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Durvalumab

Imfinzi

Extended indication Extension of indication to include IMFINZI in combination with platinum-based chemotherapy as neoadj
Therapeutic value No estimate possible yet
Registration phase Registration application pending

Product

Active substance Durvalumab
Domain Oncology
Reason of inclusion Indication extension
Main indication Lung cancer
Extended indication Extension of indication to include IMFINZI in combination with platinum-based chemotherapy as neoadjuvant treatment, followed by IMFINZI as monotherapy after surgery, for the treatment of adults with resectable (tumours ≥ 4 cm and/or node positive) NSCLC and no known EGFR mutations or ALK rearrangements.
Proprietary name Imfinzi
Manufacturer AstraZeneca
Portfolio holder AstraZeneca
Mechanism of action PD-1 / PD-L1 inhibitor
Route of administration Intravenous
Therapeutical formulation Intravenous drip
Budgetting framework Intermural (MSZ)

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
ATMP No
Submission date January 2024
Expected Registration March 2025
Orphan drug No
Registration phase Registration application pending
Additional remarks Verwachte registratie op basis van IHSI-inschatting.

Therapeutic value

Therapeutic value No estimate possible yet
References NCT03800134 (AEGEAN)

Expected patient volume per year

Patient volume

1,514 - 2,246

Market share is generally not included unless otherwise stated.
References NKR 2020 (1);
Additional remarks In totaal zijn er op basis van bovenstaande data 2.246 patiënten met stadium IB-IIIA NSCLC (1). Op dit moment wordt neo-adjuvante behandeling in Nederland enkel gegeven aan patiënten in stadium 1B en 2, dit betreft (418+206+632=1.256 patiënten). Daarnaast komt mogelijk de groep patiënten die chirurgie ontvangt bij stadium IIIA in aanmerking voor deze therapie, dit betreffen (258 patiënten). Over deze laatste groep dient echter nog te worden besloten hoe de behandelingen in de praktijk gaat lopen, gezien er ook voor kan worden gekozen om bij een grotere groep patiënten chirurgie toe te passen (maximaal alle 990 patiënten met Stadium IIIA). Om die reden zal het patiëntvolume dat in aanmerking komt 1.514 tot 2.246 patiënten betreffen.

Expected cost per patient per year

There is currently nothing known about the expected cost.

Potential total cost per year

There is currently nothing known about the possible total cost.

Off label use

There is currently nothing known about off label use.

Indication extension

There is currently nothing known about indication extensions.

Other information

There is currently no futher information available.