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市場調查報告書

癌症診斷及治療所需之生物標誌技術平台

Biomarker Technology Platforms for Cancer Diagnoses and Therapies

出版商 Trimark Publications
出版日期 2011年09月 商品編碼 214200
內容資訊 英文 342 Pages
價格
US $ 3400 PDF by E-mail (Single User License)
US $ 6800 PDF By E-mail (Unlimited User License)


癌症診斷及治療所需之生物標誌技術平台 是由出版商Trimark Publications在2011年09月所出版的。 這份英文市場調查報告書包含342 Pages 價格從美金3400起跳。

簡介

在針對癌症預防、治療及治癒等更好之治療方式開發前,早期發現及診斷為減少此疾病死亡率之最佳手段。肺癌、乳癌、結腸癌、前列腺癌等主要固體腫瘤之長期存活率因癌細胞轉移而急轉直下。而針對乳癌、結腸癌、卵巢癌、肺癌等早期發現及篩選檢查中,生物標誌之開發則更為重要。

本報告為,分析癌症生物標誌技術趨勢及新的生物標誌診斷技術、市場機會、全球收益趨勢等,以下列摘要形式闡述。

第1章 概要

第2章 癌症生物學及診斷產業之簡介

  • 生物標誌
  • 生物標誌之癌症檢出及治療
  • 癌症
  • 生技及診斷產業之發展因素
  • 腫瘤市場展望
  • 蛋白質組學
  • 癌症用外延基因標記
  • 癌症用分子診斷檢查
  • 市場機會

第3章 癌症生物標誌市場分析

  • 本章範圍
  • 生物標誌總市場之市場機會及分類
  • 商業應用中潛在之癌症生物標誌
  • 組織來源別癌症生物標誌市場展望
  • 癌症生物標誌開發人員之挑戰
  • 癌症生物標誌製品中未被滿足之需求
  • 癌症生物標誌市場之競爭情形

第4章 癌症生物標誌之主要臨床應用

  • 已經上市產品及產品線
  • CYP2C9藥物基因組學及個別化醫療之作用
  • 個別化乳癌治療
  • 個別化NSCLC治療
  • AmpliChip類個別化醫療

第5章 乳癌

  • 乳癌之概要
  • BRCA1及BRCA2基因
  • 雌激素受體及乳癌
  • HER2基因及蛋白質
  • 赫賽汀治療
  • 輔助化療所需之腫瘤檢測
  • 認識乳癌所需之基因組學使用
  • 基因分析解決方案
  • 基因微陣列表達及再發預測
  • Oncotype DX之經濟優點
  • Oncotype DX臨床之可用性增加
  • 第2代Oncotype DX
  • MammaPrint
  • Rotterdam Signature 76-Panel
  • 微陣列技術摘要
  • 質譜分析類方式
  • 展望
  • 未來發展
  • 乳癌計畫(NMP66)
  • Myriad Genetics
  • Veridex GeneSearch™乳淋巴結
  • OncoVue癌症風險測試
  • 乳癌調查用生物標誌
  • 乳癌用防用蛋白質生物標誌
  • 阿黴素之乳癌治療用生物標誌預後診斷

第6章 卵巢癌

  • 血清市場
  • 生物標誌
  • 卵巢癌用血清蛋白質生物標誌
  • 卵巢癌之分流測試

第7章 前列腺癌

  • 概要
  • 前列腺癌所含基因
  • 雄激素的獨立性
  • 前列腺癌中基因市場
  • 前立腺生物標誌之微陣列基因鑑定
  • GEArray DNA微陣列
  • Ciphergen之癌症診斷計畫
  • 胃蛋白酶
  • Matritech之前列腺癌計畫(NMP48)
  • Gen-Probe之PCA3檢測
  • 前列腺癌抗原-2(EPCA-2)
  • 質譜
  • 摘要

第8章 膀胱癌

  • 概要
  • 膀胱癌檢查
  • UroVysion膀胱癌試劑
  • Ikoniscope®機器人式數位顯微鏡平台
  • 核基質蛋白市場
  • ImmunoCyt™/uCyt+™
  • Cangen之Microsatellite DNA
  • 膀胱癌市場

第9章 結腸直腸癌

  • 概要
  • 結腸直腸癌之篩選
  • Almac Diagnostics之DSA
  • 結腸直腸癌計畫(NMP35)
  • Myriad Genetics之Colaris AP風險評估
  • 摘要

第10章 癌症診斷檢查革命所需之基因診斷

  • 概要
  • AMAS檢查
  • 主要市場中Corixa之抗體
  • Cytovision
  • Ariol System
  • Mammaglobin蛋白表達
  • L523S或KOC RNA結合蛋白
  • 由EDP生技而來之CA1-18

第11章 白血病生物標誌

  • 概要

第12章 肺癌

第13章 癌症生物標誌傳遞之可能技術

  • ACIS
  • DNA之甲基化
  • 蛋白質組學
  • 癌症生物標誌用分泌蛋白
  • 潛在主要市場中非編碼RNA
  • 結腸直腸癌發現所需之TIMP-1免疫測定建構
  • 自動顯微鏡類分析系統之開發企業
  • 腫瘤細胞隔離所需產品之開發企業
  • 提供將腫瘤細胞加上特徵之螢光標記抗體之企業
  • PerkinElmer之高通量平台

第14章 搭配診斷用於癌症治療及共同開發之生物標誌檢查

  • 概要
  • 搭配診斷
  • 結腸直腸癌及Camptostar用EGFR
  • EGFR Express及Erbitux
  • HER2及Heceptin
  • Myriad之TheraGuide 5-FU
  • TheraScreen: EGFR29
  • 搭配診斷之發展因素及阻礙
  • 特定治療標靶所需之製藥公司及夥伴關係
  • 搭配診斷之未來發展

