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        <datestamp>2026-09-29T15:38:49Z</datestamp>
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          <dc:title>Extended-release naltrexone versus buprenorphine-naloxone for opioid use disorder: a systematic review and meta-analysis of randomized controlled trials</dc:title>
          <dc:creator>Alper Mert (24653976)</dc:creator>
          <dc:creator>Duhan Kılıçkan (24654680)</dc:creator>
          <dc:creator>Maria Luiza Rodrigues Defante (20468225)</dc:creator>
          <dc:creator>Samuel Izaias dos Santos Pereira (25137700)</dc:creator>
          <dc:creator>Otavio André Farias Sousa da Silva (24654686)</dc:creator>
          <dc:creator>Jussi Jokinen (569241)</dc:creator>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Science Policy</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Opioid use disorder</dc:subject>
          <dc:subject>Extended-release naltrexone</dc:subject>
          <dc:subject>Buprenorphine-naloxone</dc:subject>
          <dc:subject>addiction</dc:subject>
          <dc:subject>Meta-analysis</dc:subject>
          <dc:description>&lt;p&gt;&lt;i&gt;Background:&lt;/i&gt; Extended-release naltrexone (XR-NTX) and buprenorphine-naloxone (BUP-NLX) are approved for opioid use disorder (OUD), but their comparative efficacy and safety are unclear.&lt;/p&gt; &lt;p&gt;&lt;i&gt;Objectives:&lt;/i&gt; We conducted a systematic review and meta-analysis of randomized controlled trials (RCTs) comparing XR-NTX and BUP-NLX.&lt;/p&gt; &lt;p&gt;&lt;i&gt;Methods:&lt;/i&gt; PubMed, Embase, and Cochrane were searched from inception to July 2025. Main efficacy outcomes were treatment initiation, retention, time to relapse, number of relapses, opioid-positive urine samples, and self-reported opioid use days. Odds ratios (OR), mean differences (MD), and hazard ratios (HR) with 95% confidence intervals (CI) were calculated. Heterogeneity was assessed with I&lt;sup&gt;2&lt;/sup&gt; and evidence certainty rated with GRADE.&lt;/p&gt; &lt;p&gt;&lt;i&gt;Results:&lt;/i&gt; Five RCTs comprising 1,043 patients (68.2% male; XR-NTX, &lt;i&gt;n&lt;/i&gt; = 512; BUP-NLX, &lt;i&gt;n&lt;/i&gt; = 531) were included. Treatment initiation was lower with XR-NTX (OR 0.27; 95% CI 0.12–0.64; &lt;i&gt;p&lt;/i&gt; = .003; I&lt;sup&gt;2&lt;/sup&gt; = 67.6%). There were no differences in treatment retention (OR 0.85; 95% CI 0.65–1.11; &lt;i&gt;p&lt;/i&gt; = .25; I&lt;sup&gt;2&lt;/sup&gt; = 0%). XR-NTX was associated with a significantly lower proportion of opioid-positive urine samples (OR 0.52; 95% CI 0.38–0.73; &lt;i&gt;p&lt;/i&gt; &lt; .001; I&lt;sup&gt;2&lt;/sup&gt; = 0%). There were no differences in relapse (OR 0.60; 95% CI 0.21–1.73; &lt;i&gt;p&lt;/i&gt; = .35; I&lt;sup&gt;2&lt;/sup&gt; = 89.9%), opioid use days in 30 days (MD − 0.99; 95% CI − 3.62 to 1.64; &lt;i&gt;p&lt;/i&gt; = .46; I&lt;sup&gt;2&lt;/sup&gt; = 63.8%), or adverse events.&lt;/p&gt; &lt;p&gt;&lt;i&gt;Conclusion:&lt;/i&gt; XR-NTX and BUP-NLX did not differ across most outcomes, though initiation was lower with XR-NTX and evidence certainty was very low to moderate. With neither clearly superior, initiating either treatment may matter most.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-29T15:38:49Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.6084/m9.figshare.33340427.v2</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Extended-release_naltrexone_versus_buprenorphine-naloxone_for_opioid_use_disorder_a_systematic_review_and_meta-analysis_of_randomized_controlled_trials/33340427</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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