What is Cervical Cancer Diagnostic Tests Market?
Cervical cancer is a type of cancer that occurs in the cells of the cervix, the lower part of the uterus that connects to the vagina. Finding cervical cancer often starts with an abnormal HPV (human papillomavirus) or Pap test result. This will lead to further tests that can diagnose cervical cancer or pre-cancer. In the next stage colposcopy and biopsy are used to further confirm the furthers. The cervical cancer diagnostic test market is witnessing considerable growth in the future due to advancements in computer-guided cervical cancer tests to minimize false-negative tests and increasing the adoption of at-home screening services.
Highlights from Cervical Cancer Diagnostic Tests Market Study
Attributes | Details |
---|
Study Period | 2018-2028 |
Base Year | 2022 |
Unit | Value (USD Million) |
Key Companies Profiled | Abbott Laboratories (United States), BD Medical (United States), Roche Molecular Diagnostics (United States), Hologic (United States), Qiagen (Germany), Quest Diagnostics (United States), BioMerieux (France), Cepheid (United States), Arbor Vita (United States), Trovagene (United States) and DaAn Gene (China) |
The increasing cases of Cervical Cancer growing the need for its testing tools in the market. The leading firms are coming with newly enhanced products with technological advancements increasing the competition between rivalries. Mergers and acquisitions have been changing business strategies in the market. Research Analyst at AMA predicts that United States Players will contribute to the maximum growth of Global Cervical Cancer Diagnostic Tests market throughout the forecasted period.
Abbott Laboratories (United States), BD Medical (United States), Roche Molecular Diagnostics (United States), Hologic (United States), Qiagen (Germany), Quest Diagnostics (United States), BioMerieux (France), Cepheid (United States), Arbor Vita (United States), Trovagene (United States) and DaAn Gene (China) are some of the key players profiled in the study. Additionally, the Players which are also part of the research are Delphi Bioscience (Singapore) and Fujirebio Diagnostics (United States). Cervical Cancer Diagnostic Tests Market Segmentation:
Scope | Sub-Segments |
---|
Application / End User | Hospitals, Specialty Clinics, Cancer and Radiation Therapy Centers, Diagnostic Centers, Homecare and Others |
Type | Pap Test, HPV Typing Test, Colposcopy, Biopsy and Bimanual Pelvic Examination |
Age Group | Age 20 - 40,Age above 40 |
On the basis of geography, the market of Cervical Cancer Diagnostic Tests has been segmented into South America (Brazil, Argentina, Rest of South America), Asia Pacific (China, Japan, India, South Korea, Taiwan, Australia, Rest of Asia-Pacific), Europe (Germany, France, Italy, United Kingdom, Netherlands, Rest of Europe), MEA (Middle East, Africa), North America (United States, Canada, Mexico). Additionally, the rising demand from SMEs and various industry verticals gives enough cushion to market growth.
Influencing Trend:
Increased Adoption of HPV Home Testing Kit and Approval and Launch of New Test
Market Growth Drivers:
Increasing Prevalence of Cervical Cancer and Technological Advancements in Diagnostic Tools and Screening Procedures
Challenges:
Uncertain Reimbursement Scenario
Restraints:
Stringent Regulatory Guidelines
Opportunities:
Rising Adoption of Cervical Cancer Diagnostic Tests for the Early Detection of Cervical Cancer and Technological Advances in Diagnosis Processes
Key Target Audience
New Entrants/Investors, Analysts and Strategic Business Planners, Cervical Cancer Diagnostic Tests Providers, Cervical Cancer Diagnostic Tests Equipment Manufacturers, Suppliers, and Distributors, Raw Material Suppliers, Government Regulatory and Research Organizations and End-Use Industries
In 2020 Roche gets FDA endorsement for Cobas HPV test for use on the Cobas 6800/8800 Systems to recognize women in danger for cervical disease, US Food and Drug Administration (FDA) endorsement for the cobas® HPV test for use on the completely computerized, high-throughput cobas® 6800/8800 Systems., and In 2018, QIAGEN N.V. announced the launch of the QIAscreen HPV PCR Test for the detection of 15 recognized high-risk genotypes of human papillomavirus (HPV), the virus considered to be the cause of cervical cancer. The assay includes both screening and genotyping functionality in one assay.
June 2020, in the Journal of the National Cancer Institute, a computer algorithm improved the accuracy and efficiency of cervical cancer screening compared with cytology (Pap test), the current standard for follow-up of women who test positive with primary human papillomavirus (HPV) screening.