PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1836593
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1836593
The brain tumor therapeutics market reached USD 3.19 billion in 2025 and is forecast to climb to USD 4.67 billion by 2030, expanding at a 7.89% CAGR.
Robust growth reflects the convergence of precision-medicine breakthroughs, fast-track approvals, and a steady pipeline of late-stage assets that shorten the bench-to-bedside journey. The commercial roll-out of Boron Neutron Capture Therapy (BNCT) alongside AI-enabled drug-repurposing tools is shifting therapeutic expectations, particularly for glioma and other high-grade tumors. Intravenous regimens still dominate clinical practice because they allow tight pharmacokinetic control, yet oral targeted agents are gaining traction as blood-brain barrier solutions improve. Investors continue to funnel record sums into neuro-oncology, with large biopharma groups allocating more than USD 53 billion to neurological assets in the past two years. However, radio-isotope supply chain disruptions and elevated therapy costs temper near-term momentum.
Regulatory speed continues to reshape the brain tumor therapeutics market. Vorasidenib's 2024 approval for grade 2 IDH-mutant glioma doubled median progression-free survival versus placebo, validating biomarker-guided development paths. Breakthrough therapy designations are compressing timelines, while investigational device exemptions now cover novel radiotherapy platforms such as Alpha DaRT's radium-224 seeds for recurrent glioblastoma. Collective momentum shortens commercialization cycles and encourages multi-arm master trials that match molecular subsets with targeted agents.
Routine testing for IDH mutation, MGMT promoter methylation, and 1p/19q codeletion now guides regimen selection in leading centers. Liquid biopsy platforms provide real-time molecular readouts, allowing therapy switches before radiographic progression. Machine-learning algorithms integrating multi-omics profiles already predict immunotherapy responses with 90%+ accuracy, a capability that is refining eligibility criteria for checkpoint blockade.
First-in-class cell and gene therapies often exceed USD 400,000 per course, while multi-agent combinations can add another USD 300,000 annually, straining payer budgets. Health systems now link reimbursement to real-world outcomes, creating coverage delays that limit early adoption in lower-income settings.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Glioblastoma held 51.23% of brain tumor therapeutics market share in 2024 and is projected to grow at an 8.45% CAGR, sustaining the largest slice of the brain tumor therapeutics market size through 2030. High mortality, limited standard-of-care options, and the emergence of tumor-treating fields help maintain investor focus.
Continued device-drug pairings, peptide vaccines, and IDH-selective inhibitors illustrate capital concentration in this segment. Meningioma follows in value terms thanks to refined radiosurgery protocols, whereas pituitary tumors benefit from novel endocrine modulators that normalize hormone levels more predictably. Pediatric-leaning subtypes such as medulloblastoma and ependymoma now integrate risk-adapted radiotherapy with molecular diagnostics, improving five-year survival yet leaving relapsed disease an urgent research priority.
The Brain Tumor Therapeutics Market Report is Segmented by Type of Brain Cancer (Glioblastoma, Meningioma, and More), Therapy (Chemotherapy, Immunotherapy, Gene & Cell Therapy, and More), Route of Administration (Oral, Intravenous, and More), and Geography (North America, Europe, Asia-Pacific, Middle East and Africa, and South America). The Market Forecasts are Provided in Terms of Value (USD).
North America maintained 40.34% market share in 2024 and enjoys unrivaled clinical-trial density, genomic testing adoption, and payer mechanisms that expedite new product uptake. The region's large installed base of Gamma Knife and BNCT systems supports combination regimens, and philanthropic funding from the Biden Cancer Moonshot sustains translational research programs.
Europe follows with steady contributions as EMA centralized approvals streamline access across member states, and public-private partnerships co-finance orphan-tumor projects. Germany, France, and Italy collectively host more than 120 ongoing brain tumor interventional studies, while pan-European registries supply real-world evidence to health technology assessment agencies.
Asia-Pacific, the fastest-growing region at 8.54% CAGR, benefits from China's regulatory modernization, where 60+ innovative drugs won clearance under accelerated pathways in 2024. Japan's early BNCT adoption makes the country a regional referral hub, and Australian institutions leverage favorable ethics timelines to recruit international patients. Improving reimbursement frameworks in South Korea and Singapore further broaden patient access to leading-edge regimens.