nach oben

Erschienen in:

Open Access 17.05.2019 | Review

How Successful is Switching from Bevacizumab or Ranibizumab to Aflibercept in Age-Related Macular Degeneration? A Systematic Overview

verfasst von: Theodoros Empeslidis, Matthew Storey, Theodoros Giannopoulos, Vassileios Konidaris, Paris G. Tranos, Evangelia S. Panagiotou, Irini C. Voudouragkaki, Anastasios G. Konstas

Erschienen in: Advances in Therapy | Ausgabe 7/2019

Abstract

Emerging anti-vascular endothelial growth factor (anti-VEGF) therapies for neovascular age-related macular degeneration (nAMD) have revolutionised medical retina practice and the management and eventual outcome of nAMD. Recent research has focused on evaluating and comparing the efficacy of the two most widely employed anti-VEGF agents, bevacizumab and ranibizumab; however, a subgroup of patients with nAMD demonstrates a suboptimal response to standard therapy. We have therefore conducted a review of pertinent studies published until August 2018 which have documented the clinical efficacy when switching to a different anti-VEGF. Evidence on baseline disease characteristics, injection frequency and disease outcome has been obtained for patients treated with ranibizumab 0.5 mg and/or bevacizumab 1.25 mg and were switched to aflibercept 2 mg. Our review identified 45 studies investigating switching to aflibercept. Our review showed a clear anatomical benefit after the switch in terms of central retinal thickness and pigment epithelium detachment characteristics, whereas the functional outcomes were variable. Remarkable heterogeneity was documented among the relevant studies with regard to several factors including the baseline characteristics of the cohorts, the non-response definition and previous treatment protocols. Larger prospective trials with appropriate control arms are therefore required to elucidate the potential benefit when switching between anti-VEGF agents in refractory nAMD.

Enhanced Digital Features

To view enhanced digital features for this article go to https://doi.org/10.6084/m9.figshare.8025965.

Introduction

Age-related macular degeneration (AMD) is a leading cause of irreversible blindness in the population over the age of 50 years in the developed world [1, 2]. The exudative, neovascular form of the disease usually results in rapid loss of vision [3]. The intravitreal use of recombinant, humanized, monoclonal antibodies Fab to neutralize all active forms of vascular endothelial growth factor A (VEGF-A) such as ranibizumab (Lucentis; Genetech, San Francisco, CA; and Novartis, West Sussex, UK) and bevacizumab (Avastin; Roche and Genentech, Basel, Switzerland) revolutionised AMD therapy and has provided significant benefits with respect to the anatomic and visual acuity (VA) outcomes as demonstrated in the MARINA and ANCHOR studies [4, 5]. A further 2008 Cochrane systematic review concluded that ranibizumab therapy was beneficial for the treatment of AMD and associated with relatively few adverse effects [6]. The ANCHOR and MARINA trials demonstrated that between 94.3% and 94.6% of patients treated with ranibizumab maintained vision at 12 months (loss of fewer than 15 letters) compared to 62.2% on placebo. Moreover, visual acuity improved by more than 15 letters in 24.8–40.3% of patients who received ranibizumab compared to only 5.0% in the placebo control group [4, 5].

Although this represents a satisfactory treatment response, approximately 5% of this group experienced significant deterioration in visual acuity (loss of more than 15 letters at 12 months) [4, 5]. The percentage of participants who experienced deterioration in visual acuity increased to approximately 10% at 24 months [7]. The CATT study reported similar visual acuity outcomes after 1 and 2 years for ranibizumab and bevacizumab under the same treatment protocol [8]. Importantly, persistent macular fluid was detected by optical coherence tomography (OCT) in 51.5% of the patients treated with monthly ranibizumab and 67.4% of those treated with monthly bevacizumab injections after 2 years. These rates were even higher when the pro re nata (PRN) protocol was used [8]. In addition, a reduction in visual acuity of more than 15 ETDRS (Early Treatment Diabetic Retinopathy Study) letters at 2 years was reported in 6.7% and 7.2% of patients treated with monthly and PRN ranibizumab respectively. The respective percentages for the bevacizumab group were 7.8% (monthly) and 11.6% (PRN) [8].

Several studies have investigated the predictive value of clinical and genetic factors in the treatment response. A poorer treatment outcome has been associated with greater age, better baseline VA, larger choroidal neovascularisation (CNV) lesion at baseline and a greater interval between onset of symptoms and initiation of treatment [9]. Moreover, extensive research has been performed to identify genetic associations with response to anti-VEGF therapies but the results are as yet inconclusive [10].

The subgroup showing resistant or refractory AMD is expected to incur significant morbidity and therefore specific research of alternative therapeutic regimens to improve outcomes is warranted. In addition to significant morbidity, AMD bears significant socioeconomic implications through direct and indirect medical and social cost [11, 12], loss of earnings, loss of healthy life [13] and a significant reduction in vision-related quality of life (VRQoL) [14, 15]. Conversely, a subsequent improvement in visual acuity is shown to be associated with improved functioning and quality of life [16].

A number of studies investigating the therapeutic potential of aflibercept, a recombinant soluble decoy receptor fusion protein with a greater affinity for VEGF-A, VEGF-B and placental growth factor [17], have been conducted. VIEW 1 and VIEW 2 multicentre studies assessed the efficacy and safety of aflibercept [18]. Various aflibercept treatment regimens have been used to optimise the AMD treatment and more recently some studies have investigated the potential of this therapy specifically in recalcitrant nAMD. The aim of this article was to critically review the success of switching from the other two antiangiogenic agents to aflibercept in individuals with refractory or recurrent AMD.

Methods

We searched Cochrane Library and MEDLINE for publications related to the review objective. Our search strategy consisted of subject headings and keywords ‘wet macular degeneration’, ‘angiogenesis inhibitors’, ‘aflibercept’, ‘VEGF trap’, ‘bevacizumab’, ‘ranibizumab’, ‘switch’, ‘refractory’, ‘resistant’, ‘transition’ and ‘recalcitrant’. Databases were last searched in August 2018.

Search results were analysed by title and abstract to determine their relevance to the review objective. Publications were included in the analysis if participants had a diagnosis of wet, neovascular or exudative AMD, previously treated with intravitreal injections of 0.5 mg ranibizumab, 1.25 mg bevacizumab or both, who were switched to treatment with aflibercept because of persistent intraretinal or subretinal fluid as determined by OCT. Exclusion criteria included a sample size of smaller than ten eyes and a follow-up period of less than 6 months. Only studies published in English were included.

Data collected from the publications included date of publication, study design, number of participants, inclusion/exclusion criteria of the study, intervention protocol, mean injection frequency, follow-up period, visual acuity and anatomical outcomes. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

Results

Our search yielded 66 studies relevant to our review objective, published between July 2013 and August 2018. Twenty-one publications were excluded from our analysis: 5 publications were review articles, 3 publications had a small sample size and 13 publications did not have a sufficient follow-up period. The remaining 45 publications were included in our data analysis. A summary of the results of our search and data collection is shown in Tables 1 and 2.

