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Version 3 (3 December 2024)
Version 2 (4 June 2024)
Version 1 (5 December 2023)
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Datopotamab deruxtecan
Extended indication
Datopotamab deruxtecan as monotherapy is indicated for the treatment of adult patients with locally
recurrent inoperable or metastatic Triple-Negative Breast Cancer (TNBC) who are not candidates for PD-1/PD-L1 inhibitor therapy.
Therapeutic value
No estimate possible yet
Registration phase
Clinical trials
Product
Active substance
Datopotamab deruxtecan
Domain
Oncology
Reason of inclusion
Indication extension
Main indication
Breast cancer
Extended indication
Datopotamab deruxtecan as monotherapy is indicated for the treatment of adult patients with locally recurrent inoperable or metastatic Triple-Negative Breast Cancer (TNBC) who are not candidates for PD-1/PD-L1 inhibitor therapy.
Manufacturer
Daiichi Sankyo
Portfolio holder
Daiichi Sankyo
Mechanism of action
Antibody-drug conjugate
Route of administration
Intravenous
Therapeutical formulation
Injection / infusion solution
Budgetting framework
Intermural (MSZ)
Registration
Registration route
Centralised (EMA)
Type of trajectory
Normal trajectory
Particularity
New therapeutical formulation
ATMP
No
Submission date
2024
Expected Registration
2025
Orphan drug
No
Registration phase
Clinical trials
Therapeutic value
Current treatment options
Single-agent chemotherapy (eribulin, capecitabine, carboplatin, paclitaxel, Nab-paclitaxel)
Therapeutic value
No estimate possible yet
Substantiation
Er zijn nog geen resultaten bekend uit deTROPION-Breast02 studie.
Frequency of administration
1 times every 3 weeks
Dosage per administration
6,0 mg/kg
References
TROPION-Breast02 (NCT05374512)
Expected patient volume per year
References
Pakketadvies sluisgeneesmiddel sacituzumab govitecan (Trodelvy®) voor de behandeling van inoperabele of uitgezaaide borstkanker, ZIN 2022
Additional remarks
In het pakketadvies wordt een patiëntvolume van 277 ingeschat.
Expected cost per patient per year
Additional remarks
Not yet known
Potential total cost per year
Additional remarks
Not yet known
Off label use
Additional remarks
There is currently nothing known about off label use.
Indication extension
Indication extension
Yes
Indication extensions
Treatment of adult patients with previously treated advanced or metastatic non-small cell lung cancer (NSCLC) with or without actionable genomic alterations (NCT04656652). Treatment of adult patients with inoperable or metastatic HR-Positive, HER2-negative Breast Cancer who have been treated with one or two prior lines of systemic chemotherapy (NCT05104866). Treatment of adult patients with advanced or metastatic NSCLC without actionable genomic alterations whose tumor has high programmed death-ligand 1 (PD-L1) expression and who have not previously received systemic therapy for advanced or metastatic NSCLC (NCT05215340).
References
Manufacturer
Other information
Additional remarks
There is currently no further information available.
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