Disclosures. Disclosures. Grand Unification: The rationale for combining immunotherapy and molecular targeted therapy 25/02/2014



Similar documents
Ovarian Cancer and Modern Immunotherapy: Regulatory Strategies for Drug Development

Melanoma and Immunotherapy

What is the Optimal Front-Line Treatment for mrcc? Michael B. Atkins, MD Deputy Director, Georgetown-Lombardi Comprehensive Cancer Center

Trials in Elderly Melanoma Patients (with a focus on immunotherapy)

Anti-PD1 Agents: Immunotherapy agents in the treatment of metastatic melanoma. Claire Vines, 2016 Pharm.D. Candidate

Immunotherapy for High-Risk and Metastatic Melanoma

Cancer Treatments Subcommittee of PTAC Meeting held 18 September (minutes for web publishing)

Predictive Biomarkers for PD1 Pathway Inhibitor Immunotherapy

Combining Immunotherapy and Targeted Therapy in Melanoma

Oncologist-to-Oncologist: How to Treat Your Patients with Immunotherapy

Combination Immunotherapies: Melanoma

NEW CLINICAL RESEARCH OPTIONS IN PANCREATIC CANCER IMMUNOTHERAPY. Alan Melcher Professor of Clinical Oncology and Biotherapy Leeds

Coordinating Immune Checkpoint Blockade For Cancer Immunotherapy In Combination

TKCC/Garvan Cancer Biology Seminars Melanoma & Cancer Immunotherapy

Foundational Issues Related to Immunotherapy and Melanoma

Immunotherapy or Molecularly Targeted Therapy: What Is the Best Initial Treatment for Stage IV BRAF-Mutant Melanoma?

Comparing Immunotherapy with High Dose IL-2 and Ipilimumab

Immune Therapy for Pancreatic Cancer

ASCO 12. PD-1 Immunotherapy Makes a Splash at ASCO

Metastatic Melanoma What You Need to Know

Media Contacts: Annick Robinson Investor Contacts: Teri Loxam (438) (908)

Cancer Immunotherapy: immune checkpoint inhibitors, cancer vaccines, and adoptive T-cell therapies - Overview

Understanding series. new. directions LungCancerAlliance.org. A guide for the patient

BOLT Hem/Onc Thought Leader Panel #38 Cancer Immunotherapy

The Past, Present & Future of Cancer Immunotherapy:

Immunotherapy Concept Turned Reality

Targeted Therapy What the Surgeon Needs to Know

Current Status of Immunotherapy For the Treatment of Metastatic Melanoma

Médecine de précision médecine personnalisée en Oncologie. Fabien Calvo, Directeur Recherche et Innovation, INCa, Directeur ITMO Cancer, AVIESAN

Update in Hematology Oncology Targeted Therapies. Mark Holguin

Your Immune System & Melanoma Treatment

New Targets and Treatments for Follicular Lymphoma. Disclosures

PROSPETTIVE FUTURE NEL TRATTAMENTO. Cinzia Ortega Dipartimento di Oncologia Medica Fondazione del Piemonte per l Oncologia I.R.C.C.S.

Oncos Therapeutics: ONCOS THERAPEUTICS Personalized Cancer Immunotherapy. March Antti Vuolanto, COO and co-founder

Predictive Biomarkers for Tumor Immunotherapy: Are we ready for clinical implementation? Howard L. Kaufman Rush University

Preliminary Results from a Phase 2 Study of ARQ 197 in Patients with Microphthalmia Transcription Factor Family (MiT) Associated Tumors

Your Immune System & Lung Cancer Treatment

The renaissance of immunotherapy is a revolution for cancer patients. Ira Mellman, Ph.D. Vice President, Cancer Immunology, Genentech

Personalized, Targeted Treatment Options Offer Hope of Multiple Myeloma as a Chronic Disease

High Grade Gliomas: Update in Treatment and Care Ryan T. Merrell, M.D. Clinical Assistant Professor of Neurology NorthShore University HealthSystem

10 th EADO Congress Vilnius, 7-10 May Ipilimumab update. Michele Maio

Cambia l algoritmo terapeutico

Latest advances in the treatment of mesothelioma

PARP Inhibitors in Lung Cancer. Primo N. Lara, Jr., MD Professor of Medicine UC Davis Comprehensive Cancer Center

Biologic Treatments for Rheumatoid Arthritis

CLINICAL POLICY Department: Medical Management Document Name: Opdivo Reference Number: CP.PHAR.121 Effective Date: 07/15

Bioinformatics for cancer immunology and immunotherapy

What You Need to Know About Lung Cancer Immunotherapy

Immunotherapy for Melanoma: The End of The Beginning. Jedd D. Wolchok, MD, PhD

A Decade of Innovation in Cancer

GENETIC PROFILES AND TARGETED TREATMENT OF CANCER - PERSONALIZED MEDICINE

Cancer and the immune system: can we beat cancer at its own game?

