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Phase II study of personalized peptide vaccination for refractory bone and soft tissue sarcoma patients
Ryuji Takahashi1, Yukinao Ishibashi, Koji Hiraoka
1Department of Surgery, Kurume University School of Medicine, Kurume, Japan.
Abstract:
Refractory bone and soft tissue sarcomas are challenging diseases to treat because of their robustness to chemotherapy. Although cancer vaccines have the potential to become an attractive treatment modality, their progress has been hampered by the presence of many subtypes of sarcomas and different human leukocyte antigen (HLA)-types. We investigated whether personalized peptide vaccination (PPV) would be feasible for the vast majority of sarcoma patients. Twenty refractory bone and soft tissue sarcoma patients with nine different subtypes and 11 different HLA-class IA phenotypes were enrolled in this study. A maximum of four HLA-matched peptides showing higher peptide-specific IgG responses in pre-vaccination plasma were selected from 31 pooled peptide candidates applicable for the HLA-A2, -A3, -A11, -A24, -A26, -A31, and -A33 types, and were subcutaneously administered weekly for 6 weeks and bi-weekly thereafter. Measurement of peptide-specific CTL and IgG responses along with other laboratory analyses were conducted before and after vaccination. No patients were excluded by either sarcoma subtypes or different HLA-types. No severe adverse events associated with PPV were observed in any patients. Peptide-specific immunological boosting was observed in the post-vaccination samples from the majority of patients. Tumor reduction of the lung metastasis and a long stable disease was observed in each case, and the median overall survival time of the 20 cases was 9.6 months. Taken together, PPV could be feasible for the vast majority of refractory sarcoma patients because of the safety and higher rates of immunological responses regardless of the presence of different sarcoma subtypes and various HLA-types.
Insights
Personalized peptide vaccination (PPV) is a safe and feasible treatment for refractory sarcomas. This approach demonstrated immunological responses and clinical benefits across diverse sarcoma subtypes and human leukocyte antigen (HLA) types.
Area of Science:
- Oncology
- Immunology
- Vaccine Development
Background:
- Refractory bone and soft tissue sarcomas present significant treatment challenges due to chemoresistance.
- Existing cancer vaccine progress is limited by sarcoma heterogeneity and diverse human leukocyte antigen (HLA) types.
Purpose of the Study:
- To assess the feasibility of personalized peptide vaccination (PPV) in a broad range of sarcoma patients.
- To evaluate the safety and immunogenicity of PPV in refractory sarcoma.
Main Methods:
- Twenty patients with refractory sarcomas received PPV targeting up to four HLA-matched peptides.
- Vaccinations were administered subcutaneously weekly for 6 weeks, then bi-weekly.
- Peptide-specific immune responses (IgG, CTL) and clinical outcomes were monitored pre- and post-vaccination.
Main Results:
- PPV was feasible for all patients, irrespective of sarcoma subtype or HLA type.
- The majority of patients showed peptide-specific immunological boosting.
- No severe adverse events were observed; clinical benefits included tumor reduction and stable disease, with a median overall survival of 9.6 months.
Conclusions:
- Personalized peptide vaccination (PPV) is a safe and viable treatment option for refractory sarcomas.
- PPV elicits robust immunological responses and clinical benefits, overcoming challenges posed by sarcoma diversity and HLA variations.
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