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©The Author(s) 2018.
World J Transplantation. Sep 10, 2018; 8(5): 150-155
Published online Sep 10, 2018. doi: 10.5500/wjt.v8.i5.150
Published online Sep 10, 2018. doi: 10.5500/wjt.v8.i5.150
Ref. | No. of subjects/follow-up | EVLtreatment | Groups | Outcomes |
ASCERTAIN[17] (2011) | 394/2 yr | Conversion to EVL with CNI elimination or minimization at mean of 5.6 yr | Gp 1: CNI elimination (EVL C0, 8-12 ng/mL), n = 127 Gp 2: CNI minimization (EVL C0, 3-8 ng/mL and CNI reduced to 80%-90% below baseline), n = 144 Gp 3: control (CsA C2, > 400 ng/mL; Tac C0, > 4 ng/mL), n = 123 | Graft survival: 96.9%, 94.6%, 95.1% (P = NS) Patient survival: 97.6%, 97.1%, 100% (P = NS) Comparable eGFR in 3 groups; recipients with baseline CrCl > 50 mL/min had greater increase in measured GFR after CNI elimination Adverse events resulted in discontinuation: 28.3%, 16.7%, 4.1% (Gp 1 vs GP 3, P < 0.001; Gp 2 vs Gp 3, P = 0.020) |
APOLLO[18] (2015) | 93/1 yr | Conversion from CNI to EVL at mean of 7 yr | Gp 1: CNI elimination (EVL C0, 6-10 ng/mL), n = 46 Gp 2: control (CsA C0, 80-150 ng/mL; Tac C0, 5-10 ng/mL), n = 47 | Graft survival: 100%, 100% Patient survival: 97.8%, 97.9% (P = NS) Adjusted eGFR was significantly higher in Gp 1 within on-treatment population Adverse events resulted in discontinuation: 32.6%, 10.6% (P < 0.01) |
Ref. | No. of subjects/follow-up | EVL treatment | Outcomes |
Morales et al[20] (2007)/ retrospective | 8/1-16 mo | Conversion to EVL with CNI elimination or reduction at mean of 5 yr | CrCl increased by 42% in recipients with CAN (grade 1 or 2) and CNI nephrotoxicity (P = 0.017) |
Sanchez-Fructuoso et al[21] (2012)/ retrospective | 220/1 yr | Conversion from CNI to EVL at mean of 69.4 mo | CrCl increased in recipients with baseline CrCl ≥ 40 mL/min and baseline proteinuria < 550 mg/d (P = 0.005) Median proteinuria increased from 304 mg/d to 458 mg/d (P < 0.001) EVL discontinuation rate was 24% |
Chow et al[22] (2015)/ open-label, single arm | 17/1 yr | Conversion to EVL with CNI minimization in recipients with CAN at mean of 4.2 yr | Mean slope of eGFR was - 4.31 mL/min/1.73 m2 per yr before conversion, as compared with 1.29 mL/min/1.73 m2 per yr at 12 mo after conversion (P = 0.036) Renal biopsy showed significant decrease of tubular atrophy (15.7% vs 7.1%, P = 0.005) and interstitial fibrosis (14.8% vs 7.2%, P = 0.013) |
Miura et al[23] (2015)/ retrospective | 13/1 yr | Conversion to EVL with Tac reduction in recipients with CNIA at mean of 43 mo | aah scores improved in 5 recipients (38%); No improvement was observed in recipients with aah3; No deterioration was observed. eGFR improved from 44.3 mL/min/1.73 m2 to 49.8 mL/min/1.73 m2 (P < 0.01). |
Uchida et al[24] (2016)/ retrospective (our report) | 26/1 yr | Conversion from antimetabolites (MMF or MZ) to EVL with CNI minimization at mean of 39.5 mo | eGFR significantly increased from 50.7 mL/min/1.73 m2 to 53.6 mL/min/1.73 m2 in the EVL continuation group EVL discontinuation rate was 42.3% |
Nojima et al[25] (2017)/ retrospective | 56/1 yr | Conversion to EVL with CNI reduction in recipients with CNI nephrotoxicity or IF/TA at mean of 7.4 yr | eGFR increased by 7% (P < 0.005) EVL discontinuation rate was 11% |
Nanmoku et al[26] (2017)/ nonrandomized | 86/ 1 yr | Conversion to EVL with Tac minimization, MMF reduction and steroid withdrawal in cases of complications such as diabetes, viral infection etc | Conventional group (n = 50); EVL group (n = 36) Biopsy-proven acute rejection rate exhibited no significant difference between these groups (12% vs 17%, P = 0.55) Serum creatinine significantly improved in the EVL group (P = 0.031) EVL discontinuation rate was 13.8% |
Advantage | Disadvantage |
Due to EVL introduction Antitumoral effect (especially on nonmelanoma skin carcinoma) Antiviral effect (especially on CMV and BKV infection) Antiproliferative effect Antiatherosclerotic effect | Due to EVL introduction Adverse events (gastrointestinal disorders, hyperlipidemia, interstitial pneumonitis, edema, mouth ulcers, proteinuria, impaired wound healing, hematotoxicity and so on) |
Due to CNI elimination or minimization Favorable graft function | Due to CNI elimination or minimization Risk of de novo DSA |
- Citation: Uchida J, Iwai T, Nakatani T. Introduction of everolimus in kidney transplant recipients at a late posttransplant stage. World J Transplantation 2018; 8(5): 150-155
- URL: https://www.wjgnet.com/2220-3230/full/v8/i5/150.htm
- DOI: https://dx.doi.org/10.5500/wjt.v8.i5.150