Safety of combining radiotherapy with immune-checkpoint inhibition

被引:0
作者
William L. Hwang
Luke R. G. Pike
Trevor J. Royce
Brandon A. Mahal
Jay S. Loeffler
机构
[1] Harvard Medical School,Harvard Radiation Oncology Program
[2] Massachusetts General Hospital,Department of Radiation Oncology
[3] Massachusetts General Hospital,Department of Neurosurgery
来源
Nature Reviews Clinical Oncology | 2018年 / 15卷
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摘要
Immune-checkpoint inhibitors targeting cytotoxic T- lymphocyte antigen 4 (CTLA-4), programmed cell death protein 1 (PD-1), or programmed cell death 1 ligand 1 (PD-L1) have transformed the care of patients with a wide range of advanced-stage malignancies. More than half of these patients will also have an indication for treatment with radiotherapy. The effects of both radiotherapy and immune-checkpoint inhibition (ICI) involve a complex interplay with the innate and adaptive immune systems, and accumulating evidence suggests that, under certain circumstances, the effects of radiotherapy synergize with those of ICI to augment the antitumour responses typically observed with either modality alone and thus improve clinical outcomes. However, the mechanisms by which radiotherapy and immune-checkpoint inhibitors synergistically modulate the immune response might also affect both the type and severity of treatment-related toxicities. Moreover, in patients receiving immune-checkpoint inhibitors, the development of immune-related adverse events has been linked with superior treatment responses and patient survival durations, suggesting a relationship between the antitumour and adverse autoimmune effects of these agents. In this Review, we discuss the emerging data on toxicity profiles related to immune-checkpoint inhibitors and radiotherapy, both separately and in combination, their potential mechanisms, and the approaches to managing these toxicities.
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页码:477 / 494
页数:17
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  • [61] Fagarasan S(2013)T-regulatory cells: key players in tumor immune escape and angiogenesis Inflamm Res. 62 201-381
  • [62] Honjo T(2009)The effect of ionizing radiation on the homeostasis and functional integrity of murine splenic regulatory T cells Clin. Cancer Res. 15 5379-148
  • [63] Shi F(2016)Fractionated but not single-dose radiotherapy induces an immune-mediated abscopal effect when combined with anti-CTLA-4 antibody Nat. Rev. Clin. Oncol. 13 516-5956
  • [64] Kataoka K(2017)Immunotherapy and stereotactic ablative radiotherapy (ISABR): a curative approach? Nat. Commun. 8 192-8868
  • [65] Nishimura H(2013)DNA exonuclease Trex1 regulates radiotherapy-induced tumour immunogenicity Curr. Opin. Immunol. 25 61-465
  • [66] Nishimura H(2011)Genetically engineered mouse models of cancer reveal new insights about the antitumor immune response Nat. Rev. Immunol. 12 371-164
  • [67] Nose M(2014)Experimental mouse tumour models: what can be learnt about human cancer immunology? Endocr. Relat. Cancer 21 139-2526
  • [68] Hiai H(2016)Endocrine-related adverse events following ipilimumab in patients with advanced melanoma: a comprehensive retrospective review from a single institution Eur. J. Cancer 54 5950-3175
  • [69] Minato N(2008)Immune-related adverse events with immune checkpoint blockade: a comprehensive review J. Clin. Oncol. 26 879-1030
  • [70] Honjo T(2012)Phase I/II study of ipilimumab for patients with metastatic melanoma Lancet Oncol. 13 459-1117