市場調查報告書
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1636731
2030 年患者衍生異質骨移植模型市場預測:按模型類型、腫瘤類型、植入方法、應用、最終用戶和地區進行的全球分析Patient-derived Xenograft Model Market Forecasts to 2030 - Global Analysis By Model Type, Tumor Type, Implantation Method, Application, End User and By Geography |
根據 Stratistics MRC 的數據,到 2024 年,患者來源的異質骨移植模型的全球市場價值將達到 4.943 億美元,預測期內複合年成長率為 14.3%,到 2030 年將達到 11.023 億美元。
在稱為患者源性異質骨移植(PDX)模型的實驗系統中,來自人類患者的腫瘤組織被移植到免疫力缺乏小鼠。該模型是癌症研究中的有用工具,因為原始腫瘤的遺傳特徵和表現型得以保留。與傳統的細胞株模型相比,PDX 模型可以更真實地描述人類癌症,並用於研究腫瘤生物學、測試療法和創建個人化醫療策略。
根據丹娜—法伯癌症研究所的一項研究,在 29 名晚期肉瘤患者中,有 16 名患者成功建立了 PDX 模型。
個人化醫療需求不斷成長
對個人化醫療的需求不斷成長正在推動患者來源的異質骨移植(PDX)模型市場。 PDX 模型使研究人員能夠研究患者特定的癌症生物學和藥物反應,這對於根據個別基因譜量身訂做治療方案至關重要。這種方法提高了治療效果並減少了副作用。癌症發生率的增加和基因組學的進步進一步增加了對個人化醫療的需求。
開發和維護成本高
建立和維護 PDX 模型需要大量的財務資源、專業知識和複雜的基礎設施。腫瘤植入和維持的複雜過程限制了其在小型研究機構中的使用。此外,免疫力缺乏動物和人類腫瘤樣本的高成本進一步增加了成本。這些經濟障礙對廣泛採用提出了挑戰。
癌症研究進展
癌症研究的進步正在為 PDX 模型市場創造機會。基於 CRISPR 的基因編輯、人工智慧主導的資料分析和人性化 PDX 模型等創新正在提高臨床前研究的準確性和效率。這些進步使研究人員能夠探索新的治療標靶,改善生物標記的發現,並加速藥物開發過程。此外,公共和私人對腫瘤學研究投資的增加正在推動對先進 PDX 模型的需求。
道德問題和監管挑戰
道德問題和監管挑戰威脅著 PDX 模型市場的成長。在研究中使用動物會引發倫理問題,並導致制定嚴格的指導方針,從而減緩或限制研究。 FDA 等監管機構正在採取措施減少對動物模型的依賴,這可能會影響市場動態。這些挑戰需要遵守複雜的通訊協定,並增加研究機構的營運成本和時限。
由於實驗室營運、供應鏈和研究資金的中斷,COVID-19 的爆發對 PDX 模型市場產生了負面影響。由於資源被轉用於 COVID-19 研究,許多腫瘤學研究被推遲。然而,這場大流行強調了個人化醫療的重要性,並強調了 PDX 模型在癌症研究中的重要性。一旦限制放鬆,人們重新專注於創新的癌症治療方法,需求就會反彈。
預計滑鼠模型產業在預測期內將是最大的。
預計滑鼠模型部分在預測期內將佔據最大的市場佔有率。小鼠被廣泛使用,因為它們與人類基因相似,易於處理,並且與其他動物相比具有成本效益。小鼠提供了一個強大的平台來研究體內腫瘤生長、藥物療效和抗藥性機制。基於小鼠的 PDX 模型已建立協議,進一步支持其在臨床前腫瘤學研究中的優勢。
生物樣本庫產業預計在預測期內複合年成長率最高。
在預測期內,生物銀行產業預計將出現最高的複合年成長率,因為它負責保存源自患者的腫瘤樣本以供將來使用。生物庫允許研究人員取得不同的腫瘤檢體,以開發新的 PDX 模型和回顧性研究。此功能加快了藥物發現過程,同時確保了實驗的可重複性。對個人化醫療的日益重視增加了對生物樣本庫服務作為臨床前研究基礎設施重要組成部分的需求。
預計北美地區在預測期內將佔據最大的市場佔有率。高癌症發病率、先進的醫療基礎設施以及對癌症研究的大量公共和私人投資等因素正在推動該地區的成長。主要產業參與者的出現進一步鞏固了北美在 PDX 模型採用方面的領導地位。此外,政府對精準醫療的支持也為此優勢做出了重大貢獻。
預計亞太地區在預測期內將實現最高成長率。快速的都市化、不斷增加的醫療支出和不斷上升的癌症發病率正在推動該地區對 PDX 模型等先進研究工具的需求。向現代醫療保健的轉變使亞太地區成為主要的成長中心。此外,中國和印度等國家正大力投資生技和藥物研發,促進市場擴張。
According to Stratistics MRC, the Global Patient-derived Xenograft Model Market is accounted for $494.3 million in 2024 and is expected to reach $1102.3 million by 2030 growing at a CAGR of 14.3% during the forecast period. An experimental system known as a patient-derived xenograft (PDX) model involves implanting tumor tissues from human patients into immunocompromised mice. This model is a useful tool for cancer research because it maintains the original tumor's genetic and phenotypic features. Compared to conventional cell line models, PDX models provide a more realistic depiction of human cancer and are utilized to investigate tumor biology, test therapeutic medications, and create personalized medicine strategies.
