The immunological landscape in pancreatic ductal adenocarcinoma and overcoming resistance to immunotherapy

被引:14
|
作者
Hilmi, Marc [1 ,2 ]
Delaye, Matthieu [1 ,2 ]
Muzzolini, Milena [3 ]
Nicolle, Remy [4 ]
Cros, Jerome [5 ]
Hammel, Pascal [6 ]
Cardot-Ruffino, Victoire [2 ]
Neuzillet, Cindy [1 ,2 ]
机构
[1] Univ Paris Saclay, Univ Versailles St Quentin, Inst Curie, Gastrointestinal Oncol,Med Oncol Dept, F-92210 St Cloud, France
[2] PSL Res Univ, Inst Curie, Mol Oncol, CNRS,UMR 144, Paris, France
[3] Univ Paris Saclay, Univ Versailles St Quentin, Ambroise Pare Hosp, APHP,Digest Surg Dept, Boulogne Billancourt, France
[4] Univ Paris Cite, Ctr Rech Inflammat CRI, INSERM, U1149,CNRS,ERL 8252, Paris, France
[5] Univ Paris C, Beaujon Hosp, AP HP, FHU MOSA,Pathol Dept, Clichy, France
[6] Univ Paris Saclay, Paul Brousse Hosp, APHP Sud, Dept Digest & Med Oncol, Villejuif, France
来源
关键词
CANCER; IMMUNE; GEMCITABINE; COMBINATION; MICROBIOME; MACROPHAGES; ONCOGENESIS; PROGRESSION; INDUCTION; EFFICACY;
D O I
10.1016/S2468-1253(23)00207-8
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Pancreatic ductal adenocarcinoma is associated with a poor prognosis and there are few treatment options. The development of immunotherapy in pancreatic ductal adenocarcinoma has been difficult, and immune checkpoint inhibitors are only effective in a very small subset of patients. Most obstacles for treatment have been related to intertumoural and intratumoural heterogeneity, the composition of tumour stroma, and crosstalk with cancer cells. Improved molecular characterisation of pancreatic ductal adenocarcinoma and a better understanding of its microenvironment have paved the way for novel immunotherapy strategies, including the identification of predictive biomarkers, the development of rational combinations to optimise effectiveness, and the targeting of new mechanisms. Future immunotherapy strategies should consider individual characteristics to move beyond the traditional immune targets and circumvent the resistance to therapies that have been developed so far.
引用
收藏
页码:1129 / 1142
页数:14
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