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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Therapeutic vaccines targeting solid tumors: A series of clinical trial analysis over the past decade
Fengqi Qiu1, Yilan Sun2, Darren Wan-Teck Lim3
1Cancer Center, Department of Pulmonary and Critical Care Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang, China; National Cancer Centre Singapore, Singapore, Singapore.
Abstract:
Therapeutic cancer vaccines hold great promise, yet their clinical efficacy in solid tumors remains modest. We systematically analyzed 86 clinical trials published between 2015 and 2025 evaluating therapeutic vaccines across mRNA, DNA, peptide, dendritic cell, virus vector, and whole tumor cell platforms to understand their clinical utility and key challenges in development. Peptide-based vaccines dominated, while mRNA vaccines showed the fastest growth, often combined with immune checkpoint inhibitors. Among 1588 patients with advanced disease, the disease control rate was 53 % and the objective response rate 18 %. In adjuvant settings, 52 % of 461 patients experienced recurrence. Although 67 % exhibited ELISPOT-positive T-cell responses, no correlation with clinical efficacy was observed. Most adverse events were mild to moderate, with pyrexia, fatigue, and injection-site reactions predominating. Therapeutic vaccines thus demonstrate favorable safety and immunogenicity, but limited monotherapy efficacy, underscoring the need for combinatorial approaches and identifying personalized immunogenic neoantigens to enhance clinical benefit.
Insights
Therapeutic cancer vaccines show promise but have modest efficacy in solid tumors. Combinatorial strategies and personalized neoantigens are needed to improve clinical benefit.
Area of Science:
- Oncology
- Immunology
- Vaccinology
Background:
- Therapeutic cancer vaccines offer potential against solid tumors, but clinical efficacy is currently limited.
- Diverse vaccine platforms exist, including mRNA, DNA, peptide, dendritic cell, virus vector, and whole tumor cell approaches.
Purpose of the Study:
- To systematically analyze clinical trials of therapeutic cancer vaccines from 2015-2025.
- To evaluate the clinical utility, safety, and challenges associated with different vaccine platforms.
Main Methods:
- Systematic review of 86 clinical trials published between 2015 and 2025.
- Analysis included patients with advanced disease and those in adjuvant settings.
- Data on vaccine platforms, response rates, recurrence, T-cell responses, and adverse events were collected.
Main Results:
- Peptide-based vaccines were most common; mRNA vaccines showed rapid growth, often with immune checkpoint inhibitors.
- In advanced disease (1588 patients), disease control rate was 53%, objective response rate was 18%.
- In adjuvant settings (461 patients), 52% experienced recurrence; 67% showed T-cell responses, but without clinical correlation. Adverse events were mostly mild.
Conclusions:
- Therapeutic cancer vaccines exhibit good safety and immunogenicity but limited monotherapy efficacy.
- Combinatorial approaches and personalized neoantigen identification are crucial for enhancing clinical benefit.
- Further research is needed to overcome challenges and improve outcomes in solid tumor treatment.
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