Two-year results for ranibizumab for radiation retinopathy (RRR): a randomized, prospective trial
Purpose To assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema. Methods Forty eyes with radiation-induced macular edema and decreased visual acuity were enrolled in the phase IIb, prospective clinical trial and randomized into 3 cohort...
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Published in | Graefe's archive for clinical and experimental ophthalmology Vol. 260; no. 1; pp. 47 - 54 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.01.2022
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0721-832X 1435-702X 1435-702X |
DOI | 10.1007/s00417-021-05281-2 |
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Abstract | Purpose
To assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema.
Methods
Forty eyes with radiation-induced macular edema and decreased visual acuity were enrolled in the phase IIb, prospective clinical trial and randomized into 3 cohorts: (A) monthly ranibizumab, (B) monthly ranibizumab with targeted retinal photocoagulation (TRP), or (C) as-needed ranibizumab and TRP. In year 2, all subjects entered a treat-and-extend protocol for ranibizumab. The primary outcome measure was mean change in early treatment diabetic retinopathy study (ETDRS) best-corrected visual acuity (BCVA) from baseline.
Results
Through year 1, the mean change in ETDRS BCVA was significantly different between the three cohorts (p < 0.001); cohort A saw the largest gain with + 4.0 letters. Significant anatomic improvements were also seen in all cohorts. Comparatively, through year 2, cohorts A, B, and C had a mean change in ETDRS BCVA of − 1.9, − 3.9, and + 1.3 letters, respectively; additionally, no significant differences were found in absolute ETDRS BCVA across time (ANOVA, p = 0.123). Overall, 90% of eyes maintained VA 20/200 or better and 33.3% of subjects gained at least one line of vision. There were no significant differences in mean central macular thickness for any cohort compared to baseline (p = 0.09). The presence of retinal hemorrhage and intraretinal exudates stayed consistent from year 1 to year 2 for all cohorts.
Conclusions
Among eyes with radiation-related macular edema, a treat-and-extend regimen with ranibizumab may not result in as many visual and anatomic improvements as monthly injections. However, treat-and-extend still may prevent serious visual complications compared to historical controls.
Trial registration
ClinicalTrials.gov Identifier: NCT02222610 |
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AbstractList | To assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema.
Forty eyes with radiation-induced macular edema and decreased visual acuity were enrolled in the phase IIb, prospective clinical trial and randomized into 3 cohorts: (A) monthly ranibizumab, (B) monthly ranibizumab with targeted retinal photocoagulation (TRP), or (C) as-needed ranibizumab and TRP. In year 2, all subjects entered a treat-and-extend protocol for ranibizumab. The primary outcome measure was mean change in early treatment diabetic retinopathy study (ETDRS) best-corrected visual acuity (BCVA) from baseline.
Through year 1, the mean change in ETDRS BCVA was significantly different between the three cohorts (p < 0.001); cohort A saw the largest gain with + 4.0 letters. Significant anatomic improvements were also seen in all cohorts. Comparatively, through year 2, cohorts A, B, and C had a mean change in ETDRS BCVA of - 1.9, - 3.9, and + 1.3 letters, respectively; additionally, no significant differences were found in absolute ETDRS BCVA across time (ANOVA, p = 0.123). Overall, 90% of eyes maintained VA 20/200 or better and 33.3% of subjects gained at least one line of vision. There were no significant differences in mean central macular thickness for any cohort compared to baseline (p = 0.09). The presence of retinal hemorrhage and intraretinal exudates stayed consistent from year 1 to year 2 for all cohorts.
Among eyes with radiation-related macular edema, a treat-and-extend regimen with ranibizumab may not result in as many visual and anatomic improvements as monthly injections. However, treat-and-extend still may prevent serious visual complications compared to historical controls.
