Abstract

Pathologic N2 non-small cell lung cancer (NSCLC) is prominently intrinsically heterogeneous. We aimed to identify homogeneous prognostic subgroups and evaluate the role of different adjuvant treatments. We retrospectively collected patients with resected pathologic T1-3N2M0 NSCLC from the Shanghai Chest Hospital as the primary cohort and randomly allocated them (3:1) to the training set and the validation set 1. We had patients from the Fudan University Shanghai Cancer Center as an external validation cohort (validation set 2) with the same inclusion and exclusion criteria. Variables significantly related to disease-free survival (DFS) were used to build an adaptive Elastic-Net Cox regression model. Nomogram was used to visualize the model. The discriminative and calibration abilities of the model were assessed by time-dependent area under the receiver operating characteristic curves (AUCs) and calibration curves. The primary cohort consisted of 1,312 patients. Tumor size, histology, grade, skip N2, involved N2 stations, lymph node ratio (LNR), and adjuvant treatment pattern were identified as significant variables associated with DFS and integrated into the adaptive Elastic-Net Cox regression model. A nomogram was developed to predict DFS. The model showed good discrimination (the median AUC in the validation set 1: 0.66, range 0.62 to 0.71; validation set 2: 0.66, range 0.61 to 0.73). We developed and validated a nomogram that contains multiple variables describing lymph node status (skip N2, involved N2 stations, and LNR) to predict the DFS of patients with resected pathologic N2 NSCLC. Through this model, we could identify a subtype of NSCLC with a more malignant clinical biological behavior and found that this subtype remained at high risk of disease recurrence after adjuvant chemoradiotherapy.

Highlights

  • Lung cancer remains the leading cause of cancer death globally [1]

  • We developed a model that combined detailed lymph node parameters to predict the risk of disease recurrence for patients with resected pathologic N2 (pN2) non-small cell lung cancer (NSCLC)

  • We developed and validated a nomogram that contained multiple lymph node parameters to predict disease-free survival (DFS) of patients with resected pN2 NSCLC individually

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Summary

Introduction

Lung cancer remains the leading cause of cancer death globally [1]. Non-small cell lung cancer (NSCLC) accounts for more than 80% of all lung cancer patients [2]. One-fifth of NSCLC patients are classified as stage III disease [3]. For resectable stage III NSCLC, surgical resection remains the main option of curative therapy, yet 5-year overall survival (OS) ranges from 16% to 42% [4, 5]. Local failure and distant metastasis can occur after surgery for patients with completely resected pathologic N2 (pN2) NSCLC. The risk of locoregional recurrence is as high as 20%–40%, and the distant metastasis rate is more than 65%, which reveals the prognostic heterogeneity of this population [6,7,8]

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