Elsevier

Journal of Thoracic Oncology

Volume 15, Issue 11, November 2020, Pages 1748-1757
Journal of Thoracic Oncology

Original Article
Translational Oncology
Multi-Institutional Prospective Validation of Prognostic mRNA Signatures in Early Stage Squamous Lung Cancer (Alliance)

https://doi.org/10.1016/j.jtho.2020.07.005Get rights and content
Under an Elsevier user license
open archive

Abstract

Introduction

Surgical resection is curative for some patients with early lung squamous cell carcinoma. Staging and clinical factors do not adequately predict recurrence risk. We sought to validate the discriminative performance of proposed prognostic gene expression signatures at a level of rigor sufficient to support clinical use.

Methods

The two-stage validation used independent core laboratories, objective quality control standards, locked test parameters, and large multi-institutional specimen and data sets. The first stage validation confirmed a signature’s ability to stratify patient survival. The second-stage validation determined which signature(s) optimally improved risk discrimination when added to baseline clinical predictors. Participants were prospectively enrolled in institutional (cohort I) or cooperative group (cohort II) biospecimen and data collection protocols. All cases underwent a central review of clinical, pathologic, and biospecimen parameters using objective criteria to determine final inclusion (cohort I: n = 249; cohort II: n = 234). Primary selection required that a signature significantly predict a 3-year survival after surgical resection in cohort I. Signatures meeting this criterion were further tested in cohort II, comparing risk prediction using baseline risk factors alone versus in combination with the signature.

Results

Male sex, advanced age, and higher stage were associated with shorter survival in cohort I and established a baseline clinical model. Of the three signatures validated in cohort I, one signature was validated in cohort II and statistically significantly enhanced the prognosis relative to the baseline model (C-index difference 0.122; p < 0.05).

Conclusions

These results represent the first rigorous validation of a test appropriate to direct adjuvant treatment or clinical trials for patients with lung squamous cell carcinoma.

Keywords

Lung squamous cell carcinoma
Prognostic gene expression signature
Surgery
Early stage NSCLC
Clinical prognostic test validation

Cited by (0)

Disclosure: Dr. Hirsch reports advisory board participation for Genentech/Roche, Bristol-Myers Squibb, AstraZeneca, Merck, Novartis, Daiichi, Amgen, OncoCyte, Eli Lilly/Loxo, and Boehringer Ingelheim outside of the submitted work. Dr. Govindan reports receiving personal fees from Inivata, Pfizer, AstraZeneca, Genentech, Millennium Pharmaceuticals, AbbVie, F. Hoffman La-Roche, NeoHealth, Janssen, Bristol-Myers Squibb, Eli Lilly, Roche, Nektar, Merck, Celgene, Janssen, Partner Therapeutics, GlaxoSmithKline, Jounce, Amgen, Achilles, and GenePlus outside of the submitted work. Dr. Merrick reports receiving grants from Bristol-Myers Squibb; and personal fees from Genentech and Roche outside of the submitted work. Dr. Bueno reports receiving grants from Genentech, Roche, Merck, Verastem, Epizyme, MedGenome, Siemens, and Gritstone outside of the submitted work. In addition, Dr. Bueno has four patents through the Brigham and Women’s Hospital (no royalties to date) and equity in a new start-up company, Navigation Sciences outside of the submitted work. The remaining authors declare no conflict of interest.