ClinicalTrials.gov Identifier: NCT02222610. PurposeTo assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema.MethodsForty eyes with radiation-induced macular edema and decreased visual acuity were enrolled in the phase IIb, prospective clinical trial and randomized into 3 cohorts: (A) monthly ranibizumab, (B) monthly ranibizumab with targeted retinal photocoagulation (TRP), or (C) as-needed ranibizumab and TRP. In year 2, all subjects entered a treat-and-extend protocol for ranibizumab. The primary outcome measure was mean change in early treatment diabetic retinopathy study (ETDRS) best-corrected visual acuity (BCVA) from baseline.ResultsThrough year 1, the mean change in ETDRS BCVA was significantly different between the three cohorts (p < 0.001); cohort A saw the largest gain with + 4.0 letters. Significant anatomic improvements were also seen in all cohorts. Comparatively, through year 2, cohorts A, B, and C had a mean change in ETDRS BCVA of − 1.9, − 3.9, and + 1.3 letters, respectively; additionally, no significant differences were found in absolute ETDRS BCVA across time (ANOVA, p = 0.123). Overall, 90% of eyes maintained VA 20/200 or better and 33.3% of subjects gained at least one line of vision. There were no significant differences in mean central macular thickness for any cohort compared to baseline (p = 0.09). The presence of retinal hemorrhage and intraretinal exudates stayed consistent from year 1 to year 2 for all cohorts.ConclusionsAmong eyes with radiation-related macular edema, a treat-and-extend regimen with ranibizumab may not result in as many visual and anatomic improvements as monthly injections. However, treat-and-extend still may prevent serious visual complications compared to historical controls. Trial registrationClinicalTrials.gov Identifier: NCT02222610 To assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema.PURPOSETo assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema.Forty eyes with radiation-induced macular edema and decreased visual acuity were enrolled in the phase IIb, prospective clinical trial and randomized into 3 cohorts: (A) monthly ranibizumab, (B) monthly ranibizumab with targeted retinal photocoagulation (TRP), or (C) as-needed ranibizumab and TRP. In year 2, all subjects entered a treat-and-extend protocol for ranibizumab. The primary outcome measure was mean change in early treatment diabetic retinopathy study (ETDRS) best-corrected visual acuity (BCVA) from baseline.METHODSForty eyes with radiation-induced macular edema and decreased visual acuity were enrolled in the phase IIb, prospective clinical trial and randomized into 3 cohorts: (A) monthly ranibizumab, (B) monthly ranibizumab with targeted retinal photocoagulation (TRP), or (C) as-needed ranibizumab and TRP. In year 2, all subjects entered a treat-and-extend protocol for ranibizumab. The primary outcome measure was mean change in early treatment diabetic retinopathy study (ETDRS) best-corrected visual acuity (BCVA) from baseline.Through year 1, the mean change in ETDRS BCVA was significantly different between the three cohorts (p < 0.001); cohort A saw the largest gain with + 4.0 letters. Significant anatomic improvements were also seen in all cohorts. Comparatively, through year 2, cohorts A, B, and C had a mean change in ETDRS BCVA of - 1.9, - 3.9, and + 1.3 letters, respectively; additionally, no significant differences were found in absolute ETDRS BCVA across time (ANOVA, p = 0.123). Overall, 90% of eyes maintained VA 20/200 or better and 33.3% of subjects gained at least one line of vision. There were no significant differences in mean central macular thickness for any cohort compared to baseline (p = 0.09). The presence of retinal hemorrhage and intraretinal exudates stayed consistent from year 1 to year 2 for all cohorts.RESULTSThrough year 1, the mean change in ETDRS BCVA was significantly different between the three cohorts (p < 0.001); cohort A saw the largest gain with + 4.0 letters. Significant anatomic improvements were also seen in all cohorts. Comparatively, through year 2, cohorts A, B, and C had a mean change in ETDRS BCVA of - 1.9, - 3.9, and + 1.3 letters, respectively; additionally, no significant differences were found in absolute ETDRS BCVA across time (ANOVA, p = 0.123). Overall, 90% of eyes maintained VA 20/200 or better and 