News Release
Alexander Perl, MD, MS

ATLANTA – An inhibitor drug that targets a specific mutation in relapsed or refractory acute myeloid leukemia (AML) helps patients live almost twice as long as those who receive chemotherapy. Researchers at the Abramson Cancer Center of the University of Pennsylvania will present the findings of ADMIRAL – a randomized clinical trial investigating the drug gilteritinib in patients with a mutation in the Fms-like tyrosine kinase 3 (FLT3) gene – today at the 2019 American Association for Cancer Research Annual Meeting in Atlanta (Abstract #7506). Alexander Perl, MD, MS, an associate professor of Hematology-Oncology in the Perelman School of Medicine at the University of Pennsylvania, led the trial and will present the results both at press briefing today as well as during a Tuesday plenary session. The drug, which is manufactured by Astellas Pharma, Inc., was recently approved by the U.S. Food and Drug Administration under the name XOSPATA® based on an interim analysis of this trial’s data.

“Patients with FLT3 mutations who have relapsed or refractory AML have very low response rates to chemotherapy at the time of relapse, and their survival is poor as a result,” Perl said. “This drug is specifically designed to help this group of patients, and now we’ve shown it can make a huge difference for those who, until recently, had no specific therapies available beyond chemotherapy.”

An estimated 19,000 patients will be diagnosed with AML in the United States this year. FLT3 is the most commonly mutated gene in AML and is found in about 30 percent of patients’ leukemia cells. The FLT3 gene is expressed in normal bone marrow cells and regulates the orderly growth of blood cells in response to daily demands. When the gene is mutated in a leukemia cell, however, the cancer cells grow in an uncontrolled manner unless the function of FLT3 is turned off by drugs like gilteritinib.

Gilteritinib is a pill patients take once a day, and previous studies have shown it can inhibit activity in AML patients with the two most common types of FLT3 mutations. The first is called FLT3 internal tandem duplication (FLT3-ITD) and is associated with aggressive disease behavior, frequent relapse, and short remission duration. The overall survival for patients with relapsed or refractory FLT3-ITD mutated AML historically has been an average of about four months with current therapies. To lower relapse risk, oncologists often recommend the most aggressive chemotherapy approaches for AML patients with FLT3-ITD, including marrow transplantation. The second FLT3 mutation gilteritinib targets occurs in the gene’s tyrosine kinase domain (TKD) and is associated with resistance to a number of previously developed FLT3 inhibitors.

In the ADMIRAL trial, 371 patients were randomized, with 247 receiving gilteritinib and 124 receiving chemotherapy. The patients who took gilteritinib had a median overall survival of 9.3 months compared to 5.6 months for the chemotherapy patients. At one year, 37 percent of patients on gilteritinib were still alive, compared to 16.7 percent of patients in the chemotherapy group. The combined rates of complete remissions (CR) or CR with partial hematologic recovery (CRh) were 34 percent for the gilteritinib arm and 15 percent for the chemotherapy arm.

“Across the board, this trial shows gilteritinib carries a clear survival benefit, meaning we now have a targeted, highly-effective, and well-tolerated treatment option for a group of truly high-risk patients,” Perl said.

The side effects of both treatments were similar, including febrile neutropenia – a fever related to white blood counts (44 percent) – as well as anemia (34 percent) and other fevers (39 percent). Severe side effects thought to be related to gilteritinib included low platelet count (24 percent), anemia (20 percent), and febrile neutropenia (15 percent). Eleven percent of patients had to discontinue the drug due to side effects.

“Although the incidence of various side effects was similar across the study arms, patients took gilteritinib for considerably longer than they underwent chemotherapy,” Perl said. “This actually means the likelihood of side effects on a daily basis is lower on this drug, and this favorable side effect profile allowed us to give gilteritinib as an outpatient treatment, a huge shift for these patients.”

Perl noted that the safety profile of the drug also means gilteritinib can be used not only to stabilize patients for a potentially curative bone marrow transplant, but also as an ongoing therapy following transplant in hopes of reducing the chance for relapse. Multicenter clinical trials of gilteritinib as part of frontline chemotherapy for newly diagnosed patients with AML and FLT3 mutations as well as maintenance therapy following bone marrow transplant have also begun. Perl is leading these trials at Penn and says focusing on preventing, rather than treating relapse by using active and well tolerated new agents early in disease course could substantially increase cure rates for this high-risk leukemia population.

Astellas Pharma, Inc., provided funding for Perl’s studies and performed statistical analysis of the data gathered by the investigators. Additional funding was provided by a National Cancer Institute Leukemia Specialized Program of Research Excellence Grant (CA100632) and by an Associazione Italiana Ricerca sul Cancro award.

The press briefing for this study will begin at 8:30 a.m. in Room B309. Tomorrow’s plenary session will begin at 10:30 a.m. in Marcus Auditorium, Building A-GWCC.

Editor’s Note: Dr. Perl has served as a consultant to Astellas Pharma, Inc.


Penn Medicine is one of the world’s leading academic medical centers, dedicated to the related missions of medical education, biomedical research, excellence in patient care, and community service. The organization consists of the University of Pennsylvania Health System and Penn’s Raymond and Ruth Perelman School of Medicine, founded in 1765 as the nation’s first medical school.

The Perelman School of Medicine is consistently among the nation's top recipients of funding from the National Institutes of Health, with $550 million awarded in the 2022 fiscal year. Home to a proud history of “firsts” in medicine, Penn Medicine teams have pioneered discoveries and innovations that have shaped modern medicine, including recent breakthroughs such as CAR T cell therapy for cancer and the mRNA technology used in COVID-19 vaccines.

The University of Pennsylvania Health System’s patient care facilities stretch from the Susquehanna River in Pennsylvania to the New Jersey shore. These include the Hospital of the University of Pennsylvania, Penn Presbyterian Medical Center, Chester County Hospital, Lancaster General Health, Penn Medicine Princeton Health, and Pennsylvania Hospital—the nation’s first hospital, founded in 1751. Additional facilities and enterprises include Good Shepherd Penn Partners, Penn Medicine at Home, Lancaster Behavioral Health Hospital, and Princeton House Behavioral Health, among others.

Penn Medicine is an $11.1 billion enterprise powered by more than 49,000 talented faculty and staff.

Share This Page: