A total of 84 patients at 25 clinical sites in Germany, Austria, and Russia participated in this randomized controlled phase II efficacy trial in recurrent glioblastoma. The trial compared the efficacy and safety of a combination therapy of asunercept and radiotherapy versus radiotherapy alone.
Patients were eligible for inclusion if they suffered from first or second relapse of glioblastoma and were refractory to standard therapy. Patients randomized into the asunercept arm were treated until further disease progression. Detailed information as well as final results of the trial were published in the peer-reviewed journal "Clinical Cancer Research" (>> publication).
Treatment with asunercept in combination with radiotherapy has shown statistically significant improvements in progression-free survival and quality of life as well as a positive trend in overall survival compared to treatment with radiotherapy alone, demonstrating the potential efficacy of asunercept in the treatment of recurrent glioblastoma. During treatment with asunercept for up to two years, no drug-related serious adverse events were observed, affirming the excellent safety profile and very good tolerability of asunercept .
Both progression-free survival at six months, the primary endpoint of the trial, and median progression-free survival were met with statistical significance. Patients having a newly-identified epigenetic biomarker associated with the CD95 ligand – the target of asunercept – experienced the greatest benefit from treatment with asunercept . The trial showed a statistically significant increase in overall survival in biomarker-positive patients treated with asunercept, with a median overall survival of 16.1 months compared to 7.7 months in patients treated with radiotherapy alone. At the end of the follow-up period, there were five surviving patients in the treatment group and one patient in the control group.
A phase II efficacy trial with asunercept to treat patients with recurrent glioblastoma has shown statistically significant improvements in progression-free survival and quality of life as well as a positive trend in overall survival.
A scientific publication confirms that the CD95 system – which is inhibited by asunercept – plays an important role in the progression of other solid tumors such as ovarian, colon, prostate, breast, bladder, and kidney cancer.
Glioblastoma belongs to the group of gliomas and is the most frequent and aggressive type of brain tumor. Glioblastoma cells are highly resistant to radiation and chemotherapy. They spread and infiltrate into the neighboring brain tissue so quickly that a complete surgical removal of the tumor is often impossible. The current standard therapy after initial diagnosis consists of surgery, followed by radiation and chemotherapy. Due to the rapid infiltration of the tumor cells into the surrounding, healthy brain tissue, recurrence is often experienced within a few months of the initial treatment.
There is currently no approved drug for the treatment of recurrent glioblastoma available in the EU, illustrating the tremendous need for new and effective therapies in this indication.