ID
45966
Beschreibung
Principal Investigator: Christopher Amos, National Institutes of Health, Bethesda, MD, USA MeSH: Lung Neoplasms,Adenocarcinoma,Neoplasms, Squamous Cell https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000876 The study was conducted under the auspices of the Transdisciplinary Research In Cancer of the Lung (TRICL) Research Team, which is a part of the Genetic Associations and MEchanisms in ONcology (GAME-ON) consortium, and associated with the International Lung Cancer Consortium (ILCCO). *Ethics* All participants provided written informed consent. All studies were reviewed and approved by institutional ethics review committees at the involved institutions. *Sequencing data* are derived from four sub-studies. The sub-studies that contributed include Harvard, Liverpool, Toronto, and IARC. The IARC and Toronto studies are described above. A description of the Harvard and Liverpool studies is provided below. **Liverpool Lung Project:** The Liverpool Lung Project (LLP)1 is a case control and cohort study, which has over 11,500 individuals, with detailed epidemiological, clinical and outcome data with associated specimens (i.e. tumour tissue, blood, plasma, sputum, bronchial lavage, EBUS and oral brushings). The participants have completed a detailed lifestyle questionnaire and updated data on clinical outcome and hospital events are collected through the Office of National Statistics, Cancer Registry and from Health Episode Statistics. The project is registered on the UK National Institute for Health Research (NIHR) lung cancer portfolio and has all the required ethical approvals and sponsorship arrangements in place. The LLP has detailed standard operating procedures (SOP) for all aspects of the recruitment, data, specimen collection as well as the data storage. The LLP Cohort study has 8,224 participants with blood and 7,761 with plasma samples. The LLP case-control samples have been incorporated into in a large number of international GWAS and molecular studies sup2,3/sup, methylation sup4-7/sup, microRNA sup8/supand next generation studies sup9-11/sup, resulting in high ranking publications, as well as forming the basis for the LLP risk prediction model sup12-14/sup which has been utilised in the UK lung cancer screening trial (UKLS) sup15-17/sup Patient and control DNAs were derived from EDTA-venous blood samples. *Harvard Samples.* David Christiani at the Harvard University School of Public Health has been directing research studies to investigate etiological factors influencing lung cancer development since 1983 and has amassed a collection of 2000 controls and 5055 lung cancer cases. He has been actively collecting and storing snap frozen tumor samples since 1992. Around 1500 tumor samples have been collected and the average wet tumor yield is about 30 grams of tumor, of which 631 cases have completely annotated clinical and survival information. Pathology confirmation is provided by two pathologists. At the time of surgery, a minimum of 30 grams of wet lung tumor tissue and 30 grams of non-involved tissue from the same lobe is sectioned, flash frozen and sent to Dr. Christiani's lab for logging and storage. A blood sample for DNA and serum is collected. A structured interview by trained research staff is conducted on each case, and clinical outcomes and treatments is extracted and entered into the molecular epidemiology data base at Harvard. Fresh frozen samples have been collected from 1451 lung cancer and are available for study. Samples from this collaborative study have played key roles in major studies, including the initial finding describing EGFR mutations in lung cancer sub22/sub. Participants in this study are patients, 18 years of age, with newly diagnosed histologically confirmed lung cancer. Samples that are included in the analysis have the following histologies: Adenocarcinoma: 8140/3, 8250/3, 8260/3, 8310/3, 8480/3 8560/3; LCC: 8012/3, 8031/3; squamous carcinoma: 8070/3, 8071/3, 8072/3, 8074/3; and other NSCLC: 8010/3, 8020/3, 8021/3, 8032/3, 8230/3. *The Toronto Study:* The Toronto study was conducted in the Great Toronto Area between 1997 and 2014. Cases were recruited at the hospitals in the network of University of Toronto and Lunenfeld- Tanenbaum Research Institute. At the time of recruitment in the clinical setting, provisional diagnoses of lung carcinoma were first assigned based on clinical criteria. Diagnoses for all cases included were histologically confirmed by the reference pathologist who is a specialist in pulmonary pathology, based on review of pathology reports from surgery, biopsy or cytology samples in 100% of cases. Diagnostic