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  4. Photodynamic therapy of subfoveal choroidal neovascularization: clinical and angiographic examples
 
research article

Photodynamic therapy of subfoveal choroidal neovascularization: clinical and angiographic examples

Schmidt-Erfurth, U.
•
Miller, J.
•
Sickenberg, M.
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1998
Graefe's Archive for Clinical and Experimental Ophthalmology

BACKGROUND: Conventional photocoagulation of subfoveal choroidal neovascularization (CNV) is often accompanied by visual loss due to thermal damage to adjacent retinal structures. Photodynamic therapy (PDT) allows vascular occlusion by selective photochemical destruction of vascular endothelial cells only. In a pilot study we evaluated the use of PDT in CNV. METHODS: In a clinical phase I/II trial, patients with subfoveal CNV were treated with PDT. Benzoporphyrin derivative monoacid ring A (BPD) was used as sensitizer at a drug dose of 6 mg/m2 or 12 mg/m2. Irradiation was performed via a diode laser emitting at 690 nm coupled into a slit lamp. Safe and maximum tolerated light doses were defined by dose escalation from 25 to 150 J/cm2. Photodynamic effects were documented ophthalmoscopically and angiographically. RESULTS: Sixty-one patients received a single course of BPD-PDT. Preliminary results suggest no damage to retinal structures within the treated area clinically. Retinal perfusion was not altered, while CNV demonstrated immediate absence of fluorescein leakage in the majority of lesions subsequent to PDT. At optimized parameters (6 mg/m2 and 50 J/cm2) complete cessation of leakage from classic CNV occurred in 100% of cases at 1 week and in 50% at week 4. In 70-80% of classic CNV, leakage reappeared at week 12, but markedly less than before treatment. CONCLUSION: PDT allows temporary absence of leakage from CNV with preservation of visual acuity. The long-term prognosis of CNV secondary to age-related macular degeneration treated with repeated courses of PDT is being evaluated in a phase III trial.

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Type
research article
DOI
10.1007/s004170050092
Author(s)
Schmidt-Erfurth, U.
Miller, J.
Sickenberg, M.
Bunse, A.
Laqua, H.
Gragoudas, E.
Zografos, L.
Birngruber, R.
van den Bergh, H.  
Strong, A.
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Date Issued

1998

Published in
Graefe's Archive for Clinical and Experimental Ophthalmology
Volume

236

Issue

5

Start page

365

End page

374

Subjects

129497-78-5 (verteporfin)

•

Photomedicine group

Note

MEDLINE

Copyright 2003 U.S. National Library of Medicine

University Eye Hospital Lubeck, Germany

8205248

(CLINICAL TRIAL); (CLINICAL TRIAL, PHASE I); (CLINICAL TRIAL, PHASE II); Journal; Article; (JOURNAL ARTICLE); (MULTICENTER STUDY)

English

1998265031

Female; Human; Male; Support, Non-U.S. Gov't

Adult; Aged; Aged, 80 and over; Capillary Permeability; *Choroid: BS, blood supply; Fluorescein Angiography; *Fovea Centralis; Fundus Oculi; Lasers; Middle Age; *Neovascularization, Pathologic: DT, drug therapy; *Photochemotherapy; Photosensitizing Agents: AE, adverse effects; *Photosensitizing Agents: TU, therapeutic use; Pilot Projects; Porphyrins: AE, adverse effects; *Porphyrins: TU, therapeutic use; Prospective Studies; Recurrence; Safety

0 (Photosensitizing Agents); 0 (Porphyrins)

Editorial or Peer reviewed

REVIEWED

Written at

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Available on Infoscience
February 1, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/63757
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