Imatinib

Imatinib (Glivec, Novartis Europharm Limited) has 9 EU-approved indications in 5 tumour types. 8 need a biomarker result: BCR::ABL1 (4), KIT (2), FIP1L1::PDGFRA (1) and PDGFR (1).
Approved indications of Imatinib
Biomarker requirementRegimenSettingConditions
Gastrointestinal stromal tumour2
KIT-positive
Monotherapy
Adj.
After resection of Kit (CD117)-positive GIST; Significant risk of relapse; patients who have a low or very low risk of recurrence should not receive adjuvant treatment
KIT-positive
Monotherapy
Any line
advanced
None
Soft tissue sarcoma1
None
Monotherapy
Any line
advanced
Dermatofibrosarcoma protuberans only; Not eligible for surgery (for recurrent and/or metastatic DFSP)
Acute lymphoblastic leukaemia2
Philadelphia chromosome (bcr-abl)
+ chemotherapy
1L
None
Philadelphia chromosome (bcr-abl)
Monotherapy
2L
Relapsed or refractory disease
Chronic myeloid leukaemia2
Philadelphia chromosome (bcr-abl)
Monotherapy
1L
Bone marrow transplantation is not considered as the first line of treatment
Philadelphia chromosome (bcr-abl)
Monotherapy
Any line
Failure of interferon-alpha therapy (for chronic phase)
Myeloid/lymphoid neoplasms with eosinophilia and TK fusions2
PDGFR fusion
Monotherapy
Any line
None
FIP1L1-PDGFRalpha rearrangement
Monotherapy
Any line
advanced
None
Full text of section 4.1 (therapeutic indications)

Glivec is indicated for the treatment of • adult and paediatric patients with newly diagnosed Philadelphia chromosome (bcr-abl) positive (Ph+) chronic myeloid leukaemia (CML) for whom bone marrow transplantation is not considered as the first line of treatment. • adult and paediatric patients with Ph+ CML in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. • adult and paediatric patients with newly diagnosed Philadelphia chromosome positive acute lymphoblastic leukaemia (Ph+ ALL) integrated with chemotherapy. • adult patients with relapsed or refractory Ph+ ALL as monotherapy. • adult patients with myelodysplastic/myeloproliferative diseases (MDS/MPD) associated with platelet-derived growth factor receptor (PDGFR) gene re-arrangements. • adult patients with advanced hypereosinophilic syndrome (HES) and/or chronic eosinophilic leukaemia (CEL) with FIP1L1-PDGFR rearrangement. The effect of Glivec on the outcome of bone marrow transplantation has not been determined. Glivec is indicated for • the treatment of adult patients with Kit (CD 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (GIST). • the adjuvant treatment of adult patients who are at significant risk of relapse following resection of Kit (CD117)-positive GIST. Patients who have a low or very low risk of recurrence should not receive adjuvant treatment. • the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (DFSP) and adult patients with recurrent and/or metastatic DFSP who are not eligible for surgery. In adult and paediatric patients, the effectiveness of Glivec is based on overall haematological and cytogenetic response rates and progression-free survival in CML, on haematological and cytogenetic response rates in Ph+ ALL, MDS/MPD, on haematological response rates in HES/CEL and on objective response rates in adult patients with unresectable and/or metastatic GIST and DFSP and on recurrence-free survival in adjuvant GIST. The experience with Glivec in patients with MDS/MPD associated with PDGFR gene re-arrangements is very limited (see section 5.1). Except in newly diagnosed chronic phase CML, there are no controlled trials demonstrating a clinical benefit or increased survival for these diseases.

Label history

84 changes to the Glivec label since 2002, 9 of them to the indications. Newest first, in the words of EMA's record of each procedure.

Changes