Diagnostic solutions in gynaecological cancers - precisely bring to light what needs to be seen

Cancer diagnosis with OSNA

Cancer staging is the step that determines the type and extent of treatment of a patient. An essential part of this staging process is an assessment of the nodal status.

Revealing the whole picture

Lymph node status is the most important prognostic factor and staging parameter in gynaecological cancer management. Whether lymph nodes are involved or not, it guides clinicians in their decision about the suitable surgical approach, the extent of the surgical intervention and what kind of additional therapy might be necessary.

Current histopathological methods have several limitations that either do not allow the provision of reliable diagnostic information in an intraoperative scenario or lack sensitivity for accurate staging. As a result, there is a risk that small metastases remain undetected leading to false negative results and inadequate treatment.

In contrast, OSNA (one step nucleic acid amplification) allows fast, sensitive and standardised molecular lymph node assessment, enabling accurate determination of the nodal status. By analysing the entire lymph node, the OSNA method provides accurate staging and a reliable basis for patient tailored treatment decisions, even during an operation, if necessary – thus helping to prevent under- or overtreatment and to improve the patient’s quality of life.

Treatment solutions in gynaecological cancers

Ovarian cancer is usually detected at later stage and is a leading cause of death from gynecological cancers. The treatment for this type of cancer has improved over the last 30- years due to better surgical approaches and improved availability of chemotherapeutic drugs. This is especially so since the introduction of platinum-based drugs and, more recently, the addition of taxanes. Despite these improvements in treatment, up to 30% of patients show no clinical remission and the majority of women will eventually relapse generally with an incurable disease. [4] Although effective surgery and treatment of the disease at an early stage are associated with an improved survival, it is impossible to predict which patient will progress or relapse during or after chemotherapy. This prediction is essential since patients who are resistant might benefit from a different combination of treatment [4] including modern targeted therapy. 

The development of genetic testing has allowed a better characterisation and understanding of ovarian cancer, its behaviour and aggressiveness as well as the patient’s risk and prognosis, thus supporting the choice of the right treatment.  

Germline mutations of the BRCA1 and BRCA2 genes lead to a high lifetime risk of ovarian cancer. They represent the predominant and most well-characterised genetic risk factors so far identified for the disease. BRCA1 and BRCA2 are involved in almost half of all families with two or more cases of ovarian cancer. As the BRCA1 and BRCA2 genes encode the proteins that are involved in DNA repair, tumours with alterations in either gene are particularly sensitive to specific anticancer agents that act by damaging DNA. [5]

Reliable assessment of the tumour’s mutational status is decisive in selecting cancer patients eligible for targeted therapy. To investigate such genetic changes, oncologists can make use of a variety of molecular genetic tests which may support them in making personalised treatment decisions. Precision diagnostics are key to selecting the right therapy at the right time for the right cancer patient.

Molecular tests for therapy selection

CytoCell FISH (Fluorescent In Situ Hybridisation) probes targeting genes MET, ROS1, CHD5, TOP2A and ZNF217 are used to aid pathologists and clinicians to understand tumour behaviour/aggressiveness and therefore patient prognosis.

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BRCA1, BRCA2, TP53, PTEN, ATM, ATR and NF1 are among the most common germline and somatic mutated genes underlying the pathogenesis of ovarian cancer that can be investigated by next generation sequencing (NGS) tests. The Sysmex solution to help characterise the overall genomic landscape of ovarian cancer is SureSeq^TM Ovarian Cancer Panel.*

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*SureSeq myPanel™ is for Research Use Only. Not for use in diagnostic procedures.
Manufacturer: CytoCell^®, SureSeq myPanel^TM are manufactured by Oxford Gene Technology IP Limited