Veracyte confirms new data on genomic alterations in thyroid cancer
Category: #health  By Mateen Dalal  Date: 2019-11-04
  • share
  • Twitter
  • Facebook
  • LinkedIn

Veracyte confirms new data on genomic alterations in thyroid cancer

 

  • The data was presented during the 89th Annual meeting of the America Thyroid Association (ATA) held this week       

Veracyte, Inc. – a California based leading genomic diagnostics company, has reportedly announced the release of data that facilitates understanding of the frequency, predictive value and simultaneous occurrence of genomic alterations that are being targeted by new investigational precision therapies for the treatment of thyroid cancer.

Apparently, these findings were provided by Afirma® Xpression Atlas analyses that utilizes RNA sequencing of Veracyte’s thyroid nodule fine-needle aspiration (FNA) samples from patients diagnosed with thyroid cancer and undergoing required evaluation.

In one such study, researchers evaluated the frequency of BRAF, ALK, NTRK and RET fusions among approximately 48,000 patients whose thyroid nodule FNA samples appeared to be suspicious for malignancy (Bethesda III/IV, V and VI categories) by cytopathology.

Reports estimate that the researchers discovered that nearly 425 (0.89%) of the FNA samples fostered one of the alterations, with NTRK fusions being the most common at 0.38% followed by RET (0.32%) then BRAF (0.13%) and finally, ALK comprising of 0.06%. Moreover, RNA whole transcriptome sequencing illustrates the differences in the prevalence of these four fusions across Bethesda categories, with the highest being Bethesda V.

University of Texas MD Anderson Cancer Centre professor, Mimi I. Hu, M.D., was reportedly quoted stating that pan-cancer FDA approval has been received for the NTRK fusion inhibitors and clinical trials have involved certain inhibitors of BRAF, ALK, NTRK, and RET, that allow their detection in patients suffering from thyroid cancer of interest to physicians.

Additionally, with the widening use of genomics in the treatment of thyroid cancer, the data holds the potential to enhance the initial phase of treatment, predict the response to the treatment and set selective targeted therapies to ensure reliable, systematic and favorable treatment, Dr. Mimi further added.

Furthermore, during the ATA meeting, Veracyte revealed its new Afirma patient report, which along with detecting suspicious cancer nodules in patients also provides personalized and actionable variant and fusion information on individual patients.

The study contains necessary information regarding risk of malignancy, risk of lymph node metastasis, correlated neoplasm type, and extrathyroidal extension; genetic counseling, presence of FDA-approved therapy and germline testing considerations. 
 

Source Credits: https://investor.veracyte.com/news-releases/news-release-details/veracyte-announces-new-data-advance-understanding-genomic

  • share
  • Twitter
  • Facebook
  • LinkedIn


About Author

Mateen Dalal    

Mateen Dalal

A qualified electronics and telecommunication engineer, Mateen Dalal embarked on his professional journey working as a quality and test engineer. Harnessing his passion for content creation however, Mateen pens down industry-rich articles for ReportsGO.com and a few o...

Read More

More News By Mateen Dalal

MyndVR-Vi unite to deliver VR care services at Palo Alto CCRCs
MyndVR-Vi unite to deliver VR care services at Palo Alto CCRCs
By Mateen Dalal

MyndVR, a leading health and wellness company providing virtual reality solutions to senior living communities, has recently announced its partnership with Vi. Vi is a leading continuing care retirement community (CCRC), which integrates sophisticate...

Quest Diagnostics announces acquisition of Blueprint Genetics
Quest Diagnostics announces acquisition of Blueprint Genetics
By Mateen Dalal

Quest Diagnostics announced the acquisition of genetic testing firm, Blueprint Genetics to extend access to actionable insights in genetic and rare diseases. The acquisition is aimed at enhancing patient care and boosting research and development of ...

The U.S. FDA authorizes Tepezza to treat thyroid eye disease in adults
The U.S. FDA authorizes Tepezza to treat thyroid eye disease in adults
By Mateen Dalal

The U.S. FDA (Food and Drug Administration), a federal agency of the U.S. Department of Health and Human Services, has reportedly approved teprotumumab-trbw (Tepezza) to treat adults suffering from thyroid eye disease. This is a rare condition in wh...