Treatment of Advanced NSCLC Patients with an Anti-Idiotypic NeuGcGM3-Based Vaccine: Immune Correlates in Long-Term Survivors
<b>Background:</b> Racotumomab-alum is an anti-idiotype vaccine targeting the NeuGcGM3 tumor-associated ganglioside. Clinical trials in advanced cancer patients have demonstrated low toxicity, high immunogenicity and clinical benefit. The goal of this study was to identify circulating biomarkers of clinical outcome. <b>Methods:</b> Eighteen patients with stage IIIb/IV non-small-cell lung cancer (NSCLC) were injected with racotumomab-alum as switch maintenance therapy after first-line chemotherapy. Treatment was administered until severe performance status worsening or toxicity. The frequencies of innate and adaptive lymphocytes were assessed by flow cytometry. Circulating factors were measured using multi-analyte flow assay kits. <b>Results:</b> The median overall survival was 16.5 months. Twenty-seven percent of patients were classified as long-term survivors. Patients with lower baseline frequencies of CD4+Tregs and central memory (CM) CD8+T cells displayed longer survival rates. Furthermore, higher baseline frequencies of NKT cells and a high CD8+T/CD4+Treg ratio were associated with longer survival. Interestingly, patients with significantly lower levels of effector memory (EM) CD8+T cells survived longer. The levels of NKT cells and terminal effector memory (EMRA) CD8+T cells were higher in long-term survivors in comparison with short-term survivors in post-immune samples. As expected, the ratio of CD8+T/CD4+Tregs showed significantly higher values during treatment in patients with clinical benefits. Regarding serum factors, pro-tumorigenic cytokines significantly increased during treatment in poor survivors. <b>Conclusions</b>: In advanced NSCLC patients receiving racotumomab-alum vaccine, longer survival could be associated with a unique profile of circulating lymphocyte subsets at baseline and during treatment. Additionally, certain pro-tumor-related cytokines increased in short-term survivors. These results should be confirmed in larger randomized clinical trials. This clinical trial was registered in the Cuban Clinical Trials Register (RPCE00000279).
Authors
- Yendry Ventura‐Carmenate (ORCID: https://orcid.org/0000-0002-5373-3414)
- Haslen Hassiul Cáceres-Lavernia (ORCID: https://orcid.org/0000-0002-5165-4472)
- Carmen Viada (ORCID: https://orcid.org/0000-0002-1604-3545)
- Leslie M. Varona-Rodríguez (ORCID: https://orcid.org/0000-0002-3305-5871)
- Elia Nenínger-Vinageras (ORCID: https://orcid.org/0000-0002-0923-1273)
- Petra Baumgaertner (ORCID: https://orcid.org/0000-0002-5979-7654)
- Sara Trabanelli (ORCID: https://orcid.org/0000-0001-8648-1324)
- Anne‐Christine Thierry
- Gisela María Suárez-Formigo
- Tania Crombet (ORCID: https://orcid.org/0000-0002-2550-7292)
- Nely Rodríguez‐Zhurbenko (ORCID: https://orcid.org/0000-0002-2070-3016)
- Camilla Jandus (ORCID: https://orcid.org/0000-0002-7405-5747)
- Zuyén González
- Zaima Mazorra
Institutions
- University of Geneva (CH)
- Center of Molecular Immunology (Cuba) (CU)
- Hermanos Ameijeiras Hospital (CU)
- Ludwig Cancer Research (CH)
- University of Lausanne (CH)
Publication Details
- Journal
- Biomedicines
- Published
- 2025-05-06
- DOI
- https://doi.org/10.3390/biomedicines13051122
- Primary Topic
- Immunotherapy and Immune Responses
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung