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OpenTrials
Completed

NCT Number: NCT00763607

Retrospective Study Evaluating IGF1R And p95HER2 as Prognostic Factors in Non Small Cell Lung Cancer (NSCLC)

Aim of the study is to evaluated the role of IGF1R and p95HER2 on prognosis in radically resected non small cell lung cancer patients

The primary objective is to correlate the expression of IGF1R and p95HER2 with survival.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Istituto Clinco Humanitas

Rozzano, Milan, 20089, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Radically resected non small cell lung cancer patients with tumor tissue available

Exclusion criteria

  • Tumor tissue not available
  • Clinical data not available

Treatment and study plan

Protein expression by immunohistochemistry and immunofluorescence

Genetic

Protein expression by immunohistochemistry and immunofluorescence

Primary outcomes

  1. Association of different biomarkers with survival

    Time frame: At the end of enrollment

Secondary outcomes

  1. Association of a specific biomarker with patient's characteristics

    Time frame: At the end of enrollment

Sponsors and collaborators

Lead sponsor

Armando Santoro, MD

Other

Registry information

Official study title

Retrospective Study Evaluating IGF1R And p95HER2 as Prognostic Factors in Radically Resected Non Small Cell Lung Cancer

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Oct 1, 2008
Registry last updated
Sep 10, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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