Tsuchimoto Akihiro, Masutani Kosuke, Omoto Kazuya, Okumi Masayoshi, Okabe Yasuhiro, Nishiki Takehiro, Ota Morihito, Nakano Toshiaki, Tsuruya Kazuhiko, Kitazono Takanari, Nakamura Masafumi, Ishida Hideki, Tanabe Kazunari
Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Division of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Clin Exp Nephrol. 2019 Apr;23(4):561-568. doi: 10.1007/s10157-018-1672-1. Epub 2018 Dec 24.
The safety of kidney transplantation (KT) for end-stage kidney disease (ESKD) after haematopoietic stem cell transplantation (HSCT) for haematological disease has not been investigated thoroughly.
In this retrospective multicentre study, we investigated the clinical courses of six ESKD patients that received KT after HSCT for various haematological diseases. Data for six such patients were obtained from three institutions in our consortium.
Two patients with chronic myeloid leukaemia, one with refractory aplastic anaemia and another one with acute lymphocytic leukaemia received bone marrow transplantation. One patients with acute lymphocytic leukaemia received umbilical cord blood transplantation, and one with mantle cell lymphoma received peripheral blood stem cell transplantation. The patients developed ESKD at a median of 133 months after HSCT. Two patients who received KT and HSCT from the same donor were temporarily treated with immunosuppressive drugs. The other patients received KT and HSCT from different donors and were treated with antibody induction using our standard regimens. For one patient with ABO-incompatible transplantation, we added rituximab, splenectomy, and plasmapheresis. In the observational period at a median of 51 months after KT, only one patient experienced acute T-cell-mediated rejection. Four patients underwent hospitalization because of infection and fully recovered. No patient experienced recurrence of their original haematological disease. All patients survived throughout the observational periods, and graft functions were preserved.
Despite the high infection frequency, survival rates and graft functions were extremely good in patients compared with previous studies. Therefore, current management contributed to favourable outcomes of these patients.
血液系统疾病造血干细胞移植(HSCT)后终末期肾病(ESKD)患者进行肾移植(KT)的安全性尚未得到充分研究。
在这项回顾性多中心研究中,我们调查了6例因各种血液系统疾病在HSCT后接受KT的ESKD患者的临床病程。这6例患者的数据来自我们联盟中的三个机构。
2例慢性髓性白血病患者、1例难治性再生障碍性贫血患者和另1例急性淋巴细胞白血病患者接受了骨髓移植。1例急性淋巴细胞白血病患者接受了脐带血移植,1例套细胞淋巴瘤患者接受了外周血干细胞移植。患者在HSCT后中位133个月出现ESKD。2例从同一供体接受KT和HSCT的患者接受了短期免疫抑制药物治疗。其他患者从不同供体接受KT和HSCT,并采用我们的标准方案进行抗体诱导治疗。对于1例ABO血型不相容移植患者,我们加用了利妥昔单抗、脾切除术和血浆置换术。在KT后中位51个月的观察期内,仅1例患者发生了急性T细胞介导的排斥反应。4例患者因感染住院并完全康复。无患者出现原血液系统疾病复发。所有患者在整个观察期内存活,移植肾功能得以保留。
尽管感染发生率较高,但与以往研究相比,患者的生存率和移植肾功能非常良好。因此,目前的治疗方法有助于这些患者获得良好的预后。