City of Hope and Osel Inc., a company developing live biotherapeutic products for modulation of the human microbiome, today announced Phase 1 trial data showing that use of the live biotherapeutic CBM588 (Clostridium butyricum MIYAIRI 588® strain) plus the immunotherapy medicine nivolumab/ipilimumab significantly improved progression-free survival in patients with metastatic kidney cancer when compared to use of nivolumab/ipilimumab alone. The study was published in Nature Medicine on Feb. 28.
CBM588 is a nonpathogenic bacteria that has multiple documented beneficial effects on the human microbiome. It produces short-chain fatty acids (mainly butyric acid), a well-known energy source for the lining of the GI tract, and has immunomodulatory properties. The bacterial strain appears to exert additional beneficial effects, including inhibiting pathogenic microorganisms and helping to restore the GI lining and decrease intestinal imbalance.
Last summer, City of Hope granted an exclusive worldwide license to Osel for intellectual property on the novel use of CBM588 to enhance the efficacy of checkpoint inhibitors to treat cancer.
In the clinical trial, 30 patients with metastatic kidney cancer (renal cell carcinoma) who had never received treatment before were randomized to receive either CBM588 orally in combination with nivolumab/ipilimumab or nivolumab/ipilimumab alone. Data showed a significant improvement in progression-free survival in patients treated with CBM588 plus nivolumab/ipilimumab (12.7 months) compared to nivolumab/ipilimumab alone (2.5 months). Additionally, use of CBM588 in combination therapy was linked to an increase in response rate when compared to use of nivolumab/ipilimumab therapy alone (58% vs. 20%).
While there was no significant difference between the treatment groups in terms of the amount of the Bifidobacterium genus bacteria, patients who responded to the CBM588 with nivolumab/ipilimumab treatment had significant increases in the Bifidobacterium species. There were no significant differences in treatment-related toxicity reported between the two groups.
“Over the last several years, the immunotherapy field has been closely studying how the GI microbiome can enhance immune checkpoint efficacy for the treatment of cancer,” said Thomas Parks, Ph.D., director of product development at Osel. “Compared to microbiome modulation using fecal transplants, CBM588 given orally is potentially a more effective, reproducible, scalable and safer method to treat patients. We look forward to supporting the world-class team at City of Hope as they advance CBM588 in additional clinical trials.”
Osel licensed the rights for the pharmaceutical use of CBM588 in the United States, Canada and Europe from Miyarisan Pharmaceutical Co., Ltd. CBM588 is manufactured under GMP (good manufacturing practice) and marketed in Japan by Miyarisan Pharmaceutical as a prescription product known as MIYA-BM (Clostridium butyricum MIYAIRI 588® strain) to treat GI indications.
“City of Hope is currently conducting another Phase 1 clinical trial of CBM588 in combination with nivolumab and tyrosine kinase inhibitor cabozantinib for the treatment of advanced or metastatic kidney cancer,” said Pal, co-director of the Kidney Cancer Program at City of Hope. “We are working to open a large, randomized Phase 3 trial of CBM588 in the future.”
Jeffrey Trent, Ph.D., Translational Genomics Research Institute (TGen) president and research director, a contributor to the study, said, “The field of microbiome research is exploding as evidenced by the clinical importance of this study, which points to the continued growth of clinical research and scientific understanding of the microbiome’s connection to disease and recovery.” TGen is an affiliate of City of Hope.
Nazli Dizman, M.D., and Luis Meza, M.D., who were both postdoctoral fellows at City of Hope when the study was conducted, were lead researchers on the trial and co-primary authors. Funding for the study, “Nivolumab plus ipilimumab with or without live bacterial supplementation in metastatic renal cell carcinoma: a randomized phase 1 trial,” was provided by a grant from the Gateway for Cancer Research.