DUBLIN, June 23, 2022 /PRNewswire/ -- The "Lung Cancer Genomic Testing Market - A Global and Regional Analysis: Focus on Product, Technology, Panel Type, Sample Type, and End User - Analysis and Forecast, 2021-2031" report has been added to ResearchAndMarkets.com's offering.
The lung cancer genomic testing medicine market was valued at $1,262.0 million in 2020 and is expected to reach $3,279.8 million by 2031, growing at a CAGR of 8.97% during the forecast period 2021-2031. The growth in the global lung cancer genomic testing market is expected to be driven by increasing awareness and adoption of the lung cancer genomic testing market, recent launches of novel lung cancer genomic testing, and the expanding research in the field of lung cancer with an emphasis on pharmacogenomics and development of companion diagnostics. The global lung cancer genomic testing market is expected to be dominated by North America, generating the highest revenue of $713.5 million. This is owing to the presence of a large number of research organizations and products and services companies in the U.S. The global lung cancer genomic testing market is still in the nascent phase. Various companies are increasing investments in research and development to facilitate the development of lung cancer genomic testing, which is expected to further increase the adoption of lung cancer genomic tests. The shift of healthcare systems toward precision diagnostic and precision medicine will drive the adoption of lung cancer genomic testing facilitating informed treatment decision making and improving healthcare outcomes. Increasing recommendations by the international oncology societies for the use of genomic testing for lung cancer diagnosis provides major opportunities in the global lung cancer genomic testing market. The presence of major in-vitro diagnostics (IVD) product providers of lung cancer genomic tests in regions such as North America and Europe has a major impact on the market. For instance, Qiagen provides therascreen Solid Tumor assays, a real-time polymerase chain reaction (PCR) test for EGFR detection in non-small cell lung cancer (NSCLC) patients. Additionally, Roche provides Cobas EGFR Mutation Test, a PCR-based test, and FoundationOne CDx by Foundation Medicine Inc., which is a next-generation sequencing (NGS) based assay for NSCLC. The presence of major laboratory developed tests (LDTs) service providers companies offer lung cancer genomic testing in regions such as North America and Europe, which has a major impact on the market. The LDTs are offered by Quest Diagnostics and Laboratory Corporation of America (Labcorp), targeting various lung cancer genes, for example, EGFR, MET, ALK, and ROS, based on Fluorescence in situ Hybridization (FISH) and NGS. The presence of these companies has a positive impact on market growth. The global lung cancer genomic testing market is dominated by the utility in diagnostic laboratories, hospitals, and clinics. During the beginning of the COVID-19 pandemic, multiple countries witnessed a complete or a partial lockdown, and all elective surgeries and procedures were halted in the healthcare settings. Since the lung cancer genomic testing is categorized under the elective procedure, the impact of the COVID-19 pandemic on the lung cancer genomic testing was negative. BIS Research analysis has concluded that the market witnessed a drop of 3.24% in the annual growth rate of global lung cancer genomic testing market. Product Type (Products, Services)
The global lung cancer genomic testing market services segment is expected to be dominated. This is owing to the easy availability, accessibility, and adaptation of LDTs, due to lower cost when compared with the product's market consisting of IVD. The global lung cancer genomic testing market by polymerase chain reaction (PCR) is expected to be dominated. This is owing to the overall cost efficiency and high sensitivity of the PCR-based genomic test for the detection of disease-causing mutations in lung cancer. Sample Type (Tissue Biopsy, Liquid Biopsy)
The global lung cancer genomic testing market by tissue biopsy sample type is expected to be dominated. This is owing to the standard healthcare practice of extracting a lung tissue biopsy for lung cancer diagnosis, which is further utilized for lung cancer genomic testing. Panel Type (Multi-Gene Panel, Single-Gene Panel)
The global lung cancer genomic testing market by multi-gene panel type is expected to be dominated. This is owing to the standard healthcare practice and familiarity of healthcare professionals with the extraction of lung tissue biopsy for lung cancer diagnosis, which is further utilized for lung cancer genomic testing. End User (Research Organization, Hospitals/Clinics, Diagnostic Laboratories, Other End Users)
The global lung cancer genomic testing market by research organization end user is expected to be dominated. This is owing to a large number of clinical research and academic organizations where lung cancer genomic testing is utilized for drug development, development of companion diagnostics, and enrolment of patients in clinical trials. Recent Developments in Global Lung Cancer Genomic Testing Market In September 2021, FDA approved Thermo Fisher Scientific's tissue-based NGS companion diagnostic for Takeda's targeted therapy for NSCLC patients with EGFR Exon20 insertion mutations- Oncomine Dx Target Test now approved as CDx for five targeted NSCLC therapies in the U.S. In May 2021, Qiagen launched the first FDA-approved tissue companion diagnostic to identify the KRAS G12C mutation in NSCLC tumors and expanded precision medicine options in lung cancer. Key Market Players and Competition Synopsis
2.4.1 Disruption in Global Lung Cancer Genomic Testing Market: Pre- and Post-COVID-19 Market Analysis 2.4.3 Interruption in Research and Clinical Development and Commercial Operation
2.4.4 Navigating Crisis Recovery and Looking to the Future
3.1 Global Legal Requirements and Regulations
3.1.1 Legal Requirements and Frameworks in the U.S.
3.1.1.1 Centers for Medicare & Medicaid Services Regulation
3.1.2 Legal Requirements and Frameworks in Europe
3.1.3 Legal Requirements and Frameworks in Asia-Pacific
3.1.4 Latin America (Brazil and Mexico)
3.2.1 Patent Filing Trend
3.2.2 Patent Analysis by Country
3.2.3 Patent Analysis by Technology
4.3.2 Advancements in the Next-Generation Technologies for Genomic Testing
4.3.3 Increasing Number of Targeted Therapies
4.3.4 Decreasing Cost of Genetic Testing Globally
4.4 Market Restraining Factors
4.4.1 Uncertain Regulatory Scenario for Genomic Testing
4.4.2 Lack of Viable Tissue Biopsy Sample
4.4.3 Uneven Reimbursement Scenario for Genomic Testing
4.5.1 Improving Global Recommendations for Lung Cancer Genomic Testing 4.5.1.1 American Society of Clinical Oncology (ASCO) Recommendations
4.5.1.2 European Society of Clinical Oncology (ESMO) Recommendations
4.5.1.3 Pan-Asia Clinical Practical Guidelines
4.5.2 Rising Investment in Research and Development
5.1 Key Strategies and Developments
5.1.1 Synergistic Activities
5.1.2 Regulatory Approvals
5.1.3 Product Launches and Upgradations
5.1.4 Mergers and Acquisitions
5.1.7 Market Share Analysis by Company
5.1.8 Growth-Share Analysis by Company
6 Global Lung Cancer Genomic Testing Market, (by Product Type), $Million, 2020-2031 7 Global Lung Cancer Genomic Testing Market, (by Technology), $Million, 2020-2031 7.3 Polymerase Chain Reaction (PCR)
7.4 Fluorescence In Situ Hybridization (FISH)/In Situ Hybridization (ISH)
8 Global Lung Cancer Genomic Testing Market, (by Panel Type), $Million, 2020-2031 9 Global Lung Cancer Genomic Testing Market, (by Sample Type), $Million, 2020-2031 10 Global Lung Cancer Genomic Testing Market, (by End User), $Million, 2020-2031 10.2 Research Organization
11 Global Lung Cancer Genomic Testing Market (by Region), $Million, 2020-2031 12.2 Role in the Global Lung Cancer Genomic Testing Market For more information about this report visit https://www.researchandmarkets.com/r/4wzxg4
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