第15章 搭配診斷及客制醫療:生物學、方式、產品線及法規趨勢

第16章 癌症生物標誌檢查部門及企業分析

第17章 產業之商業趨勢

第18章 參與癌症診斷市場中新技術平台之企業

附錄

目錄

Abstract

image1

Description

Until superior therapeutic treatments are developed to prevent, treat and cure cancer, the best means of reducing mortality and morbidity in a disease this complex is early detection and diagnosis. In the major solid cancer types such as lung, breast, colon and prostate, long-term survival rates drop precipitously once metastatis has occurred. The case is clear for development of biomarkers for early detection and screening tests for diseases such as breast, colon, ovarian and lung cancer. In addition, diagnostic measurement of cancer disease progression is essential to successful disease management. For these reasons, development of new and effective biomarkers for cancer detection and diagnosis is central to the cancer problem. The use of nucleic acid biomarker diagnostics have begun to answer these questions. Protein biomarkers are also useful. The purpose of this TriMark Publications report is to describe the specific segment of the cancer diagnostics market which develops new biomarker technology platforms for diagnosing and treating cancer. Biomarkers are useful in following the course of cancer and evaluating which therapeutic regimes are most effective for a particular type of cancer, as well as determining long-term susceptibility to cancer or recurrence. This study particularly examines those clinical measurement devices, and their reagents and supplies, which are meant to be used in hospitals, clinics, commercial laboratories and doctor' s offices to diagnose and monitor cancer. The examination also provides an in-depth discussion of the application of biomarkers in developing novel targeted cancer therapeutics, their predication response and efficacy, as well as their use in diagnosis of cancer.

Table of Contents

1. Overview

  • 1.1 Statement of Report
  • 1.2 About This Report
  • 1.3 Scope of the Report
  • 1.4 Objectives
  • 1.5 Methodology
  • 1.6 Executive Summary

2. Introduction to Cancer Biology and the Diagnostic Industry

  • 2.1 Biomarkers
    • 2.1.1 The Biomarker Market Drivers
      • 2.1.1.1 The Sector
      • 2.1.1.2 The Critical Path Opportunities
      • 2.1.1.3 Capital Markets
  • 2.2 Cancer Detection and Treatment with Biomarkers
    • 2.2.1 The Problem
  • 2.3 Cancer: The Disease
    • 2.3.1 Metastasis
    • 2.3.2 Demographics and Statistics of Cancer
  • 2.4 Drivers of the Biotech and Diagnostics Industry
    • 2.4.1 Technological Innovation
    • 2.4.2 Government Funding
    • 2.4.3 Pharmaceutical Development and Bioanalytical Services
    • 2.4.4 The War on Cancer
    • 2.4.5 Current Oncology Drug Development
  • 2.5 Outlook for Tumor Markers
  • 2.6 Focus on Proteomics
    • 2.6.1 Scientific Background
    • 2.6.2 The Relationship between Proteins and Diseases
    • 2.6.3 Limitations of Existing Diagnostic Approaches
    • 2.6.4 Addressing the Heterogeneity of Cancer
    • 2.6.5 Validation of Biomarkers Through Proper Study Design
    • 2.6.6 Exploiting the Power of MS to Improve Assay Specificity
    • 2.6.7 Creating and Maintaining a Multi-Disease Product Pipeline
    • 2.6.8 Partnerships for Developing Proteomic Biomarkes
  • 2.7 Epigenic Markers for Cancer
  • 2.8 Molecular Diagnostics Testing for Cancer
  • 2.9 Market Opportunities
    • 2.9.1 Industry Overview
    • 2.9.2 Medical Indications and Medically Useful Information
    • 2.9.3 Research Market
    • 2.9.4 Competition
    • 2.9.5 Diagnostic Services
    • 2.9.6 Clinical Image Analysis
    • 2.9.7 Research Imaging Market
    • 2.9.8 Genomic Disease Management and In Vitro Diagnostic Multivariate Index Assays (IVDMIA)
    • 2.9.9 Predictive Expression Profiles

3. Market Analysis of the Cancer Biomarkers Space

  • 3.1 Scope of this Chapter
  • 3.2 The Overall Market Opportunity and Segmentation of the Total Cancer Biomarkers Marketplace
  • 3.3 Potential Cancer Biomarker Commercial Applications
    • 3.3.1 Market for Routine Tumor Markers
    • 3.3.2 Market for Genomic Cancer Biomarkers
    • 3.3.3 Market Size and Forecasts for Companion Diagnostic Tests for Cancer Therapeutics
    • 3.3.4 SWOT Analysis of the Major Cancer Biomarker Market Segments
      • 3.3.4.1 Traditional Serum Cancer Biomarkers
      • 3.3.4.2 Proteomic Cancer Biomarkers
      • 3.3.4.3 Companion Diagnostic Cancer Biomarkers
  • 3.4 Cancer Biomarker Market Estimates by Tissue of Origin
    • 3.4.1 Colorectal
    • 3.4.2 Prostate
    • 3.4.3 Lung
    • 3.4.4 Breast
    • 3.4.5 Ovarian
  • 3.5 Challenges Facing Cancer Biomarker Developers
  • 3.6 Unmet Product Needs in the Cancer Biomarkers Space
  • 3.7 Competitive Landscape of the Cancer Biomarkers Marketplace

4. Major Clinical Applications of Cancer Biomarkers

  • 4.1 Launched Products and Pipeline
  • 4.2 CYP2C9 Pharmacogenetics and Role in Personalized Medicine
  • 4.3 Personalized Breast Cancer Therapy
  • 4.4 Personalized NSCLC Therapy
  • 4.5 AmpliChip-based Personalized Medicine

