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市場調査レポート
商品コード
1724940
転移性乳がん治療市場:治療法別、流通チャネル別、地域別、機会、予測、2018年~2032年Metastatic Breast Cancer Therapeutics Market Assessment, By Therapy, By Distribution Channel, By Region, Opportunities and Forecast, 2018-2032F |
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カスタマイズ可能
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転移性乳がん治療市場:治療法別、流通チャネル別、地域別、機会、予測、2018年~2032年 |
出版日: 2025年05月14日
発行: Market Xcel - Markets and Data
ページ情報: 英文 238 Pages
納期: 3~5営業日
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世界の転移性乳がん治療の市場規模は、2025年~2032年の予測期間中に11.27%のCAGRで拡大し、2024年の218億米ドルから2032年には512億2,000万米ドルに成長すると予測されています。転移性乳がん治療薬の世界市場は、罹患率の上昇、標的療法の進歩、研究資金の増加により拡大しています。また、認知度の向上と早期診断が治療の普及を促進し、市場関係者にさまざまな市場成長機会を提供しています。さらに、新規薬剤クラスの導入が世界の治療見通しを再構築しています。
例えば、2023年2月、Gilead Sciences, Inc.は、手術不能な局所進行性または転移性乳がんの成人患者を治療するためのトロデルヴィの米国食品医薬品局(FDA)承認を取得しました。この承認は、利用可能な治療の選択肢を増やし、乳がんに苦しむ患者の予後改善につながることが期待されます。
当レポートでは、世界の転移性乳がん治療市場について調査し、市場の概要とともに、治療法別、流通チャネル別、地域別動向、および市場に参入する企業のプロファイルなどを提供しています。
Global metastatic breast cancer therapeutics market is projected to witness a CAGR of 11.27% during the forecast period 2025-2032, growing from USD 21.80 billion in 2024 to USD 51.22 billion in 2032. The global metastatic breast cancer therapeutics market is expanding due to rising incidence rates, advancements in targeted therapies, and increased research funding. Growing awareness and early diagnosis are also driving treatment adoption and offering different market growth opportunities to market players. Additionally, the introduction of novel drug classes is reshaping the treatment landscape globally.
For instance, in February 2023, Gilead Sciences, Inc. received the U.S. Food and Drug Administration (FDA) approval for Trodelvy to treat adult patients with inoperable locally advanced or metastatic breast cancer. This approval anticipates enhancing the available treatment choices and likely leads to improved outcomes for patients suffering from breast cancer.
Increasing Prevalence of Metastatic Breast Cancer Globally
The global burden of metastatic breast cancer (MBC) is rising, driven by increasing incidence rates and extended life expectancy. According to the World Health Organization, breast cancer remains the most common cancer among women globally, with a notable portion eventually progressing to the metastatic stage. Improved screening and diagnostic technologies have increased early detection, yet many cases remain undetected until advanced stages, especially in low-resource settings. Additionally, the growing aging population contributes to higher MBC prevalence since age is a significant risk factor. These trends are propelling the demand for effective MBC therapeutics that extend survival and enhance quality of life. Consequently, pharmaceutical companies are boosting R&D efforts to address this unmet need, driving market growth. For instance, in April 2024, Eli Lilly and Company announced plans to expand its breast cancer research program, focusing on metastatic subtypes following a global rise in advanced-stage cases.
Advancements in Biologic Targeted Therapies
The development of biologic targeted therapies has significantly transformed the treatment landscape for metastatic breast cancer. These therapies, designed to target specific genetic markers such as HER2 or hormone receptors, have demonstrated improved efficacy and reduced toxicity compared to traditional chemotherapies. Monoclonal antibodies, antibody-drug conjugates, and small-molecule inhibitors have gained prominence due to their precision in targeting cancer cells while sparing healthy tissue. Biologics not only improve progression-free survival but also open pathways for combination therapies with immunotherapy or hormone therapy. The high success rate in clinical trials and growing approvals from regulatory bodies are accelerating patient access. This trend is expected to boost the global MBC therapeutics market in the coming years. For instance, in October 2023, AstraZeneca plc and Daiichi Sankyo, Inc.'s Enhertu received FDA approval for treating HER2-low metastatic breast cancer, following strong results in the DESTINY-Breast04 trial.
