Rationale and design of the OPTIMIZE trial: OPen label multicenter randomized trial comparing standard IMmunosuppression with tacrolimus and mycophenolate mofetil with a low exposure tacrolimus regimen In combination with everolimus in de novo renal transplantation in Elderly patients

被引:11
作者
de Boer, S. E. [1 ]
Sanders, J. S. F. [1 ]
Bemelman, F. J. [2 ]
Betjes, M. G. H. [3 ]
Burgerhof, J. G. M. [4 ]
Hilbrands, L. [5 ]
Kuypers, D. [6 ]
van Munster, B. C. [7 ]
Nurmohamed, S. A. [2 ]
de Vries, A. P. J. [8 ,9 ]
van Zuilen, A. D. [10 ]
Hesselink, D. A. [3 ]
Berger, S. P. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Div Nephrol, Groningen, Netherlands
[2] Univ Amsterdam, Dept Internal Med, Div Nephrol, Med Ctr, Amsterdam, Netherlands
[3] Erasmus MC, Dept Internal Med, Div Nephrol & Transplantat, Erasmus MC, Rotterdam, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
[5] Radboud Univ Nijmegen, Dept Internal Med, Div Nephrol, Med Ctr, Nijmegen, Netherlands
[6] Univ Hosp Leuven, Dept Nephrol & Renal Transplantat, Leuven, Belgium
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Div Geriatr, Groningen, Netherlands
[8] Leiden Univ, Div Nephrol, Dept Internal Med, Leiden Univ Med Ctr, Leiden, Netherlands
[9] Leiden Univ, Leiden Transplant Ctr, Leiden, Netherlands
[10] Univ Med Ctr Utrecht, Dept Internal Med, Div Nephrol, Utrecht, Netherlands
关键词
Elderly kidney transplant recipients; Reduced CNI exposure; mTOR inhibitor; Everolimus; (Health-related) quality of life; Patient-reported outcomes; Frailty; Immunosenescence; Randomized clinical trial; Multicenter trial; T-CELLS; RECIPIENTS;
D O I
10.1186/s12882-021-02409-8
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
BackgroundIn 2019, more than 30% of all newly transplanted kidney transplant recipients in The Netherlands were above 65 years of age. Elderly patients are less prone to rejection, and death censored graft loss is less frequent compared to younger recipients. Elderly recipients do have increased rates of malignancy and infection-related mortality. Poor kidney transplant function in elderly recipients may be related to both pre-existing (i.e. donor-derived) kidney damage and increased susceptibility to nephrotoxicity of calcineurin inhibitors (CNIs) in kidneys from older donors. Hence, it is pivotal to shift the focus from prevention of rejection to preservation of graft function and prevention of over-immunosuppression in the elderly. The OPTIMIZE study will test the hypothesis that reduced CNI exposure in combination with everolimus will lead to better kidney transplant function, a reduced incidence of complications and improved health-related quality of life for kidney transplant recipients aged 65 years and older, compared to standard immunosuppression.MethodsThis open label, randomized, multicenter clinical trial will include 374 elderly kidney transplant recipients (>= 65 years) and consists of two strata. Stratum A includes elderly recipients of a kidney from an elderly deceased donor and stratum B includes elderly recipients of a kidney from a living donor or from a deceased donor<65 years. In each stratum, subjects will be randomized to a standard, tacrolimus-based immunosuppressive regimen with mycophenolate mofetil and glucocorticoids or an adapted immunosuppressive regimen with reduced CNI exposure in combination with everolimus and glucocorticoids. The primary endpoint is 'successful transplantation', defined as survival with a functioning graft and an eGFR<greater than or equal to>30 ml/min per 1.73 m(2) in stratum A and >= 45 ml/min per 1.73 m(2) in stratum B, after 2 years, respectively.ConclusionsThe OPTIMIZE study will help to determine the optimal immunosuppressive regimen after kidney transplantation for elderly patients and the cost-effectiveness of this regimen. It will also provide deeper insight into immunosenescence and both subjective and objective outcomes after kidney transplantation in elderly recipients.Trial registrationClinicalTrials.gov: NCT03797196, registered January 9th, 2019. EudraCT: 2018-003194-10, registered March 19th, 2019.
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页数:10
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