Instituto Mexicano del Seguro Social, Centro Medico Nacional de Occidente, Guadalajara, Jalisco, México.
Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Ave. Eugenio Garza Sada 2501, Monterrey, N.L., 64849, México.
BMC Ophthalmol. 2023 Jul 27;23(1):335. doi: 10.1186/s12886-023-03092-z.
Ocular surface squamous neoplasia (OSSN) comprises a wide spectrum of squamous tumors, from which corneal/conjunctival intraepithelial neoplasia (CIN) is the most common one. The classic treatment is complete excision, but recurrence rates are high. Antineoplastic drugs such as mitomycin C (MMC) and interferon alpha 2b (IFNα2b) have been used as adjuvants or as primary treatment. To evaluate the efficacy and safety of topical IFNα2b and MMC in patients with CIN, a phase IIb double-blind clinical trial was performed.
Patients diagnosed with localized CIN were evaluated by slit lamp and impression cytology and were randomly given MMC 0.04% or INF2b (1 million IU/mL) 4 times daily until neoplasia resolution. Time of resolution and frequency of adverse effects were analyzed to determine the pharmacological efficacy and safety of both medications.
Seventeen patients were included. Nine patients were treated with MMC and 8 with IFNα2b. All patients responded to treatment. The resolution time in days was 59.11 ± 24.02 in patients treated with MMC and 143.50 ± 47.181 in those treated with IFNα2b (p < 0.001). In the MMC group, one recurrence was reported (11%). There were no recurrences at 2 years of follow-up in the IFNα2b group. Regarding adverse effects, one or more mild adverse reaction occurred in 77% of patients managed with MMC and in 50% of patients managed with IFNα2b (p > 0.05). No serious adverse effects were reported.
Topical chemotherapy with MMC and IFNα2b demonstrate pharmacological safety and efficacy. Therefore, these drugs could be considered as primary therapies for localized CIN .
眼表鳞状上皮肿瘤(OSSN)包括一系列的鳞状肿瘤,其中角膜/结膜上皮内瘤变(CIN)最为常见。经典的治疗方法是完全切除,但复发率很高。丝裂霉素 C(MMC)和干扰素 alpha 2b(IFNα2b)等抗肿瘤药物已被用作辅助治疗或一线治疗。为评估 CIN 患者局部应用 IFNα2b 和 MMC 的疗效和安全性,进行了一项 IIb 期双盲临床试验。
通过裂隙灯和印迹细胞学检查评估诊断为局限性 CIN 的患者,并随机给予 MMC 0.04%或 INF2b(100 万 IU/ml),每天 4 次,直至肿瘤消退。分析缓解时间和不良反应频率,以确定两种药物的药理疗效和安全性。
共纳入 17 例患者。9 例患者接受 MMC 治疗,8 例患者接受 IFNα2b 治疗。所有患者均对治疗有反应。接受 MMC 治疗的患者缓解时间为 59.11±24.02 天,接受 IFNα2b 治疗的患者为 143.50±47.181 天(p<0.001)。在 MMC 组中,有 1 例复发(11%)。在 IFNα2b 组中,2 年随访时无复发。关于不良反应,接受 MMC 治疗的患者中有 77%出现 1 种或多种轻度不良反应,而接受 IFNα2b 治疗的患者中有 50%出现 1 种或多种轻度不良反应(p>0.05)。未报告严重不良反应。
局部应用 MMC 和 IFNα2b 化疗具有药理安全性和疗效。因此,这些药物可考虑作为局限性 CIN 的一线治疗。