<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Prünte C</dc:creator>
  <dc:creator>Fajnkuchen F</dc:creator>
  <dc:creator>Mahmood S</dc:creator>
  <dc:creator>Ricci F</dc:creator>
  <dc:creator>Hatz K</dc:creator>
  <dc:creator>Studnička J</dc:creator>
  <dc:creator>Bezlyak V</dc:creator>
  <dc:creator>Parikh S</dc:creator>
  <dc:creator>Stubbings WJ</dc:creator>
  <dc:creator>Wenzel A</dc:creator>
  <dc:creator>Figueira J</dc:creator>
  <dc:date>2016</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">AIMS
To demonstrate non-inferiority of ranibizumab treat-and-extend (T&amp;E) with/without laser to ranibizumab pro re nata (PRN) for best-corrected visual acuity (BCVA) in patients with diabetic macular oedema (DMO).


METHODS
A 24-month single-masked study with patients randomised 1:1:1 to T&amp;E+laser (n=121), T&amp;E (n=128) or PRN (control; n=123). All patients received monthly injections until BCVA stabilisation. The investigator decided on re-treatment in the PRN and treatment-interval adaptations in the T&amp;E groups based on loss of BCVA stability due to DMO activity. Likewise, laser treatment was at investigator's discretion. Collectively, these features reflect a real-life scenario. Endpoints included mean average change in BCVA from baseline to months 1-12 (primary), mean BCVA change from baseline to months 12 and 24, treatment exposure and safety profile.


RESULTS
Both T&amp;E regimens were non-inferior to PRN based on mean average BCVA change from baseline to months 1-12 (T&amp;E+laser: +5.9 and T&amp;E: +6.1 vs PRN: +6.2 letters; both p&lt;0.0001). Mean BCVA change at month 24 was similar across groups (+8.3, +6.5 and +8.1 letters, respectively). The mean number of injections was 12.4 and 12.8 in the T&amp;E+laser and T&amp;E groups and 10.7 in the PRN group. The T&amp;E regimens showed 46% reduction in the number of clinic visits. Over 70% of patients maintained their BCVA, with treatment intervals of ≥2 months over 24 months. Safety profile was consistent with that described in the product information.


CONCLUSIONS
T&amp;E is a feasible treatment option for patients with DMO, with a potential to reduce treatment burden. Slightly more injections were required versus PRN, likely due to the specifics of the T&amp;E regimen applied here.


TRIAL REGISTRATION NUMBER
NCT01171976.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/299182</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1136/bjophthalmol-2015-307249</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/26453639</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>The British journal of ophthalmology. - 2016</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Clinical Trial</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Macula</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Treatment Lasers</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Treatment Medical</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Vision</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Angiogenesis Inhibitors</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Diabetic Retinopathy</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Dose-Response Relationship, Drug</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Female</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Follow-Up Studies</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Intravitreal Injections</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Macula Lutea</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Macular Edema</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Male</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Middle Aged</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Ranibizumab</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Retrospective Studies</dc:subject>
  <dc:subject xmlns:ns19="xml" ns19:lang="en">Single-Blind Method</dc:subject>
  <dc:subject xmlns:ns20="xml" ns20:lang="en">Time Factors</dc:subject>
  <dc:subject xmlns:ns21="xml" ns21:lang="en">Tomography, Optical Coherence</dc:subject>
  <dc:subject xmlns:ns22="xml" ns22:lang="en">Treatment Outcome</dc:subject>
  <dc:subject xmlns:ns23="xml" ns23:lang="en">Vascular Endothelial Growth Factor A</dc:subject>
  <dc:subject xmlns:ns24="xml" ns24:lang="en">Visual Acuity</dc:subject>
  <dc:title xmlns:ns25="xml" ns25:lang="en">Ranibizumab 0.5 mg treat-and-extend regimen for diabetic macular oedema: the RETAIN study.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