Table 1

List of prospective studies included in this review

	Study	Sample size	Follow-up (months)	Previous anti-VEGF treatment	Reason for switch	Results
	Study	Sample size	Follow-up (months)	Previous anti-VEGF treatment	Reason for switch	Outcome measure	Change
1	Aghdam et al. [20]	22	12	Ranibizumab	Persistent IRF and/or SRF	BCVA	From 45 to 59 letters (p < 0.001)
						CST	From 400 to 304 µm (p = 0.003)
						CNV area	From 0.38 to 0.28 mm² (p = 0.003)
2	Blanco-Garavito et al. [25]	84	8	Ranibizumab	Persistent PED (height > 250 µm)	BCVA	From 66.2 to 69.5 letters (p = 0.003)
						CMT	From 444 to 387 (p < 0.001)
						PED height	From 347 to 288 (p < 0.001)
3	Chang et al. [22]	49	12	Ranibizumab and/or bevacizumab	Persistent IRF or SRF	BCVA	+ 4.7 letters (p < 0.001)
3	Chang et al. [22]	49	12	Ranibizumab and/or bevacizumab	Persistent IRF or SRF	CRT	− 97.2 µm (p < 0.001)
4	Curry et al. [24]	19	12	Ranibizumab	Persistent SRF or cystoid edema	BCVA	+ 6 letters (p = 0.04)
4	Curry et al. [24]	19	12	Ranibizumab	Persistent SRF or cystoid edema	CMT	From 268 to 255 µm (p = 0.018)
5	Grewal et al. [28]	21	12	Ranibizumab or bevacizumab	Persistent IRF and/or SRF	BCVA	From 0.42 to 0.40 logMAR (non-significant)
						CFT	From 329 to 292 μm (p = 0.038)
						PED basal diameter	From 2350 to 1856 μm (p = 0.028)
						PED height	From 288 to 248 μm (p = 0.002)
6	Jorstad et al. [33]	50	24	Ranibizumab or bevacizumab	Persistent macular fluid	BCVA	From 0.25 to 0.32 logMAR (p = 0.005)
6	Jorstad et al. [33]	50	24	Ranibizumab or bevacizumab	Persistent macular fluid	CRT	From 273 to 225 µm (p < 0.001)
7	Kawashima et al. [21]	41	6	Ranibizumab	Recurrent/residual exudation	BCVA	− 0.05 logMAR (p = 0.013)
						CRT	− 39 µm (p = 0.001)
						PED	− 43.9 µm (p < 0.001)
8	Kim et al. [31]	40	12	Ranibizumab or bevacizumab	Recurrent increase in retinal edema, PED and/or SRF	BCVA	+ 4.4 letters (non-significant)
						CST	− 42 µm (p = 0.001)
						PED vol	− 0.07 mm³ (p = 0.345)
9	Mantel et al. [32]	21	12	Ranibizumab	Refractory/recurrent IRF/SRF	BCVA	− 2 letters (non-significant)
10	Sarao et al. [29]	92	12	Ranibizumab	Persistent/recurrent SRF and/or IRF	BCVA	+ 1.8 letters (p > 0.05)
10	Sarao et al. [29]	92	12	Ranibizumab	Persistent/recurrent SRF and/or IRF	CRT	− 112 µm (p < 0.001)
11	Singh et al. [23]	26	12	Ranibizumab and/or bevacizumab	Recurrent IRF/SRF/cystoid fluid or worsening PED or new haemorrhage on clinical examination	BCVA	+ 9.2 letters (p < 0.001)
11	Singh et al. [23]	26	12	Ranibizumab and/or bevacizumab		CST	− 50.2 μm (p < 0.001)
12	Sleiman [30]	17	6	Ranibizumab	Persistent SRF/IRF	BCVA	From 0.998 to 0.933 logMAR
12	Sleiman [30]	17	6	Ranibizumab	Persistent SRF/IRF	CFT	From 534 to 356 µm
13	Tiosano et al. [19]	47	6	Bevacizumab	IRF/SRF and/or PED height > 300 µm	BCVA	From 60.3 to 63.1 letters (p = 0.02)
13	Tiosano et al. [19]	47	6	Bevacizumab	IRF/SRF and/or PED height > 300 µm	CST	From 409 to 277 µm (p = 0.0002)
14	Wykoff et al. [27]	46	6	Ranibizumab	Recalcitrant wet AMD	BCVA	+ 0.2 letters (non-significant)
14	Wykoff et al. [27]	46	6	Ranibizumab	Recalcitrant wet AMD	CST	− 23.6 µm (p = 0.018)
15	Zhu et al. [26]	49	12	Ranibizumab and/or bevacizumab	Persistent SRF and/or IRF	BCVA	+ 4.7 letters (p < 0.001)
15	Zhu et al. [26]	49	12	Ranibizumab and/or bevacizumab	Persistent SRF and/or IRF	CMT	From 448 to 351 µm (p < 0.001)

The prospective studies, their main characteristics and results are shown below. The column “Change” refers to the mean change of the respective metric from the time of the switch to the final time point of follow-up

AMD age-related macular degeneration, BCVA best-corrected visual acuity, CFT central foveal thickness, CMT central macular thickness, CNV choroidal neovascularisation, CRT central retinal thickness, CST central subfield thickness, IRF intraretinal fluid, PED pigment epithelium detachment, SRF subretinal fluid

