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市場調查報告書
商品編碼
1833441
非小細胞肺癌市場機會、成長動力、產業趨勢分析及2025-2034年預測Non-Small Cell Lung Cancer Market Opportunity, Growth Drivers, Industry Trend Analysis, and Forecast 2025 - 2034 |
2024 年全球非小細胞肺癌市場價值為 202 億美元,預計將以 10.4% 的複合年成長率成長,到 2034 年達到 539 億美元。
針對特定基因突變(如 EGFR、ALK、ROS1 和 KRAS)的療法的發展已經改變了治療途徑、擴展了個人化醫療並顯著改善了特定患者群體的治療效果。
市場範圍 | |
---|---|
起始年份 | 2024 |
預測年份 | 2025-2034 |
起始值 | 202億美元 |
預測值 | 539億美元 |
複合年成長率 | 10.4% |
腺癌盛行率上升
腺癌在2024年佔據了相當大的佔有率,這得益於其高發病率,尤其是在非吸煙者和年輕患者中。腺癌是非小細胞肺癌(NSCLC)最常見的組織學亞型,通常與可操作的基因突變相關,使其成為分子標靶治療的主要關注點。
標靶治療的應用日益廣泛
標靶治療領域在2024年佔據了相當大的佔有率,其優勢在於提供個人化治療方案,在提高生存率的同時最大限度地降低全身毒性。由於多種針對EGFR、ALK、BRAF、MET和KRAS等特定致癌促進因素的藥物獲得批准,該領域發展勢頭強勁。標靶藥物通常被推薦為符合條件患者的第一線治療方案,與傳統化療相比,其無惡化存活期更長。
男性產業將獲得發展
由於男性吸菸率和職業性肺癌致癌物暴露率歷來較高,男性市場在2024年佔據了相當大的佔有率。儘管基於性別的治療方案並無顯著差異,但男性患者發病率較高,導致診斷、治療啟動和後續護理方面的需求不成比例。
北美將成為推動力地區
2025-2034年期間,北美非小細胞肺癌市場將以可觀的複合年成長率成長,這得益於強大的醫療基礎設施、廣泛的生物標記檢測以及下一代療法的早期應用。該地區也受惠於積極參與全球臨床試驗以及快速核准的監管途徑,這些途徑能夠更快地將新型療法推向市場。隨著精準腫瘤學投資的不斷增加以及政府的支持性舉措,北美預計將在非小細胞肺癌領域保持主導地位。
非小細胞肺癌產業的一些知名企業包括 Xcovery、默克公司、楊森生物技術公司、賽諾菲、艾伯維、諾華、安斯泰來製藥、輝瑞、禮來、武田、羅氏公司、百時美施貴寶公司、阿斯特捷利康、太陽製藥和 Merus。
為了鞏固在非小細胞肺癌市場的地位,各大公司正在實施一系列策略,包括擴大精準腫瘤學產品組合,並透過監管快速通道加快上市時間。重點是開發下一代抑制劑,以克服現有療法的抗藥性,尤其是在標靶治療領域。與診斷公司的合作也至關重要,因為它們可以透過伴隨診斷簡化患者識別。
The Global Non-Small Cell Lung Cancer Market was valued at USD 20.2 billion in 2024 and is estimated to grow at a CAGR of 10.4% to reach USD 53.9 billion by 2034.
The development of therapies targeting specific genetic mutations (like EGFR, ALK, ROS1, and KRAS) has transformed treatment pathways, expanded personalized medicine and significantly improved outcomes in select patient groups.
Market Scope | |
---|---|
Start Year | 2024 |
Forecast Year | 2025-2034 |
Start Value | $20.2 Billion |
Forecast Value | $53.9 Billion |
CAGR | 10.4% |
Rising Prevalence of Adenocarcinoma
The adenocarcinoma segment held a significant share in 2024, driven by its high prevalence, particularly among non-smokers and younger patients. As the most common histological subtype of NSCLC, adenocarcinoma is often associated with actionable genetic mutations, making it a prime focus for molecularly targeted therapies.
Increasing Adoption of Targeted Therapy
The targeted therapy segment held a sizeable share in 2024, backed by offering a personalized approach that improves survival while minimizing systemic toxicity. This segment has gained strong momentum due to the approval of multiple agents addressing specific oncogenic drivers like EGFR, ALK, BRAF, MET, and KRAS mutations. Targeted drugs are often preferred as first-line treatments for eligible patients, resulting in longer progression-free survival compared to traditional chemotherapy.
Male Sector to Gain Traction
The male segment generated a substantial share in 2024, owing to historically higher rates of smoking and occupational exposure to lung carcinogens among men. Although gender-based treatment protocols do not significantly differ, the higher incidence among male patients drives disproportionate demand in terms of diagnostics, therapy initiation, and follow-up care.
North America to Emerge as a Propelling Region
North America non-small cell lung cancer market will grow at a decent CAGR during 2025-2034, fueled by robust healthcare infrastructure, widespread biomarker testing, and early adoption of next-generation therapies. The region also benefits from active participation in global clinical trials and fast-track regulatory pathways that bring novel treatments to market faster. With rising investment in precision oncology and supportive government initiatives, North America is expected to maintain its dominant position in the NSCLC landscape.
Some prominent players operating in the non-small cell lung cancer industry include Xcovery, Merck & Co., Janssen Biotech, Sanofi, AbbVie, Novartis, Astellas Pharma, Pfizer, Eli Lilly, Takeda, F. Hoffmann La Roche, Bristol-Myers Squibb Company, AstraZeneca, Sun Pharmaceutical, and Merus.
To strengthen their presence in the non-small cell lung cancer market, companies are implementing a range of strategies, including expanding their precision oncology portfolios and accelerating time-to-market through regulatory fast-tracks. A major focus lies in developing next-generation inhibitors to overcome resistance to existing therapies, particularly in the targeted therapy segment. Collaborations with diagnostic firms are also key, as they enable streamlined patient identification through companion diagnostics.