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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
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.
Abstract:
Sarcomas are a relatively rare cancer, but often incurable at the late metastatic stage. Oncolytic immunotherapy has gained attention over the past years, and a wide range of oncolytic viruses have been delivered via intratumoral injection with positive safety and promising efficacy data. Here, we report preclinical and clinical results from treatment of sarcoma with oncolytic adenovirus Ad5/3-D24-GMCSF (CGTG-102). Ad5/3-D24-GMCSF is a serotype chimeric oncolytic adenovirus coding for human granulocyte-macrophage colony-stimulating factor (GM-CSF). The efficacy of Ad5/3-D24-GMCSF was evaluated on a panel of soft-tissue sarcoma (STS) cell lines and in two animal models. Sarcoma specific human data were also collected from the Advanced Therapy Access Program (ATAP), in preparation for further clinical development. Efficacy was seen in both in vitro and in vivo STS models. Fifteen patients with treatment-refractory STS (13/15) or primary bone sarcoma (2/15) were treated in ATAP, and treatments appeared safe and well-tolerated. A total of 12 radiological RECIST response evaluations were performed, and two cases of minor response, six cases of stable disease and four cases of progressive disease were detected in patients progressing prior to virus treatment. Overall, the median survival time post treatment was 170 days. One patient is still alive at 1,459 days post virus treatment. In summary, Ad5/3-D24-GMCSF appears promising for the treatment of advanced STS; a clinical trial for treatment of refractory injectable solid tumors including STS is ongoing.
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.
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