TY - JOUR
T1 - The reciprocity between radiotherapy and cancer immunotherapy
AU - Wang, Yifan
AU - Liu, Zhi Gang
AU - Yuan, Hengfeng
AU - Deng, Weiye
AU - Li, Jing
AU - Huang, Yuhui
AU - Kim, Betty Y.S.
AU - Story, Michael D.
AU - Jiang, Wen
N1 - Funding Information:
The authors thank Christine Wogan of the Division of Radiation Oncology at The University of Texas MD Anderson Cancer Center for editorial assistance. The authors thank Jordan Pietz of Creative Services, The University of Texas MD Anderson Cancer Center, and Cailian Wen of Xmagine Studio (Shenzhen, China) for artistic assistance. This work was supported in part by the American Society of Clinical Oncology (ASCO) Conquer Cancer Foundation Young Investigator Award (10804; to W. Jiang.), the Cancer Prevention and Research Institute of Texas CPRIT (RR180017; to W. Jiang.), the Mayo Clinic Center for Regenerative Medicine (to B.Y.S. Kim), the Jorge and Leslie Bacardi Fund in Regenerative Medicine (to B.Y.S. Kim), the National Institute of Neurological Disorders and Stroke Grant (R01 NS104315; to B.Y.S. Kim), the National Natural Science Foundation of China (81572500; to Z.-G. Liu), and Hunan Young Talents (2016RS3036; to Z.-G. Liu.)
Funding Information:
The authors thank Christine Wogan of the Division of Radiation Oncology at The University of Texas MD Anderson Cancer Center for editorial assistance. The authors thank Jordan Pietz of Creative Services, The University of Texas MD Anderson Cancer Center, and Cailian Wen of Xmagine Studio (Shenzhen, China) for artistic assistance. This work was supported in part by the American Society of Clinical Oncology (ASCO) Conquer Cancer Foundation Young Investigator Award (10804; to W. Jiang.), the Cancer Prevention and Research Institute of Texas CPRIT (RR180017; to W. Jiang.), the Mayo Clinic Center for Regenerative Medicine (to B.Y.S. Kim), the Jorge and Leslie Bacardi Fund in Regenerative Medicine (to B.Y.S. Kim), the National Institute of Neurological Disorders and Stroke Grant (R01 NS104315; to B.Y.S. Kim), the National Natural Science Foundation of China (81572500; to Z.-G. Liu), and Hunan Young Talents (2016RS3036; to Z.-G. Liu.) The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
Funding Information:
J. Li reports receiving commercial research grants from Bristol-Myers Squibb. No potential conflicts of interest were disclosed by the other authors.
Publisher Copyright:
© 2018 American Association for Cancer Research.
PY - 2019
Y1 - 2019
N2 - The clinical success of immune checkpoint inhibitors in treating metastatic and refractory cancers has generated significant interest in investigating their role in treating locally advanced diseases, thus requiring them to be combined with standard treatments in the hope of producing synergistic antitumor responses. Radiotherapy, in particular, has long been hypothesized to have actions complementary to those of immune checkpoint blockade, and a growing body of evidence indicates that cancer immunotherapy may also have radiosensitizing effects, which would provide unique benefit for locoregional treatments. Recent studies have demonstrated that when immune cells are activated by immunotherapeutics, they can reprogram the tumor microenvironment in ways that may potentially increase the radiosensitivity of the tumor. In this review, we highlight the evidence that supports reciprocal interactions between cancer immunotherapy and radiotherapy, where in addition to the traditional notion that radiation serves to enhance the activation of antitumor immunity, an alternative scenario also exists in which T-cell activation by cancer immunotherapy may sensitize tumors to radiation treatment through mechanisms that include normalization of the tumor vasculature and tissue hypoxia. We describe the empirical observations from preclinical models that support such effects and discuss their implications for future research and trial design.
AB - The clinical success of immune checkpoint inhibitors in treating metastatic and refractory cancers has generated significant interest in investigating their role in treating locally advanced diseases, thus requiring them to be combined with standard treatments in the hope of producing synergistic antitumor responses. Radiotherapy, in particular, has long been hypothesized to have actions complementary to those of immune checkpoint blockade, and a growing body of evidence indicates that cancer immunotherapy may also have radiosensitizing effects, which would provide unique benefit for locoregional treatments. Recent studies have demonstrated that when immune cells are activated by immunotherapeutics, they can reprogram the tumor microenvironment in ways that may potentially increase the radiosensitivity of the tumor. In this review, we highlight the evidence that supports reciprocal interactions between cancer immunotherapy and radiotherapy, where in addition to the traditional notion that radiation serves to enhance the activation of antitumor immunity, an alternative scenario also exists in which T-cell activation by cancer immunotherapy may sensitize tumors to radiation treatment through mechanisms that include normalization of the tumor vasculature and tissue hypoxia. We describe the empirical observations from preclinical models that support such effects and discuss their implications for future research and trial design.
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U2 - 10.1158/1078-0432.CCR-18-2581
DO - 10.1158/1078-0432.CCR-18-2581
M3 - Review article
C2 - 30413527
AN - SCOPUS:85062967691
SN - 1078-0432
VL - 25
SP - 1709
EP - 1717
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 6
ER -