Lymphocyte-Sparing Radiotherapy: The Rationale for Protecting Lymphocyte-rich Organs When Combining Radiotherapy With Immunotherapy

There is now strong clinical and preclinical evidence that lymphocytes, for example, CD8+ T cells, are key effectors of immunotherapy and that irradiation of large blood vessels, the heart, and lymphoid organs (including nodes, spleen, bones containing bone marrow, and thymus in children) causes tra...

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Published inSeminars in radiation oncology Vol. 30; no. 2; pp. 187 - 193
Main Authors Lambin, Philippe, Lieverse, Relinde I.Y., Eckert, Franziska, Marcus, Damiënne, Oberije, Cary, van der Wiel, Alexander M.A., Guha, Chandan, Dubois, Ludwig J., Deasy, Joseph O.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.04.2020
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Summary:There is now strong clinical and preclinical evidence that lymphocytes, for example, CD8+ T cells, are key effectors of immunotherapy and that irradiation of large blood vessels, the heart, and lymphoid organs (including nodes, spleen, bones containing bone marrow, and thymus in children) causes transient or persistent lymphopenia. Furthermore, there is extensive clinical evidence, across multiple cancer sites and treatment modalities, that lymphopenia correlates strongly with decreased overall survival. At the moment, we lack quantitative evidence to establish the relationship between dose-volume and dose-rate to critical normal structures and lymphopenia. Therefore, we propose that data should be systematically recorded to characterise a possible quantitative relationship. This might enable us to improve the efficacy of radiotherapy and develop strategies to predict and prevent treatment-related lymphopenia. In anticipation of more quantitative data, we recommend the application of the principle of As Low As Reasonably Achievable to lymphocyte-rich regions for radiotherapy treatment planning to reduce the radiation doses to these structures, thus moving toward “Lymphocyte-Sparing Radiotherapy.”
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Equal contribution
ISSN:1053-4296
1532-9461
1532-9461
DOI:10.1016/j.semradonc.2019.12.003