Completed

Detection of Occult Micrometastases in Patients With Clinical Stage I NSCLC: A Prospective Analysis

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What is being collected

Genetic Data

+ other Data

Collected from today forward - Prospective
GeneticOtherDNA Samples
Who is being recruted

Bronchial Neoplasms+7

+ Carcinoma, Bronchogenic

+ Lung Diseases

Over 18 Years
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: May 1997
See protocol details

Summary

Principal SponsorAlliance for Clinical Trials in Oncology
Last updated: June 29, 2016
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 1997

Actual date on which the first participant was enrolled.

OBJECTIVES: Determine whether the presence of occult micrometastases (OM) detected by immunohistochemistry or reverse transcriptase-polymerase chain reaction (RT-PCR) in histologically negative lymph nodes or bone marrow is associated with poorer survival among patients with stage I non-small cell lung cancer. Determine the incidence of OM in histologically negative lymph nodes and bone marrow by immunohistochemistry (staining for cytokeratins and the CEA glycoprotein) or RT-PCR (to detect CEA mRNA) in these patients. Assess the sensitivity of immunohistochemistry relative to RT-PCR for detecting OM in these patients. Determine the relationship between tumor size (or T-stage) and the presence of OM detected by immunohistochemistry or RT-PCR in these patients. Determine the relationship between the presence of OM and disease-free survival in these patients. Determine the relationship between the site of OM and incidence of recurrence, site of recurrence, and survival of these patients. OUTLINE: At the time of thoracotomy and pulmonary resection, patients have samples of bone marrow, primary tumor, and intrathoracic lymph nodes harvested. The presence of occult metastases in bone marrow and lymph nodes is assessed using immunohistochemistry or reverse transcriptase-polymerase chain reaction. Patients are followed every 6 months for 5 years.

NCT00003006
Principal SponsorAlliance for Clinical Trials in Oncology
Last updated: June 29, 2016
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

501 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Bronchial NeoplasmsCarcinoma, BronchogenicLung DiseasesNeoplasmsNeoplasms by SiteRespiratory Tract DiseasesRespiratory Tract NeoplasmsThoracic NeoplasmsCarcinoma, Non-Small-Cell LungLung Neoplasms

Criteria

Clinical stage I proven or suspected new non-small cell lung carcinoma T1 or T2 primary N1 or N2 lymph nodes <1cm on CT or negative mediastinoscopy ≥ 5 years since prior chemo or XRT; no prior mediastinal or chest XRT. ≥ 18 years of age No history of previous lung cancer or concomitant malignancy

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 10 locations

Holden Comprehensive Cancer Center at The University of Iowa

Iowa City, United StatesOpen Holden Comprehensive Cancer Center at The University of Iowa in Google Maps

Marlene &amp; Stewart Greenebaum Cancer Center, University of Maryland

Baltimore, United States

University of Minnesota Cancer Center

Minneapolis, United States

University of Minnesota Medical School

Minneapolis, United States
Completed10 Study Centers