The European Commission (EC) has approved blinatumomab monotherapy as consolidation therapy for treating adult patients with newly diagnosed Philadelphia chromosome-negative CD19-positive B-cell precursor acute lymphoblastic leukemia (B-ALL).
“This approval represents a significant advancement, offering patients the opportunity to receive blinatumomab earlier in their treatment pathway, with the potential to improve outcomes,” said Jean-Charles Soria, senior vice president of Global Oncology Development at Amgen. “The E1910 data that served as the basis of this approval adds to the growing body of evidence of the meaningful survival impact of blinatumomab.”
The Phase 3 E1910 clinical trial led by ECOG-ACRIN Cancer Research Group studied patients with newly diagnosed Philadelphia chromosome-negative B-ALL receiving postinduction consolidation treatment, which aims to deepen remission to achieve durable responses.
Study results demonstrated that blinatumomab added to multiphase consolidation chemotherapy showed superior overall survival (OS) versus chemotherapy alone. With a median follow-up of 4.5 years, the 5-year OS was 82.4% in the blinatumomab plus chemotherapy arm (n=112) and 62.5% in the chemotherapy arm (n=112).
“While there has been some treatment progress, many patients with newly diagnosed Philadelphia chromosome-negative B-ALL remain at high risk of relapse,” said Robin Foà, M.D., emeritus professor of hematology, Sapienza University of Rome.
“The E1910 study results highlight that blinatumomab has the potential to advance frontline consolidation treatment, including patients who are minimal residual disease (MRD)-negative, offering a crucial new option to achieve deeper remissions and improve long-term survival.”
Source: PR Newswire
