|Year : 2018 | Volume
| Issue : 2 | Page : 77-82
Ranibizumab combined with photodynamic therapy for the treatment of advanced-stage exudative age-related macular degeneration: Study protocol for a self-controlled trial and preliminary results
Ping Yu, Qing Wang, Ling-Ling Liu
Department of Ophthalmology, Affiliated Hospital of Qinghai University, Xining, Qinghai Province, China
|Date of Web Publication||6-Jul-2018|
Department of Ophthalmology, Affiliated Hospital of Qinghai University, Xining, Qinghai Province
Source of Support: None, Conflict of Interest: None
Background and objectives: The lack of visual field in the visual center of older adults with age-related macular degeneration (AMD) has a serious impact on daily activities. AMD is subdivided into atrophic and exudative AMD according to pathology. Patients with advanced stage exudative AMD develop aged-related degeneration in the macular area. Ranibizumab combined with photodynamic therapy is mainly used for the treatment of early exudative AMD; however, treatment outcomes in advanced stage exudative AMD are not well documented. Therefore, we attempt to analyze vision recovery, retinal thickness, and leakage of choroidal neovascular lesions in patients with advanced stage exudative AMD after treatment with ranibizumab plus photodynamic therapy. We also further explore the therapeutic efficacy of the combined therapy.
Design: A prospective self-controlled trial.
Methods: The trial will be undertaken in the Department of Ophthalmology, Affiliated Hospital of Qinghai University, China. The study population will comprise 113 patients with advanced exudative AMD who are eligible for inclusion. Photodynamic therapy combined with intravitreal injection of ranibizumab will be given as the interventional therapy.
Outcome measures and preliminary results: The primary outcome measure of the trial is visual improvement in patients 12 months after treatment. Secondary outcome measures include logarithmic visual acuity chart scores, retinal thickness, and leakage of choroidal neovascular lesions assessed monthly at 1-12 months after treatment. Adverse events are also recorded during follow-up. Pre-test results showed that at 12 months after treatment, visual acuity in 43 affected eyes was increased by ≥ 2 lines, and the average retinal thickness decreased by 111.21 μm compared with before treatment. Leakage of choroidal neovascular lesions in most affected eyes stopped or the lesions were contracted.
Discussion: Findings from the trial are expected to provide reliable data on the efficacy of ranibizumab combined with photodynamic therapy in the treatment of advanced exudative AMD. This will provide a basis for the rational use of this combined therapy in the treatment of advanced exudative AMD.
Ethics and dissemination: The study was designed in December 2017, and approved by the Ethics Committee of the Affiliated Hospital of Qinghai University (approval No. QHY001Y) in January 2018. The trial was registered with the Chinese Clinical Trial Registry in March 28, 2018. Participant recruitment was initialized in March 2018, and data analysis will be completed in December 2020. The results of this study will be disseminated by publications in peer-reviewed journals.
Trial registration: This trial was registered in the Chinese Clinical Trial Registry with registration No. ChiCTR1800015410 (protocol version 1.0).
Keywords: advanced exudative aged-related macular degeneration; vascular endothelial growth factor; ranibizumab; photodynamic therapy; visual recovery; retinal thickness; leakage of choroidal neovascular lesions; self-controlled clinical trial
|How to cite this article:|
Yu P, Wang Q, Liu LL. Ranibizumab combined with photodynamic therapy for the treatment of advanced-stage exudative age-related macular degeneration: Study protocol for a self-controlled trial and preliminary results. Clin Trials Degener Dis 2018;3:77-82
|How to cite this URL:|
Yu P, Wang Q, Liu LL. Ranibizumab combined with photodynamic therapy for the treatment of advanced-stage exudative age-related macular degeneration: Study protocol for a self-controlled trial and preliminary results. Clin Trials Degener Dis [serial online] 2018 [cited 2020 Apr 6];3:77-82. Available from: http://www.clinicaltdd.com/text.asp?2018/3/2/77/235151
| Introduction|| |
Age-related macular degeneration (AMD) is a disease that causes vision loss in the center of the visual field, and approximately 6.3 million people globally suffer from this disease. Patients with AMD usually have no obvious symptoms at the early stage of the disease; however, as the disease progresses, some patients experience a gradual loss of vision that may affect one or both eyes. Although complete blindness does not usually occur, the loss of central vision has a serious impact on daily activities.
There are two types of AMD, atrophic and exudative, based on different pathologies. Atrophic AMD causes a slow decline in visual acuity, visual deformation, atrophy of the retinal pigment epithelium in the macular area, disappearance of the central concave reflex, vitreous hernia, and fluorescent or weak light in the macular area with no fluorescent leakage, as assessed by fluorescence angiography. Exudative AMD is characterized by sudden acuity loss, shallow subretinal neovascularization with dark red hemorrhage involving the posterior pole, or even with massive vitreous hemorrhage in severe cases, and fluorescence leakage or shielding shown by fluorescence angiography. In the advanced stage of exudative AMD, degeneration of the macular area is detected. Because of the decreased phagocytic capacity of the retinal pigment epithelium, the non-digested rod outer segment of the visual cell becomes a residual body that resides in the cytoplasm of the basal cell, is excreted outside the cell and eventually deposited on the Bruch membrane, to form a drusen., Advanced exudative AMD occurs predominantly in subjects over 45 years of age and the prevalence rate increases with age. It is one of the most important causes of blindness in the elderly worldwide.
Anti-vascular endothelial growth factor (VEGF) monoclonal antibodies, bevacizumab and ranibizumab, can be used to treat exudative AMD., Laser coagulation therapy can remove drusen, but does not damage choroidal neovascularization., Practice guidelines by the American Academy of Ophthalmology, however, do not recommend this method for macular degeneration. In photodynamic therapy, specific photosensitizers are circulated into the retina and excited by 689 nm laser irradiation, thereby destroying abnormal neovascularization. Surgical methods, such as resection of subretinal neovascular membranes, macular transposition, and retinal transplantation, are also used for the treatment of exudative AMD. In recent years, the combined use of ranibizumab and photodynamic therapy (PDT) has become the main method for the treatment of exudative AMD [Table 1].
|Table 1: Combined use of ranibizumab and photodynamic therapy for exudative age-related macular degeneration in clinical practice|
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Features of the study
Previous studies have mostly concerned the combined use of ranibizumab and PDT in patients with early stage of exudative AMD,,, but not enough emphasis has been placed on the advanced stage of exudative AMD, which can cause severe visual impairment in the elderly.
The authors intend to investigate changes in vision recovery, retinal thickness, and leakage of choroidal neovascular lesions before and after treatment with ranibizumab plus PDT in patients with advanced exudative AMD, and to explore the therapeutic efficacy of the combined therapy.
| Methods/Design|| |
This prospective self-controlled clinical trial will be completed at the Department of Ophthalmology, Affiliated Hospital of Qinghai University, China. The study population will comprise 113 patients with advanced exudative AMD who meet the inclusion and exclusion criteria and will be subjected to PDT combined with intravitreal injection of ranibizumab. The primary outcome measure is the improvement rate of visual acuity at 12 months after treatment. Secondary outcome measures include monthly logarithmic visual acuity chart scores, retinal thickness, leakage of choroidal neovascular lesions, and adverse events at 1-12 months after treatment.
Recruitment will be performed by advertising for patients using posters displayed at the Department of Ophthalmology and at the Admissions office of Affiliated Hospital of Qinghai University, China. Interested patients or their relatives can contact the principal investigator by telephone, email, or WeChat. All subjects will receive the specifications of the clinical trial and will provide written informed consent to participate in the study. Each subject will be explicitly informed of the detailed information regarding the clinical trial, and can withdraw from the study at any time. Withdrawal from the trial will not influence a patient’s follow-up treatment.
All subjects will be recruited from the Department of Ophthalmology, Affiliated Hospital of Qinghai University, China.
Patients will be required to meet all of the following conditions to be included in the trial:
- Presence of choroidal neovascular lesion leakage shown by both fluorescein fundus angiography (FFA) and indocyanine green angiography
- Presence of macular retinal edema in both eyes shown by optical coherence tomography
- Visual acuityof 0.1-0.3
- Retinal thickness of 216.8-496.2 μm
- Aged 55-80 years, both sexes
- Provision of written informed consent by participants or their legal guardians
Patients presenting with any of the following conditions will be excluded from the trial:
- With polypoid choroidal vasculopathy
- With systemic or local surgical contraindications
- Having other eye diseases that involve or may involve vision, such as glaucoma, amblyopia, and diabetic retinopathy
- Receiving intraocular surgery on the affected eye within 2 months
- Pregnant or lactating women
Patients will be withdrawn from the study if they fulfill any of the following criteria:
- During the trial, subject has comorbidities or complications affecting efficacy assessment or onset of diseases affecting the outcome
- Inability to complete the follow-up
The design of the trial was completed in December 2017, and the study protocol was approved by the Ethics Committee of the Affiliated Hospital of Qinghai University (approval No. QHY001Y) in January 2018. The trial was registered with the Chinese Clinical Trial Registry in March 2018. Participant recruitment was started in March 2018, and data analysis will be completed by December 2020.
- PDT apparatus was purchased from Zeiss, Germany, and the PDT photosensitizer, benzoporphyrin derivative monoacid, was purchased from Novartis (Northwest Branch), China. PDT is characterized by the activation of photosensitizers under light irradiation to produce oxygen free radicals and singlet oxygen, triggering choroidal neovascular vasoconstriction, thrombosis, atrophy and necrosis. The PTD parameters will be: light energy 50 J/cm2, illumination time 83 seconds, and light emissivity 600 mW/cm2. The PDT treatment will be performed twice with an interval of 1 week.
- At 48-72 hours after PDT, surgery will be conducted under topical anesthesia by injection of lidocaine hydrochloride (Beijing Zizhu Pharmaceutical Co., Beijing, China). After rinsing the conjunctival sac, 0.5 mg of ranibizumab in a 0.05 mL volume (Novartis AG, Swiss; Import Drug License No. JS20100025; specification 10 mg/mL, 0.2 mL per bottle) will be injected using a No. 30 needle piercing the pars plana into the vitreous cavity of the affected eye. This injection will be performed once a month. Disinfection will be achieved through the use of antibiotic ointment followed by gauze bandaging. Three days before and 3 days after injection of ranibizumab, 0.5% levofloxacin ophthalmic solution (Noden Plant, Santen Pharmaceutical Co., Ltd., Japan; Chinese Drug Approval No. J20100046) will be dropped into the eye, six times per day.
- If signs of retinal edema are found in the affected eye after the first combination therapy, intravitreal injection of ranibizumab will be performed again [Figure 1].
|Figure 1: Combined use of ranibizumab and photodynamic therapy for the treatment of advanced-stage exudative age-related macular degeneration.|
Click here to view
Primary outcome measure
The primary outcome measure is the improvement rate of visual acuity at 12 months after treatment. Improvement of visual acuity will be defined as an increase of ≥ 2 readable lines in the logarithmic visual acuity chart at 12 months after treatment. The improvement rate of visual acuity is expressed as the percentage of improved patients relative to the total number of patients. The logarithmic visual acuity chart, also known as the 5-point logarithmic vision chart. The chart comprises five grades with 14 readable lines.
Secondary outcome measures
- Logarithmic visual acuity scales will be assessed monthly at 1-12 months after treatment.
- Retinal thickness will be assessed monthly at 1-12 months after treatment by optical coherence tomography. Ranibizumab is mainly used to improve macular edema in AMD patients., Therefore, it is necessary to use optical coherence tomography to compare macular morphological changes before and after treatment. It is very important to evaluate the efficacy of ranibizumab as well as to guide the administration frequency and dosage of the drug. Optical coherence tomography equipment was purchased from Beijing Topcon Medical Devices Co., China.
- Leakage of choroidal neovascular lesions will be assessed monthly at 1-12 months after treatment. This assessment will be done by fluorescein angiography and indocyanine green angiography.
- During the trial, all adverse events, including ocular and systemic events, will be recorded. An adverse event refers to any undesired post-treatment sign, symptom, or temporary illness associated with the medications and devices used, regardless of whether there is a causal relationship with the treatment. The following events will be regarded as serious adverse events: (1) within 7 days after treatment, a decrease of ≥ 4 readable lines of the visual acuity chart. For these patients, color fundus photographs and fluorescein fundus angiography examinations will be performed within 7 days and 12 weeks after visual loss. Moreover, these patients cannot continue to participate in the trial unless their vision returns to pre-treatment or better levels. (2)Any other ocular adverse events, including non-perfusion of retinal arterioles or venules, or extensive retinal capillary insufficiency and vitreous hemorrhage, will be considered serious adverse events.
Flow chart and outcome assessment of the trial are shown in [Figure 2] and [Table 2], respectively.
|Figure 2: Flow chart of the trial.|
Note: AMD: Age-related macular degeneration; PDT: photodynamic therapy.
Click here to view
Based on our preliminary results, it is hypothesized that the improvement rate of visual acuity at 12 months post-treatment is 90%. Taking β = 0.2, power = 80%, and α = 0.05 (two-sided), a final effective sample size of n = 94 was calculated using PASS 11.0 software (PASS, Kaysville, UT, USA). Assuming a dropout rate of 20%, a minimum of 113 subjects per group is required.
SPSS 14.0 statistical software (SPSS, Chicago, IL, USA) will be used to analyze the retinal thickness, logarithmic visual acuity, and choroidal neovascular lesion leakage in AMD patients before and after treatment. Measurement data will be described as mean values, and numerical data as a percentage. A paired t-test will be used to compare retinal thickness, logarithmic visual acuity, and choroidal neovascular lesion leakage, and a value of P < 0.05 will be considered significant.
Data collection and management
Prospective data will be collected for all enrolled patients, including physical examinations, laboratory data, perioperative clinical data, and complications, but personal information, such as names, will not be collected. During data collection and management, patients are only coded to protect their privacy.
