Imatinib
| Biomarker requirement | Regimen | Setting | Conditions |
|---|---|---|---|
| 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