The New York Eye Cancer Center, New York, New York 10065, USA.
Ophthalmic Plast Reconstr Surg. 2012 Mar-Apr;28(2):85-9. doi: 10.1097/IOP.0b013e3182392f29.
To test the safety, tolerability, and efficacy of subconjunctival ranibizumab (Lucentis [Genentech, Inc.]) for squamous cell carcinoma of the conjunctiva and cornea.
Five patients with recurrent squamous cell carcinoma of the conjunctiva and cornea enrolled in this nonrandomized, single center, phase I pilot study as an alternative to radiation or exenteration. Subconjunctival ranibizumab (0.5 mg) was given on a monthly or twice monthly basis. Patients were examined for safety, tolerability, and efficacy using visual acuity, blood pressure, urinalysis, comparative slit lamp biomicroscopy with photography, and high frequency ultrasound imaging.
Five male patients with biopsy-proven squamous conjunctival carcinoma were found to have recurrent disease. Each patient had been initially treated with combinations of primary excision (n = 1) or excision and cryotherapy (n = 4), and all (n = 5) had failed separate courses of both topical interferon a and mitomycin 0.02%. Tumors were multifocal and involved between 8 and 12 clock hours of the limbus. A median of 22 injections (range 12-27) was given over a mean 19 months (range 6-24). Three patients had a complete response (no clinically apparent disease) during the 2-year study, while 2 failed treatment despite demonstrating an initial partial response. Treatment was well-tolerated, as 4 patients demonstrated stable or improved visual acuity, and none had significant systemic or ocular side effects.
This 2-year study demonstrated that subconjunctival ranibizumab induced regression of squamous cell carcinoma of the conjunctiva and cornea. Therefore, antivascular endothelial growth factor chemotherapy may offer a new strategy, complement excision and cryotherapy, or provide an alternative to radiation and/or exenteration. Further, larger investigations utilizing a larger group of patients are needed to determine the ideal dose, route of drug delivery, and case selection.
测试结膜和角膜鳞状细胞癌患者结膜下雷珠单抗(Lucentis [Genentech,Inc.])的安全性、耐受性和疗效。
本非随机、单中心、I 期试点研究纳入 5 例复发性结膜和角膜鳞状细胞癌患者,作为放疗或眼眶内容摘除术的替代疗法。每月或每两个月给予结膜下雷珠单抗(0.5mg)。通过视力、血压、尿液分析、比较裂隙灯生物显微镜检查和摄影以及高频超声成像来评估患者的安全性、耐受性和疗效。
5 例男性患者经活检证实为结膜鳞状细胞癌,发现复发性疾病。每位患者最初均接受过原发性切除术(n=1)或切除术加冷冻疗法(n=4)的联合治疗,所有患者(n=5)均分别失败了单独使用局部干扰素 a 和丝裂霉素 0.02%的治疗。肿瘤呈多灶性,累及 8 至 12 个钟点的角膜缘。平均 19 个月(范围 6-24 个月)内共给予中位数 22 次注射(范围 12-27 次)。在 2 年的研究中,3 例患者获得完全缓解(无临床明显疾病),而 2 例患者尽管最初有部分缓解,但治疗失败。治疗耐受性良好,因为 4 例患者的视力稳定或改善,且无明显的全身或眼部副作用。
这项为期 2 年的研究表明,结膜下雷珠单抗诱导了结膜和角膜鳞状细胞癌的消退。因此,抗血管内皮生长因子化疗可能提供一种新的策略,补充切除术和冷冻疗法,或作为放疗和/或眼眶内容摘除术的替代疗法。此外,需要更大规模的研究,以确定理想的剂量、药物输送途径和病例选择,从而利用更大的患者群体进行研究。