All collected data will be recorded in case report form, and entered into an electronic data capture system (Beijing Microsignalstar Technology Development Co., Ltd., Beijing, China). All data collected before data analysis will be processed confidentially, and the final data set will be managed by the Department of Ophthalmology of the Affiliated Hospital of Qinghai University in China. Collected data will be locked and saved at least 5 years after the trial is completed.
All researchers involved in clinical practice will have abundant clinical experience for ophthalmology treatments, all the evaluators will be professionally trained and have extensive clinical evaluation experience. The researchers must receive professional training and follow uniform data recording methods and judgment standards. Data analysis will be completed by statisticians.
During the clinical trial, sponsor inspectors will conduct regular periodic visits to the research center to ensure that the trial is performed in strict adherence to all aspects of the research program. In addition, the original data will be checked to ensure that the contents of the case report forms are correct and complete.
Patients included in this trial will receive a transportation allowance and have their follow-up examination fees waived. The researchers will provide insurance coverage for all subjects, cover the costs of treatment and financial compensation for subjects suffering damage or death associated with the trial.
Ethics and dissemination
This study was approved by the Ethics Committee of the Affiliated Hospital of Qinghai University (approval No. QHY001Y), and this trial will follow the relevant laws and regulations of the Declaration of Helsinki. All the patients and their families will voluntarily participate in the trial, and will be fully informed of the study protocol and experimental process. Written informed consent will be provided with the premise of fully understanding the treatment plan. This manuscript was prepared and modified according to the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) guidelines (Additional file 1 [Additional file 1]). The results of this trial will be disseminated through presentations at scientific meetings or by publications in peer-reviewed journals. Anonymized trial data will be published at www.figshare.com.
| Preliminary Results|| |
At 12 months after treatment, the visual acuity of 43 affected eyes was improved by ≥ 2 readable lines as compared with the baseline. Optical coherence tomography showed that the mean retinal thickness decreased by 111.21 μm after treatment (P < 0.05, vs. before treatment). Fundus fluorescein angiography and indocyanine green angiography showed leakage of choroidal neovascular lesions after treatment. Leakage was completely stopped in 10 eyes (24%), reduced in 26 eyes (60%), and did not change or was increased in four eyes (9%). New lesions occurred in three eyes (7%).
| Discussion|| |
Past contributions and existing problems in the field
Laser photocoagulation and infrared laser transpupillary thermotherapy are also main treatments for AMD, and they are both directed against choroidal neovascularization.,, There have also been clinical trials for AMD involving stem cell therapy and gene-targeted therapy, but the results are not conclusive. Both ranibizumab and photodynamic therapy have a very good therapeutic effect on AMD. Ranibizumab is mainly responsible for improvement of macular edema in AMD,, while PDT is effective at destroying choroidal neovascularization.9 Improved treatment of advanced-stage exudative AMD can be achieved using a combination of ranibizumab and PDT.
Novelty of this study
The trial will focus on advanced exudative AMD, and the primary outcome measure is to observe the improvement in vision, which is the main concern of patients. Moreover, the study will recruit at least 113 patients who meet the inclusion criteria.
Limitation of this study
This study is a self-controlled trial without randomization, which will affect the accuracy of the results. Further investigation with improved experimental design will be required.
Significance of this study
Findings from this trial will provide experimental evidence for the combined use of ranibizumab and PDT in the treatment of advanced-stage exudative AMD.
Additional file 1: SPIRIT checklist.
Design of the trial: PY. Patient recruitment, screening and data collection: QW. Trial implementation and follow-up: LLL, PY. Drafting the manuscript: PY. All authors approved the final version of this manuscript for publication.
Conflicts of interest
Although ranibizumab and photodynamic therapy device will be used in the study, the authors declare that the trial will be conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Institutional review board statement
This study was approved by the Ethics Committee of the Affiliated Hospital of Qinghai University (approval No. QHY001Y). The study will be performed in accordance with the relevant laws and regulations of the Declaration of Helsinki, and the hospital’s relevant ethical principles.
Declaration of patient consent
The authors certify that they will obtain patient consent forms. In the form, patients will give their consent for their images and other clinical information to be reported in the journal. The patients will understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
This study follows the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) guidance for protocol reporting.
The statistical methods of this study were reviewed by the biostatistician of the Affiliated Hospital of Qinghai University, China.
Copyright transfer agreement
The Copyright License Agreement has been signed by all authors before publication.
Data sharing statement
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, and appendices) will be in particular shared. Study protocol and informed consent form will be promulgated within 6 months after the completion of the trial. Anonymized trial data will be available indefinitely at www.figshare.com.
Checked twice by iThenticate.
Externally peer reviewed.
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[Figure 1], [Figure 2]
[Table 1], [Table 2]