Table 2

List of retrospective studies included in this review

	Study	Sample size	Follow-up (months)	Previous anti-VEGF treatment	Reason for switch	Results
	Study	Sample size	Follow-up (months)	Previous anti-VEGF treatment	Reason for switch	Outcome measure	Change
1	Arcinue et al. [46]	63	12	Ranibizumab and/or bevacizumab	Persistent or recurrent IRF/SRF/PED/leakage on FA	BCVA	+ 2.5 letters (non-significant)
1	Arcinue et al. [46]	63	12	Ranibizumab and/or bevacizumab	Persistent or recurrent IRF/SRF/PED/leakage on FA	MRT	From 355 to 248 µm (p < 0.001)
2	Barthelmes et al. [56]	384	12	Ranibizumab and/or bevacizumab	Not defined	BCVA	From 63.4 to 63.3 letters (p = 0.17)
3	Cardoso et al. [61]	164	36	Ranibizumab and/or bevacizumab	Persistent or recurrent SRF and/or IRF or non-medical departmental reasons	BCVA (12 months)	From 56.5 to 54.6 letters (non-significant)
						CRT (12 months)	From 386 to 313 µm (p < 0.001)
						BCVA (36 months)	From 56.5 to 50.3 letters (p < 0.001)
						CRT (36 months)	From 386 to 266 µm (p < 0.001)
4	Chan et al. [34]	189	6	Ranibizumab and bevacizumab	Persistent/recurrent macular edema, SRF haemorrhage, exudates and/or PED	BCVA	− 0.081 logMAR (p < 0.001)
						CST	− 24.9 μm (p < 0.001)
						PED height	− 43.4 μm (p < 0.001)
5	Chatziralli et al. [54]	447	12	Ranibizumab	Persistent SRF/IRF or PED involving the fovea or macular haemorrhage	BCVA	From 63.7 to 63.3 letters (non-significant)
5	Chatziralli et al. [54]	447	12	Ranibizumab		CST	From 271 to 242 μm (p < 0.001)
6	Cho et al. [40]	28	6	Ranibizumab and/or bevacizumab	Persistent fluid	BCVA	From 0.52 to 0.57 logMAR (non-significant)
6	Cho et al. [40]	28	6	Ranibizumab and/or bevacizumab	Persistent fluid	CRT	From 294 to 275 μm (p = 0.008)
7	De Massougnes et al. [47]	60	9	Ranibizumab	Persistent IRF/SRF	BCVA	From 73 to 74 letters (non-significant)
7	De Massougnes et al. [47]	60	9	Ranibizumab	Persistent IRF/SRF	CST	From 372 to 321 μm (p < 0.001)
8	Dirani et al. [53]	98	12	Ranibizumab	Persistent IRF/SRF	BCVA	From 72.1 to 71.9 letters (non-significant)
8	Dirani et al. [53]	98	12	Ranibizumab	Persistent IRF/SRF	CRT	349 to 300 μm
9	Ferrone et al. [59]	221	6	Ranibizumab and bevacizumab	No criteria	BCVA	From 0.506 to 0.521 logMAR (non-significant)
9	Ferrone et al. [59]	221	6	Ranibizumab and bevacizumab	No criteria	CRT	From 261 to 237 μm (p = 0.012)
10	Gharbiya et al. [42]	31	6	Ranibizumab	Persistent IRF/SRF with/without PED	BCVA	From 42.5 to 42.8 letters (non-significant)
						CST	From 449 to 269 μm (p < 0.001)
						PED height	From 262 to 183 μm (p < 0.001)
						CT	From 192 to 167 μm (p < 0.001)
11	Hall et al. [43]	30	12	Ranibizumab and/or bevacizumab	No criteria	BCVA	From 0.506 to 0.521 (non-significant)
11	Hall et al. [43]	30	12	Ranibizumab and/or bevacizumab	No criteria	CMT	From 261 to 237 μm (p = 0.012)
12	Hirakata et al. [36]	14	12	Ranibizumab	No improvement or recurrence on OCT	BCVA	From 0.4 to 0.32 logMAR (p = 0.018)
12	Hirakata et al. [36]	14	12	Ranibizumab	No improvement or recurrence on OCT	CMT	From 273 to 208 μm (p = 0.002)
13	Homer et al. [58]	21	24	Ranibizumab and bevacizumab	Persistent exudation	BCVA	From 0.42 to 0.42 logMAR (non-significant)
						CST	From 292 to 283 μm (non-significant)
						MTI	From 37 to 57.4 days (p = 0.01)
14	Kanesa-Thasan et al. [55]	11	18	Ranibizumab	Recalcitrant PED	BCVA	From 63.7 to 63.3 letters (non-significant)
14	Kanesa-Thasan et al. [55]	11	18	Ranibizumab	Recalcitrant PED	PED vol	From 0.687 to 0.652 mm³ (p = 0.02)
15	Kocak [38]	15	12	Ranibizumab	IRF, SRF, haemorrhage or < 10% decrease in PED height or radius	BCVA	From 0.63 to 0.43 (p = 0.0049)
						PED height	From 297 to 122 μm (p = 0.0007)
						PED radius	From 2371 to 1859 μm (p = 0.0007)
16	Kumar et al. [35]	34	6	Ranibizumab	Persisting SRF and/or IRF	BCVA	From 0.57 to 0.47 logMAR (p = 0.004)
						CFT	From 416 to 248 μm (p < 0.001)
						PED height	From 260 to 214 μm (p < 0.001)
						PED diameter	From 3265 to 2949 μm (p = 0.04)
17	Lee et al. [62]	1344	6	Ranibizumab	No criteria	BCVA	Significant improvement at 2, 3 and 5 months but not 6
18	Messenger et al. [44]	109	12	Ranibizumab and/or bevacizumab	No criteria (physician’s discretion)	BCVA	From 0.506 to 0.51 logMAR (non-significant)
						CST	From 324 to 299 μm (p = 0.0047)
						NOI/year	From 7.4 to 7.2 (non-significant)
19	Moon et al. [60]	32	6	Ranibizumab	Persistent/recurrent fluid OCT or leakage on FA	BCVA	From 0.81 to 0.81 logMAR (non-significant)
19	Moon et al. [60]	32	6	Ranibizumab	Persistent/recurrent fluid OCT or leakage on FA	CMT	From 321 to 327 μm (non-significant)
20	Muftuoglu et al. [48]	81	24	Ranibizumab or bevacizumab	Persistent/recurrent IRF/SRF or leakage	BCVA	From 0.55 to 0.56 logMAR (non-significant)
20	Muftuoglu et al. [48]	81	24	Ranibizumab or bevacizumab	Persistent/recurrent IRF/SRF or leakage	CMT	Significant reduction (p < 0.001)
21	Narayan et al. [39]	192	16	Ranibizumab	Persistent macular fluid or required 4- or 6-week injection intervals to maintain a fluid-free macula	BCVA	+ 4.5 letters (p = 0.0003)
22	Nomura et al. [65]	25	12	Ranibizumab	No specific criteria (physician’s discretion)	BCVA	CVH(−): From 0.32 to 0.14 logMAR (p = 0.0001) CVH(+): From 0.21 to 0.19 logMAR (non-significant)
22	Nomura et al. [65]	25	12	Ranibizumab	No specific criteria (physician’s discretion)	CRT	CVH(−): From 273 to 161 μm (p < 0.0002) CVH(+): From 316 to 157 μm (p = 0.0037)
23	Pinheiro-Costa et al. [45]	85	12	Ranibizumab and/or bevacizumab	Persistent/recurrent IRF/SRF	BCVA	− 2 letters (non-significant)
						CRT	From 375 to 295 μm (p < 0.001)
						NOI	From 0.57 to 0.76 (p < 0.001)
24	Ricci et al. [49]	72	12	Ranibizumab	Persistent IRF/SRF	BCVA	From 64 to 67 letters (non-significant)
24	Ricci et al. [49]	72	12	Ranibizumab	Persistent IRF/SRF	CMT	From 403 to 266 μm (non-significant)
25	Thorell et al. [41]	73	6	Ranibizumab or bevacizumab	Frequent re-treatment	BCVA	From 69 to 69.5 letters (non-significant)
						CRT	− 19 μm (p < 0.001)
						NOI	− 0.6 (p < 0.001)
26	Tyagi et al. [57]	50	12	Ranibizumab	Inadequate anatomical/functional response	BCVA	+ 1.16 letters (non-significant)
						PED height	− 50.64 μm (p = 0.007)
						PED width	+ 29.7 μm (non-significant)
27	Waizel et al. [51]	96	> 6	Bevacizumab	Persisting/increasing SRF/IRF or internal non-medical policy decisions	BCVA	From 0.63 to 0.53 logMAR (non-significant)
27	Waizel et al. [51]	96	> 6	Bevacizumab		CMT	From 419 to 318 μm (p < 0.0001)
28	Warwick et al. [37]	107	12	Ranibizumab or bevacizumab	Poor OCT and visual response	BCVA	+ 3.28 letters (p = 0.0005)
28	Warwick et al. [37]	107	12	Ranibizumab or bevacizumab	Poor OCT and visual response	CRT	− 6.16 (p < 0.001)
29	You et al. [52]	33	16	Ranibizumab or bevacizumab	Persistent/recurrent exudation	BCVA	From 55.3 to 57.8 letters (non-significant)
						CFT	From 302 to 241 μm (p = 0.001)
						PED height	− 109.8 (p = 0.02)
30	Van Lancker et al. [50]	68	14–38	Ranibizumab	Persisting SRF/IRF	BCVA	From 0.57 to 0.54 logMAR (non-significant)
30	Van Lancker et al. [50]	68	14–38	Ranibizumab	Persisting SRF/IRF	CRT	− 75.6 (p = 0.001)

