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肝移植后移植后淋巴组织增生性疾病:发病率、长期生存率及血清他克莫司水平的影响

Post-transplant lymphoproliferative disorder after liver transplantation: Incidence, long-term survival and impact of serum tacrolimus level.

作者信息

Eshraghian Ahad, Imanieh Mohammad Hadi, Dehghani Seyed Mohsen, Nikeghbalian Saman, Shamsaeefar Alireza, Barshans Frouzan, Kazemi Kourosh, Geramizadeh Bita, Malek-Hosseini Seyed Ali

机构信息

Ahad Eshraghian, Mohammad Hadi Imanieh, Seyed Mohsen Dehghani, Saman Nikeghbalian, Alireza Shamsaeefar, Kourosh Kazemi, Bita Geramizadeh, Seyed Ali Malek-Hosseini, Transplant Research Center, Shiraz University of Medical Sciences, Shiraz 71937-11351, Iran.

出版信息

World J Gastroenterol. 2017 Feb 21;23(7):1224-1232. doi: 10.3748/wjg.v23.i7.1224.

Abstract

AIM

To investigate incidence and survival of post-transplant lymphoproliferative disorder (PTLD) patients after liver transplantation.

METHODS

A cross-sectional survey was conducted among patients who underwent liver transplantation at Shiraz Transplant Center (Shiraz, Iran) between August 2004 and March 2015. Clinical and laboratory data of patients were collected using a data gathering form.

RESULTS

There were 40 cases of PTLD in the pediatric age group and 13 cases in the adult group. The incidence of PTLD was 6.25% in pediatric patients and 1.18% in adult liver transplant recipients. The post-PTLD survival of patients at 6 mo was 75.1% ± 6%, at 1 year was 68.9% ± 6.5% and at 5 years was 39.2% ± 14.2%. Higher serum tacrolimus level was associated with lower post-PTLD survival in pediatric patients (OR = 1.07, 95%CI: 1.006-1.15, = 0.032). A serum tacrolimus level over 11.1 ng/mL was predictive of post PTLD survival (sensitivity = 90%, specificity = 52%, area under the curve = 0.738, = 0.035).

CONCLUSION

Incidence of PTLD in our liver transplant patients is comparable to other centers. Transplant physicians may consider adjustment of tacrolimus dose to maintain its serum level below this cutoff point.

摘要

目的

研究肝移植术后移植后淋巴细胞增生性疾病(PTLD)患者的发病率及生存率。

方法

对2004年8月至2015年3月期间在设拉子移植中心(伊朗设拉子)接受肝移植的患者进行横断面调查。使用数据收集表收集患者的临床和实验室数据。

结果

儿童年龄组有40例PTLD患者,成人组有13例。儿童患者PTLD的发病率为6.25%,成人肝移植受者为1.18%。PTLD患者6个月时的生存率为75.1%±6%,1年时为68.9%±6.5%,5年时为39.2%±14.2%。儿童患者较高的他克莫司血清水平与PTLD后较低的生存率相关(OR = 1.07,95%CI:1.006 - 1.15,P = 0.032)。他克莫司血清水平超过11.1 ng/mL可预测PTLD后的生存率(敏感性 = 90%,特异性 = 52%,曲线下面积 = 0.738,P = 0.035)。

结论

我们肝移植患者中PTLD的发病率与其他中心相当。移植医生可考虑调整他克莫司剂量,以使其血清水平维持在该临界值以下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c368/5323447/2437718c176c/WJG-23-1224-g001.jpg

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