Zijlstra Josée M, Lindauer-van der Werf Gerda, Hoekstra Otto S, Hooft Lotty, Riphagen Ingrid I, Huijgens Peter C
Department of Hematology, VU University Medical Center, 1007 MB Amsterdam, The Netherlands.
Haematologica. 2006 Apr;91(4):522-9.
Despite the increasing number of publications concerning 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) for post-treatment evaluation of lymphoma and the increasing availability of this novel diagnostic modality, its exact role in response assessment after therapy is still unknown. The aim of this study was to systematically review the literature regarding the diagnostic performance of dedicated FDG-PET in evaluation of first-line therapy of Hodgkin's disease and (aggressive) non-Hodgkin's lymphoma, and to calculate summary estimates of its sensitivity and specificity. The databases of PubMed and Embase were searched for relevant studies up to January 2004. Two reviewers independently assessed the methodological quality of each study. As a valid reference test, histology or follow-up of at least 12 months were accepted. A meta-analysis of the reported sensitivity and specificity of each study was performed. Fifteen studies, involving 705 patients, met the inclusion criteria. The studies had several design deficiencies. The majority of studies did not describe whether the reference test was interpreted without knowledge of the FDG-PET findings. In all studies, there was a description of the spectrum of patients included, i.e. all patients for post-treatment evaluation or only patients with substantial residual masses post-treatment. Pooled sensitivity and specificity for detection of residual disease in Hodgkin's lymphoma were 84% (95% CI 71-9192%) and 90% (95% CI 84-9394%), respectively. For non-Hodgkin's lymphoma, pooled sensitivity and specificity were 72% (95% CI 61-82%), and 100% (95% CI 97-100%), respectively. FDG-PET showed reasonable sensitivity and high specificity for evaluation of first-line therapy in Hodgkin's and in non-Hodgkin's lymphoma. Standardization of procedures is required before implementation in clinical practice.
尽管有关18F-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)用于淋巴瘤治疗后评估的出版物数量不断增加,且这种新型诊断方式的可及性也日益提高,但其在治疗反应评估中的确切作用仍不明确。本研究的目的是系统回顾关于专用FDG-PET在霍奇金病和(侵袭性)非霍奇金淋巴瘤一线治疗评估中的诊断性能的文献,并计算其敏感性和特异性的汇总估计值。检索了PubMed和Embase数据库中截至2004年1月的相关研究。两名研究者独立评估每项研究的方法学质量。作为有效的参考标准,接受组织学检查或至少12个月的随访。对每项研究报告的敏感性和特异性进行荟萃分析。15项研究,涉及705例患者,符合纳入标准。这些研究存在一些设计缺陷。大多数研究未描述参考标准的解读是否在不知FDG-PET结果的情况下进行。在所有研究中,均描述了纳入患者的范围,即所有用于治疗后评估的患者或仅治疗后有大量残留肿块的患者。霍奇金淋巴瘤中检测残留疾病的汇总敏感性和特异性分别为84%(95%CI 71-9192%)和90%(95%CI 84-9394%)。对于非霍奇金淋巴瘤,汇总敏感性和特异性分别为72%(95%CI 61-82%)和100%(95%CI 97-100%)。FDG-PET在霍奇金淋巴瘤和非霍奇金淋巴瘤一线治疗评估中显示出合理的敏感性和高特异性。在临床实践中实施之前需要进行程序标准化。