Jerusalem G, Beguin Y, Fassotte M F, Najjar F, Paulus P, Rigo P, Fillet G
Department of Medicine, Divisions of Oncology-Hematology and Nuclear Medicine, University of Liège, Liège, Belgium.
Blood. 1999 Jul 15;94(2):429-33.
A residual mass after treatment of lymphoma is a clinical challenge, because it may represent vital tumor as well as tissue fibrosis. Metabolic imaging by 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) offers the advantage of functional tissue characterization that is largely independent of morphologic criteria. We compared 18F-FDG PET to computed tomography (CT) in the posttreatment evaluation of 54 patients with Hodgkin's disease (HD) or intermediate/high-grade non-Hodgkin's lymphoma (NHL). Residual masses on CT were observed in 13 of 19 patients with HD and 11 of 35 patients with NHL. Five of 24 patients with residual masses on CT versus 1 of 30 patients without residual masses presented a positive 18F-FDG PET study. Relapse occurred in all 6 patients (100%) with a positive 18F-FDG PET, 5 of 19 patients (26%) with residual masses on CT but negative 18F-FDG PET, and 3 of 29 patients (10%) with negative CT scan and 18F-FDG PET studies (P </=.0001). We observed a higher relapse and death rate in patients with residual masses at CT compared with patients without residual masses at CT (progression-free survival at 1 year: 62 +/- 10 v 88 +/- 7%, P =. 0045; overall survival at 1 year: 77 +/- 5 v 95 +/- 5%, P =.0038). A positive 18F-FDG PET study was even more consistently associated with poorer survival: compared with patients with a negative 18F-FDG PET study, the 1-year progression-free survival was 0% versus 86% +/- 5% (P <.0001) and the 1-year overall survival was 50% +/- 20% versus 92% +/- 4% (P <.0001). The detection of vital tumor by 18F-FDG PET after the end of treatment has a higher predictive value for relapse than classical CT scan imaging (positive predictive value: 100% v 42%). This could help identify patients requiring intensification immediately after completion of chemotherapy. However, 18F-FDG PET mainly predicts for early progression but cannot exclude the presence of minimal residual disease, possibly leading to a later relapse.
淋巴瘤治疗后的残留肿块是一项临床挑战,因为它可能代表存活肿瘤以及组织纤维化。18F-氟脱氧葡萄糖(18F-FDG)正电子发射断层扫描(PET)进行的代谢成像具有功能组织特征化的优势,很大程度上独立于形态学标准。我们在54例霍奇金病(HD)或中/高度非霍奇金淋巴瘤(NHL)患者的治疗后评估中,将18F-FDG PET与计算机断层扫描(CT)进行了比较。19例HD患者中有13例以及35例NHL患者中有11例在CT上观察到残留肿块。CT上有残留肿块的24例患者中有5例与CT上无残留肿块的30例患者中有1例18F-FDG PET检查呈阳性。18F-FDG PET阳性的所有6例患者(100%)均出现复发,CT上有残留肿块但18F-FDG PET阴性的19例患者中有5例(26%)复发,CT扫描和18F-FDG PET检查均为阴性的29例患者中有3例(10%)复发(P≤0.0001)。我们观察到CT上有残留肿块的患者与CT上无残留肿块的患者相比,复发和死亡率更高(1年无进展生存率:62±10%对88±7%,P = 0.0045;1年总生存率:77±5%对95±5%,P = 0.0038)。18F-FDG PET检查阳性与更差的生存率更一致相关:与18F-FDG PET检查阴性的患者相比,1年无进展生存率为0%对86%±5%(P < 0.0001),1年总生存率为50%±20%对92%±4%(P < 0.0001)。治疗结束后通过18F-FDG PET检测存活肿瘤对复发的预测价值高于传统CT扫描成像(阳性预测值:100%对42%)。这有助于识别化疗完成后需要立即强化治疗的患者。然而,18F-FDG PET主要预测早期进展,但不能排除微小残留病的存在,可能导致后期复发。