Academic Unit of Oral and Maxillofacial Surgery, UCL Eastman Dental Institute, London, UK.
Division of Surgery and Interventional Science, University College London, London, UK.
Lancet Oncol. 2016 Sep;17(9):1217-29. doi: 10.1016/S1470-2045(16)30224-8. Epub 2016 Jul 28.
Photochemical internalisation, a novel minimally invasive treatment, has shown promising preclinical results in enhancing and site-directing the effect of anticancer drugs by illumination, which initiates localised chemotherapy release. We assessed the safety and tolerability of a newly developed photosensitiser, disulfonated tetraphenyl chlorin (TPCS2a), in mediating photochemical internalisation of bleomycin in patients with advanced and recurrent solid malignancies.
In this phase 1, dose-escalation, first-in-man trial, we recruited patients (aged ≥18 to <85 years) with local recurrent, advanced, or metastatic cutaneous or subcutaneous malignancies who were clinically assessed as eligible for bleomycin chemotherapy from a single centre in the UK. Patients were given TPCS2a on day 0 by slow intravenous injection, followed by a fixed dose of 15 000 IU/m(2) bleomycin by intravenous infusion on day 4. After 3 h, the surface of the target tumour was illuminated with 652 nm laser light (fixed at 60 J/cm(2)). The TPCS2a starting dose was 0·25 mg/kg and was then escalated in successive dose cohorts of three patients (0·5, 1·0, and 1·5 mg/kg). The primary endpoints were safety and tolerability of TPCS2a; other co-primary endpoints were dose-limiting toxicity and maximum tolerated dose. The primary analysis was per protocol. This study is registered with ClinicalTrials.gov, number NCT00993512, and has been completed.
Between Oct 3, 2009, and Jan 14, 2014, we recruited 22 patients into the trial. 12 patients completed the 3-month follow-up period. Adverse events related to photochemical internalisation were either local, resulting from the local inflammatory process, or systemic, mostly as a result of the skin-photosensitising effect of TPCS2a. The most common grade 3 or worse adverse events were unexpected higher transient pain response (grade 3) localised to the treatment site recorded in nine patients, and respiratory failure (grade 4) noted in two patients. One dose-limiting toxicity was reported in the 1·0 mg/kg cohort (skin photosensitivity [grade 2]). Dose-limiting toxicities were reported in two of three patients at a TPCS2a dose of 1·5 mg/kg (skin photosensitivity [grade 3] and wound infection [grade 3]); thus, the maximum tolerated dose of TPCS2a was 1·0 mg/kg. Administration of TPCS2a was found to be safe and tolerable by all patients. No deaths related to photochemical internalisation treatment occurred.
TPCS2a-mediated photochemical internalisation of bleomycin is safe and tolerable. We identified TPCS2a 0·25 mg/kg as the recommended treatment dose for future trials.
PCI Biotech.
光化学内部化是一种新型微创治疗方法,通过光照启动局部化疗释放,已显示出在增强和靶向抗癌药物方面具有有前景的临床前结果,该方法可引发局部化疗释放。我们评估了新型光敏剂二磺化四苯基氯(TPCS2a)在介导博来霉素光化学内部化治疗晚期和复发性实体恶性肿瘤患者中的安全性和耐受性。
在这项 1 期、剂量递增、首次人体试验中,我们招募了来自英国一家中心的具有局部复发性、晚期或转移性皮肤或皮下恶性肿瘤且临床评估适合博来霉素化疗的患者(年龄≥18 岁且<85 岁)。患者于第 0 天缓慢静脉注射 TPCS2a,第 4 天静脉输注固定剂量的 15000IU/m2博来霉素。3 小时后,用 652nm 激光(固定在 60J/cm2)照射目标肿瘤表面。TPCS2a 的起始剂量为 0.25mg/kg,然后按三个剂量递增组(0.5、1.0 和 1.5mg/kg)递增。主要终点是 TPCS2a 的安全性和耐受性;其他主要终点是剂量限制性毒性和最大耐受剂量。主要分析是基于方案。该研究在 ClinicalTrials.gov 注册,编号为 NCT00993512,现已完成。
2009 年 10 月 3 日至 2014 年 1 月 14 日期间,我们招募了 22 名患者入组该试验。12 名患者完成了 3 个月的随访期。与光化学内部化相关的不良事件要么是局部的,源于局部炎症过程,要么是全身性的,主要是由于 TPCS2a 的皮肤光致敏作用。最常见的 3 级或更高级别的不良事件是 9 名患者出现意外的更高的短暂疼痛反应(3 级),局部在治疗部位,2 名患者出现呼吸衰竭(4 级)。在 1.0mg/kg 组报告了 1 例剂量限制性毒性(皮肤光敏性[2 级])。在 TPCS2a 剂量为 1.5mg/kg 的 3 名患者中有 2 例出现剂量限制性毒性(皮肤光敏性[3 级]和伤口感染[3 级]);因此,TPCS2a 的最大耐受剂量为 1.0mg/kg。所有患者均认为 TPCS2a 给药安全且耐受。没有与光化学内部化治疗相关的死亡。
TPCS2a 介导的博来霉素光化学内部化是安全且耐受的。我们确定 TPCS2a 0.25mg/kg 为未来试验的推荐治疗剂量。
PCI Biotech。