Urology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Department of Epidemiology & Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
J Urol. 2023 May;209(5):863-871. doi: 10.1097/JU.0000000000003202. Epub 2023 Feb 1.
Vascular-targeted photodynamic therapy with the intravascular photosensitizing agent padeliporfin (WST-11/TOOKAD-Soluble) has demonstrated therapeutic efficacy as an ablative treatment for localized cancer with potential adaptation for endoscopic management of upper tract urothelial carcinoma. This Phase I trial (NCT03617003) evaluated the safety of vascular-targeted photodynamic therapy with WST-11 in upper tract urothelial carcinoma.
Nineteen patients underwent up to 2 endoscopic vascular-targeted photodynamic therapy treatments, with follow-up for up to 6 months. Patients who had residual or recurrent upper tract urothelial carcinoma (any grade/size) failing prior endoscopic treatment or unable or unwilling to undergo surgical resection were eligible for inclusion. The primary endpoint was to identify the maximally tolerated dose of laser light fluence. A dose escalation model was employed, with increasing light fluence (100-200 mW/cm) using a modified continual reassessment method. The secondary endpoint was treatment efficacy, defined by absence of visible tumor and negative urine cytology 30 days posttreatment.
Fourteen (74%) patients received the maximally tolerated dose of 200 mW/cm, 2 (11%) of whom experienced a dose-limiting toxicity. The initial 30-day treatment response rate was 94% (50% complete, 44% partial). Eight patients underwent a second treatment, with a final observed 68% complete response rate. Leading toxicities were flank pain (79%) and hematuria (84%), which were transient. No ureteral strictures associated with treatment were identified during follow-up.
Vascular-targeted photodynamic therapy with WST-11 has an acceptable safety profile with strong potential as an effective, kidney-sparing endoscopic management option for upper tract urothelial carcinoma. The recently initiated multicenter Phase 3 ENLIGHTED trial (NCT04620239) is expected to provide further evidence on this therapy.
血管靶向光动力疗法使用血管内光敏剂 padeliporfin(WST-11/TOOKAD-Soluble)已被证明是一种治疗局限性癌症的消融疗法,具有潜在的适应于上尿路尿路上皮癌的内镜治疗。这项 I 期试验(NCT03617003)评估了 WST-11 血管靶向光动力疗法在上尿路尿路上皮癌中的安全性。
19 名患者接受了多达 2 次内镜下血管靶向光动力疗法治疗,并进行了长达 6 个月的随访。先前内镜治疗失败或无法或不愿接受手术切除的残留或复发性上尿路尿路上皮癌(任何分级/大小)的患者符合纳入条件。主要终点是确定最大耐受激光光通量。采用递增光通量(100-200mW/cm)的剂量递增模型,使用改良连续再评估方法。次要终点是治疗效果,定义为治疗后 30 天无可见肿瘤和尿液细胞学阴性。
14 名(74%)患者接受了 200mW/cm 的最大耐受剂量,其中 2 名(11%)患者出现剂量限制毒性。初始 30 天治疗反应率为 94%(完全缓解 50%,部分缓解 44%)。8 名患者接受了第二次治疗,最终完全缓解率为 68%。主要毒性是腰痛(79%)和血尿(84%),均为一过性。在随访期间未发现与治疗相关的输尿管狭窄。
WST-11 血管靶向光动力疗法具有可接受的安全性,作为上尿路尿路上皮癌的一种有效、保肾的内镜治疗选择具有很大潜力。最近启动的多中心 III 期 ENLIGHTED 试验(NCT04620239)预计将提供该疗法的进一步证据。