Division of Adult Cardiothoracic Surgery, University of California, San Francisco.
Division of Preventive Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
JAMA Netw Open. 2019 Dec 2;2(12):e1917062. doi: 10.1001/jamanetworkopen.2019.17062.
Improved staging for non-small cell lung cancer (NSCLC) represents a critical unmet need. External validations of the eighth edition of the TNM staging system have yielded disappointing results, with persistently high mortality observed in early-stage disease.
To determine whether incorporation of a molecular prognostic classifier into conventional TNM staging for NSCLC improves estimation of disease-free survival.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study was conducted at an academic, quaternary care medical center from 2012 to 2018. A consecutive series of 238 patients underwent surgical resection of stage I to IIIC nonsquamous NSCLC and had molecular prognostic classifier testing performed. Data analysis was conducted in May 2019.
Patients were restaged according to the seventh and eighth editions of the TNM staging system and the novel TMMB staging system, which maintains the order and structure of the eighth edition of the TNM but downstages or upstages according to low or high molecular risk, respectively.
The primary outcome was disease-free survival 3 years from the time of surgical resection. Reclassification statistics were then used to evaluate performance and improvement measures of the TNM seventh and eighth editions and the TNMB staging system.
Two hundred thirty-eight patients (144 [60.5%] female; median [interquartile range] age, 70 [63-75] years) were analyzed. The median (interquartile range) follow-up was 25 (14-40) months, and the disease-free survival rate was estimated to be 58.3% (95% CI, 45.7% to 69.0%). One hundred fifty-nine patients (66.8%) were reclassified by the TNMB staging system. Overall model fit remained the same for the seventh and eighth editions of the TNM staging system, whereas the R2 statistic (change from 0.22 to 0.31), concordance index (change from 0.68 to 0.73), and log-rank χ2 (change from 38 to 108) were all associated with improvements after TNMB adoption. The TNMB system, compared with the TNM eighth edition, was associated with enhanced identification of high-risk patients and better differentiation of those without recurrence from those who had recurrence (net reclassification improvement, 0.28; 95% CI, 0.08 to 0.46; P < .001), whereas the eighth edition compared with the seventh edition was not associated with improvement of this measure (net reclassification improvement, 0.02; 95% CI, -0.18 to 0.21; P = .87).
The TNMB staging system was associated with improved estimation of disease-free survival compared with conventional TNM staging. Incorporation of a molecular prognostic classifier into staging for NSCLC may lead to better identification of high-risk patients.
非小细胞肺癌 (NSCLC) 的分期改进是一个亟待解决的重要问题。第八版 TNM 分期系统的外部验证结果令人失望,早期疾病的死亡率仍然很高。
确定将分子预后分类器纳入 NSCLC 的常规 TNM 分期是否能提高无病生存率的估计。
设计、地点和参与者:这项队列研究于 2012 年至 2018 年在一家学术性的、四级保健医疗中心进行。连续系列的 238 名患者接受了 I 期至 IIIIC 期非鳞状 NSCLC 的手术切除,并进行了分子预后分类器检测。数据分析于 2019 年 5 月进行。
根据第七版和第八版 TNM 分期系统以及新的 TMMB 分期系统对患者进行重新分期,该系统保持了第八版 TNM 的顺序和结构,但根据低或高分子风险分别下调或上调分期。
主要结果是手术切除后 3 年的无病生存率。然后使用再分类统计来评估 TNM 第七版和第八版以及 TNMB 分期系统的性能和改进措施。
共分析了 238 名患者(144 [60.5%] 为女性;中位数 [四分位间距] 年龄为 70 [63-75] 岁)。中位(四分位间距)随访时间为 25(14-40)个月,无病生存率估计为 58.3%(95%CI,45.7%至 69.0%)。159 名患者(66.8%)通过 TNMB 分期系统重新分类。第七版和第八版 TNM 分期系统的整体模型拟合保持不变,而 R2 统计量(从 0.22 变为 0.31)、一致性指数(从 0.68 变为 0.73)和对数秩 χ2(从 38 变为 108)的变化均与 TNMB 采用后的改进相关。与第八版 TNM 相比,TNMB 系统与高危患者的识别能力增强以及无复发患者与复发患者的区分能力提高有关(净再分类改善,0.28;95%CI,0.08 至 0.46;P<0.001),而第八版与第七版相比,该指标没有改善(净再分类改善,0.02;95%CI,-0.18 至 0.21;P=0.87)。
与常规 TNM 分期相比,TNMB 分期系统与无病生存率的估计改善相关。将分子预后分类器纳入 NSCLC 的分期可能会导致高危患者的识别能力提高。