The retrospective studies, their main characteristics and results are shown here. The column “Change” refers to the mean change of the respective metric from the time of the switch to the final time point of follow-up

AMD age-related macular degeneration, BCVA best-corrected visual acuity, CFT central foveal thickness, CMT central macular thickness, CNV choroidal neovascularisation, CRT central retinal thickness, CST central subfield thickness, CVH choroidal vascular hyperpermeability, IRF intraretinal fluid, MRT maximum retinal thickness, MTI mean treatment interval, NOI number of injections, PED pigment epithelium detachment, SRF subretinal fluid

Fifteen out of the 45 included studies were prospective; three of them were multicentre single-arm and one of them was a single-centre randomised with control arm. The remaining 30 were retrospective studies, one of which was a multicentre electronic medical record (EMR) review with control arm.

The inclusion and exclusion criteria for participants of the 45 studies displayed a significant degree of heterogeneity. Studies lacked a clear consensus regarding baseline participant features such as participant age, baseline visual acuity, persistent or refractory subretinal fluid, bilateral or unilateral AMD, previous intervention frequency and duration and the presence or absence of additional retinal pathology including pigment epithelial detachment (PED), subretinal fibrosis, geographic atrophy, idiopathic polypoidal choroidal vasculopathy, central serous retinopathy or cystic degeneration. In most studies performed to date refractory status was defined by the presence of intra- or subretinal fluid (IRF, SRF) and/or pigment epithelium detachment (PED), with or without macular haemorrhage despite regular treatment. The switch to aflibercept was carried out after 3–9 anti-VEGF (bevacizumab and/or ranibizumab) intravitreal injections, which were performed within a period of 3–12 months. The intervals between the last anti-VEGF injection and the first aflibercept injection was no longer than 6 weeks.

Prospective Studies

Several clinical trials have assessed the efficacy of switching to aflibercept in nAMD patients following unsatisfactory response to prior therapy (Table 1). In a multicentre prospective study, Tiosano et al. [19] studied 47 eyes from 46 nAMD patients with incomplete response to bevacizumab. Twenty-eight weeks after switching to aflibercept therapy, the mean best corrected visual acuity (BCVA) showed mild but statistical significant improvement from 60.3 to 63.1 EDTRS letters (p = 0.02), while the central subfield thickness (CST) was significantly reduced from 409 to 277 µm (p = 0.0002) [19]. When switching patients from ranibizumab to aflibercept, Aghdam et al. [20] found a significant mean BCVA increase from 45 to 59 EDTRS letters (p < 0.001) after 12 months follow-up in 22 eyes (19 patients) with nAMD. The CST was also significantly reduced from 400 to 304 µm (p = 0.003). Similarly, Kawashima et al. [21], Chang et al. [22], Singh et al. [23], Curry et al. [24], Blanco-Garavito et al. [25] and Zhu et al. [26] have demonstrated a statistically significant improvement in both BCVA and CRT following switching from ranibizumab and/or bevacizumab to aflibercept for the treatment of refractory nAMD.

In contrast, a number of studies have failed to record a significant improvement in terms of visual acuity when switching to aflibercept therapy despite identifying a significant improvement in terms of central retinal thickness (CRT). More specifically, Wykoff et al. [27] prospectively studied patients with recalcitrant nAMD initially treated with ranibizumab. Six months after switching to aflibercept therapy, there was a significant reduction of 23.6 µm in the CST (p = 0.018) but BCVA did not improve [27]. No significant gain in BCVA has been reported in four other studies, despite the significant CRT reduction [28‐31].

It is worth noting that to date the only prospective randomised clinical trial with a control arm was conducted by Mantel et al. [32]. This small study included 21 eyes (19 patients) that had been treated with ranibizumab and still required monthly injections at the end of the second year of treatment. These patients were randomised to either continue ranibizumab injections or switch to aflibercept. After 12 months, the BCVA change was not found to be significantly different between the two groups. In addition, the mean retreatment interval was 1.13 months in the aflibercept group and 1.14 months in the control group [32].

Jorstad et al. [33] evaluated prospectively the efficacy of switching from bevacizumab or ranibizumab to aflibercept in 50 eyes from 47 nAMD patients with persistent macular fluid. Notably, these authors reported a statistically significant reduction in BCVA after 2 years of follow-up, from 0.25 to 0.32 logMAR (p = 0.005), even though no significant difference was detected during the first year (0.24 logMAR) [33].

Retrospective Evidence

A large number of retrospective studies have evaluated the outcomes of transition to aflibercept therapy in nAMD (Table 2). Chan et al. [34] included 189 cases, the majority of which (82%) were refractory to bevacizumab and ranibizumab injections. They documented a significant improvement in BCVA of 0.081 logMAR (p < 0.001) and a significant reduction in CST of 24.9 μm (p < 0.001) after 6 months [34]. Further statistically significant improvements of BCVA and CRT were also reported in other studies [35‐38]. Narayan et al. [39] found a significant BCVA improvement in patients with refractory to ranibizumab therapy but with no CRT data.

In contrast, several clinical trials have reported a lack of BCVA improvement despite significantly improved anatomical outcomes [40‐53]. Chatziralli et al. [54] reported the results of large retrospective study which included 447 eyes with persistent nAMD despite treatment with ranibizumab injections. Twelve months after switching to aflibercept, the BCVA did not change (from 63.7 to 63.3 ETDRS letters), although the CST was significantly reduced from 271 to 242 μm (p < 0.001) [54]. Moreover, a non-significant VA change without any CRT data was reported by Kanesa-Thasan et al. [55], Barthelmes et al. [56] and Tyagi et al. [57].

Homer et al. [58] reported an unchanged BCVA (from 0.42 to 0.42 logMAR) and a small, non-significant reduction of CST (from 292 to 283 μm) in a small cohort of 21 eyes with persistent exudation 2 years after converting to aflibercept. Similarly, Ferrone et al. [59] and Moon et al. [60] reported non-significant functional and anatomical changes 6 months after the switch.

It is worth noting that a single study reported a significant reduction in terms of BCVA when switching from ranibizumab and/or bevacizumab to aflibercept [61]. This study demonstrated a significant BCVA reduction, from 56.5 to 50.3 letters (p < 0.001), 3 years after transition to aflibercept in 164 nAMD eyes, although vision was found to be stable 1 year after the switch. Interestingly, CRT was significantly improved at both time points [61] so one could hypothesize that other factors and the natural course of the disease may account for the ultimate reduction in vision after transition to aflibercept.

