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FDA Grants Accelerated Approval to Blinatumomab for the Treatment of B-cell Precursor ALL

It is indicated in adult and paediatric patients in first or second complete remission with minimal residual disease
30 Mar 2018
Immunotherapy
Haematological Malignancies

On 29 March 2018, the US Food and Drug Administration (FDA) granted accelerated approval to blinatumomab (Blincyto, Amgen Inc.) for the treatment of adult and paediatric patients with B-cell precursor acute lymphoblastic leukaemia (ALL) in first or second complete remission with minimal residual disease (MRD) greater than or equal to 0.1%.

Approval was based on the open label, multicentre, single-arm BLAST trial (NCT 01207388) that included 86 patients who were at least 18 years of age, had received at least 3 chemotherapy blocks of standard ALL therapy, were in complete haematologic remission (defined as < 5% blasts in bone marrow, absolute neutrophil count > 1 Gi/L, platelets > 100 Gi/L) and had MRD at a level of greater than or equal to 0.1% using an assay with a minimum sensitivity of 0.01%. Blinatumomab was administered at a constant dose of 15 mcg/m2/day (equivalent to the recommended dose of 28 mcg/day) intravenously for all treatment cycles. Patients received up to 4 cycles of treatment. Following treatment with blinatumomab, 45 out of 61 (74%) patients in CR1 and 14 out of 25 (56%) patients in CR2 underwent allogeneic haematopoietic stem cell transplantation in continuous haematologic complete remission.

Efficacy was based on both achievement of undetectable MRD within one cycle of blinatumomab treatment and haematological relapse-free survival (RFS). The assay used to assess MRD response had a sensitivity of 0.01% for 6 patients and less than or equal to 0.005% for 80 patients. Overall, undetectable MRD was achieved by 52 patients in CR1 (85%; 95% CI: 74%, 93%) and 18 patients in CR2 (72%; 95% CI: 51%, 88%). The median estimated haematological RFS with majority of patients transplanted was 35.2 (range 0.4, 53.5) months for patients in CR1 and 12.3 (range 0.7, 42.3) months for patients in CR2.

The most common adverse reactions to blinatumomab in at least 20% of patients with MRD-positive B-cell precursor ALL were pyrexia, infusion related reactions, headache, infections (pathogen unspecified), tremor, and chills. Serious adverse reactions were reported in 61% of patients. The most common serious adverse reactions in at least 2% of patients included pyrexia, tremor, encephalopathy, aphasia, lymphopenia, neutropenia, overdose, device related infection, seizure, and staphylococcal infection. Adverse reactions of grade 3 or higher were reported in 64% of patients. Discontinuation of therapy due to adverse reactions occurred in 17% of patients; neurologic events were the most frequently reported reasons for discontinuation. There were 2 fatal adverse events that occurred within 30 days of the end of blinatumomab treatment (atypical pneumonia and subdural haemorrhage).

Full Prescribing Information for recommended dose by patient weight and schedule are available here.  

FDA granted this application priority review and orphan designation. Continued approval for the new indication is contingent upon verification and description of clinical benefit in confirmatory trials.

Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine and device to FDA’s MedWatch Reporting System.

Last update: 30 Mar 2018

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