5. Breast Cancer

  • 5.1 Overview of Breast Cancer Disease
  • 5.2 BRCA1 and BRCA2 Genes
    • 5.2.1 Types of Genetic Testing Available for Breast Cancer
      • 5.2.1.1 DNA Sequencing
      • 5.2.1.2 Multi-Site Analysis
      • 5.2.1.3 Single-Site Analysis
    • 5.2.2 BRCA Test Results
      • 5.2.2.1 What Does a Positive BRCA1 or BRCA2 Test Result Mean?
      • 5.2.2.2 What Does a Negative BRCA1 or BRCA2 Test Result Mean?
      • 5.2.2.3 What Does an Ambiguous BRCA1 or BRCA2 Test Result Mean?
      • 5.2.2.4 What are the Options for a Person Who Tests Positive?
    • 5.2.3 What are Some of the Benefits of Genetic Testing for Breast Cancer Risk?
    • 5.2.4 What Are Some of the Risks of Genetic Testing for Breast and Ovarian Cancer Risk?
  • 5.3 Estrogen Receptors and Breast Cancer
    • 5.3.1 Expression and Prognostic Value of ER
    • 5.3.2 Progesterone Receptors and Breast Cancer
    • 5.3.3 ER and PR Predict Response to Endocrine Therapy
  • 5.4 HER2 Gene and Protein
    • 5.4.1 HER2 Tests
      • 5.4.1.1 IHC Test
      • 5.4.1.2 FISH Test
      • 5.4.1.3 Questions About Testing
      • 5.4.1.4 HER2 Tumor Status
  • 5.5 Herceptin Treatment
  • 5.6 Tumor Assays for Adjuvant Chemotherapy
  • 5.7 Use of Genomics to Understand Breast Cancer
  • 5.8 Genetic Analysis Solution
    • 5.8.1 The Use of Proteomics in Breast Cancer
    • 5.8.2 Tissue Microarrays
    • 5.8.3 Protein Microarrays
  • 5.9 Gene Expression Microarrays and Recurrence Prediction
    • 5.9.1 Oncotype DX
    • 5.9.2 Oncotype DX for Breast Cancer
    • 5.9.3 Risk Assessment
    • 5.9.4 Use of Chemotherapy
    • 5.9.5 Utility of the Oncotype Test
    • 5.9.6 Clinical Development and Validation of Oncotype DX
      • 5.9.6.1 Clinical Development of the Oncotype DX Recurrence Score
      • 5.9.6.2 Clinical Validation of Prediction of Recurrence and Survival in N-, ER+ Patients Treated with Tamoxifen
      • 5.9.6.3 Oncotype DX Predicts the Likelihood of Recurrence
      • 5.9.6.4 Oncotype DX Predicts the Likelihood of Breast Cancer Survival in a Community Hospital Setting
      • 5.9.6.5 Oncotype DX Predicts both Prognosis and Tamoxifen Benefit
  • 5.10 Economic Benefits of Oncotype DX
  • 5.11 Increased Clinical Utility of Oncotype DX
  • 5.12 Second Generation Oncotype DX
    • 5.12.1 Recurrence and Benefit Test for N-, ER- Breast Cancer
    • 5.12.2 Taxane Benefit Test
  • 5.13 MammaPrint
  • 5.14 Rotterdam Signature 76-Panel
  • 5.15 Summary of Microarray Technologies
  • 5.16 Mass Spectrometry-based Approaches
    • 5.16.1 Gel-based Approaches
    • 5.16.2 Non-Gel-based Approaches
      • 5.16.2.1 SELDI-TOF MS
      • 5.16.2.2 SELDI and Prognosis
      • 5.16.2.3 SELDI and Treatment Monitoring
    • 5.16.3 Limitations of Mass Spectrometry
  • 5.17 Outlook
  • 5.18 Future Perspectives
  • 5.19 Breast Cancer Program (NMP66)
  • 5.20 Myriad Genetics
  • 5.21 Veridex GeneSearch Breast Lymph Node
  • 5.22 OncoVueR Cancer Risk Test
  • 5.23 Research Biomarkers for Breast Cancer
  • 5.24 Protein Biomarkers for Breast Cancer Prevention
  • 5.25 Biomarker Prognosis of Breast Cancer Treated with Doxorubicin

6. Ovarian Cancer

  • 6.1 Serum Markers
  • 6.2 Biomarkers
    • 6.2.1 Strategies for Discovering New Cancer Biomarkers
  • 6.3 Serum Protein Biomarkers for Ovarian Cancer
    • 6.3.1 Clinical Proteomics
  • 6.4 Ovarian Cancer Triage Testing
    • 6.4.1 Vermillion' s Ovarian Cancer Triage Diagnostic Program

7. Prostate Cancer

  • 7.1 Overview
    • 7.1.1 Prevalence
    • 7.1.2 Prostate Cancer Progression and Recurrence Test
    • 7.1.3 Current Market Size
  • 7.2 Genes Involved in Prostate Cancer
  • 7.3 Androgen Independence
  • 7.4 Gene Markers in Prostate Cancer
  • 7.5 Microarray Gene Identification of Prostate Biomarkers
  • 7.6 GEArray DNA Microarrays
  • 7.7 Vermillion' s Cancer Diagnostic Program
  • 7.8 Hepsin
  • 7.9 Matritech' s Prostate Cancer Program (NMP48)
  • 7.10 Gen-Probe' s PCA3 Assay 1
  • 7.11 Early Prostate Cancer Antigen-2 (EPCA-2)
  • 7.12 Mass Spectrometry
  • 7.13 Summary

