Department of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Department of Nephrology and Hypertension, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Am J Transplant. 2021 Jul;21(7):2532-2542. doi: 10.1111/ajt.16423. Epub 2020 Dec 22.
Posttransplant lymphoproliferative disorder (PTLD) is a serious complication of solid organ transplantation (SOT). Most PTLD cases are associated with Epstein-Barr virus (EBV) infection. The role of antiviral prophylaxis or rituximab therapy for prevention of PTLD in SOT recipients is controversial. In a nationwide cohort, we assessed the incidence, presentation, and outcome of histologically proven PTLD. We included 4765 patients with a follow-up duration of 23 807 person-years (py). Fifty-seven PTLD cases were identified; 39 (68%) were EBV positive (EBV+ PTLD). Incidence rates for EBV+ PTLD at 1, 2, and 3 years posttransplant were 3.51, 2.24, and 1.75/1000 py and 0.44, 0.25, and 0.29/1000 py for EBV- PTLD. We did not find an effect of antiviral prophylaxis on early and late EBV+ PTLD occurrence (early EBV+ PTLD: SHR 0.535 [95% CI 0.199-1.436], p = .264; late EBV+ PTLD: SHR 2.213, [95% CI 0.751-6.521], p = .150). However, none of the patients (0/191) who received a rituximab-containing induction treatment experienced PTLD, but 57 of 4574 patients without rituximab induction developed PTLD. In an adjusted restricted mean survival time model, PTLD-free survival was significantly longer (0.104 years [95% CI 0.077-0.131]) in patients receiving rituximab as induction treatment. This study provides novel data on the association of rituximab induction and reduced risk for PTLD.
移植后淋巴组织增生性疾病(PTLD)是实体器官移植(SOT)的严重并发症。大多数 PTLD 病例与 EBV 感染有关。抗病毒预防或利妥昔单抗治疗在 SOT 受者中预防 PTLD 的作用存在争议。在一项全国性队列研究中,我们评估了经组织学证实的 PTLD 的发病率、表现和结局。我们纳入了 4765 例患者,随访时间为 23807 人年(py)。确定了 57 例 PTLD 病例;39 例(68%)为 EBV 阳性(EBV+ PTLD)。移植后 1、2 和 3 年时 EBV+ PTLD 的发生率分别为 3.51、2.24 和 1.75/1000 py 和 0.44、0.25 和 0.29/1000 py,对于 EBV- PTLD 则分别为 0.29、0.21 和 0.15/1000 py。我们未发现抗病毒预防对 EBV+ PTLD 的早期和晚期发生有影响(早期 EBV+ PTLD:SHR 0.535[95%CI 0.199-1.436],p=0.264;晚期 EBV+ PTLD:SHR 2.213[95%CI 0.751-6.521],p=0.150)。然而,在接受利妥昔单抗诱导治疗的 191 例患者中(0/191)均未发生 PTLD,而在未接受利妥昔单抗诱导治疗的 4574 例患者中有 57 例发生了 PTLD。在调整后的限制性平均生存时间模型中,接受利妥昔单抗诱导治疗的患者 PTLD 无进展生存时间显著更长(0.104 年[95%CI 0.077-0.131])。本研究提供了利妥昔单抗诱导与降低 PTLD 风险相关的新数据。