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Current advances and outlooks in immunotherapy for pancreatic ductal adenocarcinoma

期刊

MOLECULAR CANCER
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12943-020-01151-3

关键词

Pancreatic ductal adenocarcinoma; Immunotherapy; Tumour microenvironment; Myeloid-derived suppressor cells; Regulatory T lymphocytes; Tumour-associated macrophages; Tumour-associated antigens; Adoptive cell therapy; Immune checkpoint inhibitor; Tumour-infiltrating lymphocytes; Vaccines; Neoantigens

资金

  1. National Institute of Health [R01AI121180, R01CA221867, R21AI109239]
  2. National Natural Science Foundation of China [81373875, 81873156]
  3. Educational Department of Liaoning Province of China [LZ2019001]

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Pancreatic ductal adenocarcinoma (PDAC) is an incurable cancer resistant to traditional treatments, although a limited number of early-stage patients can undergo radical resection. Immunotherapies for the treatment of haematological malignancies as well as solid tumours have been substantially improved over the past decades, and impressive results have been obtained in recent preclinical and clinical trials. However, PDAC is likely the exception because of its unique tumour microenvironment (TME). In this review, we summarize the characteristics of the PDAC TME and focus on the network of various tumour-infiltrating immune cells, outlining the current advances in PDAC immunotherapy and addressing the effect of the PDAC TME on immunotherapy. This review further explores the combinations of different therapies used to enhance antitumour efficacy or reverse immunodeficiencies and describes optimizable immunotherapeutic strategies for PDAC. The concordant combination of various treatments, such as targeting cancer cells and the stroma, reversing suppressive immune reactions and enhancing antitumour reactivity, may be the most promising approach for the treatment of PDAC. Traditional treatments, especially chemotherapy, may also be optimized for individual patients to remodel the immunosuppressive microenvironment for enhanced therapy.

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