Department of Pediatric Hematology and Oncology, Institute of Pediatrics, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary,
Pathol Oncol Res. 2014 Jan;20(1):139-43. doi: 10.1007/s12253-013-9676-3. Epub 2013 Aug 17.
The aim of the study was to assess sensitivity and specificity of FDG-PET/CT in different forms of childhood cancer. We retrospectively evaluated the results dedicated of 162 FDG-PET/CT examinations of 86 children treated with: Hodgkin lymphoma (HL; n = 31), non-Hodgkin lymphoma (NHL; n = 30) and other high grade solid tumors (n = 25). Patients were admitted and treated in two departments of pediatric hematology and oncology in Hungary. FDG-PET/CT was performed for staging (n = 25) and for posttreatment evaluation (n = 137). Imaging was performed in three FDG-PET/CT Laboratories, using dedicated PET/CT scanners. False positive results were defined as resolution or absence of disease progression over at least 1 year on FDG-PET/CT scans without any intervention. In some cases histopathological evaluation of suspicious lesions was performed. Fals negative results were defined as negative FDG-PET/CT results in case of active malignancy. Positive predictive values (PPV) and negative predictive values (NPV) were calculated. NPV was 100%. The highest PPV was observed in high grade solid tumors (81%), followed by HL (65%) and NHL (61%). There was a major difference of PPV in different histological types of HL (50% in HL of mixed-cellularity subtype, 90% in nodular sclerosing, and 100% in lymphocyte-rich and lymphocyte depleted HL). We treated one patient with nodular lymphocyte predominant HL, who had 5 false positive FDG-PET/CT results. PPV of T- and B-lineage NHL were similar (60% and 62%, respectively). We observed an interesting difference of PPV in different stages of HL and NHL. In HL PPV was higher in early than in advanced disease forms: 66% in stage II HL and 60% in stage III HL, whereas there was an inverse relationship between PPV and disease stages in NHL 0% in stage I and II patients, 67% in stage III and 100% in stage IV patients. PPV was lower in males (54%) than in females (65%). PPV were 64% vs. 58% in patients under vs. over 10 years of age. Negative FDG-PET/CT results during follow-up reliably predict the absence of malignancy. Positive FDG-PET/CT scan results in general have a low PPV. The relatively high PPV in patients with histologically proven high grade solid tumors, advanced stages of NHL and with nodular sclerosing, lymphocyte-rich and lymphocyte depleted subtypes of HL warrant a confirmation by biopsy, whereas the watch-and-wait approach can be used in other forms of childhood cancer patients with a positive FDG-PET/CT result in course of follow-up examinations.
本研究旨在评估 FDG-PET/CT 在不同类型儿童癌症中的敏感性和特异性。我们回顾性评估了 86 名接受以下治疗的儿童的 162 次 FDG-PET/CT 检查结果:霍奇金淋巴瘤(HL;n=31)、非霍奇金淋巴瘤(NHL;n=30)和其他高级别实体瘤(n=25)。患者在匈牙利的两个儿科血液学和肿瘤学部门入院并接受治疗。FDG-PET/CT 用于分期(n=25)和治疗后评估(n=137)。成像在三个 FDG-PET/CT 实验室进行,使用专用的 PET/CT 扫描仪。假阳性结果定义为 FDG-PET/CT 扫描上至少 1 年无疾病进展的分辨率或缺失,而无任何干预。在某些情况下,对可疑病变进行了组织病理学评估。假阴性结果定义为在存在活动性恶性肿瘤的情况下 FDG-PET/CT 结果为阴性。计算了阳性预测值(PPV)和阴性预测值(NPV)。NPV 为 100%。在高级别实体瘤中观察到最高的 PPV(81%),其次是 HL(65%)和 NHL(61%)。HL 不同组织学类型的 PPV 存在显著差异(混合细胞亚型 HL 为 50%,结节性硬化为 90%,富含淋巴细胞和淋巴细胞耗竭型 HL 为 100%)。我们治疗了一名患有结节性淋巴细胞为主型 HL 的患者,该患者有 5 次 FDG-PET/CT 假阳性结果。T 细胞和 B 细胞 NHL 的 PPV 相似(分别为 60%和 62%)。我们观察到 HL 和 NHL 不同阶段的 PPV 存在有趣的差异。在 HL 中,早期疾病形式的 PPV 高于晚期:HL Ⅱ期为 66%,HL Ⅲ期为 60%,而 NHL 中 PPV 与疾病阶段呈反比关系:Ⅰ期和Ⅱ期患者为 0%,Ⅲ期为 67%,Ⅳ期为 100%。男性的 PPV(54%)低于女性(65%)。10 岁以下患者的 PPV 为 64%,10 岁以上患者的 PPV 为 58%。在随访期间,阴性 FDG-PET/CT 结果可靠地预测无恶性肿瘤。一般来说,阳性 FDG-PET/CT 扫描结果的 PPV 较低。在组织学证实的高级别实体瘤、NHL 的晚期阶段以及结节性硬化、富含淋巴细胞和淋巴细胞耗竭型 HL 患者中,PPV 相对较高,需要通过活检确认,而在其他形式的儿童癌症患者中,在随访检查中出现阳性 FDG-PET/CT 结果时,可以采用观察和等待的方法。