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2030年全球黑色素瘤诊断与治疗市场预测:按癌症类型、诊断、治疗、应用和地区进行全球分析Melanoma Diagnostics and Therapeutics Market Forecasts to 2030 - Global Analysis By Cancer Type, By Diagnosis (Dermatoscopy, Blood Tests, Computed Tomography Scan and Other Diagnosis), Therapy, Application and By Geography |
根据 Stratistics MRC 的数据,全球黑色素瘤诊断和治疗市场在预测期内将以 17.1% 的复合年增长率成长。
黑色素瘤诊断涉及识别和评估黑色素细胞病变以诊断皮肤癌。技术包括皮肤镜检查、切片检查和分析基因突变的分子测试。黑色素瘤的治疗包括手术切除、免疫治疗、标靶治疗和化疗。查核点抑制剂等免疫疗法和针对特定基因变化的标靶治疗正在发挥重要作用。早期检测和个体化治疗策略对于黑色素瘤的治疗至关重要。
据美国癌症协会称,预计2022年美国将新增约99,780例黑色素瘤病例,同年将有约7,650人死于黑色素瘤。
黑色素瘤增加
长期日晒、生活方式改变和遗传倾向等因素导致全球黑色素瘤病例增加。发病率的迅速增加需要先进的诊断工具和治疗性介入。宣传宣传活动和定期皮肤检查的增加进一步增加了对早期发现和有效治疗的需求。该行业对这些日益增长的健康问题的回应包括诊断和治疗方面的持续创新,其中黑色素瘤盛行率的上升是市场扩张的关键驱动力。
治疗费用高
与黑色素瘤的创新诊断、标靶治疗和免疫疗法相关的成本可能很高,限制了某些患者群体获得治疗的机会。这种财务障碍可能会阻碍及时和最佳的治疗并影响患者的治疗结果。此外,高成本对医疗保健系统造成负担,给个人和付款人带来经济挑战,并可能影响整体市场成长。
诊断技术的进步
高解析度成像技术、液体活检和分子分析等创新诊断工具可以实现黑色素瘤的早期、准确检测。这些技术提高的敏感性和特异性有助于及时干预并改善患者的治疗结果。此外,非侵入性和准确的诊断方法符合个人化医疗的成长趋势,并促进量身定制的治疗方法。这些技术进步不仅有助于早期诊断,而且在监测治疗反应和疾病进展方面发挥重要作用。
专门医疗保健中心的数量有限
专业医疗中心数量有限是黑色素瘤诊断和治疗市场的主要威胁。黑色素瘤通常需要专业知识才能进行准确的诊断和量身定制的治疗计划。缺乏此类中心会导致诊断延误,阻碍获得先进的治疗性介入,并限制患者的治疗效果。此外,患者可能面临地理障碍,特别是在服务不足的地区,这会影响及时获得关键诊断服务和尖端治疗方法,导致市场扩张受到限制。
COVID-19大流行对黑色素瘤诊断和治疗市场产生了重大影响。医疗保健服务的中断、资源的重新调整以及患者对前往医疗保健机构的恐惧导致黑色素瘤诊断和治疗的延误。然而,这场大流行凸显了创新远距医疗解决方案的重要性,并加速了远端医疗和数位医疗技术的采用。
预计血液检测领域在预测期内将是最大的。
由于血液检测的非侵入性和对黑色素瘤相关生物标记的有效检测,预计将成为黑色素瘤诊断市场中最大的部分。血液检测为早期检测提供了一种方便易行的方法,可以及时进行干预。液体活检技术的进步和循环肿瘤标记的鑑定正在促进该领域的兴起。随着对准确和微创诊断方法的需求增加,血液检测领域预计将占据主导地位,以满足有效黑色素瘤检测和监测日益增长的需求。
预计放射治疗产业在预测期内复合年增长率最高。
预计放射线治疗领域黑色素瘤诊断和治疗市场将出现良好成长。这种增长是由于越来越多地采用放射疗法作为黑色素瘤的有效治疗选择。强度调控放射治疗(IMRT) 和立体定位放射线手术等放射治疗技术的进步有助于提高准确性并减少副作用。人们越来越重视将放射治疗纳入综合治疗策略的联合治疗,这也推动了放射治疗的需求。
由于先进的医疗基础设施、黑色素瘤患者的高盛行率以及活跃的研发活动,预计北美将在黑色素瘤诊断和治疗市场中占据最大的市场占有率。此外,意识的提高、创新诊断技术的早期采用以及主要市场参与者的存在也有助于北美的主导地位。此外,有利的报销政策、积极的法规环境以及对个人化医疗的关注进一步支持了该地区的市场领导地位。
预计亚太地区黑色素瘤诊断和治疗市场的成长率最高。这是由于人们认识的提高、医疗基础设施的改善、可支配收入的增加以及人口高龄化导致黑色素瘤发病率上升。此外,该地区主要经济体医疗保健技术的进步、研究倡议的扩大以及对个人化医疗的关注正在进一步推动对先进诊断和治疗的需求。
According to Stratistics MRC, the Global Melanoma Diagnostics and Therapeutics Market is growing at a CAGR of 17.1% during the forecast period. Melanoma diagnostics involve the identification and assessment of melanocytic lesions to diagnose skin cancer. Techniques include dermoscopy, biopsy, and molecular testing to analyze genetic mutations. Therapeutics for melanoma comprise surgical excision, immunotherapy, targeted therapy, and chemotherapy. Immunotherapies like checkpoint inhibitors and targeted therapies addressing specific genetic alterations play a crucial role. Early detection and personalized treatment strategies are pivotal in managing melanoma.
According to the American Cancer Society, about 99,780 new melanomas will be diagnosed in the United States in 2022, and around 7,650 people are expected to die of melanoma in the same year.
