Comprehensive Genomic Profiling of Cell-Free Circulating Tumor DNA Detects Response to Ribociclib Plus Letrozole in a Patient with Metastatic Breast Cancer.
Catarina SilveiraAna Carla SousaPatrícia CorredeiraMarta MartinsAna Rita SousaArnaud Da Cruz PaulaPier SelenicaDavid N BrownMahdi GolkaramShannon KaplanShile ZhangLi LiuBritta WeigeltJorge S Reis-FilhoLuis CostaMaria Carmo-FonsecaPublished in: Biomolecules (2022)
Analysis of cell-free circulating tumor DNA obtained by liquid biopsy is a non-invasive approach that may provide clinically actionable information when conventional tissue biopsy is inaccessible or infeasible. Here, we followed a patient with hormone receptor-positive and human epidermal growth factor receptor (HER) 2-negative breast cancer who developed bone metastases seven years after mastectomy. We analyzed circulating cell-free DNA (cfDNA) extracted from plasma using high-depth massively parallel sequencing targeting 468 cancer-associated genes, and we identified a clonal hotspot missense mutation in the PIK3CA gene (3:178952085, A > G, H1047R) and amplification of the CCND1 gene. Whole-exome sequencing revealed that both alterations were present in the primary tumor. After treatment with ribociclib plus letrozole, the genetic abnormalities were no longer detected in cfDNA. These results underscore the clinical utility of combining liquid biopsy and comprehensive genomic profiling to monitor treatment response in patients with metastasized breast cancer.
Keyphrases
- circulating tumor
- cell free
- copy number
- epidermal growth factor receptor
- genome wide
- single cell
- metastatic breast cancer
- ultrasound guided
- fine needle aspiration
- genome wide identification
- case report
- tyrosine kinase
- dna methylation
- advanced non small cell lung cancer
- polycystic ovary syndrome
- endothelial cells
- ionic liquid
- circulating tumor cells
- early breast cancer
- optical coherence tomography
- healthcare
- adipose tissue
- gene expression
- health information
- social media
- autism spectrum disorder
- young adults
- protein kinase