Treat-and-extend Using Aflibercept for Type 3 Neovascularization

August 18, 2022 updated by: Kim's Eye Hospital
Type 3 neovascularization is a subtype of neovascular age-related macular degeneration (AMD) that is characterized by intraretinal neovascularization. Treat-and-extend (TAE) regimen is a widely-used, effective anti-vascular endothelial growth factor treatment regimen for neovascular AMD, regardless of subtypes of AMD. The purpose of the present study is to investigate the 18-month treatment outcome of TAE in type 3 neovascularization.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Type 3 neovascularization also called retinal angiomatous proliferation is a subtype of neovascular age-related macular degeneration (AMD) that is characterized by intraretinal neovascularization.

The incidence of type 3 neovascularization is relatively lower than other subtypes of neovascular AMD, constituting 10 to 20% of entire neovascular AMD. However, it is a very important disorder because it often leads bilateral visual deterioration. The high risk of bilateral involvement is characteristic of type 3 neovascularization. In some cases, the visual prognosis of the initially uninvolved eye with better vision, is poorer than the initially involved eye. In addition, profound visual loss may occur during the treatment course, especially in undertreated cases. Thus, preserving vision is particularly important in type 3 neovascularization, which subsequently highlights the importance of investigating more effective treatment strategies. Previous study suggested the need for proactive treatment in type 3 neovascularization to reduce the risk of abrupt visual loss.

Treat-and-extend (TAE) regimen is a widely-used, effective anti-vascular endothelial growth factor treatment regimen for neovascular age-related macular degeneration (AMD), regardless of subtypes of AMD. However, since type 3 neovascularization is at high risk of GA, there has been some debate regarding the benefit of TAE, when compared to the as-needed regimen, for treating type 3 neovascularization. Despite some controversy, reports indicated that increased injection frequency is associated with development or progression of GA. Thus, it is important to balance efficacy and efficiency when treating type 3 neovascularization.

Type 3 neovascularization is a disorder in which the treatment outcome of TAE regimen was first reported. Nevertheless, only limited evidence has been available regarding the efficacy of TAE using aflibercept in this disorder. In addition, all the previous studies were retrospective, based on relatively small study population. Moreover, results of extending the injection interval to 4 months have not yet been reported. Recently, ALTAIR study provides a scientific evidence that injection interval can be extended to 4 months when using TAE regimen. In type 3 neovascularization, extending the injection interval is not only decreases treatment burden of the patient, but also may improve long-term visual outcomes because it may decrease the injection frequency. If this regimen is found to be effective in type 3 neovascularization, it may contribute to more widespread use of TAE regimen using aflibercept for type 3 neovascularization.

In addition, there are two questions which have not been addressed in previous TAE studies for type 3 neovascularization. The first question is "Is the treatment using TAE regimen can impede the fundamental progression of the disorder?". Since visual loss in type 3 neovascularization usually develops in stage 3 disorder (eyes exhibits serous pigment epithelial detachment on OCT, it will be a very meaningful result if TAE can impede stage progression. The second question is "Is there any clues to predict the recurrence of fluid?" Since avoiding under-treatment is very important in type 3 neovascularization, it is very important to identify any factor predictive of recurrence. To address this question, it is necessary to evaluate the serial changes in vascular morphology of type 3 neovascularization lesion. Previously, however, this kind of approach cannot be performed because it requires frequent, serial indocyanine-green angiography examination. Fortunately, recent advent of OCT-angiography provides simple and safe evaluation of vascular morphology. By using OCT-angiography, any vascular morphologic changes preceding the recurrence of fluid during the TAE treatment can be evaluated.

The purpose of the present study is to investigate the 18-month treatment outcome of TAE in type 3 neovascularization. The maximum injection interval was set as 4 months. Since the ALTAIR study nicely show how to extend the interval to 4 months, the study protocol of ALTAIR study was partly adopted in the present study.

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Willing, committed, and able to return for ALL clinic visits and complete all study related procedures.
  • Able to read, (or, if unable to read due to visual impairment, be read to verbatim by the person administering the informed consent or a family member) understand and willing to sign the informed consent form.
  • Signed informed consent
  • Patients aged 50 years or older
  • Patients diagnosed with treatment naïve type 3 neovascularization
  • ETDRS BCVA letter score ≥25 letters (approximately 20/320 or better) in the study eye

Exclusion Criteria:

  • Any prior ocular (in the study eye) or systemic treatment or surgery for neovascular AMD except dietary supplements or vitamins.
  • Prior treatment with anti-VEGF agents
  • Known serious allergy to the fluorescein sodium for injection in angiography.
  • Significant media opacities, including cataract, in the study eye that might interfere with visual acuity, assessment of safety, or fundus photography.
  • Any concurrent ocular condition in the study eye which, in the opinion of the investigator, could either increase the risk to the patient beyond what is to be expected from standard procedures of intraocular injection, or which otherwise may interfere with the injection procedure or with evaluation of efficacy or safety.
  • Any ocular or periocular infection within the last 2 weeks prior to Screening in either eye.
  • Any history of uveitis in either eye.
  • Presence of definite chorioretional anastomosis
  • Subretinal hemorrhage that is either 50% or more of the total lesion area, or if the blood is under the fovea and is 1 or more disc areas in size in the study eye. (If the blood is under the fovea, then the fovea must be surrounded 270 degrees by visible CNV.)
  • Scar or fibrosis, making up > 50% of total lesion in the study eye.
  • Scar, fibrosis, or atrophy involving the center of the fovea in the study eye.
  • Presence of retinal pigment epithelial tears or rips involving the macula in the study eye.
  • History or clinical evidence of diabetic retinopathy, diabetic macular edema or any other vascular disease affecting the retina, other than AMD, in either eye.
  • Any concurrent intraocular condition in the study eye (e.g. cataract) that, in the opinion of the investigator, could require either medical or surgical intervention during the 76 week study period.
  • Prior vitrectomy in the study eye
  • Any history of macular hole of stage 2 and above in the study eye.
  • Any intraocular or periocular surgery within 3 months of Day 1 on the study eye, except lid surgery, which may not have taken place within 1 month of day 1, as long as its unlikely to interfere with the injection.
  • Prior trabeculectomy or other filtration surgery in the study eye.
  • Uncontrolled glaucoma (defined as intraocular pressure ≥ 25 mmHg despite treatment with antiglaucoma medication) in the study eye.
  • Active intraocular inflammation in either eye.
  • Active ocular or periocular infection in either eye.
  • Aphakia or pseudophakia with absence of posterior capsule (unless it occurred as a result of a yttrium aluminum garnet [YAG] posterior capsulotomy) in the study eye.
  • History of corneal transplant or corneal dystrophy in the study eye.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Treatment arm

Patients treated with aflibercept (2.0ml/0.05cc) using treat-and-extend regimen.

Three monthly loading injections followed by proactive treatment using treat-and-extend regimen. Extension of injection interval by 2 weeks. The maximum injection interval was set as 16 weeks.
Drug: Aflibercept Injection

Intravitreal injection of aflibercept using treat-and-extend regimen

:Three monthly loading injections followed by proactive treatment using TAE regimen. Extension of injection interval by 2 weeks. The maximum injection interval was set as 16 weeks.

Other Names:
  • Intravitreal injection of aflibercept (Eylea, Bayer co.)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in best-corrected visual acuity (BCVA)
Time Frame: From baseline to week 76
Change in early treatment of diabetic retinopathy score (ETDRS) BCVA from baseline to week 76
From baseline to week 76

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of patients who gain ≥15 ETDRS letters
Time Frame: from baseline to week 52 and 76
Measuring proportion of patients who gain ≥15 ETDRS letters
from baseline to week 52 and 76
Proportion of patients who loss ≥15 ETDRS letters
Time Frame: from baseline to week 52 and 76
Measuring proportion of patients who loss ≥15 ETDRS letters
from baseline to week 52 and 76
Change in BCVA to wee 52 (interim analysis)
Time Frame: from baseline to week 52
Change in ETDRS BCVA
from baseline to week 52
Change in central retinal thickness
Time Frame: from baseline to week 52 and 76
Change in central retinal thickness measured using optical coherence tomography
from baseline to week 52 and 76
Proportion of patients without fluid or hemorrhage
Time Frame: at week 52 and 76
The presence of fluid or hemorrhage is estimated using fundus photographs and optical coherence tomography images
at week 52 and 76
Incidence of geographic atrophy
Time Frame: at baseline, and at weeks 52 and 76
Geographic atrophy is idenfitied using fundus photographs and optical coherence tomography images
at baseline, and at weeks 52 and 76
Changes in size of geographic atrophy
Time Frame: from baseline to week 52 and 76
Changes in size of geographic atrophy is estimated using fundus photographs and optical coherence tomography images
from baseline to week 52 and 76
Number of injections
Time Frame: up to week 52 and 76
Number of injections were counted
up to week 52 and 76
The maximum treatment interval and the maximum next planned interval
Time Frame: during week 52 and 76
The maximum treatment interval and the maximum next planned interval of assessment at the last injection
during week 52 and 76
Proportion of patients showing fovea-involving geographic atrophy or fibrotic scar
Time Frame: at week 52 and 76
Fovea-involving geographic atrophy or fibrotic scar are idenfitied using fundus photographs and optical coherence tomography images
at week 52 and 76
Proportion of patients showing progression of stages of type 3 neovascularization
Time Frame: Through study completion, 72 weeks
Progress of disese stages are estimated using optical coherence tomography angiography images
Through study completion, 72 weeks
Proportion of patients showing tear of retinal pigment epithelium or subretinal hemorrhage
Time Frame: Through study completion, 72 weeks
Tear of retinal pigment epithelium or subretinal hemorrhage are idenfitied using fundus photographs and optical coherence tomography images
Through study completion, 72 weeks
Morphologic features of type 3 lesion
Time Frame: Through study completion, 72 weeks
Morphologic features of type 3 lesions are estimated using optical coherence tomography angiography images
Through study completion, 72 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Kim's Eye Hospital

Collaborators

Bayer

Investigators

  • Principal Investigator: Jae Hui Kim, M.D., Kim's Eye Hospital, Seoul, South Korea

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2021

Primary Completion (Anticipated)

December 20, 2023

Study Completion (Anticipated)

August 20, 2024

Study Registration Dates

First Submitted

November 23, 2020

First Submitted That Met QC Criteria

November 30, 2020

First Posted (Actual)

December 7, 2020

Study Record Updates

Last Update Posted (Actual)

August 22, 2022

Last Update Submitted That Met QC Criteria

August 18, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2020-06-003

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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