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市場調查報告書
商品編碼
2138125
2034年腫瘤精準醫療和液態生物檢體市場預測-按生物標記類型、癌症類型、技術、應用、最終用戶和地區分類的全球分析Oncology Precision Medicine & Liquid Biopsy Market Forecasts to 2034 - Global Analysis By Biomarker Type, Cancer Type, Technology, Application, End User and By Geography |
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根據 Stratistics MRC 的數據,預計到 2026 年,全球腫瘤精準醫療和液態生物檢體市場規模將達到 67 億美元,在預測期內複合年成長率將達到 25.2%,到 2034 年將達到 407 億美元。
腫瘤學中的精準醫療和液態生物檢體將個人化癌症治療與先進的分子檢測相結合,以腫瘤的生物學特徵為依據制定治療決策。此方法利用基因組資訊、生物標記和液態生物檢體技術來檢測具有臨床意義的突變,並評估癌症的長期進展。透過分析血液中循環的腫瘤DNA及其相關標記物,液態生物檢體提供了一種微創的診斷、治療選擇和後續觀察工具。這些技術的結合能夠實現個人化治療策略、持續評估,並在癌症管理的各個階段改善臨床決策。
根據世界衛生組織/國際癌症研究機構的數據,全球每年約有2,060萬例新增癌症病例和近1,000萬人死於癌症。這顯示癌症給人類帶來了巨大的疾病負擔,並凸顯了先進腫瘤診斷技術和個人化治療方案的必要性。
對個人化癌症治療的需求日益成長
對個人化癌症治療日益成長的需求正在推動腫瘤精準醫療和液態生物檢體市場的擴張。精準腫瘤學幫助醫生確定與腫瘤分子和基因特徵相符的治療方案,從而支持更具針對性的治療策略。基因測序和生物標記分析技術的進步使得識別多種癌症類型中具有臨床意義的突變變得更加容易。同時,標靶治療和伴隨診斷的日益普及促使醫院和腫瘤中心將分子檢測納入其常規癌症治療和管理策略。
詳細的腫瘤檢查高成本
高成本、高精度的腫瘤檢測仍然是「腫瘤精準醫療和液態生物檢體市場」的潛在阻礙因素。基因測序、分子譜分析、生物標記評估以及專業的診斷基礎設施都需要大量資金。檢查室處理、複雜基因組數據解讀以及聘請專業人員等相關成本會進一步增加檢測費用。在保險覆蓋範圍有限或先進診斷服務不足的地區,醫療機構在採用這些技術方面可能面臨挑戰。因此,經濟障礙可能會限制小規模醫療機構和需要個人化癌症治療的患者獲得檢測服務。
擴大多種癌症的早期檢測範圍
多癌種早期檢測方法的發展為「腫瘤精準醫療和液態生物檢體市場」帶來了機會。利用血液進行液態生物檢體可以檢測循環腫瘤DNA和其他生物標記物,從而有可能揭示與多種癌症相關的分子訊號。定序技術、生物標記識別和人工智慧的進步有望提高早期檢測癌症相關模式的準確性。透過持續的臨床研究和檢驗,液態生物檢體的應用範圍有望從治療監測擴展到更廣泛的患者群體,包括早期癌症檢測和風險評估。
監管和臨床檢驗的挑戰
監管要求和廣泛的臨床檢驗需求可能對腫瘤精準醫療和液態生物檢體市場構成挑戰。分子診斷和液態生物檢體平台必須在廣泛應用前證明其可靠的分析性能、臨床有效性和實際臨床效用。各國法規結構的差異會增加合規要求、延長研發週期並增加相關成本。此外,新發現的生物標記證據有限也會使監管評估更加複雜。這些因素可能導致產品上市延遲、投資風險增加,並使新興腫瘤技術的商業化更加困難。
新冠疫情對癌症篩檢、診斷、治療和研究活動產生了重大影響,並波及癌症精準醫療和液態生物檢體市場。根據世界衛生組織統計,2020年,42%的調查對象國家癌症治療服務受到影響;美國國家癌症研究所(NCI)報告稱,癌症臨床試驗的參與者招募人數大幅下降。由於偵測延誤和醫療資源限制,診斷活動一度受到限制。另一方面,對微創監測和靈活照護模式的需求增加,進一步提升了人們對液態生物檢體和分子檢測技術的關注。
在預測期內,循環腫瘤 DNA (ctDNA) 細分市場預計將佔據最大的市場佔有率。
循環腫瘤DNA (ctDNA) 片段預計將在預測期內佔據最大的市場佔有率,這主要得益於其在癌症分子評估和監測中的廣泛應用。透過血液檢測,ctDNA 無需進行侵入性組織取樣即可提供有關腫瘤相關基因改變的資訊。其應用包括識別具有治療價值的突變、評估治療反應、檢測分子殘留病灶以及追蹤癌症進展。基因測序和先進分子診斷技術的日益普及進一步提升了 ctDNA 在精準腫瘤學和液態生物檢體應用中的重要性。
在預測期內,「監測和復發檢測」細分市場預計將呈現最高的複合年成長率。
在預測期內,「監測和復發檢測」細分市場預計將呈現最高的成長率,這主要得益於癌症持續監測應用的不斷擴展。液態生物檢體能夠對循環腫瘤DNA及相關生物標記進行重複分析,有助於評估治療反應、識別分子水平突變以及預測潛在的疾病復發。定序靈敏度的提高和微量殘存疾病)評估技術的進步正在擴大其在治療後後續觀察的作用。對早期分子層面識別和個人化追蹤的日益重視預計將進一步推動對這些監測應用的需求。
在預測期內,北美預計將佔據最大的市場佔有率,這主要得益於其完善的癌症醫療體系、廣泛的基因組檢測以及成熟的個人化醫療能力。強大的臨床研究基礎設施和先進的分子診斷技術正在加速腫瘤學領域基於生物標記的方法的應用。該地區還擁有眾多專業的癌症醫療機構和診斷實驗室,為液態生物檢體的引入提供了支援。此外,高度發展的製藥和生物技術產業正在推動精準腫瘤學技術和液態生物檢體解決方案在整個醫療保健領域的創新、臨床檢驗和應用。
在預測期內,亞太地區預計將呈現最高的複合年成長率,這主要得益於癌症負擔的加重、醫療保健體系的改善以及分子診斷技術的普及。基因組檢測、個人化癌症治療和液態生物檢體等領域的投資增加正在推動該地區的發展。新興經濟體醫療保健覆蓋範圍的擴大正在推動這些技術的普及,而對個人化癌症治療日益成長的臨床需求則創造了更多機會。生物技術研究、診斷基礎設施和先進分子平台的進步預計將進一步推動該地區市場的持續擴張。
