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Cancer Immunotherapy: Fundamental Concepts and Emerging Role Urology Perspective

Cancer Immunotherapy: Fundamental Concepts and Emerging Role Urology Perspective. Learning Objectives. Review the evidence supporting the immune system’s role in cancer Review the characteristics of an immune response Describe mechanisms of immunotherapy

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Cancer Immunotherapy: Fundamental Concepts and Emerging Role Urology Perspective

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  1. Cancer Immunotherapy:Fundamental Concepts and Emerging Role Urology Perspective

  2. Learning Objectives • Review the evidence supporting the immune system’s role in cancer • Review the characteristics of an immune response • Describe mechanisms of immunotherapy • Discuss treatment considerations of cancer immunotherapy

  3. Program Agenda

  4. Everyday Functions of the Immune System • Principal function—prevent/eradicate infections • Continuouslysurveilsfor foreign antigens • Initial defenses are nonspecific, while specialized defenses mount a targeted response Courtesy of Science Source Courtesy of Science Source Courtesy of Science Source Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011.

  5. Immune Response: Key Components • Antigen • Substance that generates an immune response (eg, proteins of pathogens or tumors) • Antigen presenting cells (APCs) • Identify and uptake foreign antigens • Present them to T cells • T cells • Recognize and destroy cells containing foreign antigen • B cells • Produce antibodies specific to foreign antigens • Antibody • Protein that can identify and neutralize foreign antigens • Cytokines • Proteins that are naturally secreted by immune system cells Abbas AK,Lichtman AH. Basic Immunology. 3rd ed. 2011.

  6. Initiation of Immune Response: Key Components Effector cells: • Activate other immune cells • Kill “target cells” Antigenfragments Antigen NaiveT-cell Antigen receptors ActivatedT-cell Memory cells: • Circulate for months  years • Ready to rapidly respond to same antigen again Antigen presenting cell (APC) Antigenrecognition Activated APC T-cellinteraction T-cell activation T-cells become specialized Replication of antigen-specific T-cells Activation • Lymphoid Organs Adapted from Abbas AK, Lichtman AH. • Peripheral Tissues Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011.

  7. Program Agenda

  8. Hallmarks of Cancer Pathogenesis • Evading growth suppressors • Activating invasion and metastasis • Avoidingimmune • destruction Hallmarks of Cancer Pathogenesis (2011)1,2 • Enabling replicative immortality • Deregulatingcellularenergetics • Sustaining proliferative signaling • Inducingangiogenesis • Resisting cell death 1. Hanahan D, Weinberg RA. Cell. 2011;144:646-674. 2. Hanahan D, Weinberg RA. Cell. 2000;100:57-70.

  9. Increased Incidence of Cancer in Immunocompromised Individuals • Malignant tumors develop in individuals with compromised immune systems1-3 Tumor/cancer risk in transplant patients compared to general population1-3 Non-melanoma skin cancer 20-fold and beyond Non-Hodgkin’s lymphoma Kidney cancer 15-fold Melanoma 8-fold Hepatobiliary cancer 5-fold Bladder cancer 3-fold Testicular cancer Breast cancer 2-fold Prostate cancer Colon cancer 0 5 10 15 20 Fold-increase in tumor/cancer risk Kasiske BL, Wang C, et al. Am J Transplant. 2004;4(6):905-913. Le Mire L, Wojnarowska F, et al. Br J Dermatol. 2006;154(3):472-477. Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011.

  10. Immune Cells Within Tumors Predict Overall Survival • T-cell infiltration within tumors predicts overall survival (OS) in multiple cancer types including bladder cancer1-3 Infiltration of T cells Predicts Survival of Patients With Muscle-Invasive Bladder Cancer1 T cells (CD8) <8 (median=13 months) 1.0 T cells (CD8) ≥8 (median >80 months) 0.8 0.6 Prop. Surviving Without Disease 0.4 0.2 P<0.001 0.0 0 20 40 60 80 Time in Months Reprinted from Sharma P, Sato E, et al.1 Sharma P, Sato E, et al. Proc NatlAcadSci U S A. 2007;104(10): 3967-3972. Zhang L, Coukos G, et al. N Engl J Med. 2003;348(3):203-213. Galon J, Pagès F, et al. Science. 2006;313(5795):1960-1964.

  11. Immunotherapy Proven Effective in Cancer • Therapies that engage the immune system have been shown to improve patient survival in randomized, phase 3 cancer trials1-3 • Immunotherapies approved by the FDA to treat certain cancers4 • Cytokines • Monoclonal antibodies • Checkpoint inhibitors • Therapeutic vaccines Robert C, Wolchok JD, et al. N Engl J Med. 2011;364(26):2517-2526. Hodi FS, Urba WJ, et al. N Engl J Med. 2010;363(8):711-723. Kantoff PW, Schellhammer PF, et al. N Engl J Med. 2010;363(5):411-422. Mellman I, Dranoff G, et al. Nature. 2011;480 (7378):480-489.

  12. Dynamics Between Cancer and the Immune System • Immune system and cancer interact in a dynamic process, known as the 3 E’s • Elimination (immune system eradicates cancer cells) • Equilibrium (immune system controls cancer outgrowth) • Escape (cancer overwhelms the immune system) Immune Protection Immune Evasion Dunn GP, Schreiber RD, et al. Nat Rev Immunol. 2006;6(11):836-848.

  13. Elimination: Immune System Eradicates Cancer Cells1 Immune Evasion Immune Protection • A natural process involved with early disease2 Immune cells Abnormal cells/tissue Normal cells/tissue Adapted from Dunn GP, Schreiber RD, et al. Dunn GP, Schreiber RD, et al. Nat Rev Immunol. 2006;6(11):836-848. Trinchieri G. In: Cancer: Principles & Practice of Oncology. 9th ed. 2011. 13

  14. Equilibrium: Immune System Controls Cancer Cells1 Immune Protection Immune Evasion • Occurs with later stage tumors2 • Represents a balanced “dynamic” between the immune system and cancer1,2 Immune cells Abnormal cells / tissueoutgrowth controlled Adapted from Dunn GP, Schreiber RD, et al.1 Dunn GP, Schreiber RD, et al. Nat Rev Immunol. 2006;6(11):836-848. Trinchieri G. In: Cancer: Principles & Practice of Oncology. 9th ed. 2011. 14

  15. Escape: Cancer Cells Evade Immune System Immune Protection Immune Evasion • Tumor cell variants grow, resulting in progressive disease Immune cells Abnormal cells / tissue Abnormal cells / tissuecontinue to replicate Adapted from Dunn GP, Schreiber RD, et al. 15 Dunn GP, Schreiber RD, et al. Nat Rev Immunol. 2006;6(11):836-848.

  16. Features of an Effective Immune Response1,2 • Specificity • Trafficking • Adaptability • Target elimination • Durability (immune memory) Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011. Drake CG. Nat Rev Immunol. 2010;10(8);580-593.

  17. Specificity Flu Virus Year 1 • Ability to recognize and mount a specific response to distinct antigens1 • Example2 • Seasonal flu mutates surface antigens • Annual vaccination allows the immune system to effectively recognize and target the specific flu strain Flu virus surface antigens Antibodies targeted to Year 1 antigens Flu Virus Year 2 Flu virus surface antigens Antibodies targeted to Year 2 antigens AbbasAK, Lichtman AH. Basic Immunology. 3rd ed. 2011. Grebe KM, Bennink JR, et al. Microbes Infect. 2008;10(9):1024-1029.

