{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,24]],"date-time":"2026-10-24T23:11:37Z","timestamp":1792883497111,"version":"4.5.0"},"reference-count":33,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["CJASN"],"published-print":{"date-parts":[[2016,5]]},"abstract":"<jats:sec>\n                    <jats:title>Background and objectives<\/jats:title>\n                    <jats:p>The effect of mammalian target of rapamycin (mTOR) inhibitors has never been tested in patients with autosomal dominant polycystic kidney disease (ADPKD) and severe renal insufficiency.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design, setting, participants, &amp; measurements<\/jats:title>\n                    <jats:p>\n                      In this academic, prospective, randomized, open label, blinded end point, parallel group trial (ClinicalTrials.gov no. NCT01223755), 41 adults with ADPKD, CKD stage 3b or 4, and proteinuria \u22640.5 g\/24 h were randomized between September of 2010 and March of 2012 to sirolimus (3 mg\/d; serum target levels of 5\u201310 ng\/ml) added on to conventional therapy (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      =21) or conventional treatment alone (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      =20). Primary outcome was GFR (iohexol plasma clearance) change at 1 and 3 years versus baseline.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      At the 1-year preplanned interim analysis, GFR fell from 26.7\u00b15.8 to 21.3\u00b16.3 ml\/min per 1.73 m\n                      <jats:sup>2<\/jats:sup>\n                      (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001) and from 29.6\u00b15.6 to 24.9\u00b16.2 ml\/min per 1.73 m\n                      <jats:sup>2<\/jats:sup>\n                      (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001) in the sirolimus and conventional treatment groups, respectively. Albuminuria (73.8\u00b181.8 versus 154.9\u00b1152.9\n                      <jats:italic toggle=\"yes\">\u03bc<\/jats:italic>\n                      g\/min;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.02) and proteinuria (0.3\u00b10.2 versus 06\u00b10.4 g\/24 h;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.01) increased with sirolimus. Seven patients on sirolimus versus one control had\n                      <jats:italic toggle=\"yes\">de novo<\/jats:italic>\n                      proteinuria (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.04), ten versus three patients doubled proteinuria (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.02), 18 versus 11 patients had peripheral edema (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.04), and 14 versus six patients had upper respiratory tract infections (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.03). Three patients on sirolimus had angioedema, 14 patients had aphthous stomatitis, and seven patients had acne (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.01 for both versus controls). Two patients progressed to ESRD, and two patients withdrew because of worsening of proteinuria. These events were not observed in controls. Thus, the independent data and safety monitoring board recommend early trial termination for safety reasons. At 1 year, total kidney volume (assessed by contrast\u2013enhanced computed tomography imaging) increased by 9.0% from 2857.7\u00b11447.3 to 3094.6\u00b11519.5 ml on sirolimus and 4.3% from 3123.4\u00b11695.3 to 3222.6\u00b11651.4 ml on conventional therapy (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.12). On follow-up, 37% and 7% of serum sirolimus levels fell below or exceeded the therapeutic range, respectively.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Finding that sirolimus was unsafe and ineffective in patients with ADPKD and renal insufficiency suggests that mTOR inhibitor therapy may be contraindicated in this context.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.2215\/cjn.09900915","type":"journal-article","created":{"date-parts":[[2016,2,22]],"date-time":"2016-02-22T22:34:06Z","timestamp":1456180446000},"page":"785-794","source":"Crossref","is-referenced-by-count":41,"title":["Effect of Sirolimus on Disease Progression in Patients with Autosomal Dominant Polycystic Kidney Disease and CKD Stages 3b-4"],"prefix":"10.2215","volume":"11","author":[{"given":"Piero","family":"Ruggenenti","sequence":"first","affiliation":[{"name":"Clinical 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