Ricci Claudio, Casadei Riccardo, Taffurelli Giovanni, D'Ambra Marielda, Monari Francesco, Campana Davide, Tomassetti Paola, Santini Donatella, Minni Francesco
Department of Internal Medicine, Emergency and Surgery (DIMEC), Alma Mater Studiorum, University of Bologna, S.Orsola-Malpighi Hospital, Italy.
Department of Internal Medicine, Emergency and Surgery (DIMEC), Alma Mater Studiorum, University of Bologna, S.Orsola-Malpighi Hospital, Italy.
Pancreatology. 2014 Nov-Dec;14(6):539-41. doi: 10.1016/j.pan.2014.09.005. Epub 2014 Sep 16.
In 2010, the World Health Organization released a new classification system for endocrine pancreatic tumors. The new categories replaced those in the old classification.
To test the safety and accuracy of the new classification in stratifying patients, we retrospectively evaluated 64 consecutive patients, surgically R0 resected for pancreatic endocrine tumors.
In our experience, only 19/31 (61.3%) patients classified as having well-differentiated tumors were included in the new neuroendocrine tumor G1 category while the remaining 12 (38.7%) shifted into the G2 category. Moreover, 10/33 (30.3%) patients classified as affected by a malignant endocrine neoplasm in the old system were considered as G1 tumors in the new one. These differences were statistically significant (P < 0.001) and changed the risk category in 22 (33.3%) patients with well-differentiated pancreatic endocrine tumors. Multiple multivariate models were produced and the poor stratification of the new system was found to be in the G2 category which presents too wide a range of the Ki 67 index (2 to 20%). We built a model in which the G2 category was divided into two subcategories: tumors with a Ki 67 index ≥2 and <5% and tumors with a Ki index ≥5 and <20%, partially modifying the new classification. In this model, the modified classification showed a superiority with respect to the European Neuroendocrine tumor Society-Tumor-Node-Metastasis staging system in stratifying patients for recurrence, with a relative risk of 19 (P < 0.001).
The new G2 category seems too large because it includes both benign, low and high grade malignant tumors.
2010年,世界卫生组织发布了一种新的胰腺内分泌肿瘤分类系统。新类别取代了旧分类中的类别。
为了测试新分类在对患者进行分层时的安全性和准确性,我们回顾性评估了64例连续接受手术R0切除的胰腺内分泌肿瘤患者。
根据我们的经验,在新的神经内分泌肿瘤G1类别中,只有19/31(61.3%)被归类为高分化肿瘤的患者,其余12例(38.7%)被归入G2类别。此外,在旧系统中被归类为恶性内分泌肿瘤的10/33(30.3%)患者在新系统中被视为G1肿瘤。这些差异具有统计学意义(P < 0.001),并改变了22例(33.3%)高分化胰腺内分泌肿瘤患者的风险类别。构建了多个多变量模型,发现新系统分层不佳的是G2类别,其Ki 67指数范围太宽(2%至20%)。我们构建了一个模型,其中G2类别分为两个子类别:Ki 67指数≥2%且<5%的肿瘤和Ki指数≥5%且<20%的肿瘤,对新分类进行了部分修改。在该模型中,修改后的分类在对患者复发分层方面显示出优于欧洲神经内分泌肿瘤学会-肿瘤-淋巴结-转移分期系统,相对风险为19(P < 0.001)。
新的G2类别似乎太大,因为它既包括良性、低级别和高级别恶性肿瘤。