33.3% of subjects gained at least one line of vision. There were no significant differences in mean central macular thickness for any cohort compared to baseline (p = 0.09). The presence of retinal hemorrhage and intraretinal exudates stayed consistent from year 1 to year 2 for all cohorts.Among eyes with radiation-related macular edema, a treat-and-extend regimen with ranibizumab may not result in as many visual and anatomic improvements as monthly injections. However, treat-and-extend still may prevent serious visual complications compared to historical controls.CONCLUSIONSAmong eyes with radiation-related macular edema, a treat-and-extend regimen with ranibizumab may not result in as many visual and anatomic improvements as monthly injections. However, treat-and-extend still may prevent serious visual complications compared to historical controls.ClinicalTrials.gov Identifier: NCT02222610.TRIAL REGISTRATIONClinicalTrials.gov Identifier: NCT02222610. Purpose To assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema. Methods Forty eyes with radiation-induced macular edema and decreased visual acuity were enrolled in the phase IIb, prospective clinical trial and randomized into 3 cohorts: (A) monthly ranibizumab, (B) monthly ranibizumab with targeted retinal photocoagulation (TRP), or (C) as-needed ranibizumab and TRP. In year 2, all subjects entered a treat-and-extend protocol for ranibizumab. The primary outcome measure was mean change in early treatment diabetic retinopathy study (ETDRS) best-corrected visual acuity (BCVA) from baseline. Results Through year 1, the mean change in ETDRS BCVA was significantly different between the three cohorts (p < 0.001); cohort A saw the largest gain with + 4.0 letters. Significant anatomic improvements were also seen in all cohorts. Comparatively, through year 2, cohorts A, B, and C had a mean change in ETDRS BCVA of − 1.9, − 3.9, and + 1.3 letters, respectively; additionally, no significant differences were found in absolute ETDRS BCVA across time (ANOVA, p = 0.123). Overall, 90% of eyes maintained VA 20/200 or better and 33.3% of subjects gained at least one line of vision. There were no significant differences in mean central macular thickness for any cohort compared to baseline (p = 0.09). The presence of retinal hemorrhage and intraretinal exudates stayed consistent from year 1 to year 2 for all cohorts. Conclusions Among eyes with radiation-related macular edema, a treat-and-extend regimen with ranibizumab may not result in as many visual and anatomic improvements as monthly injections. However, treat-and-extend still may prevent serious visual complications compared to historical controls. Trial registration ClinicalTrials.gov Identifier: NCT02222610 |
Author | Yu, Hannah J. Munoz, Jose Anand, Rajiv Fuller, Timothy Moore, Chelsey Schefler, Amy C. Fuller, Dwain Kim, Ryan S. |
Author_xml | – sequence: 1 givenname: Hannah J. surname: Yu fullname: Yu, Hannah J. organization: Retina Consultants of Texas, Retina Consultants of America – sequence: 2 givenname: Dwain surname: Fuller fullname: Fuller, Dwain organization: Texas Retina Associates – sequence: 3 givenname: Rajiv surname: Anand fullname: Anand, Rajiv organization: Texas Retina Associates – sequence: 4 givenname: Timothy surname: Fuller fullname: Fuller, Timothy organization: Texas Retina Associates – sequence: 5 givenname: Jose surname: Munoz fullname: Munoz, Jose organization: Retina Consultants of Texas, Retina Consultants of America – sequence: 6 givenname: Chelsey surname: Moore fullname: Moore, Chelsey organization: Retina Consultants of Texas, Retina Consultants of America – sequence: 7 givenname: Ryan S. surname: Kim fullname: Kim, Ryan S. organization: Retina Consultants of Texas, Retina Consultants of America, McGovern Medical School – sequence: 8 givenname: Amy C. surname: Schefler fullname: Schefler, Amy C. email: acsmd@retinaconsultantstexas.com organization: Retina Consultants of Texas, Retina Consultants of America, Blanton Eye Institute, Houston Methodist Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34463842$$D View this record in MEDLINE/PubMed |
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Contributor | Diugnan, Karen Bretana, Maria E |
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Keywords | Targeted retinal photocoagulation Uveal melanoma Brachytherapy Macular edema Anti-vascular endothelial growth factor Radiation retinopathy |
