Orthopaedic Biomechanics Laboratory, Sunnybrook Research Institute, UB-55, 2075 Bayview Avenue, Toronto, ON M4N 3M5, Canada.
Breast Cancer Res Treat. 2012 Sep;135(2):391-401. doi: 10.1007/s10549-012-2146-x. Epub 2012 Jul 12.
Spinal metastasis commonly occurs in advanced breast cancer. Treatment is often multimodal including radiation therapy (RT), bisphosphonates (BPs), and surgery, yet alternative minimally invasive local treatments are needed. Photodynamic therapy (PDT) has been shown to ablate tumor cells and enhance bone formation secondary to metastatic breast cancer, demonstrating potential as a treatment for spinal metastasis. Combined with previous BP treatment, bone formation was further enhanced by PDT. This study aimed to determine the effects of PDT in combination with previous RT on healthy and metastatically involved vertebrae. Forty-six athymic rats underwent RT (4 Gy on day-7), twenty-three of them were inoculated with MT-1 human breast cancer cells on day 0. Thirteen healthy and ten metastatically involved rats underwent PDT treatment on day 14. All rats were sacrificed on day 21. L2 vertebrae were analyzed using μCT imaging, mechanical testing, and histological methods. In healthy vertebrae, while modest increases in trabecular structure were found in RT + PDT compared to RT only, mechanical stability was negatively affected. The 4 Gy RT dose was found to ablate all tumor cells and prevent further vertebral metastasis. As such, in metastatically involved rats, no differences in stereological or mechanical properties were detected. RT + PDT and RT-only treatment resulted in greatly improved vertebral structural and mechanical properties versus untreated or PDT-only treatment in metastatically involved rats, due to early tumor destruction in RT-treated groups. Increased amounts of woven bone and osteoid volume were found in PDT-treated vertebrae. Further investigation is needed to understand if structural improvements seen in RT + PDT treatment can translate into longer-term improvements in strength to support the potential of PDT as a viable adjuvant treatment for spinal metastasis postradiation.
脊柱转移通常发生在晚期乳腺癌中。治疗通常是多模式的,包括放射治疗(RT)、双膦酸盐(BPs)和手术,但需要替代的微创局部治疗方法。光动力疗法(PDT)已被证明可以消融肿瘤细胞,并增强转移性乳腺癌的骨形成,显示出作为脊柱转移治疗的潜力。与之前的 BP 治疗相结合,PDT 进一步增强了骨形成。本研究旨在确定 PDT 联合之前的 RT 对健康和转移性受累椎体的影响。46 只无胸腺大鼠接受 RT(第 7 天 4 Gy),其中 23 只在第 0 天接种 MT-1 人乳腺癌细胞。13 只健康和 10 只转移性受累大鼠在第 14 天接受 PDT 治疗。所有大鼠均在第 21 天处死。使用 μCT 成像、力学测试和组织学方法分析 L2 椎体。在健康椎体中,与仅接受 RT 相比,RT + PDT 虽然发现小梁结构略有增加,但力学稳定性受到负面影响。发现 4 Gy RT 剂量可消融所有肿瘤细胞并防止进一步的椎体转移。因此,在转移性受累大鼠中,未检测到立体学或力学特性的差异。与未治疗或仅 PDT 治疗相比,RT + PDT 和仅 RT 治疗在转移性受累大鼠中导致椎骨结构和力学性能大大改善,这是由于 RT 治疗组中早期肿瘤破坏。在 PDT 治疗的椎体中发现了更多的编织骨和类骨质体积。需要进一步研究以了解 RT + PDT 治疗中观察到的结构改善是否可以转化为强度的长期改善,以支持 PDT 作为放射后脊柱转移可行辅助治疗的潜力。