Data ọhụrụ nke ọgwụ mgbochi ọrịa cancer maka Tumor siri ike

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Nouscom today announced encouraging new translational data obtained from the ongoing Phase 1 trial evaluating NOUS-209. The data were presented yesterday in a Late Breaking session at the 2022 American Association for Cancer Research (AACR) Annual Meeting.

NOUS-209, Nouscom’s lead product, is an off-the-shelf cancer vaccine targeting 209 shared neoantigens. It is being investigated in a Phase 1 clinical trial, administered in combination with the anti-PD-1 checkpoint inhibitor pembrolizumab, for the treatment of Microsatellite Instable High (MSI-H) gastric, colorectal and gastro-esophageal junction solid tumors.

Previously presented interim clinical data of the combination (presented at the Society for Immunotherapy of Cancer’s (SITC) Annual Meeting in November 2021) highlighted promising early signs of clinical efficacy in 12 MSI-H patients.

The new translational data presented at AACR 2022 further supported these findings and demonstrated NOUS-209 is safe, highly immunogenic with promising signs of clinical efficacy. Key findings were as follows:

•             Vaccine immunogenicity was demonstrated by ex-vivo IFN-ɣ ELISpot assay in 67% of patients in dose level 1 (n=3), and 100% (n=7) of patients in dose level 2.

•             In 3 patients with long term PRs whose pre/post treatment tumor biopsies were available, the intratumoral TCR repertoire was expanded and diversified post treatment with NOUS-209. Increased T effector memory post treatment was observed.

•             In one of these three patients, vaccine-induced neoantigen specific TCR was tracked from periphery in the tumor biopsy post NOUS-209 treatment.

•             Results indicate that neoantigen specific CD8+ T cells, induced by NOUS-209, expand and diversify only upon treatment with NOUS-209, and successfully infiltrate the tumor microenvironment to exert anti-tumor activity.

Marwan G. Fakih, M.D., Medical Oncology Specialist at City of Hope’s Duarte California, and Study investigator said: “While we have seen progress in the treatment options for MSI-High solid tumors in recent years, there remains a significant unmet need. It is therefore extremely encouraging to see these new translational Phase 1 data illustrating how NOUS-209 induces robust T cell expansion and TCR diversification in patients demonstrating durable clinical responses. I very much look forward to the full analysis of the Phase 1 results and further clinical development.”

Dr. Elisa Scarselli, Chief Scientific Officer and Co-Founder of Nouscom, said: “The data, obtained from 12 metastatic MSI-H patients, highlights a common signature observed post vaccination in patients with durable clinical response. The signature is characterized by the TCR repertoire expansion and diversification in tumor infiltrating lymphocytes stimulated by vaccination with NOUS-209, together with a parallel increase of T cells with effector memory phenotype. Moreover, we were able to track vaccine induced T cells among those expanded post-treatment in the tumor of one of these patients.

“We look forward to building upon our compelling proof-of-concept data by leveraging important learnings from the ongoing trial to support the development of NOUS-209 as potentially the first neoantigen off-the shelf cancer vaccine targeting MSI-H tumors.”

IHE Ị GA-Ewepụ na edemede a:

  • It is being investigated in a Phase 1 clinical trial, administered in combination with the anti-PD-1 checkpoint inhibitor pembrolizumab, for the treatment of Microsatellite Instable High (MSI-H) gastric, colorectal and gastro-esophageal junction solid tumors.
  • The signature is characterized by the TCR repertoire expansion and diversification in tumor infiltrating lymphocytes stimulated by vaccination with NOUS-209, together with a parallel increase of T cells with effector memory phenotype.
  • Previously presented interim clinical data of the combination (presented at the Society for Immunotherapy of Cancer’s (SITC) Annual Meeting in November 2021) highlighted promising early signs of clinical efficacy in 12 MSI-H patients.

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Linda Hohnholz

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