Cancer Immunotherapy: Can Your Immune System Cure Cancer? Steve Emerson, MD, PhD Herbert Irving Comprehensive Cancer Center

Next Generation Sequencing in Early-Phase Clinical Trials in Cancer Filip Janku

Moving forward, where are we with Clinical Trials?

T Cell Immunotherapy for Cancer

Immuno-Oncology 2015: A New Landscape in Lung Cancer

IMMUNOTHERAPY FOR THE TREATMENT OF LUNG CANCER

Principal Investigator: Valerie W. Rusch, MD, FACS, Chief, Thoracic Surgery Memorial Sloan-Kettering Cancer Center

The EGFR mutation and precision therapy for lung cancer

The immune system. Bone marrow. Thymus. Spleen. Bone marrow. NK cell. B-cell. T-cell. Basophil Neutrophil. Eosinophil. Myeloid progenitor

Targeted immunotherapy: unleashing the immune system against cancer

Emerging Therapies for the Treatment of Advanced Melanoma: Focus on Immunotherapy

Your Immune System & Cancer Treatment

Coxsackievirus A21 (CAVATAK TM ) - mediated oncolytic immunotherapy in advanced melanoma patients

CheckMate -057, a Pivotal III Opdivo (nivolumab) Lung Cancer Trial, Stopped Early

CML. cure. A Patient s Guide. Molecular Biology Diagnosis Stem Cell Transplant Monitoring New Drugs Questions to Ask and More

Metastatic Triple Negative Breast Cancer: Ongoing Trials. Joan Albanell Hospital del Mar, Barcelona

Endpoint Selection in Phase II Oncology trials

Monoclonal Antibodies in Cancer. Ralph Schwall, PhD Associate Director, Translational Oncology Genentech, Inc.

Genomic Clinical Trials: NCI Initiatives

THE CANCER STEM CELL INHIBITORS VS-6063 AND VS-5584 EXHIBIT SYNERGISTIC ANTICANCER ACTIVITY IN PRECLINICAL MODELS OF MESOTHELIOMA

Nivolumab and Ipilimumab versus Ipilimumab in Untreated Melanoma

Pulling the Plug on Cancer Cell Communication. Stephen M. Ansell, MD, PhD Mayo Clinic

Biomarkers and Associations With the Clinical Activity of PD-L1 Blockade in a MPDL3280A Study

Genomic Medicine The Future of Cancer Care. Shayma Master Kazmi, M.D. Medical Oncology/Hematology Cancer Treatment Centers of America

Breakthrough Cancer Therapies: Directing the Immune System to Eliminate Tumor Cells. Corporate Presentation May 2015

CAR T cell therapy for lymphomas

BAP1 germline mutations A new Cutaneous Nevus Melanoma Syndrome. Thomas Wiesner

Colorectal cancer xenopatients: A preclinical platform for precision medicine

Immuno-Oncology, The New Era of Cancer Treatment. Ted Lee, MD, MPH Disease Area Head, IO, Pac Rim, Bristol Myers Squibb

Pulmonary and Critical Care Regional Symposium April 25, 2015

a Phase 2 prostate cancer clinical trial is ongoing. Table 2: Squalamine vs Standard-of-care literature

Non-Small Cell Lung Cancer

Immunotherapy of Uveal Melanoma

ROLE OF RADIATION THERAPY FOR RESECTABLE LUNG CANCER

Clinical Trial Designs for Incorporating Multiple Biomarkers in Combination Studies with Targeted Agents

Cancer Treatments Subcommittee of PTAC Meeting held 2 March (minutes for web publishing)

Transcription:

Grand Unification: The rationale for combining immunotherapy and molecular targeted therapy Ryan J. Sullivan, M.D. Massachusetts General Hospital / Harvard University Canadian Melanoma Conference February 23, 2014 Disclosures Unfortunately, I have no relevant disclosures to declare. Disclosures I have one irrelevant disclosure. 1

Disclosures I have one irrelevant disclosure. Beware of agreeing to hike with Michael Smylie Objectives (Nov 2013) Review preclinical data justifying the combo of BRAF directed therapy and immunotherapy Describe the clinical data of BRAFi/immunotherapy combinations Review ongoing and future trials of BRAFi/immunotherapy combinations Revised Objectives Briefly review BRAF/immunotherapy sequencing data Review preclinical data justifying the combo of targeted therapy and immunotherapy Describe the clinical data of BRAFi/immunotherapy combinations Review ongoing and future trials of targeted therapy/immunotherapy combinations 2

