Nivolumab Medicine 13 December 2018 Extended indication Extension of Indication to include first-line treatment of adult patients with metastatic Non-Small Cell Lung Carcinoma (NSCLC) in combination with ipilimumab. Therapeutic value No judgement Total cost Registration phase Registration application pending Product Active substance Nivolumab Domain Oncology and Hematology Reason of inclusion Indication extension IND Main indication Lung cancer Extended indication Extension of Indication to include first-line treatment of adult patients with metastatic Non-Small Cell Lung Carcinoma (NSCLC) in combination with ipilimumab. Current proprietary name Already available biosimilars / generics Proprietary name Opdivo Manufacturer BMS Portfolio holder Mechanism of action PD-1 / PD-L1 inhibitor Route of administration Intracavernous Therapeutical formulation Intravenous drip Budgetting framework Intermural (MSZ) Centre of expertise Additional remarks PD-1 remmer. Financieel arrangement van toepassing op alle indicaties. Registration Registration route Centralised (EMA) Type of trajectory Normal trajectory Particularity Unknown ATMP Unknown Submission date 2018 Expected Registration April 2019 Orphan drug No Registration phase Registration application pending Reimbursement Medicine sluice Additional remarks Checkmate 227; met PFS primary endpoint in high tumor burden. Therapeutic value Current treatment options Therapeutic value No judgement This assessment does not indicate any potential inclusion in the package. Substantiation Studieresultaten: wel een verschil in PFS maar geen verschil in OS, biomarker (tumour mutational load) daarnaast nog niet mogelijk in Nederland. Duration of treatment Median 4.2 Not found Frequency of administration 1 times every 2 weeks Dosage per administration 3 mg/kg References https://news.bms.com/press-release/bms/pivotal-phase-3-checkmate-227-study-demonstrates-superior-progression-free-surviva; Hellmann et al. N Engl J Med 2018; 378:2093-2104; NCT02477826 Additional remarks Opdivo 3 mg/kg every two weeks and low-dose Yervoy (1 mg/kg) every six weeks. Median duration of treatment is 4,2 maanden Expected patient volume per year Patient volume Market share is generally not included unless otherwise stated. Maximum patient volume for sluice References NKR 2016, GIP-databank. Additional remarks Jaarlijks presenteren er ongeveer 4.500 patiënten per jaar met NSCLC stadium IV. Hiervan zal 60% een eerstelijnsbehandeling krijgen (2.700). Deze behandeling zal zijn plaats hierin moeten veroveren. De biomarker die nodig is is nog niet overal beschikbaar in Nederland dus voorlopig zal deze behandleing nog niet ingevoerd gaan worden. Expected cost per patient per year Cost € 47,000.00 This amount gives an indication of the total cost. It is the result of the average expected patient volume times the average cost per patient. both per year. References G-standaard; Hellmann et al. N Engl J Med 2018 Additional remarks Ipilimumab 50 mg kost €4.250, ipilimumab 2.000 mg kost €17.000,00. Bij een behandelduur van 4,2 maanden worden 9 toedieningen Opdivo gebruikt: €21.871,00 (9x€2.430,00) en 3 toedieningen Yervoy: €25.500,00 (3x€8.500,00). In totaal bedraagt dit €47.371,00. Voor alle indicatie van nivolumab geldt een financieel arrangement die is voortgekomen uit de onderhandelingen in de sluis (lopend tot eind 2019). Potential total cost per year Total cost Total cost for sluice Additional remarks Off label use Off label use Unknown Indications off label use References Additional remarks Indication extension Indication extensions Unknown Indication extensions References Additional remarks Other information Additional remarks