암 치료 분야 유전체학 시장 - 세계 산업 규모, 점유율, 동향, 기회, 예측, 제품별, 기술별, 용도별, 최종사용자별, 지역별 부문, 경쟁(2020-2030년)
Genomics in Cancer Care Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Product, By Technology, By Application, By End User, By Region and Competition, 2020-2030F
상품코드 : 1691736
리서치사 : TechSci Research
발행일 : 2025년 03월
페이지 정보 : 영문 182 Pages
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한글목차

암 치료 분야 유전체학 세계 시장 규모는 2024년 157억 3,000만 달러로 평가되었고, 예측 기간 동안 402억 2,000만 달러에 달할 것으로 예상되며, 2030년까지 16.91%의 연평균 복합 성장률(CAGR)을 나타낼 것으로 예상됩니다.

세계 암 치료 분야 유전체학 시장은 정밀의료의 보급과 유전체 기술의 발전으로 큰 성장을 거듭하고 있습니다. 암 진단 및 치료에 있어 차세대 염기서열분석기(NGS), 액체생검, 인공지능의 통합은 암 치료를 혁신적으로 변화시켰습니다. 암 발병률 증가와 개인 맞춤형 치료에 대한 요구가 높아지면서 유전체 기반 솔루션에 대한 수요가 가속화되고 있습니다. 제약사, 연구기관, 진단업체들은 바이오마커 기반 암 치료제를 개발하기 위해 협력하여 치료 효과와 환자 예후를 개선하고 있습니다. 유전체 데이터 분석 도구와 바이오인포매틱스 플랫폼의 지속적인 발전은 시장 확대를 더욱 촉진하고 있으며, 유전체 분석은 현대 암 치료에 필수적인 요소로 자리 잡고 있습니다.

시장 개요
예측 기간 2026-2030년
시장 규모 : 2024년 157억 3,000만 달러
시장 규모 : 2030년 402억 2,000만 달러
CAGR : 2025-2030년 16.91%
급성장 부문 맞춤형 의료
최대 시장 북미

시장 성장 촉진요인

유전체 시퀀싱의 발전

주요 시장 이슈

비용과 접근성

주요 시장 동향

액체생검과 조기발견

목차

제1장 개요

제2장 조사 방법

제3장 주요 요약

제4장 고객의 소리

제5장 세계의 암 치료 분야 유전체학 시장 전망

제6장 북미의 암 치료 분야 유전체학 시장 전망

제7장 유럽의 암 치료 분야 유전체학 시장 전망

제8장 아시아태평양의 암 치료 분야 유전체학 시장 전망

제9장 남미의 암 치료 분야 유전체학 시장 전망

제10장 중동 및 아프리카의 암 치료 분야 유전체학 시장 전망

제11장 시장 역학

제12장 시장 동향과 발전

제13장 Porter의 Five Forces 분석

제14장 경쟁 구도

제15장 전략적 제안

제16장 리서치사에 대해 & 면책사항

LSH
영문 목차

영문목차

Global Genomics in Cancer Care Market was valued at USD 15.73 Billion in 2024 and is expected to reach USD 40.22 Billion in the forecast period with a CAGR of 16.91% through 2030. The Global Genomics in Cancer Care Market is experiencing significant growth due to the increasing adoption of precision medicine and advancements in genomic technologies. The integration of next-generation sequencing (NGS), liquid biopsy, and artificial intelligence in cancer diagnostics and treatment has transformed oncology care. Rising cancer prevalence and the growing need for personalized therapies have accelerated the demand for genomic-based solutions. Pharmaceutical companies, research institutions, and diagnostic firms are collaborating to develop biomarker-driven cancer therapies, enhancing treatment efficacy and patient outcomes. The continuous evolution of genomic data analysis tools and bioinformatics platforms further supports the market's expansion, making genomics an essential component of modern cancer care.

Market Overview
Forecast Period2026-2030
Market Size 2024USD 15.73 Billion
Market Size 2030USD 40.22 Billion
CAGR 2025-203016.91%
Fastest Growing SegmentPersonalized Medicine
Largest MarketNorth America

Key Market Drivers

Advancements in Genomic Sequencing

In the ever-evolving landscape of cancer care, genomic sequencing has emerged as a potent tool, significantly shaping the Global Genomics in Cancer Care Market. Advancements in genomic sequencing, particularly Next-Generation Sequencing (NGS), have enabled comprehensive molecular profiling of cancer. This allows researchers and healthcare providers to analyze a patient's entire genome to identify mutations, alterations, and genetic markers associated with cancer, facilitating more accurate diagnoses and tailored treatment strategies.

The Cancer Genome Atlas (TCGA), a landmark program by the National Cancer Institute (NCI), has molecularly characterized over 20,000 primary cancer and matched normal samples across 33 cancer types. This extensive dataset, comprising more than two petabytes of genomic data, is publicly available and aids the cancer research community in improving prevention, diagnosis, and treatment strategies.

Genomic sequencing allows for the identification of specific genetic mutations driving a patient's cancer, which is invaluable in developing targeted therapies. Pharmaceutical companies leverage genomic insights to create drugs that precisely target the genetic abnormalities responsible for cancer growth, increasing treatment effectiveness and reducing side effects.

Personalized medicine, based on genomic sequencing, has revolutionized cancer care. By analyzing a patient's genetic makeup, oncologists can tailor treatment plans to the individual, optimizing therapy selection and dosage. This approach not only improves patient outcomes but also enhances the overall quality of life during treatment.

Genomic sequencing also plays a crucial role in early detection and prevention. Genetic testing can identify individuals with a higher risk of developing certain cancers, enabling early interventions and proactive health management. Additionally, screening for genetic markers associated with cancer allows for earlier diagnosis and intervention, increasing the chances of successful treatment.

The wealth of data generated through genomic sequencing is a goldmine for researchers and healthcare providers. Advanced data analytics and bioinformatics tools are employed to interpret and extract meaningful insights from genomic data, leading to more informed clinical decisions and supporting ongoing research into new cancer therapies and diagnostic tools.

Advancements in genomic sequencing have driven down the cost of sequencing, making it more accessible for patients and healthcare providers. As sequencing becomes more affordable, its adoption in clinical settings becomes more widespread, further fueling market growth.

In summary, the integration of genomic sequencing into cancer care has transformed the approach to diagnosis, treatment, and prevention, driving significant advancements in the Global Genomics in Cancer Care Market.

Key Market Challenges

Cost and Accessibility

The high cost of genomic technologies and limited accessibility to advanced cancer care remain significant challenges in the Global Genomics in Cancer Care Market. Next-generation sequencing (NGS), whole genome sequencing, and other genomic profiling techniques require expensive instruments, reagents, and bioinformatics infrastructure, making them unaffordable for many healthcare providers and patients. The cost burden is further exacerbated by the need for specialized expertise to interpret complex genomic data, increasing operational expenses for diagnostic laboratories and hospitals. Many low- and middle-income countries struggle to integrate genomic-based cancer diagnostics into their healthcare systems due to budget constraints and the lack of reimbursement policies for these advanced tests.

Limited accessibility to genomic cancer care is another critical issue, particularly in remote and underserved regions. Many healthcare facilities lack the necessary infrastructure to conduct in-house genomic testing, leading to delays in diagnosis and treatment initiation. Patients in such areas often need to travel long distances to access specialized centers, increasing financial and logistical burdens. The disparity in access to genomic testing is also evident within high-income countries, where only major medical centers offer comprehensive genomic profiling, while smaller hospitals and clinics face resource limitations. The absence of standardized regulations and inconsistent reimbursement policies across different regions further hinder the widespread adoption of genomic technologies in oncology.

Key Market Trends

Liquid Biopsies and Early Detection

The Global Genomics in Cancer Care Market is experiencing a significant shift toward liquid biopsies and early detection, driven by advancements in next-generation sequencing (NGS) and circulating tumor DNA (ctDNA) analysis. Liquid biopsy is emerging as a revolutionary tool for non-invasive cancer diagnostics, enabling real-time monitoring of tumor progression and treatment response. Traditional tissue biopsies are often invasive, time-consuming, and limited in capturing tumor heterogeneity. Liquid biopsies, on the other hand, provide a comprehensive genomic profile by detecting genetic alterations in circulating biomarkers such as ctDNA, circulating tumor cells (CTCs), and extracellular vesicles in blood samples. The increasing adoption of this technology is improving early cancer detection rates, enhancing treatment personalization, and reducing the need for repeated invasive procedures.

Key Market Players

Report Scope:

In this report, the Global Genomics in Cancer Care Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Genomics in Cancer Care Market, By Product:

Genomics in Cancer Care Market, By Technology:

Genomics in Cancer Care Market, By Application:

Genomics in Cancer Care Market, By End User:

Genomics in Cancer Care Market, By Region:

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in the Global Genomics in Cancer Care Market.

Available Customizations:

Global Genomics in Cancer Care market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

Company Information

Table of Contents

1. Product Overview

2. Research Methodology

3. Executive Summary

4. Voice of Customer

5. Global Genomics in Cancer Care Market Outlook

6. North America Genomics in Cancer Care Market Outlook

7. Europe Genomics in Cancer Care Market Outlook

8. Asia-Pacific Genomics in Cancer Care Market Outlook

9. South America Genomics in Cancer Care Market Outlook

10. Middle East and Africa Genomics in Cancer Care Market Outlook

11. Market Dynamics

12. Market Trends & Developments

13. Porters Five Forces Analysis

14. Competitive Landscape

15. Strategic Recommendations

16. About Us & Disclaimer

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