– Study findings confirm the importance of improving education among clinicians and streamlining processes to increase adoption of testing in routine cancer care –
SAN FRANCISCO, May 26, 2023 /PRNewswire/ -- Invitae (NYSE: NVTA), a leading medical genetics company, today announced nine studies to be presented at the 2023 American Society of Clinical Oncology (ASCO) Annual Meeting held in Chicago from June 2-6, 2023. The new research insights highlight innovations in genetic testing in a variety of clinical settings, population groups and cancer types, and reinforce the need to reduce barriers to genetic services to help patients receive the most effective care and monitoring.
Presentation showcases learnings about the benefits of germline genetic testing for lung cancer patients (Saturday, June 3, 2023 at 12:30 p.m. CDT and Monday, June 5, 2023 at 1 p.m. CDT)
Leading lung cancer expert and Invitae research partner, Renato Martins, M.D., M.P.H., Virginia Commonwealth University (VCU) Massey Cancer Center, will present findings from a retrospective study of over 7,000 lung cancer patients who completed germline genetic testing (GGT). Results of the study showed that 14.9% of patients in this cohort had pathogenic germline variants (PGVs), nearly all of which were clinically actionable. Dr. Martins will share research highlights and key takeaways about how patients with lung cancer can benefit from precision therapies based on PGVs in addition to how this vital information informs future cancer screening and family testing, which supports consideration for GGT for patients with lung cancer.
Latest PROCLAIM trial findings illustrate how prostate cancer patients experience the impact of genetic testing (Saturday, June 3, 2023 at 1:15 p.m. CDT)
Studies have shown that uptake for GGT in prostate patients varies widely (10-60%) based on the stage of the disease, practice setting and provider type. To better understand how patients experience genetic testing, Invitae enrolled unselected prostate cancer patients from 15 community urology practices to undergo multigene panel testing and collected patient-reported outcomes via surveys at least one month post GGT.
Most patients reported that their test results reduced their concerns or did not impact their level of concern regarding their cancer diagnosis, treatment or follow up. This study shows that universal GGT was beneficial to prostate cancer patients and helped to inform their treatment and follow-up decisions.
"Educational programs for germline genetic testing (GGT) for community clinicians treating prostate cancer patients is essential so they can successfully incorporate GGT into their practices," said Neal D. Shore, M.D., F.A.C.S., from the Carolina Urologic Research Center, and lead author of the study. "When clinicians understand both the 'why' and the 'how' for a successful testing program, then patients, their families and our healthcare system will all benefit."
Population level data demonstrates support for universal germline testing after a cancer diagnosis (Monday, June 5, 2023 at 3 p.m. CDT)
A study led by Allison Kurian, M.D., M.Sc., at Stanford University, in collaboration with Invitae and others, sought to better understand the adoption of genetic testing and results across cancer types. Using the statewide Surveillance Epidemiology and End Results (SEER) registries in California and Georgia, researchers were able to link results from laboratories that provided nearly all GGT in these regions to evaluate more than 1.3 million adult patients diagnosed with all reported cancer types.
The study highlighted that GGT remains low across cancer types, falling short of guidelines, and the gaps in rates of testing and particularly the continued racial/ethnic disparities in testing are critical areas for intervention that systematic implementation of current universal testing guidelines may help to address. Genetic testing use among patients for whom universal testing is currently recommended were as follows: male breast cancer (50%), ovarian cancer (38.6%), female breast cancer (26%), pancreatic cancer (5.6%), colorectal cancer (5.6%) with testing use increasing over time from 2013 to 2019. Additionally, results showed that compared to non-Hispanic whites, patients from other racial/ethnic groups received less testing without improvement over time, underscoring the need to improve access to genetic testing for underserved groups.
"Significant gaps persist in the uptake of germline genetic testing across cancer types," stated W. Michael Korn, M.D., chief medical officer for oncology at Invitae. "We continue to see evidence that the vast majority of patients who qualify have not yet benefited from testing. System-wide implementation of existing universal testing guidelines is the most effective way to identify actionable results that are currently missed, and essential to provide patients access to germline-indicated precision therapies and clinical trials, especially for underserved populations."
"The power of linking genetic testing results to SEER registry data allows us to understand what is happening at the population level – and to pinpoint where the gaps in testing lie," said Kurian. "This is a crucial step towards closing those gaps."
Study results show that novel approaches that aim to streamline germline genetic testing can help eliminate barriers in clinical practice
The research team at University of Vermont Medical Center partnered with Invitae to explore a novel and streamlined approach to genetic testing where patients with advanced cancer were first tested and then offered genetic counseling if a PGV was identified.
Patients who had been diagnosed recently (<1 year) with metastatic cancer underwent germline testing accompanied by written educational materials. Patients received outreach from a genetic counselor only if their results showed a variant of uncertain significance (phone call) or were positive for a PGV (phone call plus invitation for clinic follow-up), while those with negative results received a summary letter.
Patients and healthcare providers were given a survey to gauge their satisfaction with the streamlined testing process. More than 94% of patients appreciated having undergone testing during an existing appointment and 82% of participants felt confident that they understood the results of their test. Every healthcare provider who completed the survey was satisfied with the testing process and 94% were interested in continuing with the new approach. The study results show that there is interest from both healthcare providers and patients to incorporate new processes that remove barriers to genetic testing and facilitate seamless integration into cancer care.
Improving access to genetic testing
Invitae is presenting additional research with its partners at ASCO that supports the company's mission to bring comprehensive genetic information into mainstream medicine to improve healthcare for all. These findings underscore the importance of incorporating genetic testing into the standard of care and improving access to testing for underrepresented groups to aid in earlier diagnoses and connect patients to clinical trials as well as precision medicines.
2023 ASCO presentations:
2023 ASCO posters:
Invitae (NYSE: NVTA) is a leading medical genetics company trusted by millions of patients and their providers to deliver timely genetic information using digital technology. We aim to provide accurate and actionable answers to strengthen medical decision-making for individuals and their families. Invitae's genetics experts apply a rigorous approach to data and research, serving as the foundation of their mission to bring comprehensive genetic information into mainstream medicine to improve healthcare for billions of people.
To learn more, visit invitae.com and follow for updates on Twitter, Instagram, Facebook and LinkedIn @Invitae.
Safe Harbor Statement
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements relating to the company's beliefs regarding the implications of its new research; that the research reinforces the critical role of germline genetic testing in oncology; and that the study findings confirm the importance of improving education among clinicians and streamlining processes to increase adoption of testing in routine cancer care. Forward-looking statements are subject to risks and uncertainties that could cause actual results to differ materially, and reported results should not be considered as an indication of future performance. These risks and uncertainties include, but are not limited to: the company's ability to grow its business in a cost-efficient manner; the company's history of losses; the company's ability to maintain important customer relationships; the company's ability to compete; the company's need to scale its infrastructure in advance of demand for its tests and to increase demand for its tests; the risk that the company may not obtain or maintain sufficient levels of reimbursement for its tests; the applicability of clinical results to actual outcomes; risks associated with litigation; the company's ability to use rapidly changing genetic data to interpret test results accurately and consistently; security breaches, loss of data and other disruptions; laws and regulations applicable to the company's business; and the other risks set forth in the company's filings with the Securities and Exchange Commission, including the risks set forth in the company's Quarterly Report on Form 10-Q for the quarter ended March 31, 2023. These forward-looking statements speak only as of the date hereof, and Invitae Corporation disclaims any obligation to update these forward-looking statements.
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SOURCE Invitae Corporation