FDA Approves Gemtuzumab Ozogamicin for AML

WEDNESDAY, NOVEMBER 1, 2017

 

The U.S. Food and Drug Administration (FDA) approved gemtuzumab ozogamicin (GO) for two patient populations: adults with newly diagnosed CD33-positive acute myeloid leukemia (AML) and children ≥2 years old with relapsed or refractory CD33-positive AML.

 

GO originally received accelerated approval in May 2000 as monotherapy for older patients with relapsed CD33-positive AML. In June 2010, the drug was voluntarily withdrawn from the market after subsequent confirmatory trials failed to verify clinical benefit and demonstrated safety concerns, including early deaths.

 

This recent approval includes a lower recommended dose, as well as new patient populations and a different dosing schedule, in combination with chemotherapy or as monotherapy. “We are approving [GO] after a careful review of the new dosing regimen, which has shown that the benefits of this treatment outweigh the risk,” said Richard Pazdur, MD, director of the FDA’s Oncology Center of Excellence and acting director of the Office of Hematology and Oncology Products in the FDA’s Center for Drug Evaluation and Research.

 

The approval was based on outcomes from three clinical trials – one investigated GO in combination with chemotherapy, and two investigated GO as a single agent. In the combination study, 271 adult patients with newly diagnosed CD33-positive AML were randomized to receive daunorubicin and cytarabine with or without GO; patients who received GO plus daunorubicin and cytarabine had a median event-free survival of 17.3 months (range not provided), compared with 9.5 months (range not provided) in those who received chemotherapy alone (p value not reported).

 

In the first monotherapy study, 237 patients with newly diagnosed AML who could not tolerate or chose not to receive intensive chemotherapy were randomized to receive GO or best supportive care. The median overall survival (OS) was 4.9 months in those receiving GO, compared with 3.6 months in those receiving best supportive care (p values not reported). In the second monotherapy trial, which was a single-arm study of 57 patients with relapsed CD33-positive AML, 26 percent of patients achieved a complete remission that lasted a median of 11.6 months (range not provided) after receiving a single course of GO.

 

The most common AEs associated with GO included pyrexia, nausea, infection, vomiting, bleeding, thrombocytopenia, stomatitis, constipation, rash, headache, elevated liver function tests, and neutropenia. Severe AEs included leukopenia, infection, liver damage, hepatic veno-occlusive disease, infusion-related reactions (IRRs), and hemorrhage.

GO previously received orphan-drug designation and carries a boxed warning that severe or fatal hepatotoxicity, including veno-occlusive disease and sinusoidal obstruction syndrome, has occurred in some patients.

 

Source: U.S. Food and Drug Administration press release, September 1, 2017.