An Era of Futility: 1975 2005 Dacarbazine High dose Interleukin 2 1980 1990 2000 2010 We ve learned that melanoma is driven by genetic changes TCGA 2012 Oncogenes in melanoma Year Target Prevalence Drug 1984 NRAS 20% tramentinib, MEK162 2002 BRAF 50% vemurafenib, LGX 818 dabrafenib; trametinib, MEK162 2005 CKIT 1% imatinib, dasatinib, nilotinib 2008 GNAQ/11 1% * selumetinib,?pkci 2012 NF1 loss 10% unknown *(80-90% of uveal) 3

X X X X X Immune (T cell) activation is not as simple as 4

Immune (T cell) activation is not as simple as Immune (T cell) activation is amazingly much more complex Pardoll. Nat Rev Cancer 2012 yet druggable! Pardoll. Nat Rev Cancer 2012 5

An Era of Futility: 1975 2005 Dacarbazine High dose Interleukin 2 1980 1990 2000 2010 An Era of Futility: 1975 2005 An Era of Hope: 2006 Nivolumab, MK 3475 Dabafenib, trametinib Dacarbazine High dose Interleukin 2 Ipilimumab vemurafenib 1980 1990 2000 2010 Immunotherapy: Ipilimumab BRAF mutant: Vemurafenib An Era of Hope: By subclass 2011 6

An Era of Hope: By subclass Immunotherapy: Ipilimumab BRAF mutant: Vemurafenib Dabafenib, trametinib 2011 2013 An Era of Hope: By subclass Immunotherapy: Ipilimumab BRAF mutant: Vemurafenib Dabafenib, trametinib MK 3475, Nivolumab. 2011 2013 2014 5 An Era of Hope: By subclass Immunotherapy: Ipilimumab BRAF mutant: Vemurafenib Dabafenib, trametinib MK 3475, Nivolumab MEK162, LGX818, cobimetinib 2011 2013 2014 5 7

An Era of Hope: By subclass Immunotherapy: Ipilimumab BRAF mutant: Vemurafenib NRAS mutant: Other mutants: Dabafenib, trametinib MK 3475, Nivolumab, other anti PD1/PDL1/checkpoint inhibitors. MEK162, LGX818, cobimetinib, ERKi MEK162, trametinib, CDKi, ERKi MEKi, PKCi, AKTi, KITi 2011 2013 2014 5 Is there an ideal sequence of immunotherapy and molecularly targeted therapy? BRAF-directed therapy is as effective before or after immunotherapy Response No Response Total ITfirst 17 13 30 MAPKi first 153 80 233 170 93 263 Ackerman et al. Cancer 2014. In Press 8

Ipilimumab does not appear to be as effective following progression on BRAF-directed therapy Ackerman et al. Cancer 2014. In Press Outcome is better with iplimumab first sequence Ascierto et al. ASCO 2013 Outcome is better with BRAFi than ipilimumab sequence Ascierto et al. ASCO 2013 though selection bias must be considered Ackerman et al. Cancer 2014. In Press 9

Intergroup Study (formerly E4613) ECOG PS 0 1 Stage IIIC (unres) or M1a/b M1c Prior therapy No Yes R A N D O M I Z E Arm 1: Ipi q3wks x 4 Arm 2: Vem 960 BID PD Vem Ipi PI: Mike Atkins Intergroup Study (formerly E4613) Dabrafenib plus trametinib Nivolumab plus ipilimumab Wolchok et al. NEJM 2012 Flaherty et al. NEJM 2012 PI: Mike Atkins Intergroup Study (formerly E4613) ECOG PS 0 1 Stage IIIC (unres) or M1a/b M1c Prior therapy No Yes R A N D O M I Z E Arm 1: Ipi/Nivo q 3wks x 4 then nivo q2wks x 42wks Arm 2: Dab 150 BID, Tram 2 qd PD Dab/Trem Ipi/Nivo PI: Mike Atkins 10

New Paradigm? New Paradigm? Ribas, Society for Melanoma Research 2012 New Paradigm? Ribas, Society for Melanoma Research 2012 11

New Paradigm? Ribas, Society for Melanoma Research 2012 Is there any reason to combine immunotherapy with molecularly targeted therapy? BRAF inhibitor therapy plus immunotherapy in BRAF mutant melanoma 12

Are BRAF inhibitors immunosuppressive? Treatment with BRAFi does not impair overall immune competance; MEKi does. BRAF inhibition does NOT affect T cell function, however MEK inhibition impairs proliferation & function Boni et al. Cancer Res 2010; Hong et al. Clin Cancer Res. 2012 BRAF/MAPK Inhibition Increases Recognition of Melanoma Cells by Antigen Specific T Cells MEK Inhibitor U0126 * * BRAF Inhibitor PLX4720 * * P<0.05 Boni et al. Cancer Res 2010 13