Rising incidence of melanoma
Factors such as prolonged sun exposure, changing lifestyles, and genetic predispositions contribute to a rising number of melanoma cases globally. This surge in incidence necessitates advanced diagnostic tools and therapeutic interventions. Increased awareness campaigns and routine skin screenings further amplify the demand for early detection and effective treatments. The industry's response to this growing health concern involves continuous innovation in diagnostics and therapeutics, positioning the rising incidence of melanoma as a crucial driver fueling market expansion.
High treatment costs
The expenses associated with innovative diagnostics, targeted therapies, and immunotherapies for melanoma can be substantial, limiting accessibility for a portion of the patient population. This financial barrier hampers timely and optimal treatment, potentially impacting patient outcomes. Additionally, high costs may strain healthcare systems and result in economic challenges for both individuals and payers, impacting overall market growth.
Advancements in diagnostic technologies
Innovative diagnostic tools, such as high-resolution imaging techniques, liquid biopsy assays, and molecular profiling, enable earlier and more accurate detection of melanoma. The enhanced sensitivity and specificity of these technologies contribute to timely interventions, improving patient outcomes. Moreover, non-invasive and precise diagnostic methods align with the growing trend of personalized medicine, facilitating tailored treatment approaches. These technological advancements not only aid in early diagnosis but also play a crucial role in monitoring treatment response and disease progression.
Limited availability of specialized healthcare centers
The limited availability of specialized healthcare centers represents a significant threat to the melanoma diagnostics and therapeutics market. Melanoma often requires specialized expertise for accurate diagnosis and tailored treatment plans. The scarcity of such centers can lead to delays in diagnosis, hinder access to advanced therapeutic interventions, and limit patient outcomes. Additionally, patients may face geographical barriers, particularly in underserved regions, impacting timely access to crucial diagnostic services and cutting-edge therapies, which limits market expansion.
The COVID-19 pandemic significantly impacted the melanoma diagnostics and therapeutics market. Disruptions in healthcare services, reprioritization of resources, and patients' concerns about visiting healthcare facilities led to delays in melanoma diagnosis and treatment. However, the pandemic underscored the importance of innovative and remote healthcare solutions, accelerating the adoption of telemedicine and digital health technologies.
