市場調查報告書
商品編碼
1388949
全球非小細胞肺癌市場:按類型、治療類型、藥物類別、通路和地區劃分的評估、機會和預測(2016-2030)Non-Small Cell Lung Cancer Market Assessment, By Type, By Treatment Type, By Drug Class, By Distribution Channel, By Region, Opportunities and Forecast, 2016-2030F |
2022 年全球非小細胞肺癌 (NSCLC) 市場規模為 106 億美元,在預測期內(2023-2030 年)複合年增長率為 9.5%,到 2030 年還將繼續增長。預計達到219億美元。 全球非小細胞肺癌市場是一個充滿活力的市場,其特點是治療、診斷的不斷進步以及對該疾病的了解不斷加深。
NSCLC是肺癌的主流,約佔所有肺癌病例的85%。 例如,根據 ACS 發布的 2023 年統計數據,預計 2023 年將診斷出約 238,340 名新肺癌患者。 這個市場是由多種因素複雜的相互作用形成的,包括技術創新、不斷發展的治療策略以及日益增強的個人化醫療意識。 精準醫學的進步正在徹底改變非小細胞肺癌的治療,轉向針對每個患者的特定基因突變和生物標記量身定制的標靶治療和免疫療法。
與傳統化療相比,免疫檢查點抑制劑、EGFR抑制劑和ALK抑制劑等標靶治療藥物的出現改善了治療效果並減少了副作用,顯著改變了治療模式。 此外,這一領域正在不斷發展,不斷進行的研究和開發旨在發現新的治療標靶、創新的聯合療法和用於早期檢測的診斷工具。 生物標記驅動的療法、液體活檢和伴隨診斷在治療選擇中發揮關鍵作用,為患者提供更精確、更有效的干預措施。 市場競爭非常激烈,製藥公司正在大力投資研究和臨床試驗,以推出新療法並擴大產品組合。 然而,挑戰依然存在,包括治療成本上升、獲取機會的差異以及需要進行全面的篩檢計劃以早期診斷非小細胞肺癌。
本報告分析了全球非小細胞肺癌市場,提供了產品概述、市場基本結構、整體市場規模趨勢展望、按細分市場和地區劃分的詳細趨勢以及背景市場信息,調查主要影響因素、主要企業概況、市場佔有率等。
為涵蓋的所有地區/國家提供每個細分市場的資訊。
上面列出的公司並非按市場份額排序,並且可能會根據研究工作中獲得的資訊進行更改。
Global non-small cell lung cancer market size was valued at USD 10.6 billion in 2022, and is expected to reach USD 21.9 billion in 2030, with a CAGR of 9.5% for the forecast period between 2023 and 2030F. The global non-small cell lung cancer market is a dynamic landscape characterized by ongoing advancements in treatment modalities, diagnosis, and a growing understanding of the disease.
NSCLC represents a predominant form of lung cancer, constituting approximately 85% of all lung cancer cases. For instance, according to the 2023 statistics published by ACS, about 238,340 new cases of lung cancer are expected to be diagnosed in 2023. This market is shaped by a complex interplay of factors, including technological innovations, evolving therapeutic strategies, and increasing awareness of personalized medicine. Advancements in precision medicine have revolutionized NSCLC treatment, with a shift towards targeted therapies and immunotherapies tailored to specific genetic mutations or biomarkers present in individual patients.
The emergence of immune checkpoint inhibitors and targeted therapies, such as EGFR and ALK inhibitors, has significantly transformed the treatment paradigm, offering improved outcomes and reduced side effects compared to traditional chemotherapy. Moreover, the landscape is continually evolving with ongoing research and development initiatives, aiming to discover novel therapeutic targets, innovative combination therapies, and diagnostic tools for early detection. Biomarker-driven therapies, liquid biopsies, and companion diagnostics play a pivotal role in treatment selection, enabling more precise and effective interventions for patients. Market competition is intense, with pharmaceutical companies investing significantly in research and clinical trials to introduce novel therapies and expand their product portfolios. However, challenges persist, including high treatment costs, access disparities, and the need for more comprehensive screening programs to diagnose NSCLC at earlier stages.
In the dynamic landscape of the global non-small cell lung cancer market, strategic collaborations have emerged as pivotal. Major players, such as pharmaceutical firms and biotech companies, are forging impactful partnerships. Recent alliances between leading diagnostic technology providers and pharmaceutical giants aim to revolutionize treatment through precision medicine and innovative therapies. These collaborations focus on joint research, development, and commercialization, leveraging collective expertise to introduce novel treatments and diagnostic solutions.
This strategic convergence fosters a synergetic approach, propelling advancements in personalized medicine, improving patient outcomes, and reshaping the paradigm of non-small cell lung cancer management globally. For instance, Bristol Myers Squibb, finalized the acquisition of Turning Point Therapeutics on March 6, 2022. Turning Point Therapeutics is a clinical-stage precision oncology company with a lineup of internally developed investigative medications aimed at overcoming major constraints of current cancer treatments. This acquisition expanded Bristol Myers Squibb's oncology portfolio by incorporating late-stage precision oncology asset.
