4.5 Article

Present and future of immunotherapy in Neuroendocrine Tumors

期刊

REVIEWS IN ENDOCRINE & METABOLIC DISORDERS
卷 22, 期 3, 页码 615-636

出版社

SPRINGER
DOI: 10.1007/s11154-021-09647-z

关键词

Immunotherapy; Immune checkpoint inhibitors; Neuroendocrine tumors; Neuroendocrine neoplasia; Merkel Cell Carcinoma; Small Cell Lung Cancer

资金

  1. Universita degli Studi di Genova within the CRUI-CARE Agreement
  2. Italian Ministry of Education, University and Research [PRIN 2017Z3N3YC]

向作者/读者索取更多资源

Despite the lack of robust evidence supporting the role of immunotherapy in the treatment of neuroendocrine neoplasms, future research should focus on strategies to make NETs more susceptible to response to immune checkpoint inhibitors (ICIs). The combination of conventional therapy, target therapy, and immunotherapy deserves attention, along with the exploration of biomarkers for patient selection in this type of treatment.
Immunotherapy, so promising in many neoplasms, still does not have a precise role in the treatment of neuroendocrine neoplasms (NENs). In this article, we provide an overview on the current knowledge about immunotherapy with immune checkpoint inhibitors (ICIs) applied to NENs, evaluating future perspectives in this setting of tumors. Evidence so far available for ICIs in gastroenteropancreatic (GEP)-NENs is definitively not as robust as for other tumors such as Small Cell Lung Cancer or Merkel Cell Carcinoma. In fact, with regard to the well-differentiated forms of NENs (NETs), the results obtained nowadays have been disappointing. However, the near future, might reserve interesting results for ICIs in GEP-NEN from a total of nine different ICI drugs, used throughout 19 randomised controlled trials. Such numbers highlight the growing attention gathering around NENs and ICIs, in response to the need of stronger evidences supporting such therapy. For the future, the most important aspect will be to study strategies that can make NETs more susceptible to response to ICI and, thus, enhance the effectiveness of these treatments. Therefore, the combination of conventional therapy, target therapy and immunotherapy deserve attention and warrant to be explored. A sequential chemotherapy, possibly inducing an increase in tumor mutational burden and tested before immunotherapy, could be a hypothesis deserving more consideration. A radiation treatment that increases tumor-infiltrating lymphocytes, could be another approach to explore before ICIs in NENs. Equally essential will be the identification of biomarkers useful for selecting patients potentially responsive to this type of treatment.

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