Prognostic impact of EGFR mutation in non-small-cell lung cancer patients with family history of lung cancer
A family history can be a valuable tool in the era of precision medicine. Although a few studies have described an association of family history of lung cancer with EGFR activating mutation, their impact on survival of lung cancer patients is unclear. The study included consecutive 829 non-small-cel...
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Published in: | PloS one Vol. 12; no. 5; p. e0177015 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Public Library of Science
09-05-2017
Public Library of Science (PLoS) |
Subjects: | |
Online Access: | Get full text |
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Summary: | A family history can be a valuable tool in the era of precision medicine. Although a few studies have described an association of family history of lung cancer with EGFR activating mutation, their impact on survival of lung cancer patients is unclear.
The study included consecutive 829 non-small-cell lung cancer patients who received analysis of EGFR mutation in a prospective lung cancer cohort. Family history of lung cancer was obtained by face-to-face interviews at the time of diagnosis. An association of EGFR activating mutation with a family history of lung cancer in first-degree relatives was evaluated with multivariate logistic regression analysis, and its association with survival was estimated with Cox's proportional hazards model.
Seventy five (9.0%) patients had family history of lung cancer. The EGFR mutation was commonly observed in patients with positive family history compared to those with no family history (46.7% v 31.3%, χ2 p = 0.007). The family history was significantly associated with the EGFR mutation (aOR and 95% CI: 2.01 and 1.18-3.60, p = 0.011). Patients with the positive family history survived longer compared to those without (MST, 17.9 v 13.0 months, log-rank p = 0.037). The presence of the EGFR mutation was associated with better survival in patients without the family history (aHR and 95% CI: 0.72 and 0.57-0.90, p = 0.005). However, this prognostic impact was not observed in patients with the positive family history (aHR and 95% CI: 1.01 and 0.50-2.36, p = 0.832).
In comparison to patients without the family history, EGFR activating mutation was common, and it did not affect prognosis in patients with positive family history. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: The authors have declared that no competing interests exist. Conceptualization: JSR.Data curation: HJK KWC MSC JHN.Formal analysis: HJK JSK.Funding acquisition: JSR.Investigation: JSK JSR.Methodology: JSK JSR.Project administration: JSK JSR HJK.Resources: HJK.Supervision: JSR HJK.Visualization: JSR KWC.Writing – original draft: JSK JSR.Writing – review & editing: JSK JSR MSC JHN. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0177015 |