PD-L1 Testing German Experience. P. Schirmacher for QuIP

Similar documents
Quality control of PD-L1 in NSCLC - Results of two German ring trials Dr. Andreas Scheel University Hospital Cologne

Santiago de Chile, September 6 th, 2018

NSCLC. Harmonization study 1. Lung cancer and other malignancies -PD-L1 assay, QuIP EQA

Atezolizumab Is a Humanized Anti-PDL1 Antibody That Inhibits the Binding of PD-L1 to PD-1 and B7.1

Corporate presentatie Maastricht UMC+ (titel presentatie)

Advances in Pathology and molecular biology of lung cancer. Lukas Bubendorf Pathologie

Biomarcatori per la immunoterapia: cosa e come cercare Paolo Graziano

Vernieuwing en diagnostiek bij NSCLC: Immunotherapy: PD-L1 analyse: waar staan we

Immunotherapy in NSCLC Pathologist role

Sabrina Schmitt: "German Biobank Node s concept for quality management"

HSL-Advanced Diagnostics 2018 / 19 Test & Service List

Lung cancer PD-L1 testing clinical impact

Biomarkers for Cancer Immunotherapy Debate

Molecular Testing Updates. Karen Rasmussen, PhD, FACMG Clinical Molecular Genetics Spectrum Medical Group, Pathology Division Portland, Maine

Molecular Testing in Lung Cancer

Patient Selection: The Search for Immunotherapy Biomarkers

Carcinoma Urotelial: La Célula Inflamatoria Clave en la Inmunoterapia Fernando López-Ríos

The Role of Immuno-Oncology Biomarkers in Lung Cancer

Implementation of nation-wide molecular testing in oncology in the French Health care system : quality assurance issues & challenges

PD-L1 Analyte Control DR

Transform genomic data into real-life results

Immune checkpoint blockade in lung cancer

Overview of the ESP Lung and Colon EQA schemes with a focus on Dutch laboratories

Giorgio V. Scagliotti Università di Torino Dipartimento di Oncologia

MICROSCOPY PREDICTIVE PROFILING

Predictive Biomarkers for Pembrolizumab. Eric H. Rubin, M.D.

Disclosures. Molecular Cytopathology. Update on Molecular Testing of Cytology Specimens: Beyond the Cell Block. Molecular Cytopathology Solid Tumor

Role of the pathologist in the diagnosis and mutational analysis of lung cancer Professor J R Gosney

Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment with Targeted Tyrosine Kinase Inhibitors

Cancer Immunotherapy Patient Forum. for the Treatment of Melanoma, Leukemia, Lymphoma, Lung and Genitourinary Cancers - November 7, 2015

Learning from the Impact of the Drug-Diagnostics Strategy in Oncology

Companion & Complementary Diagnostics: Clinical and Regulatory Perspectives

PD-L1 and Immunotherapy of GI cancers: What do you need to know

Quality assurance and quality control in pathology in breast disease centers

News from ASCO. Niven Mehra, Medical Oncologist. Radboud UMC Institute of Cancer Research and The Royal Marsden Hospital

TITLE: UK NEQAS ICC & ISH Pre-Pilot Meeting for PD-L1. Immunohistochemistry in Non-Small Cell Lung Carcinoma

Predictive markers for treatment with Immune checkpoint inhibitors - PD-L1 et al -

Molecular Diagnostics Overview JAN A. NOWAK, PHD, MD PATHOLOGY AND LABORATORY MEDICINE MOLECULAR DIAGNOSTICS LABORATORY FEBRUARY 15, 2018

Quantitative Image Analysis of HER2 Immunohistochemistry for Breast Cancer

Tissue or Liquid Biopsy? ~For Diagnosis, Monitoring and Early detection of Resistance~

Quality Indicators - Anatomic Pathology- HSC/STC Jul-Sep 2 nd Qtr. Apr-Jun 1 st Qtr

Quality Assurance and Quality Control in the Pathology Dept.