The blood tests segment is expected to be the largest during the forecast period
The blood testing segment is expected to be the largest in the melanoma diagnostics market due to its non-invasive nature and efficiency in detecting biomarkers associated with melanoma. Blood-based tests offer a convenient and accessible means for early detection, enabling timely intervention. Advancements in liquid biopsy technologies and the identification of circulating tumor markers in blood contribute to the segment's prominence. As the demand for accurate, less invasive diagnostic methods grows, the blood testing segment is anticipated to dominate, catering to the increasing need for effective melanoma detection and monitoring.
The radiotherapy segment is expected to have the highest CAGR during the forecast period
The radiotherapy segment is projected to achieve lucrative growth in the melanoma diagnostics and therapeutics market. This growth is attributed to the increasing adoption of radiotherapy as an effective treatment option for melanoma. Technological advancements in radiotherapy techniques, including intensity-modulated radiation therapy (IMRT) and stereotactic radiosurgery, contribute to enhanced precision and reduced side effects. The growing emphasis on combination therapies, where radiotherapy is integrated into comprehensive treatment strategies, further propels the demand for radiotherapy.
North America is poised to command the largest market share in the melanoma diagnostics and therapeutics market due to its advanced healthcare infrastructure, a high prevalence of melanoma cases, and robust research and development activities. Moreover, increasing awareness, early adoption of innovative diagnostic technologies, and the presence of key market players contribute to North America's dominant position. Additionally, favorable reimbursement policies, a proactive regulatory environment, and a focus on personalized medicine further drive the region's leadership in the market.
The Asia Pacific region is poised to experience the highest growth rate in the melanoma diagnostics and therapeutics market due to increasing awareness, improving healthcare infrastructure, rising disposable income, and a growing aging population that contribute to a higher prevalence of melanoma cases. Additionally, advancements in healthcare technologies, expanding research initiatives, and a focus on personalized medicine in key economies within the region further drive the demand for advanced diagnostics and therapeutics.
Some of the key players in Melanoma Diagnostics And Therapeutics Market include Abbott Diagnostics, Agilent Technologies, Amgen, Inc., AstraZeneca, Biomerieux SA, Bristol Myers Squibb, Caliber Imaging & Diagnostics, Inc., Canfield Scientific, Inc., Dermlite, DermTech, Eli Lilly and Company, Roche Holding AG, GlaxoSmithKline PLC, Merck & Co., Inc, Novartis AG, Pfizer, Inc., Qiagen and Sanofi.
In November 2023, The U.S. Food and Drug Administration (FDA) approved Eli Lilly and Company's Zepbound™ (tirzepatide) injection, the first and only obesity treatment of its kind that activates both GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 (glucagon-like peptide-1) hormone receptors.
In November 2023, Amgen announced new data reinforcing the safety and efficacy of Repatha® (evolocumab) from the FOURIER Open Label Extension (OLE) [FOURIER-OLE] trial at the American Heart Association (AHA) Scientific Sessions 2023 in Philadelphia. These presentations will focus on the reduction of a known cardiovascular disease (CVD) risk factor, LDL "bad" cholesterol (LDL-C). Amgen will also present new research from the Phase 2 OCEAN(a)-DOSE study of its investigational small interfering RNA (siRNA) olpasiran that will focus on a primarily genetically determined and presumed independent CVD risk factor, lipoprotein(a) [Lp(a)].
In October 2023, Novartis, a global leader in immuno-dermatology and rheumatology, announced that the US Food and Drug Administration (FDA) has approved Cosentyx® (secukinumab) to treat moderate to severe hidradenitis suppurativa (HS) in adults. Cosentyx is the only FDA-approved fully human biologic that directly inhibits interleukin-17A (IL-17A), a cytokine believed to be involved in the inflammation of HS.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.