PUBLISHER: Mellalta Meets LLP | PRODUCT CODE: 2117118
PUBLISHER: Mellalta Meets LLP | PRODUCT CODE: 2117118
Prostate cancer is the clearest aging-curve story in Japanese oncology: already the most common cancer in men, its incidence climbs mechanically as the male population grows older, pulling surgery capacity, hormone-therapy volumes, and imaging demand up with it. The disease also carries the newest modality question in Japanese cancer care. Pluvicto's NHI listing in November 2025 made radioligand therapy a reimbursed reality for metastatic castration-resistant disease, but the treatment is deliverable only at certified sites with nuclear-medicine infrastructure - a capacity question that will govern how quickly Japanese practice converts the global evidence into routine care.
The tension is a three-way sorting problem. Upstream, PSA testing practice in Japan remains opportunistic rather than programmatic, so stage at diagnosis varies widely by region and channel. Midstream, the androgen-receptor pathway inhibitors - abiraterone, enzalutamide, apalutamide, darolutamide - have layered onto androgen deprivation across non-metastatic and metastatic hormone-sensitive settings, with Japanese label timing and co-promotion structures shaping real use. Downstream, the castration-resistant space now stacks PARP inhibitors for HRR-altered disease, cabazitaxel, Xofigo for bone-dominant disease, and Pluvicto for PSMA-positive disease - each with its own diagnostic gate, and each competing for patients who are older and more comorbid than the trial populations that defined them.
This report maps prostate cancer in Japan from PSA testing to radioligand delivery. It lays out the detection and staging structure, the ARPI layer with its pivotal programs - LATITUDE, ARCHES, EMBARK, ARANOTE, TALAPRO-2, PROpel, STAMPEDE - and the mCRPC decision tree including VISION, PSMAfore, and the SPLASH challenger program from Lilly's POINT Biopharma. Dedicated chapters cover PSMA PET imaging supply from Lantheus, Telix, Curium, and Blue Earth Diagnostics, domestic radiopharmaceutical roles of PDRadiopharma, certified-site capacity formation, and the sequencing disputes that arise when radioligand therapy meets ARPI rechallenge.
The report serves uro-oncology BD and medical-affairs teams, hospital planners weighing RLT investment, imaging and nuclear-medicine suppliers, and investors tracking the modality's Japanese buildout. It connects the epidemiological driver to the infrastructure question, which is where Japanese prostate care will actually be decided.
Scope and Coverage: The report covers prostate cancer epidemiology, detection, staging, and treatment in Japan across hormone-sensitive and castration-resistant settings, including ARPI, PARP, radiopharmaceutical, and radioligand therapy options plus PSMA imaging infrastructure. It profiles Novartis, Johnson & Johnson, Astellas, Pfizer, Bayer, Lilly, AstraZeneca, Lantheus, Curium, Telix, Blue Earth Diagnostics, and PDRadiopharma.
Report Highlights: