Ou Sai-Hong Ignatius, Zell Jason A
Chao Family Comprehensive Cancer Center, Division of Hematology/Oncology, Department of Medicine, University of Irvine Medical Center, Orange, California 92868, USA.
J Thorac Oncol. 2008 Mar;3(3):216-27. doi: 10.1097/JTO.0b013e318164545d.
We performed a validation study of the proposed International Association for the Study of Lung Cancer (IASLC) tumor, node, metastasis (TNM) and stage grouping revisions on advanced nonbronchioloalveolar carcinoma (non-BAC) non-small cell lung cancer (NSCLC).
Twenty-three thousand five hundred eighty-three patients from the California Cancer Registry between 1999 and 2003 with histologically confirmed non-BAC NSCLC and complete TNM staging were identified and reclassified according to the IASLC proposed TNM revisions and new stage groupings. Twelve thousand nine hundred one stage IIIB and IV patients formed the primary analysis of the changes to T4 and M descriptors. Surveillance, Epidemiology, and End Results extent of disease codes were used to identify various T4 and M descriptors. Cox proportional hazards regression was used to calculate hazard ratios (HRs) among the stage groupings of the current and proposed staging system with adjustment for ethnicity, gender, age, histology, histologic grade, socioeconomic status, surgery, radiation, and chemotherapy.
The proposed changes to the T4 and M descriptors were supported by overall survival analysis. T4 due to additional nodules had significant survival advantage over other T4 and M descriptors among non-BAC NSCLC and individual histology and warrants down-staging to T3. Pericardial effusion had survival similar to M1b patients. Cox proportional hazards regression analysis supports subdividing M descriptor into M1a (versus IASLC stage IA; HR = 4.90; 95% confidence interval: 4.49-5.34) and M1b (versus IASLC stage IA; HR = 6.84; 95% confidence interval: 6.30-7.44).
IASLC has greatly improved the T4 and M descriptors allowing better prognostication of advanced non-BAC NSCLC. Pericardial effusion may be considered as M1b rather than M1a.
我们对国际肺癌研究协会(IASLC)提出的关于晚期非细支气管肺泡癌(非BAC)非小细胞肺癌(NSCLC)的肿瘤、淋巴结、转移(TNM)分期及分组修订进行了一项验证研究。
从加利福尼亚癌症登记处识别出1999年至2003年间23583例经组织学确诊为非BAC NSCLC且TNM分期完整的患者,并根据IASLC提出的TNM修订和新的分期分组进行重新分类。12901例III B期和IV期患者构成了对T4和M描述符变化的主要分析对象。利用监测、流行病学和最终结果疾病范围编码来识别各种T4和M描述符。采用Cox比例风险回归分析,在对种族、性别、年龄、组织学、组织学分级、社会经济地位、手术、放疗和化疗进行调整后,计算当前分期系统和提议分期系统的各分期分组之间的风险比(HRs)。
对T4和M描述符的提议更改得到了总生存分析的支持。在非BAC NSCLC以及各组织学类型中,因额外结节导致的T4与其他T4和M描述符相比具有显著的生存优势,值得将其降期为T3。心包积液的生存率与M1b患者相似。Cox比例风险回归分析支持将M描述符细分为M1a(相对于IASLC IA期;HR = 4.90;95%置信区间:4.49 - 5.34)和M1b(相对于IASLC IA期;HR = 6.84;95%置信区间:6.30 - 7.44)。
IASLC极大地改进了T4和M描述符,使得对晚期非BAC NSCLC的预后判断更加准确。心包积液可被视为M1b而非M1a。