Micro cone beam computed tomography for sensitive assessment of radiation-induced late lung toxicity in preclinical modelsvan Berlo, D., Khmelinskii, A., Gasparini, A., Salguero, F. J., Floot, B., de Wit, N., van de Ven, M., Song, J. Y., Coppes, R. P., Verheij, M., Sonke, J. J. & Vens, C., Sep-2019, In : Radiotherapy and Oncology. 138, p. 17-24 8 p.
Research output: Contribution to journal › Article › Academic › peer-review
Background and purpose: Preclinical models are much needed to assess the effect of novel radiosensitizers or mitigators on radiation dose limiting lung toxicity. Albeit showing radiation-induced lung pathologies, current mouse models lack the sensitivity to do so. Using micro image-guided radiotherapy (mIGRT) techniques, we aimed to establish murine models which enable the sensitive detection of lung damage aggravation and characterized functional, radiological and histological responses.
Materials and methods: Right lungs of C57Bl/6J mice were irradiated using mu IGRT with doses from 15 to 27 Gy and with 21 Gy and cisplatin as a radio-sensitizer in a second study. Mice were sacrificed for histological and pathological assessment at different time-points post-IR. Lung density was determined using the integrated micro cone-beam CT (mu CBCT). Lung function was measured by double-chamber-plethysmography.
Results: mu IGRT resulted in accurate deposition of the radiation dose in the right lung only as determined by gamma H2AX staining. Lung fibrosis was confirmed by pathological assessments and increased significantly at 21 Gy as determined by automated quantification of histochemical analyses. Lung function was affected in a dose-dependent manner. mu CBCT-determined lung densities increased significantly over time in the irradiated lungs and showed a strong radiation dose-dependence. Importantly, the mu CBCT analyses allowed the detection of additional lung damage caused by 3 Gy dose increments or by the combination with cisplatin.
Conclusion: mCBCT after right lung mIGRT enables the sensitive detection of effects inflicted by relative small dose increments or radio-sensitizers. Our preclinical model therefore facilitates the determination of lung damage exacerbation for the safety assessment of novel RT-drug combinations. (C) 2019 Elsevier B.V. All rights reserved.
|Number of pages||8|
|Journal||Radiotherapy and Oncology|
|Publication status||Published - Sep-2019|
- Preclinical lung models, Lung fibrosis, mu IGRT, Normal tissue toxicity, mu CBCT, THORACIC IRRADIATION, MOUSE LUNG, HEART IRRADIATION, DAMAGE, RADIOTHERAPY, COMBINATION, CIS-DIAMMINEDICHLOROPLATINUM(II)