Geisinger Health System
01/25/2023 | Press release | Distributed by Public on 01/25/2023 10:44
Genomic screening can help detect thyroid cancer, study finds
Medullary thyroid cancer found in 60% of patients with RET gene variants who had thyroid removed
DANVILLE, Pa. - Population-based genomic screening can facilitate early detection of medullary thyroid cancer (MTC) in patients with variants in the RET gene, a new Geisinger study found.
MTC accounts for 2% to 5% of all thyroid cancers and is responsible for 13% of all deaths related to thyroid cancer. About one-quarter of MTC cases are hereditary and can be attributed to variants in the RET gene.
The Geisinger study evaluated 75 patients who were found to have RET gene variants as part of the MyCode Community Health Initiative. None of the patients had any symptoms of thyroid cancer prior to receiving these genetic results. Twenty of these patients chose to have a thyroidectomy after learning of the RET variant; 13 also had lymph nodes removed. Of the 20 patients who chose to have surgery, cancer was detected in 12. Two additional patients had C-cell hyperplasia, a known precursor to MTC. The results were published in JAMA Otolaryngology - Head and Neck Surgery.
While genomic screening can provide opportunities for early detection and treatment of MTC, more work is needed to ensure patients have the education and resources they need to understand the condition and make decisions about their care based on their genetic risk factors, the research team said.
"It is possible that some patients in the study chose not to have surgery due to an absence of symptoms at the time of detection, or were hesitant to act upon a potential risk," said Nicholas Purdy, D.O., FACS, director of head and neck surgery in Geisinger's department of otolaryngology and a lead author of the study. "It is important to further identify barriers to care and make sure that all patients receive the information they need to make informed decisions about their care."
"Genomic screening through MyCode allows us to find previously unrecognized risks for cancer and other serious diseases and intervene early," said Adam Buchanan, M.S., MPH, chair of Geisinger's Department of Genomic Health and a co-author of the study. "But it also compels us to support patients and clinicians throughout the process and conduct research that improves the likelihood of positive health outcomes for patients and families."
MTC accounts for 2% to 5% of all thyroid cancers and is responsible for 13% of all deaths related to thyroid cancer. About one-quarter of MTC cases are hereditary and can be attributed to variants in the RET gene.
The Geisinger study evaluated 75 patients who were found to have RET gene variants as part of the MyCode Community Health Initiative. None of the patients had any symptoms of thyroid cancer prior to receiving these genetic results. Twenty of these patients chose to have a thyroidectomy after learning of the RET variant; 13 also had lymph nodes removed. Of the 20 patients who chose to have surgery, cancer was detected in 12. Two additional patients had C-cell hyperplasia, a known precursor to MTC. The results were published in JAMA Otolaryngology - Head and Neck Surgery.
While genomic screening can provide opportunities for early detection and treatment of MTC, more work is needed to ensure patients have the education and resources they need to understand the condition and make decisions about their care based on their genetic risk factors, the research team said.
"It is possible that some patients in the study chose not to have surgery due to an absence of symptoms at the time of detection, or were hesitant to act upon a potential risk," said Nicholas Purdy, D.O., FACS, director of head and neck surgery in Geisinger's department of otolaryngology and a lead author of the study. "It is important to further identify barriers to care and make sure that all patients receive the information they need to make informed decisions about their care."
"Genomic screening through MyCode allows us to find previously unrecognized risks for cancer and other serious diseases and intervene early," said Adam Buchanan, M.S., MPH, chair of Geisinger's Department of Genomic Health and a co-author of the study. "But it also compels us to support patients and clinicians throughout the process and conduct research that improves the likelihood of positive health outcomes for patients and families."
About Geisinger
Geisinger is committed to making better health easier for the more than 1 million people it serves. Founded more than 100 years ago by Abigail Geisinger, the system now includes 10 hospital campuses, a health plan with more than half a million members, a Research Institute and the Geisinger Commonwealth School of Medicine. With nearly 24,000 employees and more than 1,700 employed physicians, Geisinger boosts its hometown economies in Pennsylvania by billions of dollars annually. Learn more at Facebook, Instagram, LinkedIn and Twitter.