Abstract

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. 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.

Highlights

  • Improved staging for non–small cell lung cancer (NSCLC) represents a critical unmet need

  • Overall model fit remained the same for the seventh and eighth editions of the TNM staging system, whereas the R2 statistic, concordance index, and log-rank χ2 were all associated with improvements after TNMB adoption

  • The TNMB system, compared with the TNM eighth edition, was associated with enhanced identification of highrisk patients and better differentiation of those without recurrence from those who had recurrence, whereas the eighth edition compared with the seventh edition was not associated with improvement of this measure

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Summary

Introduction

Improved staging for non–small cell lung cancer (NSCLC) represents a critical unmet need. The eighth edition of the TNM staging system (hereafter referred to as “eighth edition”) was recently adopted in 2018.1 Despite the advances of the molecular genetic era, the TNM system remains dependent on tumor size (T), nodal status (N), and the presence of metastasis (M). External validations of the eighth edition have failed to show improvement in estimation of survival. Risk stratification of early-stage disease continues to underperform, with 5-year overall mortality rates as high as 40% to 45% in patients with pathologic stage I disease.. TNM Eighth Edition Stage and Molecular Prognostic Classifier Stage IA1 TNMB Stage Low-risk. Intermediate-risk Stage IA2 High-risk Stage IA3 Stage IB Stage IIA

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