl pox-PSA-TRICOM Bavarian Nordic Viral vector Phase 2

Editor's Notes

  1. Once metastatic androgen-independent prostate cancer (AIPC) develops, responses to alternative hormonal therapy or chemotherapy are not durable, with a median overall survival of approximately 18 months with docetaxel based chemotherapy.
  2. IL4 ?
  3. Les CD sont les seules cellules présentatrices capables d'activer les lymphocytes T naïfs lors d'une immunisation primaire, et les meilleures pour activer les lymphocytes T mémoire.
  4. very little is known about the EXIT process
  5. Cross presentation
  6. Molecules de costim pour fonction
  7. PBMC + Ag: restimulation in vitro: culture 48h centri recup surnageant ELISA
  8. Sans oublier les multiplications exvivo de virus ou la survenue de maladies autoimmune.
  9. Sipuleucel-T is manufactured APCs are seperated from other white blood cells using proprietary technology. APCs are combined with Dendreon’s Antigen Delivery Cassette for approximatively 40 hours
  10. In March,an FDA advisory committee voted 13-4 that Provenge was effective and 17-0 that Provenge was safe. It was later discovered that two of the Doctors on the panel that voted against the effectiveness of the treatment - and who also subsequently lobbied heavily for the FDA to deny Provenge approval - were found to have previously undisclosed financial interests in companies in direct competition to Dendreon