According to Dana-Farber Cancer Institute study, 16 out of 29 patients with advanced sarcoma successfully established PDX models.
Rising demand for personalized medicine
The rising demand for personalized medicine is driving the patient-derived xenograft (PDX) model market. PDX models enable researchers to study patient-specific cancer biology and drug responses, making them essential for tailoring treatments to individual genetic profiles. This approach improves therapeutic efficacy and reduces adverse effects, aligning with the growing focus on precision oncology. The increasing prevalence of cancer and advancements in genomics further amplify the need for personalized medicine.
High costs of development and maintenance
Establishing and sustaining PDX models require significant financial resources, specialized expertise, and advanced infrastructure. The complex processes involved in tumor implantation and maintenance limit accessibility for smaller research organizations. Additionally, the high cost of immunodeficient animals and human tumor samples further increases expenses. These financial barriers pose challenges to widespread adoption.
Advancements in cancer research
Advancements in cancer research are creating opportunities for the PDX model market. Innovations such as CRISPR-based gene editing, AI-driven data analysis and humanized PDX models are enhancing the accuracy and efficiency of preclinical studies. These advancements allow researchers to explore novel therapeutic targets, improve biomarker discovery, and accelerate drug development processes. Additionally, increasing public and private investments in oncology research are driving demand for advanced PDX models.
Ethical concerns and regulatory challenges
Ethical concerns and regulatory challenges threaten the growth of the PDX model market. The use of animals in research raises ethical issues, leading to stringent guidelines that can delay or restrict studies. Regulatory agencies like the FDA have introduced measures to reduce reliance on animal models, potentially affecting market dynamics. These challenges necessitate compliance with complex protocols, increasing operational costs and timeframes for research organizations.
The COVID-19 pandemic negatively impacted the PDX model market due to disruptions in laboratory operations, supply chains, and research funding. Many oncology studies were delayed as resources were diverted toward COVID-19 research. However, the pandemic underscored the importance of personalized medicine, highlighting the relevance of PDX models in cancer research. As restrictions eased, demand rebounded with renewed focus on innovative cancer therapies.
The mice models segment is expected to be the largest during the forecast period
The mice models segment is expected to account for the largest market share during the forecast period. Mice are widely used due to their genetic similarity to humans, ease of handling, and cost-effectiveness compared to other animals. They provide a robust platform for studying tumor growth, drug efficacy, and resistance mechanisms in vivo. The availability of well-established protocols for mice-based PDX models further supports their dominance in preclinical oncology research.
The biobanking segment is expected to have the highest CAGR during the forecast period
Over the forecast period, the biobanking segment is expected to witness the highest CAGR due to its role in preserving patient-derived tumor samples for future use. Biobanks enable researchers to access diverse tumor specimens for developing new PDX models and conducting retrospective studies. This capability accelerates drug discovery processes while ensuring reproducibility in experiments. The growing emphasis on personalized medicine drives demand for biobanking services as an essential component of preclinical research infrastructure.
The North America region is anticipated to account for the largest market share during the forecast period. Factors such as a high prevalence of cancer, advanced healthcare infrastructure, and significant public-private investments in oncology research drive regional growth. The presence of key industry players further strengthens North America's position as a leader in PDX model adoption. Additionally, government initiatives supporting precision medicine also contribute significantly to this dominance.
The Asia Pacific region is anticipated to register the highest growth rate over the forecast period. Rapid urbanization, increasing healthcare expenditure, and rising cancer incidence drive demand for advanced research tools like PDX models in this region. The shift toward modern healthcare practices positions Asia Pacific as a key growth hub. Furthermore, countries like China and India are investing heavily in biotechnology and pharmaceutical R&D, fostering market expansion.
Key players in the market
Some of the key players in Patient-derived Xenograft Model Market include Champions Oncology, Charles River Laboratories, Crown Bioscience, EPO Berlin-Buch, Hera BioLabs, Horizon Discovery Group, Inotiv, JSR Corporation, Oncodesign Precision Medicine, Pharmatest Services, Taconic Biosciences, The Jackson Laboratory, Urolead, WuXi AppTec, Xenopat and Xentech.
In December 2024, Can-Fite BioPharma Ltd. recently announced that its work titled The Liver Protective Effect of the Anti-Cancer Drug Candidate Namodenoson is mediated via Adiponectin will be presented at the 2025 ASCO Gastrointestinal Cancers Symposium to take place at San Francisco & On Line, January 23-25.
In October 2019, Crown Bioscience announced the launch of a new tumor organoid drug development platform with the potential to significantly improve the predictivity and speed of preclinical drug discovery. The initial phase of the platform launch features the first commercially available 3D in vitro PDX-derived organoid (PDXO) models generated from CrownBio's uniquely-characterized library of 2500+ patient-derived xenograft (PDX) models.
In May 2015, Taconic Biosciences and Cellaria Biosciences have entered into a scientific collaboration designed to improve the utility of patient-derived xenografts (PDXs) in animal models for oncology and immuno-oncology research. Cellaria's novel methodologies for generating cells from patient tumors will complement Taconic's industry-leading portfolio of tissue humanized mouse models, which are said to be well suited as hosts for PDXs.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.