Shome Debraj, Trent Jonathan, Espandar Ladan, Hatef Elham, Araujo Dejka M, Song C Diane, Kim Stella K, Esmaeli Bita
Section of Ophthalmology, Department of Head and Neck Surgery, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Ophthalmology. 2008 Mar;115(3):483-7. doi: 10.1016/j.ophtha.2007.11.016. Epub 2008 Jan 16.
Perifosine is a novel alkylphospholipid with antiproliferative properties attributed to protein kinase B inhibition. The authors describe a form of ulcerative keratitis in 5 patients with advanced gastrointestinal stromal tumor (GIST) enrolled in a phase I/II trial of perifosine in combination with imatinib.
Interventional case series.
Five patients (1 man, 4 women) with imatinib-resistant metastatic GIST who received a combination of imatinib and perifosine orally.
The medical records were reviewed retrospectively.
Ocular toxicity and ulcerative keratitis associated with perifosine.
The ocular symptoms included redness, irritation, tearing, photophobia, and a gradual decrease in vision. Slit-lamp biomicroscopy in each case revealed a peripheral, paralimbal, ring-shaped, superficial corneal stromal infiltration and ulcerative keratitis, reminiscent of the autoimmune keratitis in conditions such as rheumatoid arthritis. The ulcerative keratitis was unilateral in 3 and bilateral in 2 patients; it was National Cancer Institute grade II (symptoms interfering with function but not interfering with activities of daily living) in all patients. All 5 patients had imatinib-resistant metastatic GIST and had continued on the highest dose of imatinib tolerated and initiated therapy with perifosine 100 mg daily or 900 mg weekly. A combination of topical steroids, topical antibiotics, and lubricating drops were used to manage ulcerative keratitis. In the first 3 patients, ulcerative keratitis initially was treated with topical antibiotics without improvement, but subsequently they improved significantly after topical steroids were added.
A vision-threatening form of ulcerative keratitis may occur in patients taking perifosine. It is possible that imatinib in combination with perifosine contributes to this corneal toxicity; however, the authors are unaware of this ocular toxicity having been reported for imatinib when used without perifosine. The visual loss associated with perifosine may be reversible if detected and treated early and with judicious early use of topical steroids, topical antibiotic coverage, and lubrication.
Perifosine是一种新型烷基磷脂,具有因抑制蛋白激酶B而产生的抗增殖特性。作者描述了5例晚期胃肠道间质瘤(GIST)患者出现的一种溃疡性角膜炎,这些患者参加了perifosine联合伊马替尼的I/II期试验。
干预性病例系列。
5例对伊马替尼耐药的转移性GIST患者(1例男性,4例女性),口服伊马替尼和perifosine联合用药。
对病历进行回顾性审查。
与perifosine相关的眼部毒性和溃疡性角膜炎。
眼部症状包括眼红、刺激感、流泪、畏光以及视力逐渐下降。裂隙灯生物显微镜检查显示,每例患者均有周边、角膜缘旁、环形、浅表角膜基质浸润和溃疡性角膜炎,类似于类风湿关节炎等疾病中的自身免疫性角膜炎。溃疡性角膜炎3例为单侧,2例为双侧;所有患者均为美国国立癌症研究所II级(症状影响功能但不影响日常生活活动)。所有5例患者均为对伊马替尼耐药的转移性GIST,继续使用耐受的最高剂量伊马替尼,并开始每日服用100 mg或每周服用900 mg的perifosine治疗。使用局部类固醇、局部抗生素和润滑滴眼液联合治疗溃疡性角膜炎。在前3例患者中,溃疡性角膜炎最初用局部抗生素治疗无改善,但随后添加局部类固醇后显著改善。
服用perifosine的患者可能会出现威胁视力的溃疡性角膜炎。伊马替尼联合perifosine可能导致这种角膜毒性;然而,作者未发现单独使用伊马替尼时有这种眼部毒性的报道。如果早期发现并进行治疗,且明智地早期使用局部类固醇、局部抗生素覆盖和润滑,与perifosine相关的视力丧失可能是可逆的。