Companion Diagnostic Tests in Oncology Market Size is Set to Achieve USD 17.0 Billion by 2034, with 9.5% CAGR: Transparency Market Research Inc.

Transparency Market Research
Transparency Market Research

Exploration of novel biomarkers beyond traditional genetic mutations expands the scope of companion diagnostic tests in oncology.

Wilmington, Delaware, United States, Transparency Market Research, Inc. , Sept. 09, 2024 (GLOBE NEWSWIRE) -- The global companion diagnostic tests in oncology market (الاختبارات التشخيصية المصاحبة في سوق الأورام) is estimated to flourish at a CAGR of 9.5% from 2024 to 2034. Transparency Market Research projects that the overall sales revenue for companion diagnostic tests in oncology is estimated to reach US$ 17.0 billion by the end of 2034.

Liquid biopsy technologies are gaining traction, offering non-invasive methods to detect tumor-specific biomarkers. This approach holds promise for early cancer detection and monitoring treatment response. The incorporation of AI and machine learning algorithms enhances the interpretation of genomic data from companion diagnostic tests, improving diagnostic accuracy and personalized treatment recommendations.

Increased patient engagement and advocacy efforts are influencing market dynamics. Patients are demanding access to comprehensive genomic profiling and involvement in treatment decisions, driving demand for companion diagnostic tests. The digital transformation of healthcare systems facilitates the integration of companion diagnostic tests into electronic health records (EHRs) and clinical decision support systems, streamlining testing processes and improving accessibility.

The COVID-19 pandemic has underscored the importance of diagnostic testing and accelerated the adoption of telemedicine and remote monitoring solutions, potentially influencing the uptake of companion diagnostic tests in oncology.

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Companion Diagnostic Tests in Oncology Market: Competitive Landscape

In the dynamic realm of oncology, companion diagnostic tests play a pivotal role in guiding personalized treatment decisions. The market is fiercely competitive, with key players like Roche Diagnostics, Agilent Technologies, and Foundation Medicine dominating. Roche's extensive CDx portfolio, including the FDA-approved Ventana assays, underscores its leadership. Agilent Technologies' precision oncology solutions and Foundation Medicine's comprehensive genomic profiling services pose formidable competition.

Emerging players like Guardant Health and Thermo Fisher Scientific intensify the landscape with innovative liquid biopsy and NGS technologies. This competitive environment fosters innovation, driving advancements in precision medicine and ultimately improving outcomes for cancer patients globally. Some prominent players are as follows: