PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1836639
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1836639
The Asia-Pacific cancer vaccines market was valued at USD 2.18 billion in 2025 and is forecast to reach USD 3.77 billion by 2030, advancing at an 11.58% CAGR.
Sustained growth rests on the region's escalating cancer burden, policy-backed HPV immunisation roll-outs, and rapid breakthroughs in personalised mRNA-neoantigen platforms. Governments prioritise cervical-cancer prevention, while investors funnel capital into biotech clusters that shorten clinical timelines for new therapeutic vaccines. Contract development and manufacturing organisations (CDMOs) in China, India, and South Korea add capacity for viral-vector and mRNA production, flattening supply-chain risk and lowering unit costs. Intensifying competition from immune checkpoint inhibitors, CAR-T therapies, and emerging combination regimens tempers the speed of therapeutic uptake, yet economic analyses still favour vaccination over treatment for many tumour types. Together, these factors underpin double-digit annual expansion of the Asia-Pacific cancer vaccines market.
Asia-Pacific now shoulders 60% of global cancer cases, a figure driven by urbanisation, dietary shifts, and rapid population ageing. China reports 4.57 million new diagnoses annually, while cervical cancer incidence in India exceeds 23 per 100,000 women in several states. Region-specific malignancies-nasopharyngeal, hepatocellular, and gastric cancers-raise unique prevention needs. Economic modelling shows that vaccination can cut cervical cancer incidence by 20-76% across Vietnam, Thailand, and Indonesia, making prophylaxis more cost-effective than treatment. These dynamics sustain long-term demand for both preventive and therapeutic cancer vaccines.
China's Healthy China 2030 agenda places HPV immunisation at the centre of women's-health policy, even though coverage among girls aged 9-14 stands at just 2.24% . Japan reversed its decade-long suspension of proactive HPV recommendations, Australia already tops 90% coverage, and Indonesia's campaigns show 54-82% declines in HPV-related disease. Incremental cost-effectiveness ratios range from USD 166 to USD 450 per QALY in Mongolia, Indonesia, and Thailand, giving finance ministries confidence to fund large-scale procurement. Predictable demand volumes allow suppliers to negotiate long-term contracts and ramp regional output.
PD-1/PD-L1 inhibitors could generate USD 4 billion in China by 2025, with domestic firms moving beyond lung and liver cancer into broader solid-tumour pipelines. Claudin18.2 CAR-T protocols report 38.8% objective response and 91.8% disease-control rates in early-phase gastrointestinal trials. Acceptable safety profiles-96.1% of adverse events graded mild or moderate-bolster clinician confidence and may divert patients from vaccine based therapeutics. Combination regimens such as efti plus pembrolizumab post 32.8% response versus 26.7% for monotherapy, further crowding the immuno-oncology landscape.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Recombinant products held 48.41% of 2024 revenue, anchoring the Asia-Pacific cancer vaccines market with proven safety records and well-established GMP lines. The mRNA/neoantigen class is set to rise at 12.23% CAGR, reshaping the competitive grid as cost-efficient Chinese playersrapidly commercialise personalised candidates. Viral-vector and DNA modalities post stable mid-single-digit trajectories, serving as bridges between legacy constructs and next-generation therapies. Whole-cell and dendritic-cell vaccines remain niche, yet they retain clinical relevance for advanced solid tumours that require multi-antigen responses.
The mRNA upswing is powered by AI-driven target discovery and flexible production cycles that compress sequence-to-clinic timelines. Likang Life Sciences' LK-101 and StemiRNA's lipid-polyplex system illustrate cost-engineering advantages, enabling six-dose regimens at one-hundredth of prevailing Western prices. Regional CDMO build-outs further widen the gap by eliminating transcontinental freight and customs delays. As a result, mRNA lines are forecast to absorb a sizeable share of future approvals, particularly in cancers with high mutational loads such as melanoma and lung adenocarcinoma.
Preventive formulations controlled 91.21% of 2024 revenue, reflecting government-funded HPV programmes and broad public-health messaging. Therapeutic candidates, however, are tracking a 12.31% CAGR on rising demand for patient-specific regimens that augment checkpoint inhibitors. The Asia-Pacific cancer vaccines market size for therapeutic injections is projected to expand from USD 192 million in 2025 to roughly USD 344 million by 2030, underscoring the shift toward integrated care pathways.
Economic models continue to favour prophylaxis, with HPV programmes costing below USD 450 per QALY in multiple low- and middle-income settings. Yet second-line data for agents like BVAC-C, which delivered 19.2% objective response and 53.8% disease control in refractory cervical cancer, validate therapeutic relevance. As neoantigen selection tools mature, therapeutic cycles are expected to integrate seamlessly with standard chemoradiation, redefining downstream revenue pools.
The Asia-Pacific Cancer Vaccines Market is Segmented by Technology (Recombinant Vaccines, and More), Treatment Method (Preventive Vaccines and Therapeutic Vaccines), Cancer Type (Cervical Cancer (HPV), Melanoma and More), Delivery Route (Intramuscular, Intravenous, and More), and Geography (China, Japan, India, and More). The Market and Forecasts are Provided in Terms of Value (USD).