TGFBI expression is an independent predictor of survival in adjuvant-treated lung squamous cell carcinoma patients

M. J. Pajares, J. Agorreta, E. Salvo, C. Behrens, I. I. Wistuba, L. M. Montuenga, R. Pio, A. Rouzaut

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Background: Transforming growth factor β-induced protein (TGFBI) is a secreted protein that mediates cell anchoring to the extracellular matrix. This protein is downregulated in lung cancer, and when overexpressed, contributes to apoptotic cell death. Using a small series of stage IV non-small cell lung cancer (NSCLC) patients, we previously suggested the usefulness of TGFBI as a prognostic and predictive factor in chemotherapy-treated late-stage NSCLC. In order to validate and extend these results, we broaden the analysis and studied TGFBI expression in a large series of samples obtained from stage I-IV NSCLC patients. Methods: TGFBI expression was assessed by immunohistochemistry in 364 completely resected primary NSCLC samples: 242 adenocarcinomas (ADCs) and 122 squamous cell carcinomas (SCCs). Kaplan-Meier curves, log-rank tests and the Cox proportional hazards model were used to analyse the association between TGFBI expression and survival. Results: High TGFBI levels were associated with longer overall survival (OS, P<0.001) and progression-free survival (PFS, P<0.001) in SCC patients who received adjuvant platinium-based chemotherapy. Moreover, multivariate analysis demonstrated that high TGFBI expression is an independent predictor of better survival in patients (OS: P=0.030 and PFS: P=0.026). Conclusions: TGFBI may be useful for the identification of a subset of NSCLC who may benefit from adjuvant therapy.

Original languageEnglish (US)
Pages (from-to)1545-1551
Number of pages7
JournalBritish journal of cancer
Volume110
Issue number6
DOIs
StatePublished - Mar 18 2014

Keywords

  • TGFBI
  • adjuvant therapy
  • lung carcinoma
  • prognosis
  • survival

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

MD Anderson CCSG core facilities

  • Tissue Biospecimen and Pathology Resource

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