classification was done initially according to ICD-9, ICD-10, and ICD for oncology-2, and subsequently converted to ICD-O-3. Tumors were grouped into the major categories included in this analysis according to primary cancer type based on the ICD-3 definitions. Controls were randomly selected from individual visiting family medicine clinics and Ministry of Finance Municipal Tax Tapes. All subjects were interviewed using a standard questionnaire and information on lifestyle risk factors, occupational history, medical and family history was collected. Blood samples were collected from more than 85% of the subjects. *IARC:* The IARC data are derived from case-control studies conducted in Russia and include samples that have available tissue samples. Patient and control DNAs were derived from EDTA-venous blood samples. The lung cancer patients were classified according to ICD-O-3; SQ: 8070/3, 8071/3, 8072/3, 8074/3; AD: 8140/3, 8250/3, 8260/3, 8310/3, 8480/3, 8560/3, 8251/3, 8490/3, 8570/3, 8574/3; with tumous with overlapping histologies classified as mixed. *The Lung Cancer Transdisciplinary Research Cohort is utilized in the following dbGaP sub-studies.* To view genotypes, other molecular data, and derived variables collected in these sub-studies, please click on the following sub-studies below or in the "Sub-studies" section of this top-level study page phs000876 Lung Cancer Transdisciplinary Research Cohort.- phs000877 Meta Analysis - phs000878 CIDR Lung Cancer - phs001681 Affy Axiom Array
Link
Stichworte
Versionen (1)
- 26.03.24 26.03.24 - Madita Rudolph
Rechteinhaber
Christopher Amos, National Institutes of Health, Bethesda, MD, USA
Hochgeladen am
26. März 2024
DOI
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Lizenz
Creative Commons BY 4.0
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dbGaP phs000876 Transdisciplinary Research Into Cancer of the Lung (TRICL)
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, subject source, source subject ID, consent group, and affection status of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing" project.
- Subject ID, sample ID, sample source, source sample ID, study accession, and sample use variable of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing" project.
- Sample ID, body site where sample was obtained, analyte type, type of DNA extraction, and tumor status of sample of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing" project.
- Subject ID, study site, gender, case or control status, age, smoking status, ethnicity, history, and cigarette pack per years of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing" project.
- Subject ID, age, gender, subjects with or without lung cancer, and smoking status of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Affymetrix" project.
- Sample ID, analyte type, body site where sample was obtained, tumor status of sample, tumor subtype of samples, and source repository where subjects originate of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Affymetrix" project.
Ähnliche Modelle
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, subject source, source subject ID, consent group, and affection status of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing" project.
- Subject ID, sample ID, sample source, source sample ID, study accession, and sample use variable of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing" project.
- Sample ID, body site where sample was obtained, analyte type, type of DNA extraction, and tumor status of sample of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing" project.
- Subject ID, study site, gender, case or control status, age, smoking status, ethnicity, history, and cigarette pack per years of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing" project.
- Subject ID, age, gender, subjects with or without lung cancer, and smoking status of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Affymetrix" project.
- Sample ID, analyte type, body site where sample was obtained, tumor status of sample, tumor subtype of samples, and source repository where subjects originate of participants with or without lung cancer and involved in the "Transdisciplinary Research into Cancer of the Lung (TRICL) - Affymetrix" project.
C0680251 (UMLS CUI [1,2])
C1512693 (UMLS CUI [1,2])
C0243161 (UMLS CUI [1,3])
C0679557 (UMLS CUI [1,4])
C0242379 (UMLS CUI [1,5])
C0001418 (UMLS CUI [1,6])
C0007137 (UMLS CUI [1,7])
C0206704 (UMLS CUI [1,8])
C0206623 (UMLS CUI [1,9])
C0007131 (UMLS CUI [1,10])
C3640076 (UMLS CUI [1,2])
C0871420 (UMLS CUI [1,3])
C1519386 (UMLS CUI [1,2])
C0150103 (UMLS CUI [1,3])
C1706256 (UMLS CUI [1,4])