Abstract

Survival of gastrointestinal cancer remains dismal, especially for metastasized disease. For various cancers, especially melanoma and lung cancer, immunotherapy has been proven to confer survival benefits, but results for gastrointestinal cancer have been disappointing. Hence, there is substantial interest in exploring the usefulness of adaptive immune system education with respect to anti-cancer responses though vaccination. Encouragingly, even fairly non-specific approaches to vaccination and immune system stimulation, involving for instance influenza vaccines, have shown promising results, eliciting hopes that selection of specific antigens for vaccination may prove useful for at least a subset of gastrointestinal cancers. It is widely recognized that immune recognition and initiation of responses are hampered by a lack of T cell help, or by suppressive cancer-associated factors. In this review we will discuss the hurdles that limit efficacy of conventional cancer therapeutic vaccination methods (e.g., peptide vaccines, dendritic cell vaccination). In addition, we will outline other forms of treatment (e.g., radiotherapy, chemotherapy, oncolytic viruses) that also cause the release of antigens through immunogenic tumor cell death and can thus be considered unconventional vaccination methods (i.e., in situ vaccination). Finally, we focus on the potential additive value that vaccination strategies may have for improving the effect immunotherapy. Overall, a picture will emerge that although the field has made substantial progress, successful immunotherapy through the combination with cancer antigen vaccination, including that for gastrointestinal cancers, is still in its infancy, prompting further intensification of the research effort in this respect.

Highlights

  • Clinical management of oncological disease of the gastrointestinal tract remains very challenging especially when surgical options have been exhausted

  • Pioneering clinical results have been obtained in melanoma where response rates with a genetically modified granulocyte macrophage colony stimulating factor (GM-CSF) expressing herpes simplex based Oncolytic viruses (OV) (T-VEC) in the presence of CTLA-4 or PD-1 blockade were promising and even improved in patients treated with OV combination therapy compared to anti-CTLA4 alone [90,165,166]

  • In case of evidence of an ongoing active immune response, Immune checkpoint blockade (ICB) can be considered as a stand-alone treatment

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Summary

Introduction

Clinical management of oncological disease of the gastrointestinal tract remains very challenging especially when surgical options have been exhausted. Cancers are antigenic and evoke immunological responses, but can escape the resulting tumor destruction through a variety of mechanisms including upregulation of so-called checkpoints: inhibitory elements to limit self-damaging autoimmunity By counteracting these inhibitory signals, the cancer can be combatted. Design of vaccination strategies is complicated by the complex tumor microenvironment (TME) and other characteristics like mutational load and expression of tumor antigens, which are largely unique to various types of tumors and may vary even within tumors This is not different for gastrointestinal cancers. High neoantigen levels do not correlate with survival for pancreatic- and liver cancer per se [14,15,16] For these cancers it is rational to assume that stimulating cancer-specific immune responses will be associated with better outcomes. In the present manuscript we shall overview the most important therapeutic cancer vaccine forms, elude on non-immune related cancer therapies that may trigger systemic immunity as a side effect, and will discuss how these therapies mechanistically offer potential for combination with other forms of immunotherapy to find opportunities for treatment of gastrointestinal cancers

The Ideal Anti-Tumor Immune Response and the Limitation of Vaccination
Conventional Vaccines
Peptide Vaccine
Genetic Vaccine
Tumor Cell Vaccine
DC-Vaccine
In Situ Vaccines
Radiotherapy
Chemotherapy
Oncolytic Viruses
Conclusions
Findings
Results and Immunologic
Full Text
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