8. Bladder Cancer

  • 8.1 Overview
    • 8.1.1 Prevalence
    • 8.1.2 Progression and Recurrence
    • 8.1.3 Bladder Cancer Risk Factors
    • 8.1.4 Bladder Cancer Symptoms
  • 8.2 Bladder Cancer Tests
  • 8.3 UroVysion Bladder Cancer Kit
  • 8.4 IkoniscopeR Robotic Digital Microscopy Platform
    • 8.4.1 The CellOptics Platform
    • 8.4.2 Cell Staining and Genetic Characterization
    • 8.4.3 Ikoniscope/IkoniLAN Automated Microscopy
  • 8.5 Nuclear Matrix Protein Markers
  • 8.6 ImmunoCyt™/uCyt+™
  • 8.7 Cangen Microsatellite DNA
  • 8.8 Bladder Cancer Market
    • 8.8.1 Urologist Market
    • 8.8.2 Clinical Lab Market
    • 8.8.3 Primary Care Market
    • 8.8.4 Private and Public Sector Markets
    • 8.8.5 POC Market
    • 8.8.6 Market Distribution
  • 8.8.7 Reimbursement

9. Colorectal Cancer

  • 9.1 Overview
    • 9.1.1 Prevalence
    • 9.1.2 Progression and Recurrence
  • 9.2 Screening for CRC
    • 9.2.1 Stool-based DNA Screening
  • 9.3 Almac Diagnostics DSA™
  • 9.4 Colon Cancer Program (NMP35)
  • 9.5 Myriad Genetics COLARIS AP Risk Assessment
  • 9.6 Summary

10. Genetic Diagnostics Set to Revolutionize Cancer Diagnostic Testing

  • 10.1 Overview
    • 10.1.1 Clinicians' Need for More Information with Regard to Therapeutic Treatment Drives Demand for Pharmacogenomic Testing
    • 10.1.2 Predictive Medicine Shows Potential for Genetic Diagnostics
    • 10.1.3 Different Rates of Growth
    • 10.1.4 Effective Competitive Strategies
    • 10.1.5 Improvements in Marketing Effectiveness
    • 10.1.6 Emerging Technologies Imply Start of a New Era and Offer Tremendous Growth Opportunities
    • 10.1.7 Increased Market Share
    • 10.1.8 Technologies Used in Genetic Testing
  • 10.2 AMAS Test
  • 10.3 Corixa (now GSK) Antibodies as Tumor Markers
  • 10.4 CytoVision
  • 10.5 Ariol System
  • 10.6 Mammaglobin Protein Expression
  • 10.7 L523S or KOC RNA Binding Protein
  • 10.8 CA1-18 from EDP Biotech Corporation

11. Leukemia Biomarkers

  • 11.1 Overview
    • 11.1.1 Prevalence
      • 11.1.1.1 Progression and Recurrence

12. Lung Cancer

13. Enabling Technologies for Oncology Biomarker Discovery

  • 13.1 Automated Cellular Imaging System (ACIS)
    • 13.1.1 ACIS for HER2 Protein Expression Testing
    • 13.1.2 ACIS for ER Protein Expression Testing
    • 13.1.3 ACIS for PR Protein Expression Testing
    • 13.1.4 ACIS for Cell Proliferation Expression
    • 13.1.5 ACIS for Protein Expression
    • 13.1.6 ACIS for Protein Micrometastases in Bone Marrow
    • 13.1.7 ACIS for Protein Micrometastases in Tissue
    • 13.1.8 ACIS for TMA
    • 13.1.9 ACIS for DNA Ploidy
    • 13.1.10 ACIS for HPV
  • 13.2 DNA Methylation
    • 13.2.1 DMH
    • 13.2.2 MIRA-Assisted Microarrays for DNA Methylation Analysis and Cancer Diagnosis
  • 13.3 Proteomics
    • 13.3.1 Proteomics Technologies for Cancer Marker Discovery
    • 13.3.2 Validation of Candidate Biomarkers
    • 13.3.3 Requirements Bringing a New Marker into the Market
    • 13.3.4 Value Chain in the Development of New Cancer Biomarkers
  • 13.4 Secreted Proteins as Cancer Biomarkers
    • 13.4.1 Markers of Known Tissue Origin
    • 13.4.2 Secreted Proteins as Low Abundance Markers
    • 13.4.3 Secreted Proteins in Tissue and Blood
  • 13.5 Non-coding RNAs as Potential Tumor Markers
    • 13.5.1 miRNA Meets Microarray
    • 13.5.2 Mimetics and Inhibitors
    • 13.5.3 Clinical Patterns in Cancer
  • 13.6 Architect TIMP-1 (Tissue Inhibitor of Metalloproteinases-1) Immunoassay for CRC Detection
  • 13.7 Companies Developing Automated Microscope-based Analysis Systems
  • 13.8 Companies Developing Research Products for Tumor Cell Isolation
  • 13.9 Companies Supplying Fluorescently Labeled Antibodies to Characterize Tumor Cells
  • 13.10 PerkinElmer High-Throughput Platforms: AlphaScreenR, AequoScreenR, DELFIAR and LANCER Technologies

14. Biomarker Tests Co-developed with Cancer Therapeutics as Companion Diagnostics

  • 14.1 Sector Overview
  • 14.2 Companion Diagnostics
  • 14.3 EGFR for CRC and Camptostar (Irinotecan)
  • 14.4 EGFR Express and Erbitux (Cetuximab)
  • 14.5 HER2 and Heceptin
  • 14.6 Myriad' s TheraGuide 5-Fluorouracil (5-FU)™
  • 14.7 TheraScreen: EGFR29
  • 14.8 Drivers and Barriers to Companion Diagnostics
  • 14.9 Partnerships with Pharma Companies to Identify Therapeutic Targets
  • 14.10 Future Developments for Companion Diagnostics

15. Companion Diagnostics and Personalized Medicine: Biology, Approaches, Pipeline and Regulatory Trends

  • 15.1 Scope of this Chapter
  • 15.2 Introduction to Companion Diagnostics and Personalized Medicine
  • 15.3 The Compelling Case for Personalized Medicine
  • 15.4 Drug Metabolism and Implications for Companion Diagnostics and Personalized Medicine
  • 15.5 Examples of Personalized Medicine
  • 15.6 Personalized Medicine and Companion Diagnostics Testing Product Pipeline
  • 15.7 The Personalized Medicine Coalition
  • 15.8 Regulatory Trends and Guidelines in the Personalized Medicine Space
  • 15.8.1 The Changing Regulatory Landscape for Personalized Medicine
  • 15.9 Patenting Personalized Medicine
  • 15.10 The Leading Edge of Personalized Medicine: Specific Examples of Clinical Situations Where Personalized Medicine and Companion Diagnostics are Appropriate and Being Deployed
    • 15.10.1 EGFR Assay
    • 15.10.2 Individualized Warfarin Therapy
    • 15.10.3 UGT1A1 Molecular Assay for Camptosar
    • 15.10.4 Response to Gleevec in Gastrointestinal Stromal Tumors
    • 15.10.5 LabCorp/ARCA Personalized Medicine Deal for Cardiovascular Diseases
    • 15.10.6 Osmetech Licenses Epidauros Biotechnologie AG CYP2D6 Biomarker to Push into Companion Diagnostics
  • 15.11 Companion Diagnostics and Personalized Medicine: Qualitative and Quantitative Market Analysis
    • 15.11.1 Market Analysis of Molecular Diagnostics and Companion Diagnostics and Personalized Medicine
    • 15.11.2 Diagnostics vs. Pharmaceuticals
    • 15.11.3 Molecular Diagnostic Market
    • 15.11.4 Molecular Diagnostics Technology Platforms and their Impact on Personalized Medicine
  • 15.12 Snapshot of Companion Diagnostics Industry Structure
  • 15.13 The Case for Theranostics (Therapeutic/Companion Diagnostic)
  • 15.14 Personalized Medicine Market Analysis - Market Survey Data Characterizing the Qualitative and Quantitative Industry Parameters
  • 15.15 How the Market Segregates Today
  • 15.16 Timeline for Impact of Various Segments in Personalized Medicine
  • 15.17 Challenges for Personalized Therapeutics and Companion Diagnostics Development
  • 15.18 Macro Trends in Personalized Medicine
  • 15.19 Personalized Medicine and Companion Diagnostics: Industry SWOT Analysis

16. Cancer Biomarker Testing Sector and Company Analysis

  • 16.1 Abbott Molecular, Inc.
  • 16.2 Agendia
  • 16.3 Agilent Technologies
  • 16.4 AMDL, Inc.
  • 16.5 Applied Biosystems
  • 16.6 Aureon Laboratories, Inc.
  • 16.7 BioCurex
  • 16.8 Biomarker Technologies
  • 16.9 Biomedical Diagnostics LLC
  • 16.10 Biomerica
  • 16.11 Biomira, Inc.
  • 16.12 Biomoda
  • 16.13 Byk Gulden
  • 16.14 Clarient (now a GE Healthcare Company)
  • 16.15 Correlogic Systems, Inc.
  • 16.16 Cytogen Corporation
  • 16.17 Dako (Formerly Dako Cytomation)
  • 16.18 diaDexus
  • 16.19 Diagnocure, Inc. (ImmunoCyt/uCyt+)
  • 16.20 DxS Ltd. (Acquired by QIAGEN)
  • 16.21 Epigenomics
  • 16.22 Exagen Diagnostics, Inc.
  • 16.23 Genesis Genomics
  • 16.24 Gen-Probe
  • 16.25 Health Discovery Corporation
  • 16.26 Illumina
  • 16.27 Immunicon
  • 16.28 Ipsogen
  • 16.29 InterGenetics
  • 16.30 Life Technologies
  • 16.31 Miraculins, Inc.
  • 16.32 Myriad Genetics, Inc.
  • 16.33 Orion Genomics
  • 16.34 Pacific Biosciences
  • 16.35 Power3 Medical Products
  • 16.36 Qiagen N.V.
  • 16.37 Roche Molecular Diagnostics
  • 16.38 SuperArray Bioscience Corporation (now SABiosciences)
  • 16.39 Upstream Biosciences, Inc.
  • 16.40 Ventana Medical Systems, Inc.
  • 16.41 Veridex
  • 16.42 Vermillion, Inc.

17. Business Trends in the Industry

  • 17.1 Industry Consolidation
  • 17.2 Breadth of Product Offering and Pricing
  • 17.3 Government Regulation of Medical Devices
  • 17.3.1 FDA Guidance on Drug Test Co-development
  • 17.4 Strategic Business and Marketing Considerations
  • 17.5 Commercial Opportunities in Cancer Markers
    • 17.5.1 Licensing and Intellectual Property Constraints and how they will Impact New Product Development
  • 17.6 Moderators of Growth
    • 17.6.1 Roadblocks to Integrating Cancer Biomarkers into Clinical Practice
  • 17.7 Biotechnology Industry Trends
  • 17.8 Pharmaceutical Industry Trends
  • 17.9 Sales and Marketing Strategies for Tumor Marker Tests
    • 17.9.1 North American Market
    • 17.9.2 International Markets
      • 17.9.2.1 Europe
      • 17.9.2.2 Central and South America
      • 17.9.2.3 Asia/Pacific
  • 17.10 Product Commercialization
  • 17.11 Reimbursement
  • 17.12 Self Referral Rules
  • 17.13 Health Insurance Portability and Accountability Act
  • 17.14 Clinical Laboratory Improvement Amendments
  • 17.15 In-Vitro Diagnostic Directive and Medical Device Regulations
  • 17.16 FDA' s Quality System Regulation
  • 17.17 FDA' s OIVD on IVDMIAs
  • 17.18 FDA' s Qualification of Cancer Biomarkers
    • 17.18.1 Regulatory Perspectives of Biomarker Validation
  • 17.19 Genetic Tests and Medical Records
    • 17.19.1 Laws against Genetic Discrimination
  • 17.20 Medicare Reimbursement
    • 17.20.1 Medicare Spending Trends
  • 17.21 Global Drivers of Clinical Laboratory Testing
  • 17.22 Global Outlook for Cancer Biomarkers
    • 17.22.1 Which Companies are Utilizing Cutting-Edge Technologies to Develop, Validate and Implement Cancer Biomarkers for Clinical Use?
    • 17.22.2 What Impediments Still Exist to Incorporating Promising Research into Clinical Practice?
    • 17.22.3 Which Biomarkers Show the Most Promise for Approval?
    • 17.22.4 How can Regulatory Oversight Drive Approval and Adoption of New Technologies?
    • 17.22.5 Which Alliances Show the Greatest Synergy in Bringing Valid Biomarkers to Market?
    • 17.22.6 Which Shared Technologies are Driving the Most Encouraging Development?
    • 17.22.7 How Strategic Alliances and Interdisciplinary Involvement Drive Development and Implementation of Emerging Biomarker Technologies
  • 17.23 Oncology Biomarker Qualification Initiative
  • 17.24 FDA Critical Path
  • 17.25 FDA Criteria for a Valid Biomarker

