PDGFR
3 EU-approved indications of 2 drugs need a PDGFR result, in 2 tumour types, most of them in myeloid/lymphoid neoplasms with eosinophilia and TK fusions and gastrointestinal stromal tumour.
Approved indications3
| Drug | Biomarker requirement | Regimen | Setting | Conditions |
|---|---|---|---|---|
| Gastrointestinal stromal tumour1 | ||||
Ayvakytconditional | D842V | Monotherapy | Any line advanced | None |
| Myeloid/lymphoid neoplasms with eosinophilia and TK fusions2 | ||||
Glivec | Monotherapy | Any line | None | |
Glivec | FIP1L1-PDGFRalpha rearrangement | Monotherapy | Any line advanced | None |
PDGFR by tumour
Label wording3
The sentence from section 4.1 of the SmPC that each indication above comes from.
- Avapritinib (Ayvakyt)
AYVAKYT is indicated as monotherapy for the treatment of adult patients with unresectable or metastatic gastrointestinal stromal tumours (GIST) harbouring the platelet-derived growth factor receptor alpha (PDGFRA) D842V mutation.
- Imatinib (Glivec)
adult patients with myelodysplastic/myeloproliferative diseases (MDS/MPD) associated with platelet-derived growth factor receptor (PDGFR) gene re-arrangements.
- Imatinib (Glivec)
adult patients with advanced hypereosinophilic syndrome (HES) and/or chronic eosinophilic leukaemia (CEL) with FIP1L1-PDGFRα rearrangement.