J Korean Ophthalmol Soc.  2009 Oct;50(10):1475-1482. 10.3341/jkos.2009.50.10.1475.

The Effects of a Subtenoncapsular Injection of Bevacizumab for Ocular Surface Disease With Corneal Neovascularization

Affiliations
  • 1Department of Ophthalmology, Chung-Ang University College of Medicine, Seoul, Korea. jck50ey@kornet.net

Abstract

PURPOSE
To investigate the effect of an injection of bevacizumab into the sub-Tenon's capsule on ocular surface neovascularization disease including pterygium and corneal neovascularization.
METHODS
Twenty-five eyes of 21 patients with pterygium and 19 eyes of 15 patients with corneal neovascularization were given an injection of 5 mg bevacizumab into the sub-Tenon's capsule. The clinical effects and complications were evaluated by analyzing the changes in anterior segment photo, visual acuity, and intraocular pressure at week one, week two, week four, and every month thereafter.
RESULTS
After injections of bevacizumab, partial remission of corneal neovascularized lesion was observed in five eyes (20%) of the pterygium group, and there were no significant changes in the visual acuity and no complications. In the corneal neovascularization group, corneal neovascularized lesions of 18 eyes (95%: 2 eyes, complete remission 16 eyes, partial remission) improved after injections of the bevacizumab and the scores of extent and severity of corneal neovascularized lesion improved significantly, unlike the pterygium group. The visual acuity of two eyes (11%) improved more than two lines of Yong-Han Jin's distance visual acuity test and there were no systemic side effects. Localized side effects included four eyes (21%) with punctate epithelial erosions and two eyes (11%) with temporary, elevated intraocular pressure in the corneal neovascularization group. The side effects improved without any additional treatment.
CONCLUSIONS
An injection of bevacizumab into the sub-Tenon's capsule is more effective in fresh lesions of corneal neovascularization disease than in old and stable lesions of pterygium. Therefore, it could be used as a prominent treatment of various corneal neovascularization diseases.

Keyword

Bevacizumab; Clinical effects; Corneal neovascularization; Subtenon injection

MeSH Terms

Antibodies, Monoclonal, Humanized
Corneal Neovascularization
Eye
Humans
Intraocular Pressure
Pterygium
Visual Acuity
Bevacizumab
Antibodies, Monoclonal, Humanized

Figure

  • Figure 1. Comparison of the changes in the average scores of corneal neovascularizaion before and after sub-Tenon’s capsule injections of bevacizumab. (A) There was a significant decrease of the score of corneal neovascularization extent in the corneal neovascularization group. (B) There was a significant decrease of the score of corneal neovascularization severity in the corneal neovascularization group.*

  • Figure 2. Thirty-eight-year-old man with a history of pterygium over 10 years. Color photographs of his right eye before bevacizumab injection (A), 2 weeks after the first injection (B), 1 month after the second injection (C), 2 months after the third injection (D). Conjunctival injection was subsided slightly but magnified photographs of pterygium head showed unchanged lesion of corneal neovascularizaion (extent 1, severity 1.5) at before bevacizumab injection (E), 1 month after the second injection (F), 2 months after the third injection (G).

  • Figure 3. Fifty-one-year-old woman with a month history of herpes zoster keratoconjunctivitis. Before bevacizumab injection, (A) Left eye showed some of small, round stromal opacities(arrow heads) (extent 1). (B) Slight limbal elevation with injection of conjunctiva (arrow) was noted. (C) Magnified photograph of superior cornea showed severity 1. Two weeks after the first injection, (D) stromal opacities, (E) limbal elevated lesion, and conjunctival injection disappeared. (F) Corneal neovascularized lesion disappeared completely (extent 0 and severity 0) until 6 months.

  • Figure 4. Sixty-three-year-old man with one-month history of herpes stromal keratitis. Before bevacizumab injection (A) Left eye showed corneal neovascularization at the inferior portion (extent 2). (B, C) Magnified photograph of inferior cornea showed severity 2. (D, E, F) Two weeks after the first injection, inferior corneal neovascularized lesion disappeared completely (extent 0 and severity 0) until 6 months.

  • Figure 5. Twenty-five-year-old woman with one-year history of ocular surface disease caused by Stevens-Johnson syndrome. (A) Right eye showed epithelial and stromal opacification at the central cornea with total peripheral corneal neovascularization (extent 12) before bevacizumab injection. (B) One month after the fifth injection, it showed marked reduction of corneal opacification, with significant disappearance of blood vessels (extent 6.5). (C) Magnified photograph of superior cornea before bevacizumab injection showed severity 4 and (D) 1 month after the fifth injection showed severity 3. Her best corrected visual acuity (BCVA) was 20/500 before bevacizumab injection, and eventually it improved to 20/100.

  • Figure 6. Forty-five-year-old woman with 3-month history of ocular surface disease caused by rejected corneal graft. (A) Photograph of right eye showed central stromal opacity with nearly total peripheral corneal neovascularization (extent 11) before bevacizumab injection.(B) One month after the fifth injection, it showed marked reduction of central corneal opacity with significant disappearance of blood vessels (extent 6). (C) Magnified photograph of nasal cornea before bevacizumab injection showed severity 3.5 and (D) 1 month after the fifth injection showed severity 3. Her best corrected visual acuity (BCVA) was 20/100 before bevacizumab injection, and eventually it improved to 20/50.


Cited by  2 articles

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Yong Il Kim, Geun Young Lee, Eun Joo Kim, Yeoun Hee Kim, Kyoo Won Lee, Young Jeung Park
J Korean Ophthalmol Soc. 2015;56(6):847-855.    doi: 10.3341/jkos.2015.56.6.847.

Prognostic Factors Affecting Visual Recovery in Terson Syndrome with Aneurysmal Subarachnoid Hemorrhage
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J Neurocrit Care. 2017;10(2):99-106.    doi: 10.18700/jnc.170026.


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