The global non-small cell lung cancer market has seen significant technological advancements, revolutionizing treatment approaches. Targeted therapies, such as immunotherapies and precision medicine, have reshaped the landscape. Immunotherapies like checkpoint inhibitors (PD-1/PD-L1 inhibitors) have shown remarkable efficacy in managing advanced NSCLC by enhancing the body's immune response against cancer cells. Additionally, the emergence of personalized medicine, utilizing genetic testing to identify specific mutations or biomarkers, has led to the development of drugs tailored to individual patients.
Liquid biopsies, a minimally invasive diagnostic technique, is gaining prominence for monitoring treatment response and detecting mutations. Furthermore, advancements in imaging technologies like PET scans and MRI have improved early detection and monitoring of NSCLC. In January 2023, Novocure announced the LUNAR study, which assessed the safety and effectiveness of Tumor Treating Fields (TTFields) in combination with standard treatments for stage 4 non-small cell lung cancer (NSCLC) after progression following or during platinum-based therapy, successfully achieved its main objective.
The non-small cell lung cancer market has witnessed groundbreaking innovations aimed at revolutionizing treatment. Immunotherapies like checkpoint inhibitors, such as Pembrolizumab and Nivolumab, have reshaped the landscape by targeting specific proteins to enhance the immune response against cancer cells. Furthermore, targeted therapies like Osimertinib have shown efficacy in specific genetic mutations like EGFR, improving outcomes for patients. Liquid biopsy techniques are emerging, offering less invasive methods to detect genetic mutations, aiding in treatment decisions.
Advancements in precision medicine and biomarker testing are fostering personalized treatment approaches, optimizing therapies for individual patients. Additionally, advancements in combination therapies and innovative drug delivery systems are showing promising results in enhancing treatment efficacy and reducing side effects. During December 2022, the FDA in the United States, provided accelerated approval to Mirati's Krazati (adagrasib), offering a targeted treatment for adult patients diagnosed with KRAS-mutated locally advanced or metastatic non-small cell lung cancer.
The global non-small cell lung cancer market is witnessing a significant uptick in investment by companies aimed at developing more effective therapies. This surge in investment underscores a commitment to advancing the field of oncology and addressing the unmet medical needs of patients. Companies are allocating resources to research and develop innovative treatments that encompass targeted therapies, immunotherapies, and precision medicine approaches. The increased focus is driven by a growing understanding of the molecular complexities of non-small cell lung cancer, leading to the identification of new drug targets and treatment strategies.
For example, during January 2023, DeuterOncology, a clinical-stage pharmaceutical firm, concluded a Series A financing round, securing approx. USD 6.1 million (EUR 5.65 million). This investment empowers the company to commence the phase I clinical investigation for its primary product DO-2, an enhanced MET kinase inhibitor designed as a promising targeted therapy for lung cancer, striving to be a top-tier treatment option. Recently, MET inhibitors have gained approval for treating patients with Non-Small Cell Lung Cancer (NSCLC) exhibiting the MET exon 14 skipping mutation.
The growth of the non-small cell lung cancer market has been significantly impacted by COVID-19. Specifically, the pandemic led to the cessation of over 200 interventional studies, as indicated by clinicaltrials.gov until July 2021, resulting in a deceleration of market expansion. Nevertheless, with the easing of restrictions and the resumption of services, there has been a renewed emphasis on conducting clinical trials for non-small cell lung cancer treatment. Notably, in October 2022, Daiichi Sankyo, Inc., in collaboration with AstraZeneca, initiated a Phase II clinical trial to assess the safety and effectiveness of trastuzumab deruxtecan in treating HER2-mutated metastatic non-small cell lung cancer (NSCLC). These endeavors are anticipated to propel market growth throughout the projected period.
The non-small cell lung cancer market is characterized by fragmentation and competitiveness, featuring numerous major players. These companies are implementing diverse strategic approaches like collaborations, partnerships, new product introductions, and other initiatives to maintain their standing in the market. The market features a competitive landscape with several key players driving innovation and therapeutic advancements. Immunotherapies and targeted therapies remain a focus, with ongoing clinical trials and the development of combination therapies. The market outlook is promising, with an increasing emphasis on early detection methods, liquid biopsy technologies, and the exploration of innovative drug delivery systems. Collaboration between key players, academic institutions, and biotech firms continues to drive the evolution of treatment options, underscoring a future of diversified, more effective, and personalized therapies for NSCLC patients.
In June 2022, the European Commission granted approval to Novartis's Tabrecta (capmatinib) as a standalone treatment for adults dealing with advanced non-small cell lung cancer, necessitating systemic therapy after prior treatment with immunotherapy and/or platinum-based chemotherapy.
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Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.