Bedini Amedeo Vittorio, Andreani Stefano Michele, Tavecchio Luca, Fabbri Alessandra, Giardini Roberto, Camerini Tiziana, Bufalino Rosaria, Morabito Alberto, Rosai Juan
Thoracic Surgery Unit, University of Milan, S. Paolo Hospital, Milan, Italy.
Ann Thorac Surg. 2005 Dec;80(6):1994-2000. doi: 10.1016/j.athoracsur.2005.07.019.
We designed and assessed a new TNM staging system (herein called the INT [Istituto Nazionale Tumori] system) for thymic epithelial tumors in order to overcome the perceived drawbacks of Masaoka's system, which represents the current standard.
In all, 123 cases were evaluated. The histologic types according to the World Health Organization (WHO) classification were as follows: subtype A: 5 cases; AB: 40; B1: 16; B2: 29; B3: 16; and C: 17 cases. There were 45 Masaoka's stage I, 33 stage II, 26 stage III, and 19 stage IV cases. A total of 11 INT definitions were grouped into three stages: locally restricted disease (75 cases), which included Masaoka's stage I and selected stage II cases (no pleural invasion); locally advanced disease (37 cases), which included Masaoka's stage III cases plus those staged II owing to pleural invasion and those staged IV owing to intrathoracic nodal or limited pleuropericardial involvement; and systemic disease (11 cases), which included the remaining Masaoka's stage IV cases.
Completeness of resection, WHO types, and both staging systems were significant prognostic factors (p < 0.0001) on univariate analysis. The 95-month progression-free survival rates according to Masaoka's system were stage I: 100%; II: 93.6%; III: 46.3%; and IV: 23.2%. The INT system corresponding figures were as follows: locally restricted disease: 98.6%; locally advanced disease: 46.9%; and systemic disease: 11.7%. The INT system was the prognostic factor with the greatest impact (p = 0.0218) on multivariate analysis (Masaoka's system: p = 0.2012; completeness of resection: p = 0.6855; histology: p = 0.9386).
The INT system allows finer disease descriptions than Masaoka's system, resulting in a stage grouping with higher prognostic distinctiveness.
我们设计并评估了一种新的胸腺上皮肿瘤TNM分期系统(在此称为INT[国家肿瘤研究所]系统),以克服目前作为标准的Masaoka系统所存在的明显缺陷。
共评估了123例病例。根据世界卫生组织(WHO)分类的组织学类型如下:A亚型:5例;AB型:40例;B1型:16例;B2型:29例;B3型:16例;C型:17例。Masaoka分期为I期45例,II期33例,III期26例,IV期19例。INT系统共11个定义分为三个阶段:局部受限疾病(75例),包括Masaoka I期及部分II期病例(无胸膜侵犯);局部进展期疾病(37例),包括Masaoka III期病例以及因胸膜侵犯而分期为II期的病例和因胸内淋巴结受累或有限的胸膜心包受累而分期为IV期的病例;全身疾病(11例),包括其余的Masaoka IV期病例。
单因素分析显示,手术切除完整性、WHO类型以及两种分期系统均为显著的预后因素(p<0.0001)。根据Masaoka系统,95个月无进展生存率分别为:I期:100%;II期:93.6%;III期:46.3%;IV期:23.2%。INT系统相应的数据如下:局部受限疾病:98.6%;局部进展期疾病:46.9%;全身疾病:11.7%。多因素分析显示INT系统是影响最大的预后因素(p=0.0218)(Masaoka系统:p=0.2012;手术切除完整性:p=0.6855;组织学:p=0.9386)。
与Masaoka系统相比,INT系统能够更精细地描述疾病,从而使分期分组具有更高的预后区分度。