18. Companies Entering the Cancer Diagnostics Market with Novel Technology Platforms

  • 18.1 Abbott Diagnostics
  • 18.2 Affymetrix, Inc.
  • 18.3 Agendia BV
  • 18.4 Agensys, Inc.
  • 18.5 Agilent Technologies
  • 18.6 Almac Group
  • 18.7 AMDL, Inc.
  • 18.8 Aureon Laboratories, Inc.
  • 18.9 Bayer Diagnostics Corporation
  • 18.10 Beckman Coulter, Inc.
  • 18.11 Biocode Hycel S.A.
  • 18.12 BioCurex, Inc.
  • 18.13 Biomarker Technologies LLC
  • 18.14 Biomedical Diagnostics LLC
  • 18.15 Biomerica
  • 18.16 bioMerieux
  • 18.17 Biomira, Inc.
  • 18.18 Biomoda, Inc.
  • 18.19 Bruker Daltonics, Inc.
  • 18.20 Byk Gulden
  • 18.21 Cangen Biotechnologies, Inc.
  • 18.22 Caprion Proteomics
  • 18.23 Celera Diagnostics
  • 18.24 Cepheid
  • 18.25 Clarient, Inc.
  • 18.26 Claros Diagnostics, Inc.
  • 18.27 Clinical Data, Inc.: PGxHealth and Cogenics
  • 18.28 Correlogic Systems, Inc.
  • 18.29 CytoCore (Formerly Molecular Diagnostics, Inc.)
  • 18.30 Cytogen Corporation
  • 18.31 Dako (Formerly Dako Cytomation)
  • 18.32 diaDexus LLC
  • 18.33 DiagnoCure, Inc.
  • 18.34 Diagnostic Products Corporation (now Siemens)
  • 18.35 Diagnostic Systems Laboratories, Inc.
  • 18.36 DRG International, Inc.
  • 18.37 DxS Ltd. (Acquired by Qiagen)
  • 18.38 EDP Biotech Corporation
  • 18.39 Eisai Co., Ltd.
  • 18.40 Epigenomics
  • 18.41 Exact Sciences Corporation
  • 18.42 Exagen Diagnostics, Inc.
  • 18.43 Gene Logic, Inc.
  • 18.44 Genesis Genomics, Inc. (Mitomics)
  • 18.45 Genomic Health, Inc.
  • 18.46 Gen-Probe, Inc.
  • 18.47 Health Discovery Corporation
  • 18.48 Hologic, Inc. (Formerly Cytyc Corporation)
  • 18.49 Ikonisys, Inc.
  • 18.50 Illumina
  • 18.51 Immunicon Corporation
  • 18.52 Immunomedics, Inc.
  • 18.53 Incyte Pharmaceuticals, Inc.
  • 18.54 InterGenetics
  • 18.55 Ipsogen
  • 18.56 LabCorp
  • 18.57 Life Technologies Corporation
  • 18.58 Matritech, Inc.
  • 18.59 Miraculins, Inc.
  • 18.60 Mitsubishi Kagaku Medical
  • 18.61 Myriad Genetics, Inc.
  • 18.62 NimbleGen Systems, Inc.
  • 18.63 Northwest Biotherapeutics, Inc.
  • 18.64 Oncotech, Inc.
  • 18.65 Orion Genomics
  • 18.66 Oxford BioTherapeutics
  • 18.67 Pacific Biosciences
  • 18.68 Panacea Pharmaceuticals, Inc.
  • 18.69 Polymedco, Inc.
  • 18.70 Power3 Medical Products
  • 18.71 Proteome Systems Ltd.
  • 18.72 Qiagen N.V.
  • 18.73 Roche Diagnostics
  • 18.74 Upstream Biosciences, Inc.
  • 18.75 Ventana Medical Systems, Inc.
  • 18.76 Veridex LLC
  • 18.77 Vermillion, Inc. (Formerly Ciphergen)

Appendix 1: Cancer Biomarker Centers of Research

Appendix 2: Myriad Patents on Genes BRCA-1 and BRCA-2

Appendix 3: Cancer Markers Currently in Common Clinical Use

Appendix 4: International Federation of Gynecology and Obstetrics (FIGO) Staging System for Primary Carcinoma of the Ovary