PLENARY SESSION 1: CLINICAL TRIAL DESIGN IN AN ERA OF HORIZONTAL DRUG DEVELOPMENT Industry Perspective

CDx in oncology Prof. Christophe Le Tourneau, MD, PhD FEAM Geneva September 27, 2018

Data Sharing Consortiums and Large Datasets to Inform Cancer Diagnosis

Patient Leader Education Summit. Precision Medicine: Today and Tomorrow March 31, 2017

Innovation, Uncertainty and Reimbursement Processes in Precision Medicine: The Case of PD-L1

Breast cancer pathology

How could molecular profiling impact histology independent labels in the future?

Regulatory Landscape for Precision Medicine

Colon cancer: practical molecular diagnostics. Wade S. Samowitz, M.D. University of Utah and ARUP

Overview of Biomarker Development for Immune PD-1/L1 Checkpoint Blockade

Roche Pharma Day 2015

O DESAFIO DA INOVAÇÃO EM ONCOLOGIA EM PORTUGAL The Challenges of innovative oncology care in Portugal. Gabriela Sousa Oncologia Médica IPO Coimbra

Lung Cancer Update on Pathology Zhaolin Xu, MD, FRCPC, FCAP

LUNG CANCER. pathology & molecular biology. Izidor Kern University Clinic Golnik, Slovenia

NGS ONCOPANELS: FDA S PERSPECTIVE

Product Introduction. Product Codes: HCL029, HCL030 and HCL031. Issue

Guideline. Associated Documents ASCO CAP 2018 GUIDELINES and SUPPLEMENTS -

HistoCyte Laboratories Ltd

METASTATIC COLORECTAL CANCER: TUMOR MUTATIONAL ANALYSIS AND ITS IMPACT ON CHEMOTHERAPY SUMA SATTI, MD

Brain mets under I.O.

NGS IN ONCOLOGY: FDA S PERSPECTIVE

Results you can trust

IDH1 R132H/ATRX Immunohistochemical validation

Product Introduction

Version 2 of these Guidelines were drafted in response to published updated ASCO/CAP HER2 test Guideline Recommendations-

Infrastructure for Clinical Data Exchange

Evolution of Pathology

Emerging Tissue and Serum Markers

NSCLC 2 nd and further line therapies. Egbert F. Smit MD PhD. Dept. Thoracic Oncology, Netherlands Cancer Institute

21 st Century Slide Based Pathology & Molecular Diagnostics: From the Laboratory to the Patient

HER2 status assessment in breast cancer. Marc van de Vijver Academic Medical Centre (AMC), Amsterdam

Il ruolo di PD-L1 (42%) tra la prima e la seconda linea di trattamento

Andreas Wicki. University Hospital Basel Switzerland

NGS in Lung Cancer Cytology

Innovation and value creation. Severin Schwan, CEO Roche Group. Zurich, January 2015

Emerging biomarkers for immunotherapy in lung cancer

How close are we to standardised extended RAS gene mutation testing? The UK NEQAS experience

PATIENT SELECTION CORRELATION OF PD-L1 EXPRESSION AND OUTCOME? THE ONCOLOGIST VIEW ON LUNG CANCER

Importance of Methodology Certification and Accreditations to Perform Assays. Stan Hamilton, MD Head, Pathology and Laboratory Medicine

Agilent companion diagnostics for cancer immunotherapy

Media Release. Basel, 07 December 2017

Valida5on of a Microsatellite Instability Assay by NGS

Clinical Utility of Diagnostic Tests

NeoTYPE Cancer Profiles

Immunotherapy for NSCLC: Current State of the Art and Future Directions. H. Jack West, MD Swedish Cancer Institute Seattle, Washington, United States

Assessment performed on Tuesday, July 29, 2014, at Lions Gate Hospital, North Vancouver

Role of the Pathologist in Guiding Immuno-oncological Therapies. Scott Rodig MD, PhD

