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JCSE01 - Perspectives for Lung Cancer Early Detection (ID 779)
- Event: WCLC 2018
- Type: Joint IASLC/CSCO/CAALC Session
- Track: Screening and Early Detection
- Presentations: 1
- Coordinates: 9/23/2018, 07:30 - 11:15, Room 202 BD
JCSE01.16 - Positive Correlation Between Whole Genomic Copy Number Variant Scoring and the Grading System in Lung Non-Mucinous Invasive Adenocarcinoma (ID 14705)
11:15 - 11:15 | Author(s): Shenglei Li
Grading systems of Lung adenocarcinoma have been proposed by Sica and Kadota in stage I tumors,but the predominant architectural subtypes grading system is applicable for resection samples mostly. The correlation between the histological subtypes and grading with whole genomic copy number variation(WGCNV) is unknown, and was investigated in lung non-mucinous invasive adenocarcinoma (LNMIA) at this study.The predominant histological subtype from 58 resection specimens of LNMIA and 20 para-cancerous lung tissues were collected by laser microdissection from HE staining FrameSlides PEN-Membrane slides.7 of 58 specimens,two predominant subtypes in one cancerous nodule were collected simultaneously. Whole genome amplification followed by high-throughput sequencing was used to deteted WGCNV with the para-cancerous lung tissues as normal reference set and WGCNV was scored by a particular formula.
The letters above the figure show the results of Chi-squared test, and same letters mean no significant difference.
WGCNV median scores of 5 histological subtypes of LNMIA with three tiered architectural grades are shown in Table1. The WGCNV scores have a positive correlation with either histological subtypes and architectural grading system (Figure1 A and B). The differences of WGCNV scores are detected betweem two predominant subtypes in one cancerous nodule.GWCNV scores display a positive correlation with three tiered architectural grading system and may has a potential value to predict prognosis in LNMIA. a9ded1e5ce5d75814730bb4caaf49419
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P1.09 - Pathology (Not CME Accredited Session) (ID 941)
- Event: WCLC 2018
- Type: Poster Viewing in the Exhibit Hall
- Presentations: 1
- Coordinates: 9/24/2018, 16:45 - 18:00, Exhibit Hall
P1.09-20 - Correlation Between Whole Genomic Copy Number Variant Scoring and Pathological Classification, Staging in Lung Non-Mucinous Adenocarcinoma (ID 12126)
16:45 - 18:00 | Author(s): Shenglei Li
The new classification of lung adenocarcinoma composing of adenocarcinoma in situ (AIS), minimally invasive adenocarcinoma (MIA) and invasive adenocarcinoma (IA) has been applicable worldwide. Both the histological classification and TNM staging of lung adenocarcinoma have important values in indicating prognosis, but their correlations with whole genomic copy number variation (WGCNV) are still unknown.a9ded1e5ce5d75814730bb4caaf49419 Method
Lung non-mucinous adenocarcinoma(LNMA) including AIS, MIA and IA resection specimens, malignant pleural effusion (MPE), metastatic nodules (MN) biopsy and 20 para-cancerous non-tumor lung tissue samples were selected. The cells of predominant histological subtype from each LNMA and non-tumor smaples were collected by laser microdissection from HE staining FrameSlides PEN-Membrane slides. Whole genome amplification followed by high-throughput sequencing was used to detect the somatic CNV with the para-cancerous lung tissues as normal reference set. WGCNV was scored by a particular formula.4c3880bb027f159e801041b1021e88e8 Result
WGCNV median scores and distributions of pathological subcategories and TNM staging were shown in Table 1 and their trends were displayed in Figure 1.WGCNV scores display the positive correlation or significant differences among diversified histological subcategories of LNMA, but not in T & TMN staging8eea62084ca7e541d918e823422bd82e Conclusion
WGCNV scoring displays the positive correlation or significant differences among diversified subcategories and may has a potential value prediecting prognosis in LNMA.6f8b794f3246b0c1e1780bb4d4d5dc53