Bintrafusp alfa for patients with recurrent or metastatic olfactory neuroblastoma

Nyall R London1,2, Dara Bracken-Clarke3, Elisabetta Xue3

  • 1Sinonasal and Skull Base Tumor Section, Surgical Oncology Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Abstract

Insights

This study evaluated bintrafusp alfa (BA) for recurrent/metastatic olfactory neuroblastoma (ONB), a rare cancer. While no objective responses were seen, some patients experienced stable disease and a manageable safety profile, supporting further immunotherapy research.

Area of Science:

  • Oncology
  • Immunotherapy
  • Clinical Trials

Background:

  • Recurrent/metastatic (R/M) olfactory neuroblastoma (ONB) lacks established treatments.
  • This study represents the first immunotherapy clinical trial for R/M ONB.
  • The trial evaluated bintrafusp alfa (BA), a bifunctional TGF-β trap/anti-PD-L1 fusion protein.

Purpose of the Study:

  • To assess the activity of bintrafusp alfa (BA) in patients with R/M ONB.
  • To evaluate the overall response rate (ORR) as the primary endpoint.
  • To determine safety, progression-free survival (PFS), and overall survival (OS).

Main Methods:

  • 11 patients with R/M ONB received intravenous bintrafusp alfa (1200 mg) every 2 weeks.
  • Patients were stratified into two cohorts based on prior immunotherapy exposure.
  • Enrollment was halted due to bintrafusp alfa development discontinuation.

Main Results:

  • No objective responses were observed in the trial.
  • In the cohort without prior immunotherapy (n=9), 50% (4/8 evaluable) achieved stable disease (SD), with three long-lasting.
  • One patient with SD demonstrated a complete metabolic response on 68Ga-DOTATATE imaging. Grade 3/4 adverse events included immune-mediated diabetes and hemorrhage.

Conclusions:

  • Bintrafusp alfa demonstrated a manageable safety profile in R/M ONB patients.
  • A subset of patients experienced clinical benefit, including prolonged stable disease and one complete metabolic response.
  • This trial confirms the feasibility of conducting systemic therapy trials in R/M ONB and supports further combinatorial immunotherapy research.