The only retrospective study with a control arm was reported by Lee et al. [62]. It was a multicentre study comparing the outcomes of 448 eyes that were switched to aflibercept after 6 monthly ranibizumab injections as opposed to 896 eyes which continued ranibizumab therapy. Despite an initial improvement in BCVA after switching to aflibercept therapy, this benefit was not detected 6 months after the switch [62].

Pigment Epithelial Detachment (PED)

In terms of PED characteristics, such as PED height and volume, several studies showed significant improvement when switching to aflibercept [21, 25, 28, 34, 38, 42, 52, 55]. In contrast, Kim et al. [31] reported a stable PED volume 12 months after conversion to aflibercept in cases with refractory PED. Tyagi et al. [57] found a significant reduction in PED height but not PED width in 50 cases, 12 months after switching from ranibizumab to aflibercept.

Number of Injections

With regard to the number of injections, several studies have shown a significant reduction in the number of injections after a therapeutic switch to aflibercept [29, 41, 45, 56, 58], while others have reported a non-significant change in the overall number of injections [32, 44, 53]. Sarao et al. [29] also found an improvement in the mean injection interval, from 5.3 to 13.6 weeks, in a study of 50 cases that were switched from ranibizumab to aflibercept and were followed up for 1 year.

Quality of Life

As for the impact of switching intravitreal therapies on quality of life, Zhu et al. [26] prospectively assessed the changes in vision-related quality of life in 49 patients with refractory nAMD with the use of the National Eye Institute Visual Functioning Questionnaire 25 (NEI VFQ-25). The NEI VFQ-25 composite scores improved significantly after 1 year and this improvement correlated with the significant changes in BCVA but not CMT [26].

Discussion

Various contributing factors have been implicated in the suboptimal response to anti-VEGF treatment for patients suffering from exudative AMD [9, 10]. The hypothesis of reduced anti-VEGF efficacy with repeated injections or a form of treatment-related tachyphylaxis may apply and has resulted in switching between anti-VEGF treatments as a logical management step in clinical practice [63]. Amoaku et al. [63] proposed a grading system for the response of patients with exudative AMD to anti-VEGF treatment based on functional and morphological criteria. The response was categorized as good, partial poor and no response in terms of visual acuity and OCT parameters including subretinal/intraretinal fluid, pigment epithelial detachment and central retinal thickness. The authors suggested that switching between anti-VEGF agents is justified only when there is evidence of poor or inadequate response in either function or morphology [63].

Several conclusions regarding the success of switching from ranibizumab or bevacizumab to aflibercept in patients with exudative AMD can be drawn from our review. In terms of visual acuity many studies suggest a meaningful improvement after the switch. However, the only two comparative studies that have been conducted failed to identify a significant visual difference following treatment change as opposed to continuing with the same agent (ranibizumab) [32, 62]. In addition, a large retrospective study by Lee et al. [62] demonstrated a significant improvement in terms of VA immediately after switching to aflibercept; however, this improvement was not sustained after 6 months. The authors suggest that this result is due to tachyphylaxis to ranibizumab rather than to superiority of aflibercept. Moreover, Mantel et al. [32] showed a non-significant deterioration in VA in patients that switched to aflibercept when compared to controls. Long-term visual outcomes do not appear to be more favourable either [33, 61] but there may be many compounding factors beyond 2 years of follow-up. Jorstad et al. [33] and Cardoso et al. [61] found a significant deterioration in VA at 24 and 36 months respectively after switching to aflibercept, despite stability in their 12-month results [33, 61]. Since there was no control group in either study, the result can probably be attributed to the natural course of the disease rather than to the actual switch to aflibercept.

In contrast, the majority of switch studies show a significant improvement in anatomical outcomes immediately after the switch that has been maintained throughout the follow-up period [19, 21‐29, 31, 33‐36, 38, 40‐48, 50‐55, 59‐61, 64, 65]. Anatomical features including CRT and PED measured by OCT are consistently improved to a significant degree in almost all of the reviewed studies.

In addition, the injection interval appears to be increased or at least remained stable after the switch in all the pertinent studies. Moreover, the only study that assessed the quality of life showed significant improvement as an additional benefit of the therapeutic switch to aflibercept [26].

Overall most of the studies support the concept of switching to aflibercept in those patients that show an insufficient response to the other anti-VEGF agents based on improved anatomical outcomes, reduction in intraretinal fluid, subretinal fluid, PED and potentially extended injection intervals. Various studies have shown improvement or stabilization of visual outcomes when switching to aflibercept after suboptimal response to the other two anti-VEGF agents. Nevertheless, it should be emphasized that nonrandomised, retrospective case series on switching are difficult and challenging to interpret because of the plethora of technical biases, lack of controls and the presence of confounding factors. Furthermore, the methodological heterogeneity of the studies creates much uncertainty when trying to answer a specific clinical question such as the one dealt with here. However, case series have a place in preliminary investigational research and are informative in understanding potential strategies for optimising patient care.

Furthermore, the lack of subgroup analysis data, AMD phenotype classification and uniform design of the studies makes any interpretation of benefits a challenging task. The absence of comparative arm in most published studies to date makes interpretation of the findings difficult. Regrettably, the two studies with control arms have been either retrospective or underpowered because of a small sample size [32, 62]. The absence of masking in the interpretation of fundus fluorescein angiograms and optical coherence tomography examinations is also a methodological setback. Moreover, registration of changes in refractive errors and documentation of cataract were absent in most of the studies performed to date. Additionally, overall one has to consider whether optimal timely and sufficient treatment has been provided to patients with refractive AMD and exclude all possible causes of non-response including masking syndromes.

Conclusions

The present review attempted to critically summarise current evidence and success rate when switching from ranibizumab or bevacizumab to aflibercept patients with exudative AMD. Although there is a significant body of literature reporting variable results, the cumulative evidence suggests that there may be a benefit. Patients with exudative AMD refractory to other anti-VEGF agents may gain substantial benefit from switching to aflibercept in terms of anatomical outcome and interval between injections; however, there is still uncertainty regarding the visual outcome. Adequately powered randomised controlled trials with appropriate controls are required to address the real benefits of the switch between anti-VEGF agents and establish treatment guidelines for better anatomical and functional outcome.

Acknowledgements

Funding

No funding or sponsorship was received for this study or publication of this article.

Authorship

All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.

Disclosures

Theodoros Empeslidis: honoraria and travel grants from Novartis and Bayer. Theodoros Giannopoulos: research funding from Pharmaten and Bayer; travel support from Novartis and Bayer. Vassileios Konidaris: honoraria and travel grants from Novartis and Bayer. Paris G. Tranos: research funding from Novartis and Bayer; honoraria from Bayer, Allergan and Novartis. Irini C. Voudouragkaki: travel support from Vianex and Bayer. Anastasios G. Konstas: research funding from Allergan, Bayer and Santen; travel support from Vianex; honoraria from Allergan, Mundipharma, Santen and Vianex. Evangelia S. Panagiotou and Matthew Storey have nothing to disclose.

Compliance with Ethics Guidelines

This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

Data Availability

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Unsere Produktempfehlungen

e.Med Interdisziplinär

Kombi-Abonnement

Für Ihren Erfolg in Klinik und Praxis - Die beste Hilfe in Ihrem Arbeitsalltag

Mit e.Med Interdisziplinär erhalten Sie Zugang zu allen CME-Fortbildungen und Fachzeitschriften auf SpringerMedizin.de.

