Abstract 99P
Background
In recent years, comprehensive genetic profiling (CGP) became a widespread procedure performed in many cases of metastatic and non-metastatic malignancies. Commercial CGP kits provide information covering hundreds of cancer-related genes along with additional information on genomic stability, large-scale rearrangements and tumor mutational burden. The reports generated following CGP can serve as a diagnostic tool for the characterization of tumors according to their molecular traits. Though molecular reports may influence the diagnosis, routinely they are not sent to pathologists for review, but rather to oncologists who rely on the primary pathological diagnosis. We aim to investigate the potential impact of the integration of CGP reports as an ancillary pathology diagnosis.
Methods
We analyzed 170 CGPs in our unit since its establishment and searched for cases in which the molecular data contributed to the mere pathologic diagnosis.
Results
While in most cases CGP reports either did not affect or supported the primary diagnosis, in 8 cases (4.7%) molecular data substantially affected the primary pathologic diagnosis and contributed to the mere pathologic diagnosis.
Conclusions
We conclude that CGP reports may serve as a valuable component of pathology reports and diagnosis. This is especially true in cases of unknown primary origin and other uncertain diagnoses. It is therefore suggested to routinely review CGP results with the diagnosing pathologists for reassessment. Beyond revealing potential treatment options, CGP results may affect the mere pathological diagnosis.
Editorial acknowledgement
Clinical trial identification
Legal entity responsible for the study
The author.
Funding
Has not received any funding.
Disclosure
The author has declared no conflicts of interest.
Resources from the same session
10P - An adapted CGP-based model to interpret POLE mutations in endometrial cancer
Presenter: Rita Trozzi
Session: Cocktail & Poster Display session
Resources:
Abstract
11P - Reconstructing tumour evolution of single cells using both somatic mutations and copy-number alterations
Presenter: Rija Zaidi
Session: Cocktail & Poster Display session
Resources:
Abstract
12P - Swiss-PO: Molecular modelling for precision oncology
Presenter: Fanny Krebs
Session: Cocktail & Poster Display session
Resources:
Abstract
13P - A novel algorithm for predicting variant detectability in oncogenomic analysis
Presenter: Alper Akkuş
Session: Cocktail & Poster Display session
Resources:
Abstract
14P - expHRD: An algorithm for the transcriptome-based estimation of homologous recombination deficiency score
Presenter: Jin-Ku Lee
Session: Cocktail & Poster Display session
Resources:
Abstract
15P - ClinBioNGS: An integrated clinical bioinformatics pipeline for the analysis of somatic NGS cancer panels
Presenter: Xavier Sole
Session: Cocktail & Poster Display session
Resources:
Abstract
16P - Investigation of c-MYC role in DNA-PK-mediated activation of STING pathway in SCLC
Presenter: Caterina de Rosa
Session: Cocktail & Poster Display session
Resources:
Abstract
17P - NRF2 activation promotes HER2-targeted tolerance and resistance in oesophageal adenocarcinoma through metabolic reprogramming to glutathione
Presenter: Wei Zhang
Session: Cocktail & Poster Display session
Resources:
Abstract
18P - AURKB inhibition radiosensitises NSCLC by altering mitotic fate
Presenter: Kathryn Egerton
Session: Cocktail & Poster Display session
Resources:
Abstract
19P - Stratified control study on neuroendocrine differentiation and potential clinical markers in patients with limited-stage small-cell lung cancer
Presenter: Li Liu
Session: Cocktail & Poster Display session
Resources:
Abstract