Extended indication

Durvalumab in combination with carboplatin and paclitaxel is indicated for the first-line treatment

Therapeutic value

No estimate possible yet

Registration phase

Registered

Product

Active substance

Durvalumab

Domain

Oncology

Reason of inclusion

Indication extension

Main indication

Cervical cancer

Extended indication

Durvalumab in combination with carboplatin and paclitaxel is indicated for the first-line treatment of adults with primary advanced or recurrent endometrial cancer​ who are candidates for systemic therapy, followed by maintenance treatment with: - as monotherapy in endometrial cancer that is mismatch repair deficient (dMMR) - combination with olaparib in endometrial cancer that is mismatch repair proficient (pMMR).

Proprietary name

Imfinzi

Manufacturer

AstraZeneca

Mechanism of action

PD-1 / PD-L1 inhibitor

Route of administration

Intravenous

Budgetting framework

Intermural (MSZ)

Registration

ATMP

No

Submission date

2024

Expected Registration

September 2024

Orphan drug

No

Registration phase

Registered

Therapeutic value

Therapeutic value

No estimate possible yet

Expected patient volume per year

Patient volume

149 - 155

Market share is generally not included unless otherwise stated.

References
NKR (1); Advies - vergoed dostarlimab (Jemperli®) voor de behandeling van baarmoederkanker. Zorginstituut. 2024 (2).
Additional remarks
Jaarlijks worden ruim 2.000 nieuwe gevallen van endometriumcarcinoom gediagnosticeerd (1). Volgens de budget impactanalyse van de vergoeding van dostarlimab voor dezelfde indicatie als dit middel wordt een patiëntvolume van 149 tot 155 per jaar geschat (2).

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.