  18. Trafficking • Ability of activated immune system cells to migrate to particular antigens throughout the body1,2 • Example • Following exposure to activated APCs, naive T cells become activated1 • Activated T cells are mobilized to areas containing antigen1,2 Reinhardt RL, Jenkins MK, et al. Nature. 2001;410(6824):101-105. Drake CG. Nat Rev Immunol. 2010;10(8):580-593. Courtesy of Science Source

  19. Adaptability • Allows for a broader immune response1 (eg, immune response to additional antigens) 2 PSMA PSCA Tumor PAP ActivatedAPC Antigen 2 Tumor Antigen 1 APC MUC-1 Naive T cell T cell Activated T-cell target and kill tumor cell APC takes up additional released antigens Activated APC presents antigen to naive T cell Adapted from Gulley JL. Hum Vaccin Immunother. 2013;9(1):1-3. PSMA, prostate-specific membrane antigen; PSCA, prostate stem cell antigen; PAP, prostatic acid phosphatase; MUC-1, mucin-1. Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011. Nesslinger NJ, Gulley JL, et al. Clin Cancer Res. 2010;16(15):4046-4056.

  20. Immune Response: Target Elimination • Ability of immune cells to destroy their target (eg, cancer cells)1,2 • Usually via induction of apoptosis3 Target cell death3: Scanning Electron Micrograph showing T cells inducing a target cell to undergo apoptosis T cell T Cell Apoptotic Bodies Target Cell (eg, cancer cell) Courtesy of sciencesource.com Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011. Boissonnas A, Amigorena S, et al. J Exp Med. 2007;204(2):345-356. Trapani JA, Smyth MJ. Nat Rev Immunol. 2002;2(10):735-747.

  21. Durability (Immune Memory) • Ability of immune system to recognize an antigen to which it has previously been exposed and provide long-lasting protection against it1 Shown is the durable virus-specific T-cell response after smallpox vaccination2 Percentage 1. Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011. 2. Hammarlund E, Slifka MK, et al. Nat Med. 2003;9(9):1131-1137.

  22. Program Agenda

  23. Immunotherapy • Treatment to boost or restore the ability of the immune system to fight cancer, infections, and other diseases • Cytokines • Monoclonal antibodies • Checkpoint inhibitors • Therapeutic vaccines National Cancer Institute. Cancer terms. http://www.cancer.gov/dictionary/?print=1&cdrid=45729. Accessed October 5, 2012. Mellman I, Dranoff G, et al. Nature. 2011;480(7378):480-489.

  24. The Renaissance of Immunotherapy1-5 Enthusiasm Phase Skepticism Phase Renaissance Phase 1978-1985 1985-1997 1997- 20101st cellular immunotherapy approved for CA 1992IL-2 (cytokine) approved for CA 1986IFN-α (cytokine) approved for CA 19851st study with adoptive T-cell transfer in CA 19761st study with BCG in bladder CA 1890s 1st CA vaccine developed (Coley) 1990s Discovery of role of checkpoint inhibitors in CA 1978 Discovery of tumor specific mABs 20111st checkpoint inhibitor approved for CA 1997 1st mAB approved for CA 1973 Discovery of the dendritic cell (Steinman) Adapted with permission from Lesterhuis WJ, Punt CJ, et al2 and Kirkwood JM, Gogas HJ, et al. J ClinOncol. 2008;26(20):3445-3455. BCG, Bacille Calmette-Guerin; mABs, monoclonal antibodies; CA, cancer; IFN-α, interferon alpha; IL-2, interleukin-2 Kirkwood JM, Ferrone S, et al. CA Cancer J Clin. 2012;62(5):309-335. Lesterhuis WJ, Punt CJ, et al. Nat Rev Drug Discov. 2011;10(8):591-600. Krummel MF, Allison JP. J Exp Med. 1995;182(2):459-465. Lotze M. In: Cancer: Principles & Practice of Oncology. 9th ed. 2011 Leget GA, Czuczman MS. CurrOpinOncol. 1998;10(6):548-551.

  25. Cytokines • Proteins that are naturally secreted by immune system cells1 • Mechanism of action2 • Interleukin-2 (IL-2) stimulates T-cell proliferation • Examples2 • Interleukins, interferons • Efficacy3 • IL-2 demonstrated activity in a number of cancer types (eg, colon, breast, renal cell carcinoma [RCC]) • ~7% of RCC patients show a complete response; this response may also be durable IL-2 Stimulation of T-cell Proliferation2 IL2 Receptor Cell Proliferation • Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011. • Bachmann MF, Oxenius A. EMBO Rep. 2007;8(12):1142-1148. • Lotze M. In: Cancer: Principles & Practice of Oncology. 9th ed. 2011.

