Effectiveness and Patient Experiences of Rhenium Skin Cancer Therapy for Nonmelanoma Skin Cancer: Interim Results from the EPIC-Skin Study.

Siddhartha Baxi, Saima Vohra, Angela Hong, Nicola Mulholland, Martin Heuschkel, Gerhard Dahlhoff, Giuseppe Cardaci, Siroos Mirzaei, Mike Sathekge
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Abstract

Nonmelanoma skin cancer and its treatment represent a significant global cancer burden for health care systems and patients. Rhenium skin cancer therapy (Rhenium SCT) is a novel noninvasive radionuclide nonmelanoma skin cancer treatment, which can be provided in a single outpatient session. The aim of this prospective, multicenter, single-arm, international, phase IV study (EPIC-Skin) is to assess clinic- and patient-reported outcomes of Rhenium SCT as a treatment for basal cell carcinoma (BCC) and squamous cell carcinoma (SCC). Methods: Eligible patients had biopsy-proven stage I or stage II BCC or SCC lesions no more than 3 mm deep and no larger than 8 cm2 in area. Rhenium SCT resin was applied to an adhesive foil affixed to the target lesion in a single session. Interim efficacy and safety analysis were planned once 50% of target patients had recorded a 6-mo follow-up visit. Primary outcome is the proportion of lesions achieving complete response using modified RECIST. Secondary and other outcome measures include patient-reported quality of life (QoL), treatment comfort, and cosmesis. Results: A total of 182 patients was enrolled and administered Rhenium SCT (50 Gy dose to deepest point of target) to at least 1 BCC or SCC. Of 81 patients who reached the 6-mo posttreatment follow-up, it was found that 97.2% (103/106) of lesions showed complete responses and 2.8% (3/106) had partial responses. Improvements in QoL were also reported, whereas no patients reported any pain or discomfort during treatment. Adverse events were reported in 15.9% (29/182) of patients and were rated grade 1 (n = 19), grade 2 (n = 9), or grade 3 (n = 1). Conclusion: This preliminary analysis of the EPIC-Skin study indicates that Rhenium SCT is safe and effective for the treatment of BCC and SCC and is associated with significant QoL improvements. It will be particularly beneficial for lesions that are difficult to treat surgically because of size and location. It is also beneficial for patients with comorbidities or those unable to receive conventional fractionated radiotherapy.

铼皮肤癌疗法治疗非黑色素瘤皮肤癌的效果和患者体验:EPIC-皮肤研究的中期结果。
非黑色素瘤皮肤癌及其治疗给全球医疗系统和患者带来了沉重的负担。[188Re]树脂皮肤癌疗法(Rhenium SCT)是一种新型的非侵入性放射性核素非黑色素瘤皮肤癌治疗方法,只需在门诊进行一次治疗即可。这项前瞻性、多中心、单臂、国际 IV 期研究(EPIC-Skin)旨在评估铼 SCT 治疗基底细胞癌(BCC)和鳞状细胞癌(SCC)的临床和患者报告结果。治疗方法符合条件的患者均为活检证实的 I 期或 II 期 BCC 或 SCC 病变,病变深度不超过 3 毫米,面积不超过 8 平方厘米。将铼SCT树脂涂抹在贴在目标病灶上的粘合箔上,只需一次治疗。计划在 50% 的目标患者接受 6 个月随访后进行中期疗效和安全性分析。主要结果是使用改良 RECIST 获得完全应答的病变比例。次要和其他结果指标包括患者报告的生活质量(QoL)、治疗舒适度和外观。结果:共有 182 名患者入组,并对至少 1 个 BCC 或 SCC 进行了铼 SCT(50 Gy 剂量至目标最深点)治疗。在治疗后6个月随访的81名患者中,发现97.2%(103/106)的病灶有完全反应,2.8%(3/106)有部分反应。患者的生活质量也有所改善,没有患者报告治疗期间有任何疼痛或不适。15.9%的患者(29/182)报告了不良反应,分级为1级(19人)、2级(9人)或3级(1人)。结论EPIC-Skin研究的初步分析表明,铼SCT治疗BCC和SCC安全有效,并能显著改善患者的生活质量。它对因病变大小和位置而难以手术治疗的病变尤其有益。它还有利于合并症患者或无法接受常规分次放疗的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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