Appendix 5: FDA Guidance for Industry: Pharmacogenomic Data Submission

  • A5.1 Introduction
  • A5.2 Background
  • A5.3 Submission Policy
  • A5.3.1 General Principles
  • A5.3.2 Specific Uses of Pharmacogenomic Data in Drug Development and Labeling
  • A5.3.3 Benefits of Voluntary Submissions to Sponsors and FDA
  • A5.4 Submission of Pharmacogenomic Data
  • A5.4.1 Submission of Pharmacogenomic Data During the IND Phase
  • A5.4.2 Submission of Pharmacogenomic Data to a New NDA, BLA or Supplement
  • A5.4.3 Submission to a Previously Approved NDA or BLA
  • A5.4.4 Compliance with 21 CFR Part 58
  • A5.4.5 Submission of Voluntary Genomic Data from Application-Independent Research
  • A5.5 Format and Content of a VGDS
  • A5.6 Process for Submitting Pharmacogenomic Data
  • A5.7 Agency Review of VGDSs

Glossary

INDEX OF FIGURES

  • Figure 3.1: Potential Market for Cancer Biomarkers
  • Figure 3.2: Segmentation of the Cancer Biomarkers Marketplace Based on Commercial Offerings - Products and Services
  • Figure 3.3: Geographical Distribution of Cancer Tumor Diagnostic Testing
  • Figure 3.4: Cancer Biomarkers Research Market, 2006-2016
  • Figure 3.5: Breast Cancer Biomarker Market Potential, 2010
  • Figure 3.6: Challenges in the Study or Utilization of Proteomic Cancer Biomarkers
  • Figure 3.7: Challenges in the Study or Utilization of Companion Diagnostic Cancer Biomarkers
  • Figure 3.8: Challenges in the Study or Utilization of Serum Cancer Markers
  • Figure 3.9: Top Unmet Needs in Commercial Products in the Cancer Biomarkers Space
  • Figure 5.1: Hybridization Process
  • Figure 5.2: FISH Test Procedure
  • Figure 5.3: Gene Expression Profiling
  • Figure 15.1: Phase I and II Processes of Drug Metabolism
  • Figure 15.2: Human Phase I Enzymes
  • Figure 15.3: Human Phase II Enzymes
  • Figure 15.4: Hepatic Distribution of Human CYP450
  • Figure 15.5: Relative Contribution of CYP450 Enzymes to Drug Metabolism
  • Figure 15.6: Genetic Components Determine Drug Metabolism
  • Figure 15.7: From Genetic Content to Personalized Medicine
  • Figure 15.8: Remuneration for Diagnostics
  • Figure 15.9: Breakout of the Molecular Diagnostics Marketplace
  • Figure 15.10: Molecular Diagnostics Market Segmentation
  • Figure 15.11: Molecular Diagnostics Market Segmentation by Technology
  • Figure 15.12: Market Survey Respondent Demographics
  • Figure 15.13: Breakout of the Respondent Pool by Affiliation
  • Figure 15.14: Segmentation of the Personalized Medicine Market
  • Figure 15.15: Personalized Medicine Market Drivers
  • Figure 15.16: Challenges in the Personalized Medicine Space
  • Figure 16.1: Epigenomics Product Development Pipeline
  • Figure 17.1: Medicare Spending on Clinical Laboratory Services per Enrollee, 2000-2010