Technology appraisal guidance Published: 16 May 2018 nice.org.uk/guidance/ta520

Case Studies. Ravi Salgia, MD, PhD

FAQs for UK Pathology Departments

Current Status of Biomarkers (including DNA Tumor Markers and Immunohistochemistry in the Laboratory Diagnosis of Tumors)

See how you can guide the path her cancer takes

Clinical Utility of Actionable Genome Information in Precision Oncology Clinic

Immunotherapy for the Treatment of Head and Neck Cancers. Barbara Burtness, MD Yale University

NCCN Non-Small Cell Lung Cancer V Meeting June 15, 2018

Liquid biopsy: the experience of real life case studies

Predictive biomarker profiling of > 1,900 sarcomas: Identification of potential novel treatment modalities

Structured Immuno-Oncology Combination Strategies To Maximize Efficacy

Transcription:

PD-L1 Testing German Experience P. Schirmacher for QuIP

Quality Management Molecular Diagnostics Method/Inter-Center-Optimisation/Validation Preclinical Validation/internal QM Accreditation Institutes (DAkkS; ISO 9001 DIN 17020) National Round Robins (QuIP)

QuiP (DGP) Independent Self administered Non commercial Expert guided (Panels) Extensive RR-Expertise (> 300 RRs) High acceptance (diagnostic community, clinicians, industry, politics) International (in selected indications) ESP-LOA and cooperation

Principle: Free Choice of Methods Free Choice of Method, e.g. Sanger Pyro-Sequencing Mutation-spezifische PCR NGS (Deep/Panel Sequencing) Reflection of technology Evaluation by diagnostic result

Constant Round Robins 2010 2011 2012 2013 2014 2015 2016 2017 2018 RfB BRAF 600 BRAF 600 BRAF 600 BRAF 600 RfB CD117 CD117 CD117 CD117 CD117 CD117 CD117 CD117 RfB EGFR EGFR EGFR RfB Erez/PRez Erez/PRez Erez/PRez Erez/PRez Erez/PRez Erez/PRez Erez/PRez RfB GIST GIST GIST GIST GIST RfB HER2n IHC HER2n IHC HER2n IHC HER2n IHC HER2n IHC RfB HER2n ISH HER2n ISH HER2n ISH HER2n ISH HER2n ISH RfB Keratine Keratine Keratine Keratine Keratine Keratine Keratine Keratine RfB KlonML KlonML KlonML KlonML KlonML KlonML KlonML RfB KRAS RfB Lymphome Lymphome Lymphome Lymphome Lymphome Lymphome Lymphome Lymphome RfB MMRD MMRD MMRD MMRD MMRD MMRD MMRD MMRD RfB MSI MSI MSI MSI MSI MSI MSI RfB NEM NEM NEM NEM NEM NEM NEM NEM RfB RAS RAS RAS RAS multiblock ER ER ER ER ER ER ER ER multiblock PR PR PR PR PR PR PR PR multiblock Her2-IM Her2-IM Her2-IM Her2-IM Her2-IM Her2-IM Her2-IM Her2-IM multiblock Her2-ISH Her2-ISH Her2-ISH Her2-ISH Her2-ISH Her2-ISH Her2-ISH Her2-ISH multiblock Ki-67 Ki-67 Ki-67 Ki-67 Ki-67 Ki-67 Ki-67 Ki-67 provitro HPV HPV HPV HPV HPV HPV HPV HPV provitro TBc TBc TBc TBc TBc TBc TBc TBc RfB T790M T790M RfB PD-L1MM RfB PD-L1 NSCLC PD-L1 NSCLC EGFR IHC RfB sqnsclc RfB BRCA1/2 BRCA1/2 RfB BRAF 600 Lunge

Prototypic Round Robins Round Robin Status Round Robin Status T790M 2016 PD-L1 NSCLC EGFR IHC sqnsclc PD-L1 Melanoma (2) finished final report final report final report MLH1 ROS1 IDH1(R132H) Consideration QuIP-Board Consideration QuIP-Board Consideration QuIP-Board T790M 2017 (2) ongoing Q1-Q2 PD-L1 NSCLC (2) ongoing Q1-Q2 BRAF V600 (2) BRCA 1/2 (2) planned Q3-Q4 planned Q3-Q4

