Ritch P S, Hansen R M, Heuer D K
Cancer. 1983 Feb 1;51(3):430-2. doi: 10.1002/1097-0142(19830201)51:3<430::aid-cncr2820510313>3.0.co;2-5.
A patient with refractory acute myelogenous leukemia was treated with high-dose cytosine arabinoside (3.0 g/m2 every 12 hours). Following ten doses over five days the patient developed excessive tearing, photophobia, burning ocular pain, and blurred vision. Ophthalmologic examination revealed conjunctival injection, central punctate corneal opacities with subepithelial granular deposits, and decreased visual acuity. Symptoms gradually resolved over the following four days; however, impaired visual acuity persisted for two weeks and corneal opacification did not disappear until four weeks following therapy. Prior and subsequent administration of cytosine arabinoside according to the same dose schedule for only four doses over two days and eight doses over four days were well tolerated and did not produce ocular toxicity. It is suggested that ocular toxicity results from inhibition of corneal epithelial DNA synthesis and is related to both drug dosage and duration of drug exposure. Strategies should be explored to eliminate this treatment-limiting adverse effect of potentially effective therapy.
一名难治性急性髓性白血病患者接受了大剂量阿糖胞苷治疗(每12小时3.0 g/m²)。在五天内给予十剂后,患者出现流泪过多、畏光、眼部灼痛和视力模糊。眼科检查发现结膜充血、中央点状角膜混浊伴上皮下颗粒状沉积物以及视力下降。症状在接下来的四天内逐渐缓解;然而,视力受损持续了两周,角膜混浊直到治疗后四周才消失。之前和之后按照相同剂量方案在两天内仅给予四剂阿糖胞苷以及在四天内给予八剂阿糖胞苷,患者耐受性良好,未产生眼部毒性。提示眼部毒性是由于角膜上皮DNA合成受抑制所致,且与药物剂量和药物暴露时间有关。应探索策略以消除这种潜在有效治疗的限制治疗的不良反应。