Serotype chimeric oncolytic adenovirus coding for GM-CSF for treatment of sarcoma in rodents and humans

Simona Bramante1, Anniina Koski, Anja Kipar

  • 1Cancer Gene Therapy Group Department of Pathology and Transplantation Laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland.

Insights

Oncolytic adenovirus therapy shows promise for advanced sarcomas. This oncolytic immunotherapy, Ad5/3-D24-GMCSF, demonstrated safety and efficacy in preclinical models and a small patient group with treatment-refractory soft-tissue sarcomas.

Area of Science:

  • Oncology
  • Virology
  • Immunotherapy

Background:

  • Sarcomas are rare cancers, often incurable at the metastatic stage.
  • Oncolytic immunotherapy, using oncolytic viruses, is a promising treatment strategy.
  • Intratumoral delivery of oncolytic viruses has shown positive safety and efficacy.

Purpose of the Study:

  • To evaluate the preclinical and clinical efficacy of oncolytic adenovirus Ad5/3-D24-GMCSF (CGTG-102) for sarcoma treatment.
  • To assess the safety and tolerability of Ad5/3-D24-GMCSF in patients with advanced sarcomas.

Main Methods:

  • Ad5/3-D24-GMCSF efficacy was tested on soft-tissue sarcoma (STS) cell lines and in animal models.
  • Human data from the Advanced Therapy Access Program (ATAP) were collected for patients with treatment-refractory STS or primary bone sarcoma.
  • Radiological RECIST evaluations were performed on treated patients.

Main Results:

  • Ad5/3-D24-GMCSF demonstrated efficacy in both in vitro and in vivo STS models.
  • Fifteen patients with refractory STS or bone sarcoma received treatment, which was safe and well-tolerated.
  • Among evaluable patients, two showed minor responses, six had stable disease, and four progressed; median survival was 170 days, with one long-term survivor.

Conclusions:

  • Ad5/3-D24-GMCSF shows promise for treating advanced soft-tissue sarcomas.
  • Further clinical development is warranted, with a trial for refractory injectable solid tumors, including STS, currently ongoing.