a Department of Nuclear Medicine and Molecular Imaging , University Hospitals Leuven , Leuven , Belgium.
b Department of Haematology , University Hospitals Leuven , Leuven , Belgium.
Acta Oncol. 2019 Jul;58(7):1041-1047. doi: 10.1080/0284186X.2019.1598622. Epub 2019 Apr 29.
Fluorine-18-fluorodeoxyglucose positron emission tomography (PET) has an established and central role in diagnosis, staging and response evaluation of lymphoproliferative diseases. It has shown a high sensitivity and specificity at diagnosis in posttransplant lymphoproliferative disorders (PTLDs). However, little is known about the performance of interim and end of treatment (EOT) PET in PTLD patients with regards to response assessment, relapse prediction and outcome. We performed a single-center retrospective study in which we analyzed consecutive patients diagnosed with CD20-positive PTLD after solid organ transplantation between 2008 and 2017, who all received risk-stratified sequential treatment according to the PTLD-1 phase II trial. Interim and EOT PET studies were scored according to the Deauville criteria. Forty-one patients were included with median follow-up of 41.5 months (range 1-108). Positive and negative predictive values for disease recurrence were 13% and 85% for interim and 33% and 87% for EOT PET, respectively. There was no significant difference in overall survival, progression-free survival nor time to progression between negative versus positive patients on interim and EOT scans. Negative interim and/or negative end of treatment PET identify PTLD patients with low risk of disease recurrence.
氟-18-氟代脱氧葡萄糖正电子发射断层扫描(PET)在淋巴增生性疾病的诊断、分期和反应评估中具有既定且核心的作用。它在移植后淋巴增生性疾病(PTLD)的诊断中显示出较高的敏感性和特异性。然而,对于 PTLD 患者的中期和治疗结束(EOT)PET 在反应评估、复发预测和结果方面的性能知之甚少。我们进行了一项单中心回顾性研究,分析了 2008 年至 2017 年间在实体器官移植后诊断为 CD20 阳性 PTLD 的连续患者,他们均根据 PTLD-1 二期试验接受了分层的序贯治疗。中期和 EOT PET 研究根据 Deauville 标准进行评分。共纳入 41 例患者,中位随访时间为 41.5 个月(范围 1-108)。中期和 EOT PET 的疾病复发阳性和阴性预测值分别为 13%和 85%、33%和 87%。中期和 EOT 扫描阴性的患者与阳性患者在总生存、无进展生存或进展时间方面没有显著差异。阴性的中期和/或阴性的 EOT PET 可识别出复发风险较低的 PTLD 患者。