Jetzt testen ¹

e.Med Innere Medizin

Kombi-Abonnement

Mit e.Med Innere Medizin erhalten Sie Zugang zu CME-Fortbildungen des Fachgebietes Innere Medizin, den Premium-Inhalten der internistischen Fachzeitschriften, inklusive einer gedruckten internistischen Zeitschrift Ihrer Wahl.

Jetzt testen ²

e.Med Allgemeinmedizin

Kombi-Abonnement

Mit e.Med Allgemeinmedizin erhalten Sie Zugang zu allen CME-Fortbildungen und Premium-Inhalten der allgemeinmedizinischen Zeitschriften, inklusive einer gedruckten Allgemeinmedizin-Zeitschrift Ihrer Wahl.

Jetzt testen ³

Bressler N. Age-related macular degeneration is the leading cause of blindness. JAMA. 2004;291(15):1900–1.CrossRefPubMed

Friedman D, O’Colmain B, Munoz B, et al. Prevalence of age-related macular degeneration in the United States. Arch Ophthalmol. 2004;122(4):564–72.CrossRefPubMed

Lim LS, Mitchell P, Seddon JM, Holz FG, Wong TY. Age-related macular degeneration. Lancet. 2012;379(9827):1728–38.CrossRefPubMed

Rosenfeld P, Brown D, Heier J, et al. Ranibizumab for neovascular age-related macular degeneration. N Engl J Med. 2006;355:1419–31.CrossRefPubMed

Brown D, Kaiser P, Michels M, et al. Ranibizumab versus verteporfin for neovascular age-related macular degeneration. N Engl J Med. 2006;335:1432–44.CrossRef

Vedula SS, Krzystolik MG. Antiangiogenic therapy with anti-vascular endothelial growth factor modalities for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2008;2:CD005139.

Rosenfeld PJ, Shapiro H, Tuomi L, et al. Characteristics of patients losing vision after 2 years of monthly dosing in the phase III ranibizumab clinical trials. Ophthalmology. 2011;118(3):523–30.CrossRefPubMed

Martin DF, Maguire MG, Fine SL, et al. Ranibizumab and bevacizumab for treatment of neovascular age-related macular degeneration: two-year results: comparison of age-related macular degeneration treatments trials research group. Ophthalmology. 2012;119(7):1388–98.CrossRefPubMed

Zhang X, Lai TYY. Baseline predictors of visual acuity outcome in patients with wet age-related macular degeneration. Biomed Res Int. 2018;2018:9640131.PubMedPubMedCentral

10.

Lores-Motta L, de Jong EK, den Hollander AI. Exploring the use of molecular biomarkers for precision medicine in age-related macular degeneration. Mol Diagn Ther. 2018;22(3):315–43.CrossRefPubMedPubMedCentral

11.

Rein D, Zhang P, Wirth K, et al. The economic burden of major adult visual disorders in the United States. Arch Ophthalmol. 2006;124:1754–60.CrossRefPubMed

12.

Husler S, Schmid H. Coping with wet age-related macular degeneration: a study from Switzerland. Klin Monbl Augenheilkd. 2013;230(12):1251–6.CrossRefPubMed

13.

Taylor HR, Pezzullo ML, Keeffe JE. The economic impact and cost of visual impairment in Australia. Br J Ophthalmol. 2006;90(3):272–5.CrossRefPubMedPubMedCentral

14.

Lin JC, Yu JH. Assessment of quality of life among Taiwanese patients with visual impairment. J Formos Med Assoc. 2012;111(10):572–9.CrossRefPubMed

15.

Brown G, Sharma S, Brown M, Kistler J. Utility values and age-related macular degeneration. Arch Ophthalmol. 2000;118(1):47–51.CrossRefPubMed

16.

Bressler NM, Chang TS, Suner IJ, et al. Vision-related function after ranibizumab treatment by better- or worse-seeing eye: clinical trial results from MARINA and ANCHOR. Ophthalmology. 2010;117(4):747–56.CrossRefPubMed

17.

Hanout M, Ferraz D, Ansari M, et al. Therapies for neovascular age-related macular degeneration: current approaches and pharmacologic agents in development. Biomed Res Int. 2013;2013:830837.CrossRefPubMedPubMedCentral

18.

Schmidt-Erfurth U, Kaiser PK, Korobelnik JF, et al. Intravitreal aflibercept injection for neovascular age-related macular degeneration: ninety-six-week results of the VIEW studies. Ophthalmology. 2014;121(1):193–201.CrossRefPubMed

19.

Tiosano L, Segal O, Mathalone N, et al. Aflibercept as a second line therapy for neovascular age related macular degeneration in Israel (ASLI) study. Eye (Lond). 2017;31(6):890–8.CrossRef

20.

Aghdam KA, Pielen A, Framme C, Junker B. Visual and anatomic outcomes after conversion to aflibercept in neovascular age-related macular degeneration: 12-month results. Eur J Ophthalmol. 2016;26(5):473–8.CrossRefPubMed

21.

Kawashima Y, Oishi A, Tsujikawa A, et al. Effects of aflibercept for ranibizumab-resistant neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. Graefes Arch Clin Exp Ophthalmol. 2014;253(9):1471–7.CrossRefPubMed

22.

Chang AA, Broadhead GK, Hong T, et al. Intravitreal aflibercept for treatment-resistant neovascular age-related macular degeneration: 12-month safety and efficacy outcomes. Ophthalmic Res. 2015;55(2):84–90.CrossRefPubMed

23.

Singh RP, Srivastava SK, Ehlers JP, et al. A single-arm, investigator-initiated study of the efficacy, safety, and tolerability of intravitreal aflibercept injection in subjects with exudative age-related macular degeneration previously treated with ranibizumab or bevacizumab (ASSESS study): 12-month analysis. Clin Ophthalmol. 2015;9:1759–66.CrossRefPubMedPubMedCentral

24.

Curry B, Bylsma G, Hewitt AW, Verma N. The VEGF treatment of AMD switch study (The vTAS Study). Asia Pac J Ophthalmol (Phila). 2017;6(6):481–7.

25.

Blanco-Garavito R, Jung C, Uzzan J, et al. Aflibercept after ranibiumab intravitreal injections in exudative age-related macular degeneration: the ARI2 Study. Retina. 2017;00:1–8.CrossRef

26.

Zhu M, Wijeyakumar W, Syed AR, et al. Vision-related quality of life: 12-month aflibercept treatment in patients with treatment-resistant neovascular age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol. 2017;255(3):475–84.CrossRefPubMed

27.

Wykoff CC, Brown DM, Maldonado ME, Croft DE. Aflibercept treatment for patients with exudative age-related macular degeneration who were incomplete responders to multiple ranibizumab injections (TURF trial). Br J Ophthalmol. 2014;98(7):951–5.CrossRefPubMed

28.

Grewal DS, Gill MK, Sarezky D, Lyon AT, Mirza RG. Visual and anatomical outcomes following intravitreal aflibercept in eyes with recalcitrant neovascular age-related macular degeneration: 12-month results. Eye (Lond). 2014;28(7):895–9.CrossRef

29.