According to Stratistics MRC, the Global Oncology Precision Medicine & Liquid Biopsy Market is accounted for $6.7 billion in 2026 and is expected to reach $40.7 billion by 2034 growing at a CAGR of 25.2% during the forecast period. Oncology Precision Medicine & Liquid Biopsy combines personalized cancer care with advanced molecular testing to guide treatment based on the biological features of tumors. The approach uses genomic information, biomarkers, and liquid biopsy methods to detect clinically relevant alterations and evaluate changes in cancer over time. By examining circulating tumor DNA and related markers in blood, liquid biopsies provide minimally invasive opportunities for diagnosis, therapy selection, and monitoring. Together, these technologies enable individualized treatment strategies, ongoing assessment, and improved clinical decision-making across different stages of cancer management.
According to WHO/IARC, an estimated 20.6 million new cancer cases and nearly 10 million cancer deaths occurred globally each year, highlighting the substantial disease burden supporting demand for advanced oncology diagnostics and personalized treatment approaches.
Growing demand for personalized cancer treatment
Rising demand for individualized cancer care is supporting the expansion of the Oncology Precision Medicine & Liquid Biopsy Market. Precision oncology helps physicians match treatments with the molecular and genetic profiles of tumors, supporting more targeted therapeutic decisions. Improvements in genomic sequencing and biomarker analysis are making it easier to identify clinically meaningful mutations across diverse cancers. At the same time, growing use of targeted medicines and companion diagnostic technologies is encouraging hospitals and oncology centers to incorporate molecular testing into routine cancer treatment and management strategies.
High cost of precision oncology testing
Expensive precision oncology testing remains a potential limitation for the Oncology Precision Medicine & Liquid Biopsy Market. Genomic sequencing, molecular profiling, biomarker evaluation, and specialized diagnostic infrastructure can require considerable financial resources. Additional expenses related to laboratory processing, interpretation of complex genomic data, and skilled professionals may further increase testing costs. Where reimbursement coverage is limited or advanced diagnostic services are less accessible, healthcare providers may face challenges adopting these technologies. Consequently, financial barriers can restrict utilization among smaller healthcare facilities and patients requiring personalized oncology care.
Expansion of multi-cancer early detection
Growing development of multi-cancer early detection approaches presents an opportunity for the Oncology Precision Medicine & Liquid Biopsy Market. Blood-based liquid biopsy methods can examine circulating tumor DNA and other biomarkers that may reveal molecular signals linked with different cancers. Progress in sequencing technologies, biomarker identification, and artificial intelligence could strengthen the detection of cancer-associated patterns at earlier stages. With continued clinical research and validation, liquid biopsy applications may extend beyond therapy monitoring to include earlier cancer detection and risk evaluation across wider patient groups.