Implementation of new Diagnostic Assays Information about approval of new drug with predictive molecular testing (1-3 months ahead) Implementation Validation and optimisation of testing modalities Solutions for open scientific issues Diagnostic recommendations, information, discussion with clinical societies Diagnostics for early accession/ compassionate use programs Broad/nationwide availability (methodology, expertise, training) Agreement on reimbursement issues Local issues Others (e.g. legal issues) Quality Management Panel-establishment and -validation (> 3 m) Establishment of expert panel (n~5-8; Lead- Institutes; other Panel centers) Consent about approach (methodology, time schedule, testing conditions etc.) Identification and selection of suitable test cases Cross validation by lead institutes Testing/validation of panel centers; evaluation; set-up of RR conditions National/international round robin (> 2 m) announcement/feed-back; application preparation by Lead-institutes, RfB Probe mailing, testing, test results mailed Evaluation and publication Implementation without regulatory, financial and intellectual framework but decisive for drug/therapy success (system relevant). Requires Competence Center System (Peers) and more attention by industry and regulatory authorities

PD-L1 IHC German Strategy for Roll-out and QM National Harmonisation Study (DGP) Validation Harmonisation Recommendation National QA Measures (QuIP) Quality Assurance Teaching and Training National Improvement Activity (nngm/dkh)

PD-L1 IHC in NSCLC National Harmonisation-Study Pathology: Reinhard Büttner Manfred Dietel Lukas Heukamp Korinna Jöhrens Thomas Kirchner Simone Reu Josef Rüschoff Andreas Scheel Hans-Ulrich Schildhaus Peter Schirmacher Markus Tiemann Arne Warth Wilko Weichert Industrial Partners BMS MSD Roche AstraZeneca Ventana Dako Targos

Response to Anti PD-1 (Pembrolizumab) and Expression of PD-L1 in NSCLC

Different Antibodies and Antibody Reactivities Scheel et al., 2016

Tumorimmunotherapy: PDL-1-Testing

BIRCH: PD-L1 TC and IC Selection Criteria TC2/3 IC2/3 Intrinsic PD-L1 expression in tumor cells (TC) 34% of screened patients between Jan. 2014 and Dec. 2014 Adaptive PD-L1 expression in tumor-infiltrating immune cells (IC) BIRCH enrolled patients with tumors that were PD-L1 TC2/3 or IC2/3 VENTANA SP142 IHC assay was used to determine PD-L1 expression on both TC and IC Archival or freshly collected tumor specimens were required for PD-L1 testing at a central laboratory PD-L1 as a predictive biomarker: PD-L1 expression on TC and IC was independently predictive of response in patients with previously treated NSCLC (i.e., POPLAR) 1,2 TC3 or IC3 = TC 50% or IC 10% PD-L1+ cells; TC2/3 or IC2/3 = TC or IC 5% PD-L1+ cells, respectively. 1. Horn L, et al. ASCO 2015; 2. Vansteenkiste J, et al. ECC 2015. Besse et al, Oral Presentation at ECC 2015

A Global NSCLC-PDL1 Score? Scheel et al., 2016

Interobserver-Validation (Phase I) Scheel et al., 2016

Harmonisation Study: Immune Cells Scheel AH et al., Modern Pathology 2016

Phase 2 Assays: - Performance in multiple Institutes / Reliability - Staining pattern - validation of Phase 1; fixed assay vs. open protocol - Inter-lab concordance Evaluation: - Validation proportional score (6-step) - Local vs. central evaluation

Phase 2 Targos Molecular Pathology; - Project management Phase 2 - NSCLC-TMAs (project specific): - 'TMA-Master' (3DHistotech) - 1.5 mm cores - Central provision of slides 8 Pathology Institutes - Trial analog protocols Dako 22C3, 28-8 Ventana SP142, SP263 - Open protocol: 22C3, 28-8 (local protocols) - 3 institutes per protocol