Sarao V, Parravano M, Veritti D, Arias L, Varano M, Lanzetta P. Intravitreal aflibercept for choroidal neovascularization due to age-related macular degeneration unresponsive to ranibiumab therapy. Retina. 2016;36:770–7.CrossRefPubMed

30.

Sleiman A. Aflibercept in refractory wet AMD treated with ranibizumab: anatomical and visual outcome. Saudi J Ophthalmol. 2016;30(4):227–32.CrossRef

31.

Kim K, Kim E, Kim Y, Yang J, Yu S, Kwak H. Outcome of intravitreal aflibercept for refractory pigment epithelial detachment with or without subretinal fluid and secondary to age-related macular degeneration. Retina. 2017;1:1–11.CrossRef

32.

Mantel I, Gianniou C, Dirani A. Conversion to aflibercept therapy versus continuing with ranibizumab therapy for neovascular age-related macular degeneration dependent on monthly ranibizumab treatment. Retina. 2016;6:53–8.CrossRef

33.

Jorstad OK, Faber RT, Moe MC. Two-year functional and anatomical results after converting treatment resistant eyes with exudative age-related macular degeneration to aflibercept in accordance with a treat and extend protocol. Acta Ophthalmol. 2017;95(5):460–3.CrossRefPubMed

34.

Chan C, Jain A, Sadda S, Varshney N. Optical coherence tomographic and visual results at six months after transitioning to aflibercept for patients on prior ranibizumab or bevacizumab treatment for exudative age-related macular degeneration (an American Ophthlmological Society thesis). Trans Am Ophthalmol Soc. 2014;112:160–98.PubMedPubMedCentral

35.

Kumar N, Marsiglia M, Mrejen S, et al. Visual and anatomical outcomes of intravitreal aflibercept in eyes with persistent subfoveal fluid despite previous treatments with ranbizumab in patients with neovascular age-related macular degeneration. Retina. 2013;33:1605–12.CrossRefPubMed

36.

Hirakata T, Fujinami K, Watanabe K, Sasaki M, Noda T, Akiyama K. One-year outcome of intravitreal aflibercept injection for age-related macular degeneration resistant to ranibizumab: rapid morphologic recovery and subsequent visual improvement. Clin Ophthalmol. 2016;10:969–77.CrossRefPubMedPubMedCentral

37.

Warwick AN, Leaver HH, Lotery AJ, Goverdhan SV. Fixed bimonthly aflibercept in naive and switched neovascular age-related macular degeneration patients: 1 year outcomes. Int J Ophthalmol. 2016;9(8):1156–62.PubMedPubMedCentral

38.

Kocak I. Intravitreal aflibercept in treatment-resistant pigment epithelial detachment. Int Ophthalmol. 2017;37(3):531–7.CrossRefPubMed

39.

Narayan DS, Muecke J. Intravitreal aflibercept treatment in eyes with exudative age-related macular degeneration following prior treatment with intravitreal ranibizumab. Indian J Ophthalmol. 2015;63(11):832–6.CrossRefPubMedPubMedCentral

40.

Cho H, Shah CP, Weber M, Heier JS. Aflibercept for exudative AMD with persistent fluid on ranibizumab and/or bevacizumab. Br J Ophthalmol. 2013;97(8):1032–5.CrossRefPubMed

41.

Thorell MR, Nunes RP, Chen GW, et al. Response to aflibercept after frequent re-treatment with bevacizumab or ranibizumab in eyes with neovascular AMD. Ophthalmic Surg Lasers Imaging Retina. 2014;45(6):526–33.CrossRefPubMed

42.

Gharbiya M, Iannetti L, Parisi F, De Vico U, Mungo ML, Marenco M. Visual and anatomical outcomes of intravitreal aflibercept for treatment-resistant neovascular age-related macular degeneration. Biomed Res Int. 2014;2014:273754.CrossRefPubMedPubMedCentral

43.

Hall LB, Zebardast N, Huang JJ, Adelman RA. Aflibercept in the treatment of neovascular age-related macular degeneration in previously treated patients. J Ocul Pharmacol Ther. 2014;30(4):346–52.CrossRefPubMed

44.

Messenger WB, Campbell JP, Faridi A, et al. Injection frequency and anatomic outcomes 1 year following conversion to aflibercept in patients with neovascular age-related macular degeneration. Br J Ophthalmol. 2014;98(9):1205–7.CrossRefPubMed

45.

Pinheiro-Costa J, Costa JM, Beato JN, et al. Switch to aflibercept in the treatment of neovascular AMD: one-year results in clinical practice. Ophthalmologica. 2015;233(3–4):155–61.CrossRefPubMed

46.

Arcinue CA, Ma F, Barteselli G, Sharpsten L, Gomez ML, Freeman WR. One-year outcomes of aflibercept in recurrent or persistent neovascular age-related macular degeneration. Am J Ophthalmol. 2015;159(3):426–36.CrossRefPubMed

47.

De Massougnes S, Dirani A, Ambresin A, Delugis D, Marchionno L, Mantel I. Pigment epithelial detachment response to aflibercept in neovascular age-related macular degeneration refractory to ranibizumab. Retina. 2016;36:881–8.CrossRefPubMed

48.

Muftuoglu IK, Arcinue CA, Tsai FF, et al. Long-term results of pro re nata regimen of aflibercept treatment in persistent neovascular age-related macular degeneration. Am J Ophthalmol. 2016;167:1–9.CrossRefPubMed

49.

Ricci F, Parravano M, Regine F, et al. Aflibercept in persistent neovascular AMD: comparison of different treatment strategies in switching therapy. Eye (Lond). 2016;30(8):1077–83.CrossRef

50.

Van Lancker L, Petrarca R, Moutsouris K, Masaoutis P, Kampougeris G. Clinical experience of switching anti-VEGF therapy from ranibizumab to aflibercept in age-related choroidal neovascularization. Eur J Ophthalmol. 2017;27(3):342–5.CrossRefPubMed

51.

Waizel M, Todorova MG, Masyk M, et al. Switch to aflibercept or ranibizumab after initial treatment with bevacizumab in eyes with neovascular AMD. BMC Ophthalmol. 2017;17(1):79.CrossRefPubMedPubMedCentral

52.

You Q, Gaber R, Meshi A, et al. High-dose high-frequency aflibercept for recalcitrant neovascular age-related macular degeneration. Retina. 2018;38:1156–65.CrossRefPubMed

53.

Dirani A, Mantel I. Ranibizumab treatment history as predictor of the switch-response to aflibercept: evidence for drug tolerance. Clin Ophthalmol. 2018;12:593–600.CrossRefPubMedPubMedCentral

54.

Chatziralli I, Nicholson L, Vrizidou E, et al. Predictors of outcome in patients with neovascular age-related macular degeneration switched from ranibizumab to 8-weekly aflibercept. Ophthalmology. 2016;123(8):1762–70.CrossRefPubMed

55.

Kanesa-Thasan A, Grewal D, Gill M, Lyon A, Mirza R. Quantification of change in pigment epithelial detachment volume and morphology after transition to intravitreal aflibercept in eyes with recalcitrant neovascular AMD: 18-month results. Ophthalmic Surg Lasers Imaging Retina. 2015;46(6):638–41.CrossRefPubMed

56.

