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全球肿瘤学伴随诊断测试市场研究报告 - 2024 年至 2032 年行业分析、规模、份额、成长、趋势和预测Global Companion Diagnostic Tests in Oncology Market Research Report - Industry Analysis, Size, Share, Growth, Trends and Forecast 2024 to 2032 |
预计到 2032 年,全球肿瘤市场伴随诊断测试的市场规模将从 2023 年的 58.9 亿美元达到近 139.9 亿美元,2024-2032 年研究期间复合年增长率为 10.09%。
肿瘤学中的伴随诊断测试旨在识别与患者的癌症诊断或预后相关的特定生物标记或分子标靶。这些测试与标靶癌症疗法一起使用,以个性化治疗决策、预测治疗反应并监测疾病进展。这些测试分析生物样本,如组织活检、血液样本或循环肿瘤 DNA,以检测基因突变、基因扩增、蛋白质表现量或其他指示癌症亚型、分期或治疗反应的分子变化。透过提供有关患者肿瘤生物学的可行信息,伴随诊断测试使肿瘤学家能够在精准肿瘤学实践中製定治疗策略、优化治疗选择并改善患者的治疗效果。
全球癌症的流行,加上分子生物学和基因组学的进步,正在推动用于个人化癌症治疗的伴随诊断测试的开发和采用。此外,对精准医疗和基于价值的医疗保健的日益重视推动了对辅助诊断测试的需求,这些测试有助于优化治疗结果、最大限度地减少不良反应并降低医疗成本。此外,监管机构简化药物审批流程和鼓励标靶治疗开发的措施正在推动对伴随诊断测试开发和商业化的投资。此外,製药公司、诊断实验室和研究机构之间的合作和伙伴关係推动创新并加速针对新兴生物标记和治疗标靶的伴随诊断测试的开发。此外,液体活检和新一代定序 (NGS) 技术的日益普及正在扩大伴随诊断测试的范围和能力,从而能够对肿瘤进行非侵入性和全面的分析,以实现精准肿瘤学应用。然而,不断变化的监管环境和报销挑战可能会对未来几年肿瘤学市场成长的伴随诊断测试提出挑战。
研究报告涵盖波特五力模型、市场吸引力分析和价值链分析。这些工具有助于清晰地了解行业结构并评估全球范围内的竞争吸引力。此外,这些工具还对全球肿瘤学伴随诊断测试市场的每个细分市场进行了包容性评估。肿瘤学产业伴随诊断测试的成长和趋势为这项研究提供了整体方法。
肿瘤学市场报告中的伴随诊断测试的这一部分提供了国家和区域层面细分市场的详细资料,从而帮助策略师确定相应产品或服务的目标人群以及即将到来的机会。
本节涵盖区域前景,重点介绍北美、欧洲、亚太地区、拉丁美洲以及中东和非洲肿瘤学伴随诊断测试市场当前和未来的需求。此外,该报告重点关注所有主要地区各个应用领域的需求、估计和预测。
该研究报告还涵盖了市场主要参与者的全面概况以及对全球竞争格局的深入了解。肿瘤伴随诊断测试市场的主要参与者包括 Abbott、F. Hoffmann-LA Roche AG、Genomic Health, Inc.、Qiagen、Agilent Technologies, Inc.、Agendia NV、bioMerieux SA、Illumina, Inc.、Siemens Healthineers、赛默飞世尔科技公司、BioGenex。本节包含竞争格局的整体视图,包括各种策略发展,例如关键併购、未来产能、合作伙伴关係、财务概况、合作、新产品开发、新产品发布和其他发展。
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The global demand for Companion Diagnostic Tests in Oncology Market is presumed to reach the market size of nearly USD 13.99 Billion by 2032 from USD 5.89 Billion in 2023 with a CAGR of 10.09% under the study period 2024 - 2032.
Companion diagnostic tests in oncology are designed to identify specific biomarkers or molecular targets associated with a patient's cancer diagnosis or prognosis. These tests are used with targeted cancer therapies to personalize treatment decisions, predict treatment response, and monitor disease progression. These tests analyze biological samples such as tissue biopsies, blood samples, or circulating tumor DNA to detect genetic mutations, gene amplifications, protein expression levels, or other molecular alterations indicative of cancer subtype, stage, or treatment response. By providing actionable information about a patient's tumor biology, companion diagnostic tests enable oncologists to tailor treatment strategies, optimize therapy selection, and improve patient outcomes in precision oncology practice.
The spurring prevalence of cancer worldwide, coupled with advancements in molecular biology and genomics, is driving the development and adoption of companion diagnostic tests for personalized cancer treatment. Additionally, the escalating emphasis on precision medicine and value-based healthcare drives demand for companion diagnostic tests that help optimize treatment outcomes, minimize adverse effects, and reduce healthcare costs. Moreover, regulatory agencies' initiatives to streamline drug approval processes and encourage the development of targeted therapies are driving investment in companion diagnostic test development and commercialization. Furthermore, collaborations and partnerships between pharmaceutical companies, diagnostic laboratories, and research institutions drive innovation and accelerate the development of companion diagnostic tests for emerging biomarkers and therapeutic targets. Additionally, the growing adoption of liquid biopsy and next-generation sequencing (NGS) technologies is expanding the scope and capabilities of companion diagnostic tests, enabling non-invasive and comprehensive profiling of tumors for precision oncology applications. However, the evolving regulatory landscape and reimbursement challenges may challenge the companion diagnostic tests in oncology market growth in the coming years.
The research report covers Porter's Five Forces Model, Market Attractiveness Analysis, and Value Chain analysis. These tools help to get a clear picture of the industry's structure and evaluate the competition attractiveness at a global level. Additionally, these tools also give an inclusive assessment of each segment in the global market of companion diagnostic tests in oncology. The growth and trends of companion diagnostic tests in oncology industry provide a holistic approach to this study.
This section of the companion diagnostic tests in oncology market report provides detailed data on the segments at country and regional level, thereby assisting the strategist in identifying the target demographics for the respective product or services with the upcoming opportunities.
This section covers the regional outlook, which accentuates current and future demand for the Companion Diagnostic Tests in Oncology market across North America, Europe, Asia-Pacific, Latin America, and Middle East & Africa. Further, the report focuses on demand, estimation, and forecast for individual application segments across all the prominent regions.
The research report also covers the comprehensive profiles of the key players in the market and an in-depth view of the competitive landscape worldwide. The major players in the Companion Diagnostic Tests in Oncology market include Abbott, F. Hoffmann-LA Roche AG, Genomic Health, Inc., Qiagen, Agilent Technologies, Inc., Agendia N.V., bioMerieux SA, Illumina, Inc., Siemens Healthineers, Thermo Fisher Scientific Inc., BioGenex. This section consists of a holistic view of the competitive landscape that includes various strategic developments such as key mergers & acquisitions, future capacities, partnerships, financial overviews, collaborations, new product developments, new product launches, and other developments.
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