PD-L1 Testing + Robust, broadly available technology (IHC) Good antibodies; alternatives exist Robust, relatively stable assay Consented algorithm - Stand-alone assay/ no methodical convergence Singular analyses Algorithm/reporting complexity; dynamic Heterogenous expression; 1% threshold problematic Insufficient refunding

Prototypic Round Robin PD-L1-NSCLC (1) 28.4.16 Decision for RR, Lead- and Panel Institutes 6.16 Coordination of Lead Institutes, selection of cases, trilateral validation 15.7-26.7. Testing of the Panel Institutes (internal RR) 27.7. -29.7. Evaluation of internal RRresults, Lead/Panel-Institute; meeting, decision for open RR 15.9 Public PD-L1 training meeting (Charite) End of 9.16 Open RR Lead Institutes: Berlin, Cologne, Göttingen Panel Institutes: Hannover, Heidelberg, Jena, Munich TU, Munich LMU Composition: 10 cases; 2 points each, 18 points necessary for certificate No methodical restriction, sections provided Optional reporting of methodology Option to challenge and for educational

Prototypic Round Robin Participants: 83 (76 D, 4 A, 3 CH) Successful: 60 Success rate: 72% PD-L1-NSCLC (1) Composition < 1%: 3 cases 1%-49%: 2 cases 50-100 %: 5 cases

PD-L1-NSCLC Round Robin Antibodies

PD-L1-NSCLC Challenge Challenged result: 18 Institutes 1 Institute post hoc success 4 Institutes: Interpretation problems 13 Institutes: Staining problems

Prototypic Round Robin Malignant Melanoma (1) 3.8 Panel-Institutes.16 Decision for RR 22.8.16 Decision on Lead- and Panel Institutes 9/10.16 Coordination of Lead Institutes, Case selection and reciprocal testing 14-28.10 Testing of Panel Institutes (internal RR) 9/10 Announcement of open RR 9.-25.11.16 open RR 28.11-2.12. Evaluation of open RR; announcement of results Lead Institutes: Berlin, Heidelberg, TU Munich Panel Institutes: Hannover, Munich LMU, Cologne, Hamburg, Göttingen, Würzburg Composition: 10 cases; 2 points each, 18 points necessary for certificate No methodical restriction, sections provided Optional reporting of methodology Option to challenge and for educational

Prototypic Round Robin PD-L1-Melanoma Participants: 44 Successful: 37 Success rate: 84% Composition <5%: 5 cases >5%: 5 cases

PD-L1-Melanoma Round Robin Antibodies

PD-L1-NSCLC and MM Round Robin Other Conclusions Diverse use of primary antibodies 28-8 and SP263 stain stronger 22C3 stains rather weaker Discrepancies are rather towards lower staining intensities Establishment using tonsil tissue suggested

Future and Ongoing Activities PD-L1-NSCLC (2) ongoing (until 15.5.) PD-L1 Bladder Cancer in preparation PD-L1 MM (2) in discussion

Other/Better Markers!? PD-L1 Gene CNV/expression MSI Mutational load Immunophenotyping Combinations RESISTANCE MARKERS

PD-L1 Amplifications/Deletions and/or Mutational Load Increasing number of mutations n=78 n=40 WGS/WES? Panels? Others? Budczies et al. 2016

Immune Cell Infiltration and Response to Conventional and Personalized Treatment Lasitschka, F, Schirmacher P, Jäger D, Halama N, et al.

Constant Round Robins Participants 2016 Participants 2016 RR RR BRAF 58 ER 186 CD117 66 PR 177 GIST 39 Her2-IM 198 Her2nlHC 88 Her2-ISH 103 Her2nlSH 52 Ki-67 177 RAS 71 Lymphone 71 HPV 7 MMRD 84 TBC 14 MSI 45 Keratine 88 KlonML 29 NEM 69 EGFR 48