Barthelmes D, Campain A, Nguyen P, et al. Effects of switching from ranibizumab to aflibercept in eyes with exudative age-related macular degeneration. Br J Ophthalmol. 2016;100(12):1640–5.CrossRefPubMed

57.

Tyagi P, Juma Z, Hor YK, Scott NW, Ionean A, Santiago C. Clinical response of pigment epithelial detachment associated with neovascular age-related macular degeneration in switching treatment from ranibizumab to aflibercept. BMC Ophthalmol. 2018;18(1):148.CrossRefPubMedPubMedCentral

58.

Homer N, Grewal DS, Mirza RG, Lyon AT, Gill MK. Transitioning to intravitreal aflibercept following a previous treat-and-extend dosing regimen in neovascular age-related macular degeneration: 24-month results. Eye (Lond). 2015;29(9):1152–5.CrossRef

59.

Ferrone PJ, Anwar F, Naysan J, et al. Early initial clinical experience with intravitreal aflibercept for wet age-related macular degeneration. Br J Ophthalmol. 2014;98(Suppl 1):i17–21.CrossRefPubMed

60.

Moon DRC, Lee DK, Kim SH, You YS, Kwon OW. Aflibercept treatment for neovascular age-related macular degeneration and polypoidal choroidal vasculopathy refractory to anti-vascular endothelial growth factor. Korean J Ophthalmol. 2015;29(4):226–32.CrossRefPubMedPubMedCentral

61.

Cardoso P, Pinheiro AF, Meira J, et al. Switch to aflibercept in the treatment of neovascular AMD: long-term results. J Ophthalmol. 2017;2017:6835782.

62.

Lee C, Kim A, Baughman D, et al. Visual acuity improvement when switching from ranibizumab to aflibercept is not sustained. Retina. 2017;1:1–6.

63.

Amoaku WM, Chakravarthy U, Gale R, et al. Defining response to anti-VEGF therapies in neovascular AMD. Eye (Lond). 2015;29(6):721–31.CrossRef

64.

Abri Aghdam K, Seidensticker F, Pielen A, Framme C, Junker B. The short-term effects of aflibercept on the size of choroidal neovascularization lesion in treatment-resistant neovascular age-related macular degeneration as determined by spectral-domain optical coherence tomography. Lasers Surg Med. 2016;48(7):668–77.CrossRefPubMed

65.

Nomura Y, Yanagi Y. Intravitreal aflibercept for ranibizumab-resistant exudative age-related macular degeneration with choroidal vascular hyperpermeability. Jpn J Ophthalmol. 2015;59(4):261–5.CrossRefPubMed

Titel: How Successful is Switching from Bevacizumab or Ranibizumab to Aflibercept in Age-Related Macular Degeneration? A Systematic Overview
verfasst von: Theodoros Empeslidis
Matthew Storey
Theodoros Giannopoulos
Vassileios Konidaris
Paris G. Tranos
Evangelia S. Panagiotou
Irini C. Voudouragkaki
Anastasios G. Konstas
Publikationsdatum: 17.05.2019
Verlag: Springer Healthcare
Erschienen in: Advances in Therapy / Ausgabe 7/2019
Print ISSN: 0741-238X
Elektronische ISSN: 1865-8652
DOI: https://doi.org/10.1007/s12325-019-00971-0

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

^{Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag}

Kostenlos registrieren

Neu im Fachgebiet Innere Medizin

Vorhofflimmern bei Jüngeren gefährlicher als gedacht

06.05.2024 Vorhofflimmern Nachrichten

Immer mehr jüngere Menschen leiden unter Vorhofflimmern. Betroffene unter 65 Jahren haben viele Risikofaktoren und ein signifikant erhöhtes Sterberisiko verglichen mit Gleichaltrigen ohne die Erkrankung.

Chronisches Koronarsyndrom: Gefahr von Hospitalisierung wegen Herzinsuffizienz

06.05.2024 Herzinsuffizienz Nachrichten

Obwohl ein rezidivierender Herzinfarkt bei chronischem Koronarsyndrom wahrscheinlich die Hauptsorge sowohl der Patienten als auch der Ärzte ist, sind andere Ereignisse womöglich gefährlicher. Laut einer französischen Studie stellt eine Hospitalisation wegen Herzinsuffizienz eine größere Gefahr dar.

„Restriktion auf vier Wochen Therapie bei Schlaflosigkeit ist absurd!“

06.05.2024 Insomnie Nachrichten

Chronische Insomnie als eigenständiges Krankheitsbild ernst nehmen und adäquat nach dem aktuellen Forschungsstand behandeln: Das forderte der Schlafmediziner Dr. Dieter Kunz von der Berliner Charité beim Praxis Update.

GLP-1-Rezeptoragonisten und SGLT-2-Hemmer: zusammen besser

06.05.2024 Typ-2-Diabetes Nachrichten

Immer häufiger wird ein Typ-2-Diabetes sowohl mit einem GLP-1-Rezeptor-Agonisten als auch mit einem SGLT-2-Inhibitor behandelt. Wie sich das verglichen mit den Einzeltherapien auf kardiovaskuläre und renale Komplikationen auswirkt, wurde anhand von Praxisdaten aus Großbritannien untersucht.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

Newsletter bestellen

Live-Webinar "Chronische Unterbauch- und Viszeralschmerzen in der Praxis managen"

Springer Medizin

Abstract

Enhanced Digital Features

Introduction

Methods

Results

Prospective Studies

Retrospective Evidence

Pigment Epithelial Detachment (PED)

Number of Injections

Quality of Life

Discussion

Conclusions

Acknowledgements

Funding

Authorship

Disclosures

Compliance with Ethics Guidelines

Data Availability

Unsere Produktempfehlungen

e.Med Interdisziplinär

e.Med Innere Medizin

e.Med Allgemeinmedizin

Weitere Artikel der Ausgabe 7/2019

Objective and Subjective Effects of a Prototype Nasal Dilator Strip on Sleep in Subjects with Chronic Nocturnal Nasal Congestion

Second-Generation Trabecular Micro-Bypass Stents as Standalone Treatment for Glaucoma: A 36-Month Prospective Study

Extended Stability of Reconstituted and Diluted SB3 (Trastuzumab Biosimilar) Assessed by Physicochemical and Biological Properties

Advances in Clinical Cardiology 2018: A Summary of Key Clinical Trials

A Structured Literature Review of the Epidemiology and Disease Burden of Non-Alcoholic Steatohepatitis (NASH)

Improving the Timely Detection of Bladder and Kidney Cancer in Primary Care

Leitlinien kompakt für die Innere Medizin

Neu im Fachgebiet Innere Medizin

Vorhofflimmern bei Jüngeren gefährlicher als gedacht

Chronisches Koronarsyndrom: Gefahr von Hospitalisierung wegen Herzinsuffizienz

„Restriktion auf vier Wochen Therapie bei Schlaflosigkeit ist absurd!“

GLP-1-Rezeptoragonisten und SGLT-2-Hemmer: zusammen besser

Update Innere Medizin