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Molecular pathologic substaging in 244 stage I non-small-cell lung cancer patients: clinical implications.

Publication ,  Journal Article
Kwiatkowski, DJ; Harpole, DH; Godleski, J; Herndon, JE; Shieh, DB; Richards, W; Blanco, R; Xu, HJ; Strauss, GM; Sugarbaker, DJ
Published in: J Clin Oncol
July 1998

PURPOSE: To retrospectively construct a comprehensive multivariate model of cancer recurrence and to design a molecular pathologic substaging system in stage I non-small-cell lung cancer (NSCLC). METHODS: All patients with stage I NSCLC resected at Brigham and Women's Hospital (Boston, MA) between 1984 and 1992 with adequate clinical follow-up were studied. The importance of three demographic characteristics, surgical extent, 11 pathologic features, and seven molecular factors on cancer-free survival was examined. RESULTS: Two hundred forty-four patients were studied, with 25 noncancer deaths and 80 patients with recurrent disease. Significant univariate predictors (P < .05) of cancer recurrence were age older than 60 years, male sex, wedge resection, World Health Organization (WHO) adenocarcinoma subtype solid tumor with mucin, lymphatic invasion, and p53 expression. Multivariate analysis identified nine independent predictors of recurrence: solid tumor with mucin, a wedge resection, tumor diameter of 4 cm or greater, lymphatic invasion, age older than 60 years, male sex, p53 expression, K-ras codon 12 mutation, and absence of H-ras p21 expression. Multivariate cancer-free survival (CFS) analysis in the 180 patients who underwent lobectomy or pneumonectomy led to the elimination of sex and age, which left six independent factors. CONCLUSION: Lobectomy or pneumonectomy should be performed in stage I NSCLC. Using the six independent factors for recurrent disease, we propose a pathologic molecular substaging system. Patients with two factors or less are graded Ia, with a 5-year CFS rate of 87%; those with three factors are graded Ib, with a 5-year CFS rate of 58%; and those with four factors or more are graded Ic, with a 5-year CFS rate of 21%.

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Published In

J Clin Oncol

DOI

ISSN

0732-183X

Publication Date

July 1998

Volume

16

Issue

7

Start / End Page

2468 / 2477

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Survival Analysis
  • Risk Factors
  • Retrospective Studies
  • Prospective Studies
  • Prognosis
  • Predictive Value of Tests
  • Oncology & Carcinogenesis
  • Neoplasm Staging
  • Mutation
 

Citation

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Kwiatkowski, D. J., Harpole, D. H., Godleski, J., Herndon, J. E., Shieh, D. B., Richards, W., … Sugarbaker, D. J. (1998). Molecular pathologic substaging in 244 stage I non-small-cell lung cancer patients: clinical implications. J Clin Oncol, 16(7), 2468–2477. https://doi.org/10.1200/JCO.1998.16.7.2468
Kwiatkowski, D. J., D. H. Harpole, J. Godleski, J. E. Herndon, D. B. Shieh, W. Richards, R. Blanco, H. J. Xu, G. M. Strauss, and D. J. Sugarbaker. “Molecular pathologic substaging in 244 stage I non-small-cell lung cancer patients: clinical implications.J Clin Oncol 16, no. 7 (July 1998): 2468–77. https://doi.org/10.1200/JCO.1998.16.7.2468.
Kwiatkowski DJ, Harpole DH, Godleski J, Herndon JE, Shieh DB, Richards W, et al. Molecular pathologic substaging in 244 stage I non-small-cell lung cancer patients: clinical implications. J Clin Oncol. 1998 Jul;16(7):2468–77.
Kwiatkowski, D. J., et al. “Molecular pathologic substaging in 244 stage I non-small-cell lung cancer patients: clinical implications.J Clin Oncol, vol. 16, no. 7, July 1998, pp. 2468–77. Pubmed, doi:10.1200/JCO.1998.16.7.2468.
Kwiatkowski DJ, Harpole DH, Godleski J, Herndon JE, Shieh DB, Richards W, Blanco R, Xu HJ, Strauss GM, Sugarbaker DJ. Molecular pathologic substaging in 244 stage I non-small-cell lung cancer patients: clinical implications. J Clin Oncol. 1998 Jul;16(7):2468–2477.

Published In

J Clin Oncol

DOI

ISSN

0732-183X

Publication Date

July 1998

Volume

16

Issue

7

Start / End Page

2468 / 2477

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Survival Analysis
  • Risk Factors
  • Retrospective Studies
  • Prospective Studies
  • Prognosis
  • Predictive Value of Tests
  • Oncology & Carcinogenesis
  • Neoplasm Staging
  • Mutation