Yamada Masakazu, Kamao Tomoyuki, Shiraishi Atsushi, Sakai Jo, Ohashi Yuichi
Department of Ophthalmology, Kyorin University School of Medicine, 6-20-2 Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
Department of Ophthalmology, Ehime University Graduate School of Medicine, Toon, Japan.
Jpn J Ophthalmol. 2025 Mar 17. doi: 10.1007/s10384-025-01180-9.
S-1 is an orally active anticancer drug known to cause ocular adverse events (AEs), including lacrimal passage obstruction and corneal complications. This study investigated tear concentrations of 5-fluorouracil (5-FU) and tegafur (FT) in patients receiving S-1 treatment and their relationship with ocular AEs.
Multicenter prospective cohort study.
We recruited patients scheduled for S-1 chemotherapy. After initial ophthalmologic examinations at enrollment, serial examinations were performed during the courses of S-1 administration for up to 1 year. Tear samples were collected using Schirmer test strips at the end of the first course of S-1 treatment. 5-FU and FT concentrations were measured using high-performance liquid chromatography.
The study cohort comprised 94 patients among whom 38 (40.4%) developed ocular AEs, including 32 (34.0%) corneal AEs, 13 (13.8%) lacrimal AEs, and 7 (7.4%) patients who developed both. The tear FT concentrations in the ocular AE group were significantly higher compared with the group without ocular AEs (3.15 ± 3.09 vs. 1.86 ± 1.56 µg/mL; p = 0.017). There was no difference in tear 5-FU concentration between the 2 groups. The FT concentration in tears in the corneal and lacrimal AE groups was significantly higher than in the group without ocular AEs (p = 0.013 and 0.030, respectively).
FT concentration in tears due to oral S-1 therapy is associated with corneal or lacrimal AEs. Measuring FT concentration in tears or plasma may be useful for predicting the onset of ocular AEs.
S-1是一种口服活性抗癌药物,已知会引起眼部不良事件(AE),包括泪道阻塞和角膜并发症。本研究调查了接受S-1治疗的患者泪液中5-氟尿嘧啶(5-FU)和替加氟(FT)的浓度及其与眼部AE的关系。
多中心前瞻性队列研究。
我们招募了计划接受S-1化疗的患者。在入组时进行初始眼科检查后,在S-1给药过程中进行长达1年的系列检查。在S-1治疗的第一个疗程结束时,使用泪液试纸收集泪液样本。使用高效液相色谱法测量5-FU和FT的浓度。
研究队列包括94名患者,其中38名(40.4%)出现眼部AE,包括32名(34.0%)角膜AE、13名(13.8%)泪腺AE和7名(7.4%)同时出现两种AE的患者。眼部AE组的泪液FT浓度显著高于无眼部AE组(3.15±3.09 vs. 1.86±1.56 µg/mL;p = 0.017)。两组之间的泪液5-FU浓度没有差异。角膜和泪腺AE组的泪液FT浓度显著高于无眼部AE组(分别为p = 0.013和0.030)。
口服S-1治疗导致的泪液中FT浓度与角膜或泪腺AE相关。测量泪液或血浆中的FT浓度可能有助于预测眼部AE的发生。