Cytomegalovirus retinitis after hematopoietic stem cell transplantation with alemtuzumab

被引:18
|
作者
Song, Won Kyung [1 ]
Min, Yoo Hong [2 ]
Kim, Yu Ri [2 ]
Lee, Sung Chul [1 ]
机构
[1] Yonsei Univ, Coll Med, Dept Ophthalmol, Inst Vis Res, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Med, Dept Hematol, Seoul 120752, South Korea
关键词
D O I
10.1016/j.ophtha.2008.04.015
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objective: To report on the clinical characteristics and treatment outcomes of cytomegalovirus (CMV) retinitis cases that occurred after allogeneic hematopoietic stem cell transplantation (HSCT) using an alemtuzumab-based (Campath-1H, Genzyme, Cambridge, MA) conditioning regimen. Design: A retrospective noncomparative interventional case series. Participants: Seven eyes of 4 patients in whom CMV retinitis developed after allogeneic HSCT using alemtuzumab. Methods: A retrospective chart review was performed. CMV retinitis was diagnosed by the presence of characteristic ophthalmoscopic findings and confirmed by polymerase chain reaction-based detection of CMV in vitreal biopsy specimens. The affected eyes received intravitreal injections of 2 mg/0.1 mL of ganciclovir twice weekly during induction therapy until the lesions were inactive, followed by weekly injections as maintenance therapy. Maintenance intravitreal therapy continued until the lesions consisted of an atrophic retina with pigment epithelium mottling and attenuated vessels. Main Outcome Measures: Visual acuity, response of retinitis lesions, and postoperative complications. Results: From 1999 to 2007, 294 patients received allogeneic HSCTs at our institution. Among the HSCTs, 65 were unrelated transplants, and of these, 17 were performed using alemtuzumab-based conditioning regimens. Only 4 patients went on to develop CMV retinitis. These 4 patients had several features in common. All patients received transplants from unrelated donors after an alemtuzumab-conditioning regimen for acute leukemia. One patient died before initiation of treatment. Three patients exhibited a bilateral disease, and 3 patients had neutropenia. Patients underwent a mean of 8.3 intravitreal ganciclovir injections in each eye. All 3 treated patients showed a good response. The treatment was well tolerated without serious adverse events during the mean follow-up period of 8.5 months (range, 4.5-16 months). Conclusions: An increased incidence of CMV retinitis was noted in unrelated patients undergoing HSCT using a nonmyeloablative alemtuzumab-based conditioning regimen. Intravitreal ganciclovir therapy seems to be an acceptable therapeutic option in these patients given the nature of their systemic illness, which prohibits the use of typical systemic anti-CMV drugs.
引用
收藏
页码:1766 / 1770
页数:5
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