Medical Technology

GE Healthcare receives US FDA clearance for low dose CT lung cancer screening

GE Healthcare, a leading provider of transformational medical technologies and services, has become the first company with a low dose computed tomography (CT) lung cancer screening option that is cleared by the US FDA for lung cancer screening.GE-Healthcare

Both the US Preventative Services Task Force (USPSTF) and the Centers for Medicare and Medicaid Services (CMS) recommend the use of low dose CT lung cancer screening for high-risk individuals.

Additionally, Medicare has approved insurance reimbursement for its beneficiaries who are eligible for the use of low dose CT lung cancer screening in high-risk patients. Early detection from an annual lung cancer screening with low dose CT in high-risk persons can prevent a substantial number of lung cancer–related deaths.

“Bringing low dose CT screening to patients at a high risk for lung cancer will reduce death from the most deadly cancer worldwide,” said Dr. Ella Kazerooni, chair of committee on lung cancer screening, American College of Radiology.

“Performing low dose CT with attention to high image quality at the lowest radiation exposure to detect early cancer is at the core of a successful screening programme, and requires collaboration with imaging partners to bring technology to bear for this purpose. The FDA’s clearance of these CT scanners for this purpose illustrates that commitment.”

Physicians using low dose CT for lung cancer screening will now have access to the benefits from a screening indication, including GE Healthcare’s new low-dose screening reference protocols. These new protocols are tailored to the CT system, patient size, and the most current recommendations from a wide range of professional medical and governmental organisations. Now, qualified GE Healthcare CT scanners can be confidently used by physicians within their FDA cleared indications for use, delivering low dose, short scan times, and clear and sharp images for the detection of small lung nodules. These nodules are critical in identifying lung cancer at its earliest stages when it is the most treatable and curable.

The landmark National Lung Screening Trial (NLST) was conducted at 33 medical institutions with over 53,000 older, otherwise healthy patients at high-risk due to smoking history. Half of the participants were screened using low dose CT, the other half were screened using chest X-ray. The trial demonstrated that the use of low dose CT screening decisively reduced the mortality rate from lung cancer by 20 per cent compared to use of chest X-ray. The NLST also revealed a significant 6.7 per cent reduction in the rate of death from any cause using low dose CT screening.

All new 64-slice and greater CT scanners, and virtually all of the 16-slice CT scanners that GE Healthcare sells are qualified systems and will include the screening option. The solution that GE Healthcare developed is also available to thousands of qualified GE scanners currently in use, increasing access to the quality scanners that satisfy both patient and physician needs. The new protocols are able to utilise GE Healthcare’s industry-leading technologies such as ASiR, ASiR-V and Veo that are designed to reduce image noise, which is undesirable for physicians looking for small nodules.

In the United States, lung cancer is the third most common cancer and the leading cause of cancer deaths; it kills almost twice as many women as breast cancer and three times as many men as prostate cancer. Survival rates from lung cancer are highly correlated to its initial stage at the time of first diagnosis. The overall five-year survival rate for lung cancer is among the lowest (17 per cent) of all types of cancer but is significantly higher when the cancer is diagnosed at an early stage (54 per cent). However, currently only 15 per cent of lung cancer cases are diagnosed at such an early stage. The use of low dose CT lung cancer screening increases this percentage of early stage detection, providing patients a much better prognosis.

“This is the first time in history that any CT device has received FDA clearance for any screening indication,” said Henry Hummel, president and chief executive officer of molecular imaging and CT at GE Healthcare.

“GE Healthcare is thrilled to be the first CT vendor who can help clinicians establish low dose CT lung screening programmes in order to continue improving the health of their patients. Healthcare providers are looking for solutions beyond just imaging equipment; we look forward to helping them establish low dose CT lung cancer screening programmes that will inevitably save lives through earlier diagnosis and treatment for patients.

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