Abstract

Spinal metastases often occur in the advanced stages of breast, lung or prostate cancer, resulting in a significant impact on the patient’s quality of life. Current treatment modalities for spinal metastases include both systemic and localized treatments that aim to decrease pain, improve mobility and structural stability, and control tumour growth. With the development of non-toxic photosensitizer drugs, photodynamic therapy (PDT) has shown promise as a minimally invasive non-thermal alternative in oncology, including for spinal metastases. To apply PDT to spinal metastases, predictive algorithms that optimize tumour treatment and minimize the risk of spinal cord damage are needed to assess the feasibility of the treatment and encourage a broad acceptance of PDT in clinical trials. This work presents a framework for PDT modelling and planning, and simulates the feasibility of using a BPD-MA mediated PDT to treat bone metastases at two different wavelengths (690 nm and 565 nm). An open-source software for PDT planning, PDT-SPACE, is used to evaluate different configurations of light diffusers (cut-end and cylindrical) fibres with optimized power allocation in order to minimize the damage to spinal cord or maximize tumour destruction. The work is simulated on three CT images of metastatically involved vertebrae acquired from three patients with spinal metastases secondary to colorectal or lung cancer. Simulation results show that PDT at a 565 nm wavelength has the ability to treat 90% of the metastatic lesion with less than 17% damage to the spinal cord. However, the energy required, and hence treatment time, to achieve this outcome with the 565 nm is infeasible. The energy required and treatment time for the longer wavelength of 690 nm is feasible ({sim },40 min), but treatment aimed at 90% of the metastatic lesion would severely damage the proximal spinal cord. PDT-SPACE provides a simulation platform that can be used to optimize PDT delivery in the metastatic spine. While this work serves as a prospective methodology to analyze the feasibility of PDT for tumour ablation in the spine, preclinical studies in an animal model are ongoing to elucidate the spinal cord damage extent as a function of PDT dose, and the resulting short and long term functional impairments. These will be required before there can be any consideration of clinical trials.

Highlights

  • MethodsPatient identifiers were removed prior to using these imaging datasets from three patients with spinal metastases treated with stereotactic body radiation therapy (Department of Radiation Oncology, Sunnybrook Health Sciences Centre, Toronto, ON, Canada)

  • For the cut-end fibres scenario, less than 18% of the spinal cord is damaged at 90% damage to the tumour with only 3.7 kJ needed

  • PDT is increasingly being utilized as a focal oncology therapy, with recent approvals for prostate and brain tumours in various jurisdictions including Europe, the USA and Japan

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Summary

Methods

Patient identifiers were removed prior to using these imaging datasets from three patients with spinal metastases treated with stereotactic body radiation therapy (Department of Radiation Oncology, Sunnybrook Health Sciences Centre, Toronto, ON, Canada). This is a retrospective study utilizing the imaging datasets. Guided by the contours from the SBRT plan, target structures and organs at risks were segmented using ITK-SNAP27, including the metastasis, spinal cord, normal surrounding bone, and muscle. Note that the latter two structures were manually segmented as they were not explicitly contoured. Other surrounding structures were omitted as they are not expected to be significantly impacted by PDT, because they were distal to the target and were exposed only to a low photon density, or they have a limited vasculature and do Scientific Reports | (2021) 11:17871 |

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