Kumar Rakesh, Xiu Yan, Potenta Scott, Mavi Ayse, Zhuang Hongming, Yu Jian Q, Dhurairaj Thiruvekatasamy, Dadparvar Simin, Alavi Abass
Division of Nuclear Medicine, Department of Radiology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
J Nucl Med. 2004 Nov;45(11):1796-803.
(18)F-FDG PET is highly sensitive and specific for evaluation of the treatment response of nodal and extranodal diseases in patients with malignant lymphomas. However, no data are available in the literature with regard to (18)F-FDG PET for evaluation of the treatment response in patients with lymphomas with gastrointestinal tract (GIT) involvement. This study was undertaken to investigate the usefulness of (18)F-FDG PET in monitoring the response to the treatment of lymphomas in this setting.
We retrospectively analyzed 19 patients with different types of lymphomas (10 diffuse large B-cell lymphomas, 4 follicular lymphomas, 3 mantle cell lymphomas, and 2 Hodgkin's disease) involving GIT. Among 19 patients, 4 had gastric involvement, 13 had small bowel involvement, and 2 had small bowel plus colon involvement by lymphomas. All patients underwent (18)F-FDG PET before and after the completion of therapy. The results of (18)F-FDG PET were compared with the results of CT and clinical outcome; the presence of relapse was determined on the basis of positive biopsy results or clinical follow-up data.
Of the 19 posttreatment PET scans, 13 showed no pathologic (18)F-FDG uptake, whereas 6 showed persistent (18)F-FDG uptake. Among the 13 patients who had negative PET scans, only 1 patient (7.7%) relapsed, whereas all 6 patients (100%) who had persistent abnormal (18)F-FDG uptake on posttherapy PET scans relapsed. Posttreatment CT scans were negative for 10 patients but showed persistent disease in the remaining 9 patients. Among the 10 patients who had negative CT scans, 9 remained in remission and 1 (10%) relapsed. Of the 9 patients who showed persistent disease, 6 (67%) relapsed and 3 (33%) remained in remission after the mean follow-up of 20 mo. The sensitivity, specificity, positive and negative predictive values, and accuracy of posttherapy (18)F-FDG PET were 86%, 100%, 100%, 92%, and 95%, respectively. The corresponding values for CT were 67%, 75%, 75%, 90%, and 79%, respectively. Patients with positive (18)F-FDG PET results had statistically significantly lower disease-free survival (DFS) (0%) than did those with positive CT results (33%) (P = 0.04). There was no statistically significant difference in DFS between patients with negative (18)F-FDG PET results and patients with negative CT results.
A positive (18)F-FDG PET scan after the completion of chemotherapy in patients with lymphomas with GIT involvement is a strong predictor of relapse. (18)F-FDG PET has higher diagnostic accuracy than CT in the detection of residual disease after therapy. Despite the mild physiologic (18)F-FDG uptake in the GIT, (18)F-FDG PET has potential value in monitoring the response to treatment in patients with GIT lymphomas, particularly when pretreatment PET results are positive.
(18)F-FDG PET对评估恶性淋巴瘤患者淋巴结和结外疾病的治疗反应具有高度敏感性和特异性。然而,文献中尚无关于(18)F-FDG PET评估胃肠道(GIT)受累淋巴瘤患者治疗反应的数据。本研究旨在探讨(18)F-FDG PET在监测此类淋巴瘤治疗反应中的作用。
我们回顾性分析了19例不同类型淋巴瘤(10例弥漫性大B细胞淋巴瘤、4例滤泡性淋巴瘤、3例套细胞淋巴瘤和2例霍奇金病)累及GIT的患者。19例患者中,4例胃部受累,13例小肠受累,2例小肠加结肠受累。所有患者在治疗完成前后均接受了(18)F-FDG PET检查。将(18)F-FDG PET结果与CT结果及临床结局进行比较;根据活检阳性结果或临床随访数据确定复发情况。
在19次治疗后PET扫描中,13例显示无病理性(18)F-FDG摄取,而6例显示持续性(18)F-FDG摄取。在PET扫描阴性的13例患者中,仅1例(7.7%)复发,而治疗后PET扫描显示持续性异常(18)F-FDG摄取的所有6例患者(100%)均复发。治疗后CT扫描10例为阴性,但其余9例显示疾病持续存在。在CT扫描阴性的10例患者中,9例仍处于缓解期,1例(10%)复发。在显示疾病持续存在的9例患者中,6例(67%)复发,3例(33%)在平均随访20个月后仍处于缓解期。治疗后(18)F-FDG PET的敏感性、特异性、阳性和阴性预测值及准确性分别为86%、100%、100%、92%和95%。CT的相应值分别为67%、75%、75%、90%和79%。(18)F-FDG PET结果阳性的患者无病生存率(DFS)(0%)在统计学上显著低于CT结果阳性的患者(33%)(P = 0.04)。(18)F-FDG PET结果阴性的患者与CT结果阴性的患者在DFS方面无统计学显著差异。
GIT受累淋巴瘤患者化疗完成后(18)F-FDG PET扫描阳性是复发的有力预测指标。(18)F-FDG PET在检测治疗后残留疾病方面比CT具有更高的诊断准确性。尽管GIT存在轻度生理性(18)F-FDG摄取,但(18)F-FDG PET在监测GIT淋巴瘤患者的治疗反应方面具有潜在价值,特别是当治疗前PET结果为阳性时。