ESMO Congress

Lung cancer: initial results from an experimental vaccine show survival rates have almost doubled

Oncologist Cappuzzo: “The drug is a genuine molecular trainer that teaches the immune system how to recognise and destroy cancer cells without increasing toxicity”

3' min read

Translated by AI
Versione italiana

3' min read

Translated by AI
Versione italiana

Traditional treatments sometimes fail to halt the progression of advanced-stage lung cancer, and the priority is therefore to identify innovative strategies capable of improving survival without increasing side effects. This is the aim of peptide vaccines – also known as therapeutic vaccines – which seek to boost the immune response whilst the disease is already present. One such new-generation peptide vaccine, currently undergoing trials, is demonstrating unprecedented efficacy in patients with advanced non-small cell lung cancer receiving second-line treatment. The data show a doubling of one-year survival, reaching 47 per cent when combined with docetaxel-based chemotherapy and 46 per cent when combined with immunotherapy (nivolumab), compared with just 29 per cent achieved with traditional docetaxel-only therapy.

Data from the Phase 2 Combi-TED trial on the Tedopi (OSE2101) vaccine, sponsored by the Fondazione Ricerca Traslazionale (FoRT), will be presented on 25 October by Federico Cappuzzo, Director of Medical Oncology 2 at the Regina Elena National Cancer Institute in Rome, President of the FoRT Foundation and lead author of the study, as part of the congress of the European Society for Medical Oncology (ESMO). The research involved international collaboration between 17 centres of excellence in oncology across Italia, France and Spain, confirming the leading role of the Italian research network in the testing of therapeutic vaccines.

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Over 40,000 diagnoses a year

These results mark a fundamental turning point for a disease which, in Italia alone, accounts for around 40,000 new diagnoses each year, confirming its status as one of the leading causes of cancer and the number one cause of cancer-related deaths in our country. In particular, the ‘non-small cell’ (NSCLC) form accounts for around 85 per cent of all lung cancer cases. Against this backdrop, treatment options for advanced disease remain extremely limited, with traditional chemotherapy still the standard of care despite its modest efficacy and marked toxicity.

“Unlike traditional protein-based or preventative vaccines, the peptide vaccine consists of a synthetic combination of 10 short amino acid fragments (peptides) selected from tumour antigens,” explains Cappuzzo. The drug acts as a veritable molecular trainer for the immune system: in HLA-A2-positive patients (human leukocyte antigen), it presents these 10 ‘identikit’ profiles to the T-lymphocytes – the body’s defence cells – teaching them to recognise and destroy tumour cells with surgical precision and without any increase in toxicity compared with standard treatments.”

The limitations of current treatments

The study stems from the clinical need to overcome the limitations of current second-line treatments, which often yield modest results. “The only drug commonly used in clinical practice at this stage is docetaxel, a toxic molecule with limited efficacy,” emphasises Cappuzzo. “In a previous study, the peptide vaccine has already been shown to be potentially superior to docetaxel, and its definitive validation is currently underway in the phase 3 ARTEMIA trial.”

In the Combi-TED trial, 106 patients with disease progression following first-line chemo-immunotherapy were divided into three treatment groups to evaluate the administration of the peptide vaccine in combination with chemotherapy, the vaccine in combination with the immunotherapy drug nivolumab, or standard docetaxel-based chemotherapy alone. “The patients were divided into three arms: one treated conventionally with docetaxel alone, one with docetaxel in combination with the peptide vaccine, and a third which evaluated the combination of the vaccine with the continuation of the immunotherapy already received as first-line treatment,” explains Cappuzzo. The results are extremely positive: in patients receiving the vaccine, one-year survival is practically double that of the group treated with traditional therapy alone, without any increase in side effects.”

Innovation at the Combi-TED practice

The innovative strategy that has emerged from the Combi-TED study also directly addresses a real need expressed on a daily basis by patients in oncology wards, offering a concrete clinical solution to those facing disease progression. “In clinical practice, when a patient’s disease progresses after first-line chemo-immunotherapy, they very often ask us if they can continue with immunotherapy,” concludes Cappuzzo. “The key finding from our study is that even patients who continued immunotherapy whilst adding the peptide vaccine derived a substantial benefit in terms of survival.”

The data presented at ESMO could therefore herald a new era in the use of peptide vaccines in immuno-oncology, demonstrating that targeted training of the immune system can bring about a tangible change in the therapeutic outlook for patients with advanced lung cancer.

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