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Customized Cancer Medicine • All Treatments are Customized at the point of delivery • All Treatments Are Designed to Take advantage of Differences between Cancer Cells and Normal Cells • Some of these differences are Generic and some are more Specific to the Type of Cancer, the Subtype, or even to the Individual Person Customized Cancer Medicine • Generic Treatments – Cancer Starts from One Cell in One Place • Surgery- Early Detection – Cancer Cells Divide Faster • Chemotherapy and Radiotherapy • Cancer Type Specific Treatments – Hormone Responsive • Prostate/Breast – Tissue Type • Thyroid – Receptors • Monoclonal Antibodies Customized Cancer Medicine • Personalized Treatments – Not All People Are The Same • Match The Treatment For the Person’s Inherited Genes – Pharmacogenomics – Not All Tumors Are The Same • Match The Treatment For the Tumor That Person Has – Tumor Phenotyping – Gene Expression Profiling – The Relationship between the Immune System of the Person and Their Tumor Is Variable • Re Educate the Immune System – Monoclonal Antibodies – Transplanted Immune Cells – Tumor Vaccines Two Arms of the Immune System B cells T cells antibody foreign substance (antigen) Abnormal cell B cell T cell Function: Make Antibodies Kill abnormal cells Lymphoma Tumors Have A Special Target transformation Normal B cells B lymphoma cells Monoclonal Antibody Therapy Custom Made Anti-idiotype antibody Tumor Idiotype Lymphoma B cell New England Journal of Medicine, 306:517. 1982 Treatment of B Cell Lymphoma with Monoclonal Anti Idiotype Antibody Richard A Miller, David G. Maloney, Roger Warnke, and Ronald Levy 7 Monoclonal Antibody Therapy Once Size Fits All Anti-idiotype antibody Tumor Idiotype Rituximab CD20 Lymphoma B cell Aren’t antibodies wholesome, natural and without side effects FDA Approved Monoclonal Antibodies YEAR Product Target Indication 1986 Orthoclone CD3 Transplant Rejection 1994 ReoPro GPIIa/IIIb Angioplasty 1997 Rituxan CD20 B Cell Lymphoma 1998 Zenapax IL2R Transplant Rejection 1998 Simulect IL2R Transplant Rejection 1998 Remicade TNF Crohn’s, RA 1998 Herceptin Her2 Breast Cancer 2000 Mylotarg CD33 AML 2001 Campath CD52 CLL 2002 Zevalin CD20 B Cell Lymphoma 2003 Bexxar CD20 B Cell Lymphoma 2003 Raptiva CD11a Psoriasis 2004 Avastin VEGF Colon Cancer 2004 Erbitux EGFR Colon Cancer Rituximab Anti-tumor Effect: Proposed Mechanisms 1) Apoptosis, Anti-proliferation 2) Complement-mediated Killing Tumor Cell T Cells CD20 or other tumor Ags FcR Natural Killler Cells Monocytes 3) Antibody-dependent Cellular Cytotoxicity (ADCC) FcR Dendritic Cells 4) Antigen Presentation and Cross-priming Response to Antibodies Depends On Your Genes Rituximab Clinical Response Determined by Genetics FcgR IIIA 158 V/F polymorphism p=0.037 15 V/V V/F F/F 8/10 (80%) 12/28 (43%) 9/23 (39%) F Carriers 21/51 (41%) Monoclonal Antibody Conclusions • Antibodies are Effective Drugs • Improved versions will be Found • New Targets will be Found • New Disease Indications Will be Found • ? Mechanisms of Action and Resistance • ? Prediction of Efficacy 16 A Therapeutic Vaccine for Lymphoma “Rescue hybridization” Myeloma cell + Tumor Biopsy Vaccine Production 3 2 1 Immunization KLH carrier protein Id Adjuvant (SAF) Tumor Id Protein Genitope Phase III Trial Treatment Schedule Enrollment Randomize 2/1 CVP Recovery 26 weeks Monthly Vaccines x7 Immunization: 28 weeks Follow for Time to Progression Idiotype Vaccine Can A Custom Vaccine Be Practical? Idiotype Vaccine Production Via Recombinant DNA Recombinant Id proteins Mammalian or insect cells Bacteria Genetic Id Vaccines Plants Naked DNA Cell Free Whole Immunoglobulin Immunoglobulin Fragments Recombinant Viruses 1. Lymphoma Biopsy Vaccine Just in Time 2. Amplify Ig V genes Insert into Vector (~ 3 Days) 4. Vaccinate 3. Express Cell-Free /Purify (~ 2 days) Customized Cancer Medicine • Personalized Treatments Are Problematic – Drug Industry • Mass produced products for mass markets • High margins between cost of goods and sales price • Intellectual Property favors composition over use – Health Care Delivery Organizations • Standard Operating Procedures • Risk/Reward better for acute interventions • HMO model shifts financial risk to the provider – Regulatory Bodies • Accustomed to manufacturing issues and large scale trials – Privacy Concerns • Work against genetic testing • Work against use of medical records to develop predictive tests Future Doctor “Take some immunotherapy and call me in the morning” Using The Immune System To Treat Cancer: 2005 • Antibodies, Antibodies and more Antibodies • Therapeutic Vaccination – Dendritic Cells • Adoptive Cellular Therapy – Allogeneic Bone Marrow Transplantation – Autologous T Cells • Inhibition of Suppressor T Cells Dendritic Cells • Most potent “antigen-presenting cells” • Reside in tissues to collect antigen -> travel to lymph nodes • Co-culture with antigens -> cellular vaccine Myeloma cell + 1 Fusion Tumor Biopsy Vaccine Production Leukapheresis 2 + Immunization 4 Dendritic Cells Antigen-Pulsed Dendritic Cells Tumor Id Protein Co-culture 3 Idiotype-pulsed dendritic cell vaccination Pre-vaccine 11 months post-vaccine In situ Vaccination with DC Chemotherapy 2 Leukapheresis 1 3 Intratumor Injection Dendritic Cells Freedom From Progression Follicular Lymphoma first remission PROBABILITY (%) 100 80 60 Responders (n=14) 40 p<0.0001 non-Responders (n=18) 20 0 0 2 4 6 TIME (YEARS) 8 10 Rituximab Publications 180 160 Publications 140 Genentech (DNA) stock price 120 IDEC (IDPH) stock price 240 220 200 180 160 140 120 100 80 60 40 20 0 Stock price ($) Number of publications 200 100 80 60 40 20 0 Jan/91 92 Year 30 93 94 95 1st clinical trial 96 97 98 99 00 Pivotal FDA approval trial results Norman Klinman 1970 Monoclonal Antibody Imaging 111In-Labeled Zevalin™ 4 hours 3 days 6 days Abdominal SPECT 106-00-158RS Abdominal CT Hybridoma Technology Making Antibodies Immortal Antigen Cells Fuse into a Hybridoma Antibody-producing Plasma Cell 34 Monoclonial Antibodies Cancerous Plasma Cell