  26. Monoclonal Antibodies (mABs) • Proteins designed to bind to specific substances in the body1 • Mechanism of action2,3 • Differs between agents • Bind to their specific target antigen ultimately causing cell death • Efficacy • Demonstrated improvement in survival in different cancers4,5 • Demonstrated prevention of skeletal-related events5 Potential mechanisms of mABs in cancer T cell Cytokine-mAb Tumor cell Toxin-mAb Drug-mAb Receptor Tumor cell death Adapted from Kirkwood JM, Ferrone S, et al. CA Cancer J Clin. 2012;62(5):309-335. • NCI. www.cancer.gov/dictionary. Accessed January 11, 2013. • Cheson BD, Leonard JP. N Engl J Med. 2008;359(6):613-626. • Weiner LM, Wang S. Nat Rev Immunol. 2010;10(5):317-327. • Slamon DJ, Norton L, et al. N Engl J Med. 2001;344(11):783-792. • Smith MR, Goessl C, et al. Lancet. 2012;379(9810):39-46.

  27. Checkpoint Inhibitors • Inhibit tumor-induced suppression of T-cell activation or function1,2 • Mechanism of action1,2 • Antibodies target immune checkpoints to enhance antitumor response • Examples1,2 • CTLA-4 and PD1 • Efficacy3-6 • Extends OS in certain metastatic diseases • A significant effect on PFS not consistently observed Activated APC CTLA4 receptor Naive T cell CTLA4 antibodies Adapted with permission from Sharma P, Allison JP, et al.2 • CTLA4 and PD1 blunt immune response to tumor • Checkpoint inhibitors direct antibodies against them to enhance antitumor response PD1 receptor PD1 antibodies • CTLA-4, cytotoxic T lymphocyte-associated antigen 4; PD1, programmed death 1 • Pardoll D. Nat Rev Cancer. 2012;12(4):252-264. • Sharma P, Allison JP, et al. Nat Rev Cancer. 2011;11(11):805-812. • Hodi FS, Urba WJ, et al. N Engl J Med. 2010;363(8):711-723. • Robert C, Wolchok JD, et al. N Engl J Med. 2011;364(26):2517-2526. • Brahmer JR, Wigginton JM, et al. N Engl J Med. 2012;366(26):2455-2465. • Topalian SL, Sznol M, et al. N Engl J Med. 2012;366(26):2443-2454.

  28. Therapeutic Cancer Vaccines • Mechanism of action1 • Activation of T cells to seek out and destroy target cancer cells • Efficacy2,3 • Significantly extended OS in certain metastatic diseases without an effect on PFS Naive T cell Activated APC Activated T cell Normal cells/tissue Abnormal cells/tissue • Drake CG. Nat Rev Immunol. 2010;10(8):580-593. • Kantoff PW, Schellhammer PF, et al. N Engl J Med. 2010;363(5):411-422. • Kantoff PW, Godfrey WR, et al. J Clin Oncol. 2010;28(7):1099-1105.

  29. Goal of Therapeutic Cancer Vaccines “Cancer treatment vaccines are designed to treat cancers that have already developed. They are intended to delay or stop cancer cell growth; to cause tumor shrinkage; to prevent cancer from coming back; or to eliminate cancer cells that have not been killed by other forms of treatment." - NCI (2011) National Cancer Institute. Cancer vaccines. http://www.cancer.gov/cancertopics/factsheet/Therapy/. Accessed December 15, 2012.

  30. Characteristics of Immunotherapy Rescigno M, Curigliano G, et al. BiochimBiophysActa. 2007;1776(1):108-123.

  31. Characteristics of Therapeutic Vaccines1,2 • Gulley JL. Hum Vaccin Immunother. 2013;9(1):1-3. • Slovin S. Clin Adv HematolOncol. 2012;10(2):90-100.

