Umehara S, Nakagawa A, Matthay K K, Lukens J N, Seeger R C, Stram D O, Gerbing R B, Shimada H
Department of Pathology and Laboratory Medicine, Childrens Hospital Los Angeles, CA 91066-6012, USA.
Cancer. 2000 Sep 1;89(5):1150-61.
Ganglioneuroblastoma, nodular (GNBn) is a rare subtype of the family of neuroblastic tumors (neuroblastoma, ganglioneuroblastoma, and ganglioneuroma) that are classified in the unfavorable histology group according to the International Neuroblastoma Pathology Classification (Shimada system). Tumors of this subtype have been considered to represent a prototypic example of biologically and clinically nonaggressive (Schwannian stroma-rich and stroma-dominant) components combined with biologically and clinically aggressive nodular (Schwannian stroma-poor) components. However, detailed histopathologic analysis as well as thorough prognostic evaluation of patients with this subtype has not been reported.
Pathology slides and reports from a total of 70 GNBn patients from the Children's Cancer Group (CCG)-3881 and CCG-3891 studies were reviewed. Sixty-eight tumors were classified in the favorable subset (FS) or the unfavorable subset (US) based on the evaluation of nodular components by applying the same histopathologic criteria (patient age, grade of neuroblastic differentiation, mitosis-karyorrhexis index) that are used for neuroblastomas in the International Neuroblastoma Pathology Classification. Patient prognosis as well as clinical and biologic characteristics within the subsets were analyzed, and the results were compared with those from 654 non-GNBn patients who were enrolled in the same CCG studies during the same period.
Patients with GNBn tumors, usually diagnosed at age > 1 year, had a significantly lower overall 5-year event free survival (EFS) rate than patients with non-GNBn subtypes (44.7% EFS vs. 65.0% EFS; P = 0. 0073). A significant difference in the outcome of the patients between the FS (22 patients; 86.1% EFS; 95.0% survival rate) and the US (46 patients; 29.0% EFS; 40.7% survival rate) of the GNBn subtype (P < 0.0005) was shown. When the cohort of patients with GNBn tumors was subdivided into FS and US, the outcomes were similar to those of patients with tumors of favorable histology (397 patients; 90.5% EFS; 97.6% survival rate) and with tumors of unfavorable histology (257 patients; 27.0% EFS; 35.7% survival rate) of the non-GNBn type. The patients with US tumors frequently (63.0%) presented with distant metastasis.
The current study demonstrates that the nodular components in GNBn tumors are not always aggressive. The prognosis of these patients can be determined by the analysis of age-linked histopathologic features.
结节型神经节神经母细胞瘤(GNBn)是神经母细胞瘤家族(神经母细胞瘤、神经节神经母细胞瘤和神经节神经瘤)中一种罕见的亚型,根据国际神经母细胞瘤病理分类(岛田系统),其被归类于预后不良的组织学组。该亚型肿瘤被认为是生物学和临床侵袭性较弱(富含施万细胞基质且基质占主导)的成分与生物学和临床侵袭性较强的结节状(施万细胞基质较少)成分相结合的典型例子。然而,尚未有关于该亚型患者详细的组织病理学分析以及全面预后评估的报道。
回顾了儿童癌症组(CCG)-3881和CCG-3891研究中70例GNBn患者的病理切片和报告。根据应用国际神经母细胞瘤病理分类中用于神经母细胞瘤的相同组织病理学标准(患者年龄、神经母细胞分化程度、有丝分裂-核溶解指数)对结节成分进行评估,将68例肿瘤分为预后良好亚组(FS)或预后不良亚组(US)。分析了亚组内患者的预后以及临床和生物学特征,并将结果与同期参加相同CCG研究的654例非GNBn患者的结果进行比较。
GNBn肿瘤患者通常在1岁以后确诊,其5年总无事件生存率(EFS)显著低于非GNBn亚型患者(EFS为44.7% vs. 65.0%;P = 0.0073)。GNBn亚型的FS(22例患者;EFS为86.1%;生存率为95.0%)和US(46例患者;EFS为29.0%;生存率为40.7%)之间患者结局存在显著差异(P < 0.0005)。当将GNBn肿瘤患者队列分为FS和US时,其结局与非GNBn型预后良好组织学肿瘤(397例患者;EFS为90.5%;生存率为97.6%)和预后不良组织学肿瘤(257例患者;EFS为27.0%;生存率为35.7%)的患者相似。US肿瘤患者经常(63.0%)出现远处转移。
当前研究表明,GNBn肿瘤中的结节成分并非总是具有侵袭性。这些患者的预后可通过分析与年龄相关的组织病理学特征来确定。