TY - JOUR
T1 - LymphoDose
T2 - a lymphocyte dose estimation framework—application to brain radiotherapy
AU - de Kermenguy, François
AU - Benzazon, Nathan
AU - Maury, Pauline
AU - Vauclin, Rémi
AU - M’hamdi, Meissane
AU - Cifliku, Vjona
AU - Limkin, Elaine
AU - Diallo, Ibrahima
AU - Morel, Daphné
AU - Milewski, Candice
AU - Clémenson, Céline
AU - Mondini, Michele
AU - Deutsch, Eric
AU - Robert, Charlotte
N1 - Publisher Copyright:
© 2024 The Author(s). Published on behalf of Institute of Physics and Engineering in Medicine by IOP Publishing Ltd.
PY - 2024/5/21
Y1 - 2024/5/21
N2 - Objective. Severe radiation-induced lymphopenia occurs in 40% of patients treated for primary brain tumors and is an independent risk factor of poor survival outcomes. We developed an in-silico framework that estimates the radiation doses received by lymphocytes during volumetric modulated arc therapy brain irradiation. Approach. We implemented a simulation consisting of two interconnected compartmental models describing the slow recirculation of lymphocytes between lymphoid organs ( M 1 ) and the bloodstream ( M 2 ). We used dosimetry data from 33 patients treated with chemo-radiation for glioblastoma to compare three cases of the model, corresponding to different physical and biological scenarios: (H1) lymphocytes circulation only in the bloodstream i.e. circulation in M 2 only; (H2) lymphocytes recirculation between lymphoid organs i.e. circulation in M 1 and M 2 interconnected; (H3) lymphocytes recirculation between lymphoid organs and deep-learning computed out-of-field (OOF) dose to head and neck (H&N) lymphoid structures. A sensitivity analysis of the model’s parameters was also performed. Main results. For H1, H2 and H3 cases respectively, the irradiated fraction of lymphocytes was 99.8 ± 0.7%, 40.4 ± 10.2% et 97.6 ± 2.5%, and the average dose to irradiated pool was 309.9 ± 74.7 mGy, 52.6 ± 21.1 mGy and 265.6 ± 48.5 mGy. The recirculation process considered in the H2 case implied that irradiated lymphocytes were irradiated in the field only 1.58 ± 0.91 times on average after treatment. The OOF irradiation of H&N lymphoid structures considered in H3 was an important contribution to lymphocytes dose. In all cases, the estimated doses are low compared with lymphocytes radiosensitivity, and other mechanisms could explain high prevalence of RIL in patients with brain tumors. Significance. Our framework is the first to take into account OOF doses and recirculation in lymphocyte dose assessment during brain irradiation. Our results demonstrate the need to clarify the indirect effects of irradiation on lymphopenia, in order to potentiate the combination of radio-immunotherapy or the abscopal effect.
AB - Objective. Severe radiation-induced lymphopenia occurs in 40% of patients treated for primary brain tumors and is an independent risk factor of poor survival outcomes. We developed an in-silico framework that estimates the radiation doses received by lymphocytes during volumetric modulated arc therapy brain irradiation. Approach. We implemented a simulation consisting of two interconnected compartmental models describing the slow recirculation of lymphocytes between lymphoid organs ( M 1 ) and the bloodstream ( M 2 ). We used dosimetry data from 33 patients treated with chemo-radiation for glioblastoma to compare three cases of the model, corresponding to different physical and biological scenarios: (H1) lymphocytes circulation only in the bloodstream i.e. circulation in M 2 only; (H2) lymphocytes recirculation between lymphoid organs i.e. circulation in M 1 and M 2 interconnected; (H3) lymphocytes recirculation between lymphoid organs and deep-learning computed out-of-field (OOF) dose to head and neck (H&N) lymphoid structures. A sensitivity analysis of the model’s parameters was also performed. Main results. For H1, H2 and H3 cases respectively, the irradiated fraction of lymphocytes was 99.8 ± 0.7%, 40.4 ± 10.2% et 97.6 ± 2.5%, and the average dose to irradiated pool was 309.9 ± 74.7 mGy, 52.6 ± 21.1 mGy and 265.6 ± 48.5 mGy. The recirculation process considered in the H2 case implied that irradiated lymphocytes were irradiated in the field only 1.58 ± 0.91 times on average after treatment. The OOF irradiation of H&N lymphoid structures considered in H3 was an important contribution to lymphocytes dose. In all cases, the estimated doses are low compared with lymphocytes radiosensitivity, and other mechanisms could explain high prevalence of RIL in patients with brain tumors. Significance. Our framework is the first to take into account OOF doses and recirculation in lymphocyte dose assessment during brain irradiation. Our results demonstrate the need to clarify the indirect effects of irradiation on lymphopenia, in order to potentiate the combination of radio-immunotherapy or the abscopal effect.
KW - Markov chain
KW - brain tumor
KW - compartments model
KW - lymphocyte-sparing radiotherapy
KW - lymphocytes
KW - lymphopenia
UR - http://www.scopus.com/inward/record.url?scp=85191899113&partnerID=8YFLogxK
U2 - 10.1088/1361-6560/ad3c8d
DO - 10.1088/1361-6560/ad3c8d
M3 - Article
C2 - 38593817
AN - SCOPUS:85191899113
SN - 0031-9155
VL - 69
JO - Physics in Medicine and Biology
JF - Physics in Medicine and Biology
IS - 10
M1 - 105009
ER -