TY - JOUR
T1 - The tumour microenvironment in pancreatic cancer — clinical challenges and opportunities
AU - Ho, Won Jin
AU - Jaffee, Elizabeth M.
AU - Zheng, Lei
N1 - Funding Information:
W.J.H. is the recipient of an ASCO Young Investigator Award and an AACR Incyte Immuno-Oncology Research Fellowship, and is supported by NIH T32CA00971-38.
Funding Information:
W.J.H. could potentially receive patent-related royalties from Rodeo Therapeutics. E.M.J. receives commercial research grants from Aduro Biotech, Amgen, Bristol–Myers Squibb, Corvus and Hertix, has ownership interest in Aduro Biotech, and is a consultant and/or advisory board member for Achilles Therapeutics, Adaptive Biotechnologies, CStone Pharmaceuticals, Dragonfly Therapeutics, Genocea and the Parker Institute for Cancer Immunotherapy. She is a member of the National Cancer Advisory Board and the Chief Medical Advisor for the Lustgarten Foundation. L.Z. receives grant support from Amgen, Bristol–Myers Squibb, Halozyme, Inxmed, iTeos, Merck and NovaRock, and received royalties for licensing GVAX to Aduro Biotech. He is a paid consultant and/or advisory board member for Akrevia, Alphamab, Biosion, Datarevive, Foundation Medicine, Fusun Biopharmaceutical, Mingruzhiyao, NovaRock and Sound Biologics, and holds shares in Alphamab and Mingruzhiyao.
Publisher Copyright:
© 2020, Springer Nature Limited.
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Metastatic pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal solid tumours despite the use of multi-agent conventional chemotherapy regimens. Such poor outcomes have fuelled ongoing efforts to exploit the tumour microenvironment (TME) for therapy, but strategies aimed at deconstructing the surrounding desmoplastic stroma and targeting the immunosuppressive pathways have largely failed. In fact, evidence has now shown that the stroma is multi-faceted, which illustrates the complexity of exploring features of the TME as isolated targets. In this Review, we describe ways in which the PDAC microenvironment has been targeted and note the current understanding of the clinical outcomes that have unexpectedly contradicted preclinical observations. We also consider the more sophisticated therapeutic strategies under active investigation — multi-modal treatment approaches and exploitation of biologically integrated targets — which aim to remodel the TME against PDAC.
AB - Metastatic pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal solid tumours despite the use of multi-agent conventional chemotherapy regimens. Such poor outcomes have fuelled ongoing efforts to exploit the tumour microenvironment (TME) for therapy, but strategies aimed at deconstructing the surrounding desmoplastic stroma and targeting the immunosuppressive pathways have largely failed. In fact, evidence has now shown that the stroma is multi-faceted, which illustrates the complexity of exploring features of the TME as isolated targets. In this Review, we describe ways in which the PDAC microenvironment has been targeted and note the current understanding of the clinical outcomes that have unexpectedly contradicted preclinical observations. We also consider the more sophisticated therapeutic strategies under active investigation — multi-modal treatment approaches and exploitation of biologically integrated targets — which aim to remodel the TME against PDAC.
UR - http://www.scopus.com/inward/record.url?scp=85084454263&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85084454263&partnerID=8YFLogxK
U2 - 10.1038/s41571-020-0363-5
DO - 10.1038/s41571-020-0363-5
M3 - Review article
C2 - 32398706
AN - SCOPUS:85084454263
SN - 1759-4774
VL - 17
SP - 527
EP - 540
JO - Nature Reviews Clinical Oncology
JF - Nature Reviews Clinical Oncology
IS - 9
ER -