What are the effects of BRAF inhibitors on tumors? Treatment with BRAFi increases MDI expression in tumors of patients with melanoma Frederick et al. Clin Cancer Res 2013 Treatment with BRAFi increases CD8+ T Cell infiltrate in tumors of patients with melanoma Frederick et al. Clin Cancer Res 2013 14

Treatment with BRAFi reduce immunosuppressive cytokines but increases immuno exhaustion Frederick et al. Clin Cancer Res 2013 Preclinical data predicts synergy of BRAF inhibitor plus anti PDL1/PD1 combinations Cooper et al SMR 2012 Clinical trials of BRAF/MEK inhibitors and immunotherapy IFN a IL2 ACT Ipilimumab nivolumab MK3475 MPDL 3280A MEDI 4736 BRAF inhibitors Vemurafenib (V) Dabrafenib (D) 3 3 1 2* 0 0 1** 0 MEK inhibitors Cobimetinib (C) Trametinib (T) 0 0 0 0 0 0 1 0 Combined T +/ D; D +/ T 1 0 0 2 0 0 0 1 Ribas et al. NEJM 2013*; Hamid et al. ASCO 2013** 15

The combination of vemurafenib and ipilimumab leads to significant hepatotoxicity 6/10 patients enrolled who received the combination had Grade 3 ALT/AST elevation Ribas et al. NEJM 2013 MPDL3280A + Vemurafenib Preliminary Safety MPDL3280A 20 mg/kg Q3W + 720 mg vemurafenib BID Treatment Start Cycle (Q3W) 1 2 3 4+ 3/3 Patients: Rash (Gr 3) AST/ALT elevation (Gr 1-3) Flu-like symptoms (Gr 1-2) 1 Resolved with vemurafenib hold/reduction 2/2 Active Patients 2 : AST/ALT elevation (Gr 3) Resolved with vemurafenib hold/reduction Rash and flu-like symptoms did not recur 2/2 Active Patients: AST elevation Gr 1 Patient status: 1 patient D/C due to PD Cycle 8 1 patient active (Cycle 12+; CR) 1 Included fever, headache, sore throat, arthralgia, chills, fatigue 2 One patient with PD at 8 weeks 1 PR, 1 CR Hamid et al. ASCO 2013 Summary of BRAF inhibition and immunotherapy BRAFi lead to: Increase melanocyte derived antigen expression Reduced immunosuppressive cytokine production Flooding of CD8+, T lymphocytes Increased PDL1 expression Combined BRAFi/immunotherapy In vivo synergy in murine models Higher than predicted toxicity in two phase I trials of vemurafenib plus immune checkpoint inhibitors Many ongoing studies with more planned 16

NRAS mutations, MITF, and immunotherapy MAPK suppresses MITF and MDA expression Haq, Johnson et al. SMR 2013 MAPK suppresses MITF and MDA expression Haq, Johnson et al. SMR 2013 17

MAPK suppresses MITF and MDA expression Haq, Johnson et al. SMR 2013 MAPK suppresses MITF and MDA expression Haq, Johnson et al. SMR 2013 Differential patterns of MITF amplification in BRAF and NRAS mutations and NF1 loss TCGA 2012 18

MITF amplification is commonly seen in BRAF mutant melanoma TCGA 2012 MITF amplification is never seen in NRAS mutant or NF1 loss melanoma Melanocyte gene expression from BRAF mutant, MITF amplified cells is more similar to NRAS mutant cells than BRAF mutant, MITF non amplified Haq, Johnson et al. SMR 2013 19

Mutational Status and HD IL-2 Joseph, Sullivan et al. JIT 2012 NRAS mutation is associated with higher response rate and improved outcome compared to WT/WT Johnson et al. ASCO 2013 Survival in the setting of immunotherapy: BRAF vs NRAS mutant 20

Next Steps 1. Determine the mechanism Next Steps 1. Determine the mechanism 2. Clinical trials MEDI 4736 + trametinib MPDL3280A + cobimetinib Acknowledgments MGH Center for Melanoma Keith Flaherty Donald Lawrence Rizwan Haq Fisher Lab David Fisher Rizwan Haq Sullivan Lab Dennie Frederick MDACC Jen Wargo Zachary Cooper Mike Davies Vanderbilt Ingram Cancer Center Jeff Sosman Doug Johnson Christine Lovly MSKCC Rich Carvajal MIA Oliver Klein Georgina Long BIDMC David McDermott Alison Ackerman 21