Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2014-09-30
2017-09-30
Brief Summary
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Telomere biology is activated aberrantly is most lung cancers but has not been studied in early stages to the best of our knowledge.
The objective of this study is to evaluate telomere length and activity with suspected early stage adenocarcinoma of the lung.
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Detailed Description
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The clinical presentation of early adenocarcinoma subtypes is highly variable ranging from a small solitary nodule to extensive lobar consolidation. Many peripheral lesions have a characteristic ground glass opacity appearance on Chest CT, which may correlate with an improved prognosis. The reported five-year disease-free survival after resection for isolated lesions may approaches 100%.
Preoperative diagnosis of such lesions is complicated by several limitations. First, the differential diagnosis is broad including an extensive number of inflammatory and infectious processes. Second, positron emission tomography (PET), which identifies regions of increased metabolic activity, may be falsely negative due to the slow growth of early adenocarcinoma lesions. Transbronchial needle biopsy is also unreliable to confirm or exclude disease in non-solid type lesions.
The proportion of lung cancers classified as adenocarcinoma has steadily increased and now comprises nearly ½ of cases. However, the proportion of adenocarcinoma in situ is uncertain. Previous reports range from 5-10% in a large series to as high as 24% in the large Surveillance, Epidemiology and End Results database. Thus, these early adenocarcinoma lesions may represent a disproportionately large number of lung cancers which are PET negative yet carry an excellent prognosis after early resection. The early adenocarcinoma subtypes represent a clinical entity requiring further characterization to distinguish lesions more likely to be malignant from benign.
Telomerase is activated aberrantly in most lung cancers and mutations in telomerase components predispose to solid malignancies. For patients with non-small cell lung cancer, numerous studies correlate increased tumor telomerase activity with increased likelihood of Stage IIIB and Stage IV disease and/or reduced survival. Furthermore, telomerase inhibition is currently being studied in clinical trials of patients with advanced non-small lung cancer.
Problem:
The semi-solid lung lesion may represent early stage adenocarcinoma which has an excellent prognosis upon early diagnosis and prompt surgical resection. However, the semi-solid lesion has a broad differential diagnosis and preoperative features characteristic of adenocarcinoma are needed to distinguish malignant from benign lesions.
Objective:
To study telomere length and telomerase activity in patients with suspected early adenocarcinoma of the lung whom are referred for surgical biopsy of lung lesions.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Suspected Adenocarcinoma of the Lung
Patients with suspected adenocarcinoma of the lung referred for surgical lung biopsy after multi-disciplinary team recommendation.
No interventions assigned to this group
Healthy Control
Age and sex-matched patients with no known lung disease or other chronic inflammatory disease or malignancy
No interventions assigned to this group
Age-matched controls with proven solid lung malignancy
Patients with biopsy-proven advanced solid malignancy of the lung
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
Patients with other chronic inflammatory disease requiring immunosuppressive therapy or known extra-pulmonary malignancy.
18 Years
90 Years
ALL
Yes
Sponsors
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Meir Medical Center
OTHER
Responsible Party
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Locations
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Soroka University Medical Center
Beersheba, , Israel
Meir Medical Center
Kfar Saba, , Israel
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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0067-14-MMC
Identifier Type: -
Identifier Source: org_study_id
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