19 Oct 2023 - 20 Oct 2023
ESMO | Congress 2023
20 Oct 2023 - 24 Oct 2023
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NEXT-GENERATION SEQUENCING (NGS)
Cancer is a great burden for public health worldwide, and one of the strategies to reduce this burden is by conducting cancer screening and early diagnosis. Some screening methods, such as the use of mammograms to detect breast cancer or the use of the Pap test to detect cervical cancer, are proven methods of preventing these cancers. Because all of these screening methods are specific to unique tumour types, for more extensive cancer screening among healthy individuals, a more general and cost-effective approach must be developed.
New possibilities for improved cancer care are on offer from an advanced technology already demonstrating its significance—next-generation sequencing (NGS). NGS is a high-throughput technology that can allow integration of molecular tumor profiles into clinical decision-making as part of precision oncology. It can be carried out using targeted gene panels, whole-exome sequencing, or whole-genome sequencing. This refined testing has the potential to allow for more focused and highly personalized treatment. NGS may enable more focused and highly personalized cancer treatment, with the National Comprehensive Cancer Network and European Society for Medical Oncology guidelines now recommending NGS for daily clinical practice for several tumor types.
There are questions about affordability and accessibility: the cost of sequencing in lower-income countries can be five times higher than in high-income countries because of taxes and the high cost of analysis, shipment, and infrastructure. Recent technologies have improved the speed and read length of NGS as well as improved data analysis with a decrease in price, but there is a disincentive for drug manufacturers to develop tests for a more well-defined target population because this might affect their existing sales. There are questions over privacy and confidentiality, and the ethical implications must still be defined to inform patients or their relatives about the potential risks or genes associated with future disease development. There are also questions about how to determine which drug is likely to work best on the basis of the molecular profile of a patient’s tumour, which are complicated further by varied patterns of availability on individual markets, where a suitable product might not be registered for a particular indication, potentially encouraging off-label prescription and leaving it subject to reimbursement limitations.