van de Laar Stijn C, de Weerd Annelies E, Bemelman Frederike J, Idu Mirza M, de Vries Aiko P J, Alwayn Ian P J, Berger Stefan P, Pol Robert A, van Zuilen Arjan D, Toorop Raechel J, Hilbrands Luuk B, Poyck Paul P C, Christiaans Maarten H L, van Laanen Jorinde H H, van de Wetering Jacqueline, Kimenai Hendrikus J A N, Reinders Marlies E J, Porte Robert J, Dor Frank J M F, Minnee Robert C
Division of HPB and Transplant Surgery, Department of Surgery, Erasmus MC Transplant Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
Imperial College Renal and Transplant Centre, Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, United Kingdom.
Clin J Am Soc Nephrol. 2025 Mar 1;20(3):440-450. doi: 10.2215/CJN.0000000611. Epub 2025 Jan 29.
KEP recipients have comparable long-term graft survival to direct living donor kidney transplantation recipients, which underscores the need to prioritize KEP over other's therapies. Our outcomes can be achieved regardless of whether the donor travels or the graft is transported, offering flexibility in program implementation.
KEPs (kidney exchange programs) facilitate living donor kidney transplantations (LDKTs) for patients with incompatible donors, who are typically at higher risk than non-KEP patients because of higher sensitization and longer dialysis vintage. We conducted a comparative analysis of graft outcomes and risk factors for both KEP and non-KEP living donor kidney transplants.
All LDKTs performed in The Netherlands between 2004 and 2021 were included. The primary outcome measures were 1-, 5-, and 10-year death-censored graft survival. The secondary outcome measures were delayed graft function, graft function, rejection rates, and patient survival. We used a propensity score–matching model to account for differences at baseline.
Of 7536 LDKTs, 694 (9%) were transplanted through the KEP. Ten-year graft survival was similar for KEP (0.916; 95% confidence interval, 0.894 to 0.939) and non-KEP (0.919; 0.912 to 0.926, = 0.82). We found significant differences in 5-year rejection (12% versus 7%) and 5-year patient survival (KEP: 84%, non-KEP: 90%), which was nonsignificant after propensity score matching. Significant risk factors of lower graft survival included high donor age, retransplantations, extended dialysis vintage, higher panel reactive antibodies, and nephrotic syndrome as the cause of ESKD.
Transplantation through KEP offers a viable alternative for patients lacking compatible donors, avoiding specific and invasive pre- and post-transplant treatments. KEP's similar survival rate to non-KEPs suggests prioritizing KEP LDKTs over deceased donor kidney transplantation, desensitization, and dialysis. However, clinicians should consider the identified risk factors when planning and managing pre- and post-transplant care to enhance patient outcomes. Thus, we advocate for the broad adoption of KEP and establishment in regions lacking such programs, alongside initiation and expansion of international collaborations.
肾脏交换计划(KEP)受者的长期移植肾存活率与直接活体供肾移植受者相当,这突出了将KEP置于其他治疗方法之上的必要性。无论供体是否出行或移植肾是否运输,我们都能取得相应结果,这为项目实施提供了灵活性。
肾脏交换计划(KEP)有助于为供体不相容的患者进行活体供肾移植(LDKT),这些患者由于致敏性较高和透析时间较长,通常比非KEP患者面临更高的风险。我们对KEP和非KEP活体供肾移植的移植肾结果及风险因素进行了比较分析。
纳入2004年至2021年在荷兰进行的所有LDKT。主要结局指标为1年、5年和10年的死亡删失移植肾存活率。次要结局指标为移植肾延迟功能、移植肾功能、排斥反应发生率和患者生存率。我们使用倾向评分匹配模型来考虑基线差异。
在7536例LDKT中,694例(9%)通过KEP进行移植。KEP组10年移植肾存活率为0.916(95%置信区间为0.894至0.939),非KEP组为0.919(0.912至0.926,P = 0.82)。我们发现5年排斥反应发生率(12%对7%)和5年患者生存率(KEP组:84%,非KEP组:90%)存在显著差异,倾向评分匹配后差异无统计学意义。移植肾存活率较低的显著风险因素包括供体年龄较大、再次移植、透析时间延长、群体反应性抗体较高以及肾病综合征作为终末期肾病的病因。
对于缺乏相容供体的患者,通过KEP进行移植提供了一种可行的替代方案,避免了特定的、侵入性的移植前和移植后治疗。KEP与非KEP相似的存活率表明,应优先考虑KEP的LDKT,而非尸体供肾移植、脱敏治疗和透析。然而,临床医生在规划和管理移植前和移植后护理时应考虑已确定的风险因素,以提高患者结局。因此,我们主张广泛采用KEP,并在缺乏此类项目的地区建立KEP,同时启动和扩大国际合作。