Allogeneic fresh frozen plasma eye drops for the treatment of ocular Graft-versus-Host disease: prospective open-label study.

Yoav Nahum, Noa Golomb, Ronit Goldman-Levi, Michael Mimouni, Eitan Livny, Mali Rubinstein, Irit Bahar, Liat Shargian, Pia Raanani, Vered Yahalom, Moshe Yeshurun
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Abstract

Purpose: To evaluate the safety and efficacy of allogeneic fresh frozen plasma drops for the treatment of chronic ocular graft-versus-host disease (oGVHD).

Methods: In this prospective open-label institutional study, adult oGVHD patients were administered allogeneic fresh frozen 100% plasma (FFP) eye drops QID or more for 3 months, in addition to the patients' usual treatment. The drops were prepared using a closed sterile tubing system (COL© System, Biomed Device Srl., Italy). The main outcome measures included the Ocular Surface Disease Index (OSDI), corneal fluorescein staining National Eye Institute (NEI) scale, basal tear secretion test, and functional assessment of cancer therapy-bone marrow transplant (FACT-BMT) questionnaire.

Results: This study included 25 patients (49 eyes). OSDI scores decreased from 53 ± 26 at baseline to 32 ± 22 after 1 month and 30 ± 23 after 3 months (P < 0.0001), and fluorescein staining NEI grade decreased from 7.04 ± 3.51 at baseline to 5.5 ± 3.1 after 1 month (P < 0.0001) and 5.3 + 3.1 after 3 months (baseline to 3 months, P < 0.0001; one month to 3 months, P = 0.64). Mean basal tear secretion was 4.65 ± 3.4 mm at baseline and 6.5 ± 4.7 mm after 3 months (P = 0.002). The FACT-BMT scores did not change significantly from baseline to 3 months (106.3 ± 22 vs. 112 ± 20, P = 0.08). A subset of eight patients who were using scleral or bandage contact lenses concurrently showed significant improvement, and four of them were managed without lenses during the study period. No significant adverse events were noted.

Conclusion: Allogeneic FFP eye drops are safe and effective in the treatment of chronic oGVHD.

Trial registration: The trial is listed from 10/2020 in the Israeli Ministry of Health Clinical Trials Registry (MOH_2021-09-30_010276).

同种异体新鲜冷冻血浆滴眼液治疗眼部移植物抗宿主病:前瞻性开放标签研究
目的:评价同种异体新鲜冷冻血浆滴剂治疗慢性眼部移植物抗宿主病(oGVHD)的安全性和有效性。方法:在这项前瞻性开放标签机构研究中,成人oGVHD患者在患者常规治疗的基础上,给予异基因新鲜冷冻100%血浆(FFP)滴眼液QID或更多,持续3个月。滴剂使用封闭无菌管系统(COL©system, Biomed Device Srl)制备。、意大利)。主要观察指标包括眼表疾病指数(OSDI)、角膜荧光素染色美国国家眼科研究所(NEI)量表、基础泪液分泌试验和癌症治疗-骨髓移植功能评估(FACT-BMT)问卷。结果:本研究纳入25例患者(49眼)。OSDI评分由基线时的53±26分降至1个月后的32±22分,3个月后的30±23分(P)。结论:同种异体FFP滴眼液治疗慢性oGVHD安全有效。试验注册:该试验从2020年10月开始在以色列卫生部临床试验登记处(MOH_2021-09-30_010276)登记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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