LCC-CARIS-01: Molecular Profiling in Gynaecological Cancer

The concept of molecular profiling leading to personalised medicine is based on the hypothesis that using treatments selected by a molecular profiling approach favourably changes the clinical course for an individual patient. In order to best determine the next steps in a particular patient's clinical course, it is necessary to understand not only how that patient has been diagnosed, treated and responded to treatment in the past, but also to fully characterize the molecular profile of the patient's tumour, so that the maximum information on potential positive and negative treatment outcome can be gathered.

In this pilot feasibility study, the treatment plans devised for individual patients by their treating oncologists will be assessed. The primary endpoint is the frequency at which the oncologist changes a treatment plan based on the tumour's molecular phenotype and the respective drugs considered to be associated with higher likelihood of benefit or lack of benefit. Ultimately however, the treatment decision remains in the hands of the treating physicians and the study protocol does not prescribe or dictate the use of any particular treatment.

In patients with recurrent ovarian cancer or other gynecological malignancies in which no standard of care is defined, treatments are currently chosen empirically based on population-based response rates. With the use of molecular profiling treating physicians will get a chance to revise their treatment plans and consider the individual molecular profile of each patient's tumour in light of the known predictive power of biomarkers for the efficacy of certain drugs.

Inclusion criteria

• Patients with recurrent epithelial ovarian, primary peritoneal or fallopian tube cancer OR patients with other gynaecological malignancy in whom the treating physician has made a decision to commence further systemic treatment with hormones or cytotoxic chemotherapy.
• Patient must be fit and willing to receive further treatment
• Plan to commence chemotherapy within 4 weeks of trial entry.
• Adequate tumour tissue, obtained within 36 months of study, must be available for molecular profiling.
• Age ≥ 18 years
• Patients who have fully understood the information provided and who have provided written informed consent.
• Patients for whom relevant pathology specimens are held by Leeds Teaching Hospitals Trust.

Exclusion criteria

• Patients receiving treatment as part of a therapeutic trial in which physicians are not able to select any appropriate treatment option.
• Patients who lack capacity to consent to study participation.
• Patients with symptoms that mean it is clinically inappropriate to delay treatment.