  32. Program Agenda

  33. Immunotherapy: Treatment Considerations • Relative efficacy of immunotherapy may be greater with lower tumor burden1,2 • Patient given immunotherapy earlier in disease course might have a better outcome3 Tumor Growth Rate † † † Expected clinical outcome if no treatment is provided B † Death A A Patient given a vaccine earlier Tumor Burden B Patient given a vaccine later Time Adapted with permission from Gulley JL, Drake CG.3 • Kirkwood JM, Ferrone S, et al. CA Cancer J Clin. 2012;62(5):309-335. • Drake CG. Nat Rev Immunol. 2010;10(8):580-593. • Gulley JL, Drake CG. Clin Cancer Res. 2011;17(12):3884-3891.

  34. Potential Role In Combination Therapy • Standard practice in oncology is the use of combination agents with different mechanisms of action1-3 • Chemotherapy and mABs • Radiation and chemotherapy • Multiple chemotherapy regimens • Immunotherapy offers potential for synergy with other therapies1-6 Drake CG, Adler AJ, et al. Cancer Cell. 2005;7(3):239-249. Mercader M, Kwon ED, et al. Proc NatlAcadSci USA. 2001;98(25):14565-14570. Aragon-Ching JB, Gulley JL, et al. Front Biosci. 2007;12:4957-4971. Vermorken JB, Hitt R, et al. N Engl J Med. 2008;359(11):1116-1127. Slamon DJ, Norton L, et al. N Engl J Med. 2001;344(11):783-792. Gulley JL, Drake CG. Clin Cancer Res. 2011;17(12):3884-3891.

  35. Immunotherapy: An Established Treatment Strategy • More than a dozen different immunotherapy agents have been approveda, with the majority over the last decade1-5 • Immunotherapy agents currently approved target >10 different cancer types1-5 aNot inclusive of all immunotherapy classes. Mellman I, Dranoff G, et al. Nature. 2011;480(7378):480-489. Kirkwood JM, Ferrone S, et al. CA Cancer J Clin. 2012;62(5):309-335. Lotze M. In: Cancer: Principles & Practice of Oncology. 9th ed. 2011. Sondak VK, Hauschild A, et al. In: Cancer: Principles & Practice of Oncology. 9th ed. 2011. Robinson MK, Weiner LM, et al. In: Cancer: Principles & Practice of Oncology. 9th ed. 2011. 35

  36. Immunotherapy: Future Promise • Rapid increase in immunotherapy clinical research • Doubling of abstracts at major conferences from 2009 to 20121 • Approximately 800 clinical trials in various phases ongoing2 • eg, breast, colon, head and neck, kidney • Trials utilize agents alone and in combination with conventional therapies2 Courtesy of sciencephoto.com • SeekingAlpha.com. http://seekingalpha.com/article/667581-immunotherapy-comes-of-age-at-asco-2012. Accessed January 4, 2013. • ClinicalTrials.gov. http://clinicaltrials.gov/. Accessed January 4, 2013.

  37. Summary • The immune system plays a critical role in controlling cancer1 • Key features of an effective immune response include2 • Specificity • Adaptability • Durability (immune memory) • Future clinical considerations • May elicit better immune system response if used earlier in disease3,4 • Potential for durable clinical effects and synergy with subsequent therapies5-8 • Vermorken JB, Hitt R, et al. N Engl J Med. 2008;359(11):1116-1127. • Slamon DJ, Norton L, et al. N Engl J Med. 2001;344(11):783-792. • Robert C, Wolchok JD, et al. N Engl J Med. 2011;364(26):2517-2526. • Mercader M, Kwon ED, et al. Proc NatlAcadSci USA. 2001;96(25):14565-14570. • Dunn GP, Schreiber RD, et al. Nat Rev Immunol. 2006;6(11):836-848. • Abbas AK, Lichtman AH. Basic Immunology. 3rd ed. 2011. • Kirkwood JM, Ferrone S, et al. CA Cancer J Clin. 2012;62(5):309-335. • Drake CG. Nat Rev Immunol. 2010;10(8):580-593.

  38. Questions? MA-01.13.06.02

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