Segmental Growth Driven by Hormone Therapy Adoption
Hormone therapy is a key segment in metastatic breast cancer therapeutics, especially for patients with hormone receptor-positive (HR+) tumors, which constitute a significant share of MBC cases. This therapy works by blocking or lowering estrogen levels to slow down cancer growth. The widespread use of selective estrogen receptor modulators (SERMs), aromatase inhibitors, and estrogen receptor degraders has led to improved disease control with fewer side effects compared to chemotherapy. Additionally, hormone therapies are frequently used as first-line treatments, delaying the need for more aggressive interventions. Recent innovations such as oral SERDs (Selective Estrogen Receptor Degraders) are gaining regulatory attention, further expanding this segment. For instance, in January, 2023, the Food and Drug Administration (FDA) approved elacestrant (Orserdu, Stemline Therapeutics, Inc.) for use in postmenopausal women and adult men diagnosed with ER-positive, HER2-negative, ESR1-mutated advanced or metastatic breast cancer who have experienced disease progression after at least one line of endocrine therapy. Additionally, the FDA approved the Guardant360 CDx assay as a companion diagnostic tool to help identify breast cancer patients eligible for treatment with elacestrant.
North America Maintains Market Leadership
North America holds the largest share in the metastatic breast cancer therapeutics market, primarily due to the region's well-established healthcare infrastructure, higher awareness levels, and extensive R&D activities. The United States accounts for a significant portion, driven by favorable reimbursement policies, availability of advanced diagnostics, and a strong presence of key pharmaceutical players. Furthermore, government and private sector investments in cancer research and clinical trials have spurred innovation and early market entry for new therapies. The higher prevalence of lifestyle-related risk factors, such as obesity and delayed childbearing, also contributes to the rising incidence, thereby increasing treatment demand. For instance, in November 2023, Truqap (capivasertib) plus Faslodex was approved in the U.S. for patients to cure advanced HR-positive breast cancer.
Future Market Scenario (2025-2032F)
The global metastatic breast cancer therapeutics market is poised for substantial growth due to rising disease incidence, improved diagnostic accuracy, and rapid advancements in precision medicine. Increasing investments in clinical research and the development of targeted therapies, including antibody-drug conjugates and oral selective estrogen receptor degraders, are expanding treatment options and improving patient outcomes. Additionally, the integration of artificial intelligence in drug discovery and personalized medicine approaches is expected to drive innovation. With a growing focus on patient-centric care and expansion of access through online pharmacies and cancer centers, the market is likely to witness accelerated growth globally. Emerging economies, particularly in Asia-Pacific and Latin America, are anticipated to offer lucrative opportunities as healthcare infrastructure and awareness improve.
Key Players Landscape and Outlook
The key players in the market are significantly investing in the development of metastatic breast cancer therapeutics and are utilizing strategies such as mergers, acquisitions, partnerships, and new product launches to improve their services and competitiveness.
Such efforts will propel significant growth in the market, allowing large-cap industry players to increase their presence and, therefore, find new opportunities in this market.
For example, in 2024, the FDA approved a triple therapy that integrates the small molecule medication inavolisib (Itovebi) with fulvestrant (Faslodex), a hormone treatment, and palbociclib (Ibrance), another small molecule drug, aimed at specific patients suffering from advanced or metastatic HR-positive breast cancer with genetic mutations affecting a protein known as PI3K. Inavolisib inhibits the excessively active variants of PI3K, whereas palbociclib obstructs the functions of the CDK4 and CDK6 proteins, which are responsible for regulating cell growth.
All segments will be provided for all regions and countries covered
Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.