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Published on: September 20, 2016
Whole Recombinant Saccharomyces cerevisiae Yeast Expressing Ras Mutations as Treatment for Patients With Solid Tumors
Allen Cohn1, Michael A Morse2, Bert O'Neil3
1Rocky Mountain Cancer Center.
Abstract:
We are developing whole, heat-killed, recombinant Saccharomyces cerevisiae yeast, engineered to encode target proteins, which stimulate immune responses against malignant cells expressing those targets. This phase 1 trial, enrolling patients with advanced colorectal or pancreas cancer, was designed to evaluate safety, immunogenicity, response, and overall survival of ascending doses of the GI-4000 series of products, which express 3 different forms of mutated Ras proteins. The study enrolled 33 heavily pretreated subjects (14 with pancreas and 19 with colorectal cancer), whose tumors were genotyped before enrollment to identify the specific ras mutation and thereby to identify which GI-4000 product to administer. No dose limiting toxicities were observed and no subject discontinued treatment due to a GI-4000 related adverse event (AE). The majority of AEs and all fatal events were due to underlying disease progression and AE frequencies were not significantly different among dose groups. GI-4000 was immunogenic, as Ras mutation-specific immune responses were detected on treatment in ∼60% of subjects. No objective tumor responses were observed but based on imaging, clinical status and/or biochemical markers, stable disease was observed in 6 subjects (18%) on day 29, while 1 subject had stable disease at days 57 and 85 follow-up visits. The median overall survival was 3.3 months (95% confidence interval, 2.3-5.3 mo), and 5 subjects survived past the 48-week follow-up period. No significant dose-dependent trends for survival were observed. This first clinical trial in humans with GI-4000 demonstrated a favorable safety profile and immunogenicity in the majority of subjects.
Insights
This Phase 1 trial of GI-4000, a novel cancer immunotherapy, showed it was safe and triggered immune responses in patients with advanced colorectal or pancreas cancer. While no tumors shrunk, some patients experienced stable disease, indicating potential therapeutic benefit.
Area of Science:
- Oncology
- Immunotherapy
- Cancer Vaccines
Background:
- Developing novel immunotherapies for advanced cancers like colorectal and pancreas cancer is crucial.
- Targeting mutated Ras proteins with recombinant yeast vaccines offers a potential strategy to stimulate anti-tumor immunity.
Purpose of the Study:
- To evaluate the safety, immunogenicity, and preliminary efficacy of ascending doses of GI-4000 in patients with advanced colorectal or pancreas cancer.
- To assess the overall survival and response rates in patients treated with GI-4000, a heat-killed recombinant Saccharomyces cerevisiae yeast vaccine.
Main Methods:
- Phase 1 clinical trial design with ascending doses of GI-4000.
- Enrollment of 33 heavily pretreated patients with advanced colorectal or pancreas cancer.
- Tumor genotyping to identify specific Ras mutations for personalized GI-4000 product selection.
Main Results:
- GI-4000 demonstrated a favorable safety profile with no dose-limiting toxicities or treatment discontinuations due to adverse events.
- Immunogenicity was observed in approximately 60% of subjects, with detectable Ras mutation-specific immune responses.
- While no objective tumor responses were seen, 18% of subjects achieved stable disease at day 29, with some maintaining it longer.
Conclusions:
- GI-4000 is safe and immunogenic in patients with advanced colorectal and pancreas cancer.
- The vaccine elicits Ras mutation-specific immune responses, supporting its further development.
- Further investigation is warranted to determine the clinical benefit and optimal use of GI-4000 in cancer treatment.
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