INDEX OF TABLES

  • Table 2.1: Cancer Biomarkers at the Nexus Point
  • Table 2.2: Drug Development by Type of Cancer
  • Table 2.3: Organ-Specific Medicines in Development for Cancer
  • Table 2.4: Estimates for the Leading Types of New Cancer Cases and Deaths in the U.S. by Sex
  • Table 2.5: Estimated New Cancer Cases and Deaths by Sex for All Types of Cancer
  • Table 2.6: New Cancer Cases and Associated Deaths by World Region
  • Table 2.7: Cancer Death Rates per 100,000 Population (and Rank) for All Cancer Sites by Country
  • Table 2.8: Cancer Associated Genes
  • Table 2.9: Carcinogens in the Workplace
  • Table 2.10: Cancer Biomarker Markets
  • Table 2.11: Private Funding for Biotechnology and Medical Devices and Equipment, 1999-2010, U.S.
  • Table 2.12: Global Pharmaceutical Industry R&D Spending, 1995-2010
  • Table 2.13: U.S. Government NIH Research Budget, 1995 to 2011
  • Table 2.14: Tumor Markers Currently in Common Use
  • Table 2.15: Herceptin Worldwide Sales, 2000 to 2016
  • Table 2.16: Classes of Drugs Used to Treat Breast Cancer
  • Table 2.17: Solutions to Biomarker Developments
  • Table 2.18: Vermillion Collaborations
  • Table 2.19: Uses of Molecular Diagnostics in Detection and Management of Cancer
  • Table 2.20: U.S. Cancer Diagnostic Testing Market Size, 2005-2016
  • Table 2.21: Market Opportunities for Cancer Biomarker Technology Platforms
  • Table 3.1: Characteristics of Different Cancer Biomarker Types and Associated Market Opportunities
  • Table 3.2: Segmentation of the Cancer Biomarker Market by Type/Lineage of Cancer Biomarkers and Market Size
  • Table 3.3: In Vitro Cancer Marker Market Segments Worldwide, 2012
  • Table 3.4: Worldwide Market Size in Dollar Volume for Tumor Marker Assays Product Market, 2001-2016
  • Table 3.5: U.S. Market Size in Dollar Volume for Tumor Marker Assays Product Market, 2001-2016
  • Table 3.6: Worldwide In Vitro Cancer Tumor Marker Diagnostics Market Size, 2001-2016
  • Table 3.7: U.S. In Vitro Cancer Tumor Marker Diagnostics Market Size, 2001-2016
  • Table 3.8: Japanese In Vitro Cancer Tumor Marker Diagnostics Market Size, 2001-2016 58
  • Table 3.9: European In Vitro Cancer Tumor Marker Diagnostics Market Size, 2001-2016
  • Table 3.10: Global Distribution of IVD Cancer Tumor Marker Diagnostic Testing, 2010
  • Table 3.11: Estimated Market Share of Major Competitors in U.S. Cancer Tumor Marker Diagnostics Market
  • Table 3.12: Major Presence in Cancer Tumor Marker Diagnostics Markets 60
  • Table 3.13: Worldwide CEA Sales, 2001-2016
  • Table 3.14: U.S. CEA Sales, 2001-2016
  • Table 3.15: Cancer Genomic Biomarker Markets, 2002-2016
  • Table 3.16: Cancer Biomarkers Research Market Forecast, 2006-2016
  • Table 3.17: Cancer Biomarker Market Estimates by Tissue of Origin
  • Table 3.18: Companies Developing New Proteomic Cancer Biomarker Technology Platforms
  • Table 4.1: Cancer Biomarkers Used to Maximize Likelihood of Response
  • Table 4.2: Biomarkers for Monitoring Therapeutic Effectiveness and Resistance
  • Table 4.3: Biomarkers for Dose Response of Therapy
  • Table 4.4: Decision on Optimal Duration of Therapy
  • Table 5.1: Number of New Breast Cancer Patients in the U.S., 2005-2010
  • Table 5.2: BRCA Development Model
  • Table 5.3: BRCA Test Development and Commercialization
  • Table 5.4: BRAC Analysis
  • Table 5.5: Revenue for BRACAnalysis Risk Assessment Test, 2002-2011
  • Table 5.6: GEArray DNA Microarrays and RT2 Profiler PCR Arrays
  • Table 5.7: Product Development Opportunities in Breast Cancer
  • Table 5.8: Concentration of Some Abundant Proteins, New Cancer Biomarkers Identified by SELDI-TOF and Classical Cancer Biomarkers in Serum
  • Table 5.9: Questions Related to Diagnostic SELDI-TOF Technology
  • Table 6.1: Worldwide CA-125 Sales, 2001-2016
  • Table 6.2: U.S. CA-125 Sales, 2001-2016
  • Table 6.3: Some Clinically Established Cancer Serum Markers Currently in Use for Cancer
  • Table 6.4: Pathophysiology of Ovarian Cancer and Characterization of Ovarian Epithelial Tumors
  • Table 7.1: Worldwide PSA Sales, 2000-2016
  • Table 7.2: U.S. PSA Sales, 2000-2016
  • Table 7.3: Molecular Gene Markers for Prostate Cancer
  • Table 8.1: Worldwide Bladder Cancer Marker Sales, 2001-2016
  • Table 8.2: U.S. Bladder Cancer Marker Sales, 2001-2016
  • Table 8.3: Worldwide NMP22 Sales, 2001-2016
  • Table 8.4: Summary of Matritech' s Product Development Programs
  • Table 8.5: Opportunities for Bladder Cancer Biomarkers 151
  • Table 9.1: TNM Staging for CRC
  • Table 10.1: Genetic Diagnostics Market, 2004-2016
  • Table 13.1: Genomic and Proteomic Technologies
  • Table 14.1: Potential Benefits of Biomarkers as Companion Diagnostics
  • Table 14.2: Utility of Biomarker as Companion Diagnostics to Dru Development
  • Table 14.3: Device Submission Elements for the FDA
  • Table 14.4: Summary of Biomarker Use in the Commercialization of Novel Oncology Pharmacotherapeutics
  • Table 14.5: Pharmacoeconomic Challenges to the Implementation of Biomarkers as Companion Diagnostic Tests
  • Table 15.1: Percentage of Non-Responders in Various Drug Classes
  • Table 15.2: High Profile Drug Withdrawals from the Marketplace
  • Table 15.3: Drug Metabolism Drives Drug Efficacy/Toxicity
  • Table 15.4: Population Frequency of the Various Cytochromes
  • Table 15.5: Selected List of Personalized Medicine Tests
  • Table 15.6: Personalized Medicine and Companion Diagnostics Product Pipeline
  • Table 15.7: Marketed Personalized Therapies
  • Table 15.8: Members of the Personalized Medicine Coalition
  • Table 15.9: Various Molecular Diagnostics Technologies: Timeline for Impact
  • Table 15.10: Various Molecular Diagnostics Technologies: Impact on Different Therapeutic Areas in Personalized Medicine
  • Table 15.11: Technical Challenges in the Deployment for Personalized Medicine
  • Table 15.12: Classification of Diagnostics by Risk
  • Table 15.13: Areas in Personalized Medicine - Timeline of Impact
  • Table 15.14: Impact of Personalized Medicine on Various Therapeutic Areas
  • Table 15.15: Hurdles in Personalized Medicine and Companion Diagnostics Development in Various Therapeutic Areas
  • Table 15.16: Market Opportunities in Personalized Medicine
  • Table 15.17: Challenges for Market Adoption of the Various Personalized Medicine Tests
  • Table 15.18: Personalized Medicine Industry SWOT
  • Table 16.1: Opportunities for Biomarkers in Cancer Diagnosis and Treatment
  • Table 17.1: List and Discounted Prices for Abbott Tumor Marker Tests
  • Table 17.2: Increases in Total Allowed Charges for Laboratory Services per Enrollee, 2000-2010
  • Table 17.3: Incurred Reimbursement Amounts for Laboratory Services, 2000-2010
  • Table 17.4: Medicare Part B Benefit Payments, 2003-2010
  • Table 18.1: Tumor Diagnosis Immunoassay
  • Table 18.2: Tumor Diagnosis Radioimmunoassay
  • Table 18.3: Summary of Matritech' s Product Development Programs
  • Table A1: Team Descriptions
  • Table A3: Cancer Markers in Use
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