Effect of ciliary neurotrophic factor on retinal neurodegeneration in patients with macular telangiectasia type 2: a randomized clinical trial
Ophthalmology, 2019•Elsevier
Purpose To test the effects of an encapsulated cell-based delivery of a neuroprotective
agent, ciliary neurotrophic factor (CNTF), on progression of macular telangiectasia type 2, a
neurodegenerative disease with no proven effective therapy. Design Randomized sham-
controlled clinical trial. Participants Ninety-nine study eyes of 67 eligible participants were
enrolled. Methods Single-masked randomized clinical trial of 24 months' duration conducted
from May 2014 through April 2017 in 11 clinical centers of retinal specialists in the United …
agent, ciliary neurotrophic factor (CNTF), on progression of macular telangiectasia type 2, a
neurodegenerative disease with no proven effective therapy. Design Randomized sham-
controlled clinical trial. Participants Ninety-nine study eyes of 67 eligible participants were
enrolled. Methods Single-masked randomized clinical trial of 24 months' duration conducted
from May 2014 through April 2017 in 11 clinical centers of retinal specialists in the United …
Purpose
To test the effects of an encapsulated cell-based delivery of a neuroprotective agent, ciliary neurotrophic factor (CNTF), on progression of macular telangiectasia type 2, a neurodegenerative disease with no proven effective therapy.
Design
Randomized sham-controlled clinical trial.
Participants
Ninety-nine study eyes of 67 eligible participants were enrolled.
Methods
Single-masked randomized clinical trial of 24 months’ duration conducted from May 2014 through April 2017 in 11 clinical centers of retinal specialists in the United States and Australia. Participants were randomized 1:1 to surgical implantation of intravitreal sustained delivery of human CNTF versus a sham procedure.
Main Outcome Measures
The primary outcome was the difference in the area of neurodegeneration as measured in the area of the ellipsoid zone disruption (or photoreceptor loss) measured on spectral-domain (SD) OCT images at 24 months from baseline between the treated and untreated groups. Secondary outcomes included comparison of visual function changes between treatment groups.
Results
Among the 67 participants who were randomized (mean age, 62±8.9 years; 41 women [61%]; 58 white persons [86%]), 65 (97%) completed the study. Two participants (3 study eyes) died and 3 participants (4 eyes) were found ineligible. The eyes receiving sham treatment had 31% greater progression of neurodegeneration than the CNTF-treated eyes. The difference in mean area of photoreceptor loss was 0.05±0.03 mm2 (P = 0.04) at 24 months. Retinal sensitivity changes, measured using microperimetry, were correlated highly with the changes in the area of photoreceptor loss (r = 0.86; P < 0.0001). The mean retinal sensitivity loss of the sham group was 45% greater than that of the treated group (decrease, 15.81±8.93 dB; P = 0.07). Reading speed deteriorated in the sham group (–13.9 words per minute) with no loss in the treated group (P = 0.02). Serious adverse ocular effects were found in 2 of 51 persons (4%) in the sham group and 2 of 48 persons (4%) in the treated group.
Conclusions
In participants with macular telangiectasia type 2, a surgical implant that released CNTF into the vitreous cavity, compared with a sham procedure, slowed the progression of retinal degeneration. Further research is needed to assess longer-term clinical outcomes and safety.
Elsevier