Second opinion cancer diagnostics with genomics entails using advanced genomic sequencing to analyze a patient's cancer cells, providing a detailed understanding of the tumour's genetic makeup to guide personalized treatment decisions.
Second Opinion Cancer Diagnostic with Genomics
This process begins with the collection of a tissue sample from the patient's cancer, followed by genomic sequencing to analyse the DNA of the cancer cells. Our oncologists then interpret the genomic data to identify specific genetic mutations, alterations, or biomarkers that may influence the behaviour of the cancer and its response to treatment.
This comprehensive approach to cancer diagnosis and treatment planning can provide additional perspectives and recommendations, leading to more personalised and potentially optimised treatment strategies tailored to the individual characteristics of the patient's cancer.
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