Regulatory and clinical validation challenges
Regulatory requirements and the need for extensive clinical validation may create challenges for the Oncology Precision Medicine & Liquid Biopsy Market. Molecular diagnostics and liquid biopsy platforms need to establish dependable analytical performance, clinical validity, and practical clinical usefulness before widespread adoption. Variations in regulatory frameworks between countries can increase compliance requirements, development periods, and associated expenses. Additionally, limited evidence surrounding newly identified biomarkers can complicate regulatory evaluation. Such factors may postpone product launches, increase investment risks, and make commercialization of emerging oncology technologies more difficult.
The COVID-19 outbreak significantly affected cancer screening, diagnosis, treatment, and research activities, influencing the oncology precision medicine and liquid biopsy market. According to WHO, cancer treatment services were disrupted in 42% of surveyed countries during 2020, while the NCI reported major reductions in enrollment across cancer clinical trials. Delayed procedures and constrained healthcare resources temporarily limited diagnostic activity. At the same time, demand for less invasive monitoring and adaptable care models encouraged greater attention toward liquid biopsy and molecular testing technologies.
The circulating tumor DNA (ctDNA) segment is expected to be the largest during the forecast period
The circulating tumor DNA (ctDNA) segment is expected to account for the largest market share during the forecast period, supported by its extensive use in molecular cancer assessment and monitoring. Through blood-based testing, ctDNA can provide information about tumor-related genetic changes without requiring invasive tissue collection. Its applications include identifying actionable alterations, evaluating therapeutic response, detecting molecular residual disease, and tracking cancer progression. Growing adoption of genomic sequencing and advanced molecular diagnostic techniques continues to enhance the importance of ctDNA within precision oncology and liquid biopsy applications.
The monitoring & recurrence detection segment is expected to have the highest CAGR during the forecast period
Over the forecast period, the monitoring & recurrence detection segment is predicted to witness the highest growth rate, driven by expanding applications for continuous cancer monitoring. Liquid biopsy allows repeated analysis of circulating tumor DNA and related biomarkers, helping evaluate therapeutic response, identify molecular changes, and recognize possible disease recurrence. Improvements in sequencing sensitivity and minimal residual disease assessment are broadening its role in post-treatment surveillance. Growing emphasis on early molecular identification and individualized patient follow-up is expected to further strengthen demand for these monitoring applications.
During the forecast period, the North America region is expected to hold the largest market share, driven by developed cancer-care systems, widespread genomic testing, and established personalized medicine capabilities. Strong clinical research infrastructure and advanced molecular diagnostics facilitate the use of biomarker-guided approaches in oncology. The region also has numerous specialized cancer institutions and diagnostic laboratories that support liquid biopsy adoption. In addition, its well-developed pharmaceutical and biotechnology sectors encourage innovation, clinical validation, and implementation of precision oncology technologies and liquid biopsy solutions throughout healthcare settings.
Over the forecast period, the Asia Pacific region is anticipated to exhibit the highest CAGR, driven by rising cancer burden, improving healthcare systems, and wider use of molecular diagnostic technologies. Increasing investments in genomic testing, personalized oncology, and liquid biopsy are strengthening regional development. Expanding healthcare availability in emerging countries is supporting adoption, while growing clinical demand for individualized cancer therapies is creating further opportunities. Improvements in biotechnology research, diagnostic infrastructure, and advanced molecular platforms are expected to reinforce the region's continued market expansion.
Key players in the market
Some of the key players in Oncology Precision Medicine & Liquid Biopsy Market include F. Hoffmann-La Roche Ltd, Guardant Health, Illumina, Inc., Thermo Fisher Scientific Inc., QIAGEN N.V., Myriad Genetics, Inc., Sysmex Corporation, Bio-Rad Laboratories, Inc., Agilent Technologies, Inc., NeoGenomics Laboratories, Menarini Silicon Biosystems, Natera, Abbott Laboratories, Adaptive Biotechnologies, CelLBxHealth PLC, Tempus AI, SOPHiA GENETICS and Freenome.
In November 2025, Abbott and Exact Sciences announced a definitive agreement for Abbott to acquire Exact Sciences, which will enable it to enter and lead in fast-growing cancer diagnostics segments, serving millions more people. Under the terms of the agreement, Exact Sciences shareholders will receive $105 per common share, representing a total equity value of approximately $21 billion.
In October 2025, Thermo Fisher Scientific Inc. has agreed to acquire Clario Holdings Inc., a provider of digital endpoint data solutions for clinical trials. The deal includes potential additional earnout and other payments contingent on future performance. Clario's platform integrates clinical trial endpoint data from devices, sites, and patients, enabling pharmaceutical and biotechnology companies to digitally collect, manage, and analyze clinical evidence across all phases of drug development.
Note: Tables for North America, Europe, APAC, South America, and Rest of the World (RoW) Regions are also represented in the same manner as above.