Banerjee Shramana M, El-Sheikh Soha, Malhotra Anmol, Mosse Charles A, Parker Sweta, Williams Norman R, MacRobert Alexander J, Hamoudi Rifat, Bown Stephen G, Keshtgar Mo Rs
Breast Unit and Royal Free London NHS Foundation Trust, London NW3 2QG, UK.
Division of Surgery and Interventional Science, University College London, London W1W 7TY, UK.
J Clin Med. 2020 Feb 10;9(2):483. doi: 10.3390/jcm9020483.
Photodynamic therapy (PDT) is a technique for producing localized necrosis with light after prior administration of a photosensitizing agent. This study investigates the nature, safety, and efficacy of PDT for image-guided treatment of primary breast cancer. We performed a phase I/IIa dose escalation study in 12 female patients with a new diagnosis of invasive ductal breast cancer and scheduled to undergo mastectomy as a first treatment. The photosensitizer verteporfin (0.4 mg/kg) was administered intravenously followed by exposure to escalating light doses (20, 30, 40, 50 J; 3 patients per dose) delivered via a laser fiber positioned interstitially under ultrasound guidance. MRI (magnetic resonance imaging) scans were performed prior to and 4 days after PDT. Histological examination of the excised tissue was performed. PDT was well tolerated, with no adverse events. PDT effects were detected by MRI in 7 patients and histology in 8 patients, increasing in extent with the delivered light dose, with good correlation between the 2 modalities. Histologically, there were distinctive features of PDT necrosis, in contrast to spontaneous necrosis. Apoptosis was detected in adjacent normal tissue. Median follow-up of 50 months revealed no adverse effects and outcomes no worse than a comparable control population. This study confirms a potential role for PDT in the management of early breast cancer.
光动力疗法(PDT)是一种在预先给予光敏剂后利用光产生局部坏死的技术。本研究调查了PDT用于影像引导下原发性乳腺癌治疗的性质、安全性和疗效。我们对12例新诊断为浸润性导管癌且计划接受乳房切除术作为首次治疗的女性患者进行了I/IIa期剂量递增研究。静脉注射光敏剂维替泊芬(0.4mg/kg),随后通过在超声引导下经皮间质放置的激光光纤给予递增的光剂量(20、30、40、50J;每个剂量3例患者)。在PDT治疗前和治疗后4天进行MRI(磁共振成像)扫描。对切除组织进行组织学检查。PDT耐受性良好,未出现不良事件。7例患者通过MRI检测到PDT效应,8例患者通过组织学检测到PDT效应,效应程度随给予的光剂量增加,两种检测方式之间具有良好的相关性。组织学上,与自发性坏死相比,PDT坏死有明显特征。在相邻正常组织中检测到凋亡。50个月的中位随访显示无不良反应,结果不比可比的对照组人群差。本研究证实了PDT在早期乳腺癌治疗中的潜在作用。