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References_xml | – reference: HaasAPinterOPapaefthymiouGIncidence of radiation retinopathy after high-dosage single-fraction gamma knife radiosurgery for choroidal melanomaOphthalmology200210990991310.1016/s0161-6420(02)01011-411986096 – reference: BergKPedersenTRSandvikLBragadóttirRComparison of ranibizumab and bevacizumab for neovascular age-related macular degeneration according to LUCAS treat-and-extend protocolOphthalmology201512214615210.1016/j.ophtha.2014.07.04125227499 – reference: SchachatAPRyan’s retina20186New YorkElsevier, Edinburgh – reference: FlaxelCJAdelmanRABaileySTAge-related macular degeneration Preferred Practice Pattern®Ophthalmology2020127P1P6510.1016/j.ophtha.2019.09.02431757502 – reference: WykoffCCOuWCBrownDMRandomized trial of treat-and-extend versus monthly dosing for neovascular age-related macular degenerationOphthalmol Retina2017131432110.1016/j.oret.2016.12.00431047517 – reference: Finger PT, Chin KJ, Duvall G, Palladium-103 for Choroidal Melanoma Study GroupPalladium-103 ophthalmic plaque radiation therapy for choroidal melanoma: 400 treated patientsOphthalmology2009116790–796796.e110.1016/j.ophtha.2008.12.027 – reference: FingerPTChinKJSemenovaEAIntravitreal anti-VEGF therapy for macular radiation retinopathy: a 10-year studyEur J Ophthalmol201626606610.5301/ejo.500067026391167 – reference: MasonJOAlbertMAPersaudTOVailRSIntravitreal bevacizumab treatment for radiation macular edema after plaque radiotherapy for choroidal melanomaRetina Phila Pa20072790390710.1097/IAE.0b013e31806e6042 – reference: KinyounJLLong-term visual acuity results of treated and untreated radiation retinopathy (an AOS thesis)Trans Am Ophthalmol Soc2008106325335192772442646429 – reference: Feder RS, Chuck RS, Dunn SP, et al (2019) Diabetic retinopathy preferred practice pattern – reference: FingerPTChinKJHigh-dose (2.0 mg) intravitreal ranibizumab for recalcitrant radiation retinopathyEur J Ophthalmol20132385085610.5301/ejo.500033323813109 – reference: CraftsTDJensenARBlocher-SmithECMarkelTAVascular endothelial growth factor: therapeutic possibilities and challenges for the treatment of ischemiaCytokine20157138539310.1016/j.cyto.2014.08.00525240960 – reference: FingerPTMukkamalaSKIntravitreal anti-VEGF bevacizumab (Avastin) for external beam related radiation retinopathyEur J Ophthalmol20112144645110.5301/EJO.2011.621321218391 – reference: KimIKLaneAMJainPRanibizumab for the prevention of radiation complications in patients treated with proton beam irradiation for choroidal melanomaTrans Am Ophthalmol Soc2016114T2276303735012854 – reference: KremaHSomaniSSahgalAStereotactic radiotherapy for treatment of juxtapapillary choroidal melanoma: 3-year follow-upBr J Ophthalmol2009931172117610.1136/bjo.2008.15342919414441 – reference: PayneJFWykoffCCClarkWLRandomized trial of treat and extend ranibizumab with and without navigated laser versus monthly dosing for diabetic macular edema: TREX-DME 2-year outcomesAm J Ophthalmol2019202919910.1016/j.ajo.2019.02.00530771333 – reference: PayneJFWykoffCCClarkWLRandomized trial of treat and extend ranibizumab with and without navigated laser for diabetic macular edemaOphthalmology2017124748110.1016/j.ophtha.2016.09.02127836430 – reference: ShieldsCLDalvinLAChangMVisual outcome at 4 years following plaque radiotherapy and prophylactic intravitreal bevacizumab (every 4 months for 2 years) for uveal melanoma: comparison with nonrandomized historical control individualsJAMA Ophthalmol201910.1001/jamaophthalmol.2019.5132317258406990869 – reference: ScheflerACFullerDAnandRRandomized trial of monthly versus as-needed intravitreal ranibizumab for radiation retinopathy-related macular edema: 1 Year OutcomesAm J Ophthalmol202010.1016/j.ajo.2020.03.04532278771 – reference: RamakrishnanSAnandVRoySVascular endothelial growth factor signaling in hypoxia and inflammationJ Neuroimmune Pharmacol Off J Soc NeuroImmune Pharmacol2014914216010.1007/s11481-014-9531-7 – reference: Wykoff CC, Clark WL, Nielsen JS, et al (2018) Optimizing anti-VEGF treatment outcomes for patients with neovascular age-related macular degeneration. J Manag Care Spec Pharm 24:S3–S15. https://doi.org/10.18553/jmcp.2018.24.2-a.s3 – reference: MeliaBMAbramsonDHAlbertDMCollaborative ocular melanoma study (COMS) randomized trial of I-125 brachytherapy for medium choroidal melanoma. I. Visual acuity after 3 years COMS report no. 16Ophthalmology200110834836610.1016/s0161-6420(00)00526-111158813 – reference: BusbeeBGHoACBrownDMTwelve-month efficacy and safety of 0.5 mg or 2.0 mg ranibizumab in patients with subfoveal neovascular age-related macular degenerationOphthalmology20131201046105610.1016/j.ophtha.2012.10.01423352196 – volume: 21 start-page: 446 year: 2011 ident: 5281_CR11 publication-title: Eur J Ophthalmol doi: 10.5301/EJO.2011.6213 – volume: 93 start-page: 1172 year: 2009 ident: 5281_CR3 publication-title: Br J Ophthalmol doi: 10.1136/bjo.2008.153429 – volume: 1 start-page: 314 year: 2017 ident: 5281_CR18 publication-title: Ophthalmol Retina doi: 10.1016/j.oret.2016.12.004 – volume: 71 start-page: 385 year: 2015 ident: 5281_CR8 publication-title: Cytokine doi: 10.1016/j.cyto.2014.08.005 – volume: 26 start-page: 60 year: 2016 ident: 5281_CR13 publication-title: Eur J Ophthalmol doi: 10.5301/ejo.5000670 – volume: 106 start-page: 325 year: 2008 ident: 5281_CR12 publication-title: Trans Am Ophthalmol Soc – volume: 202 start-page: 91 year: 2019 ident: 5281_CR20 publication-title: Am J Ophthalmol doi: 10.1016/j.ajo.2019.02.005 – volume: 120 start-page: 1046 year: 2013 ident: 5281_CR22 publication-title: Ophthalmology doi: 10.1016/j.ophtha.2012.10.014 – volume: 114 start-page: T2 year: 2016 ident: 5281_CR6 publication-title: Trans Am Ophthalmol Soc – volume: 27 start-page: 903 year: 2007 ident: 5281_CR10 publication-title: Retina Phila Pa doi: 10.1097/IAE.0b013e31806e6042 – volume: 116 start-page: 796.e1 issue: 790–796 year: 2009 ident: 5281_CR2 publication-title: Ophthalmology doi: 10.1016/j.ophtha.2008.12.027 – volume: 127 start-page: P1 year: 2020 ident: 5281_CR16 publication-title: Ophthalmology doi: 10.1016/j.ophtha.2019.09.024 – volume-title: Ryan’s retina year: 2018 ident: 5281_CR1 – year: 2019 ident: 5281_CR23 publication-title: JAMA Ophthalmol doi: 10.1001/jamaophthalmol.2019.5132 – ident: 5281_CR15 – volume: 9 start-page: 142 year: 2014 ident: 5281_CR7 publication-title: J Neuroimmune Pharmacol Off J Soc NeuroImmune Pharmacol doi: 10.1007/s11481-014-9531-7 – volume: 122 start-page: 146 year: 2015 ident: 5281_CR17 publication-title: Ophthalmology doi: 10.1016/j.ophtha.2014.07.041 – volume: 109 start-page: 909 year: 2002 ident: 5281_CR4 publication-title: Ophthalmology doi: 10.1016/s0161-6420(02)01011-4 – year: 2020 ident: 5281_CR14 publication-title: Am J Ophthalmol doi: 10.1016/j.ajo.2020.03.045 – volume: 23 start-page: 850 year: 2013 ident: 5281_CR9 publication-title: Eur J Ophthalmol doi: 10.5301/ejo.5000333 – ident: 5281_CR21 doi: 10.18553/jmcp.2018.24.2-a.s3 – volume: 108 start-page: 348 year: 2001 ident: 5281_CR5 publication-title: Ophthalmology doi: 10.1016/s0161-6420(00)00526-1 – volume: 124 start-page: 74 year: 2017 ident: 5281_CR19 publication-title: Ophthalmology doi: 10.1016/j.ophtha.2016.09.021 |
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Snippet | Purpose
To assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema.
Methods
Forty eyes with... To assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema. Forty eyes with radiation-induced... PurposeTo assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema.MethodsForty eyes with... To assess the efficacy of a treat-and-extend strategy with intravitreal ranibizumab for radiation-related macular edema.PURPOSETo assess the efficacy of a... |
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SubjectTerms | Acuity Angiogenesis Inhibitors - therapeutic use Diabetes mellitus Diabetic retinopathy Edema Exudates Eye Hemorrhage Humans Intravitreal Injections Laser Coagulation Macular Edema - diagnosis Macular Edema - drug therapy Macular Edema - etiology Medicine Medicine & Public Health Monoclonal antibodies Ophthalmology Prospective Studies Radiation Ranibizumab - therapeutic use Retina Retinal Disorders Retinopathy Tomography, Optical Coherence Treatment Outcome Vascular Endothelial Growth Factor A Visual Acuity |
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Title | Two-year results for ranibizumab for radiation retinopathy (RRR): a randomized, prospective trial |
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