Exploring the Link Between Cancer Genetics and PPSP

NCT ID: NCT04007861

Last Updated: 2019-07-05

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 104 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-07-31
• Study Completion Date: 2019-12-31

Brief Summary

Pain is common in cancer, affecting between 40 and 60% of patients depending on tumour type and stage of disease, and represents a major area of unmet need in cancer survivors. Despite advances in treatment, there has been no significant reduction in those who experience pain. Breast cancer is common. It represents 10% of newly diagnosed cancers globally and is often associated with pain.

Exact physiological mechanisms for cancer pain are not yet fully established. There is a complex relationship between a malignant lesion and its micro-environment; a tumour does not exist in isolation but has a dynamic relationship with host cells. There is a growing interest in delineating the relationship between tumour manifestations and pain.

By retrospectively identifying individuals who have been referred to specialist pain clinics at a cancer centre and matching them to controls, the investigators can identify two groups of patients (those who experienced significant problems with pain and those who did not). Accessing paraffin-embedded tissue samples from those that have had surgical resections, will allow the investigators to compare tissue samples, in particular the metabolic and genetic differences, between the two groups.

No new tissue samples will be required for this study.

Pain is a major area of unmet need in cancer survivors. The investigators propose that this project would provide valuable knowledge and pilot data regarding the link between pain and tumour genetics. It has the potential to identify tumour genes or mutations that are associated with greater incidences of pain and ultimately potentially guide targeted interventions to help reduce the frequency and impact of pain on patients living with and beyond cancer.

Detailed Description

This study will be a retrospective, case-control study. There will be two groups of patients identified retrospectively:

The first group will be patients who have been referred to the pain management team for persistent-post surgical pain following breast cancer treatment.

The second group, will consist of patients who have been matched for age, procedure and time-lapsed since operation. These patients will not have persistent post-surgical pain.

Archived paraffin-embedded tissue samples, that have previously been taken from these patients, will be required. Samples accessed will be from patients who have previously provided consent for their samples to be used for research purposes. Once appropriate samples have been identified by the tissue banks, all data will be pseudonymised. This will include details that patients have consented to providing for research purposes via the Pain Management Database, which has Trust (CCR 442) and Research Ethics Committee (REC 16/LO/1989) approval.

Laboratory studies will then be conducted to A) investigate the underlying variations of the PIK3CA gene of tumours within the two cohorts of patients, B) investigate other genetic variations between these two groups and C) establish the key genetic and signalling pathway alterations between these two groups.

The methods by which these investigations will be conducted will be by performing PIK3CA genomics, genetic profiling, next generation sequencing and finally immunohistochemistry for activation of signalling pathways.

This study will analyse archived paraffin embedded tissue samples in a laboratory only.

The anticipated time-scale for this project would be approximately one year.

Conditions

Cancer-related Pain; Chronic Post Cancer Surgery Pain; Breast Cancer

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: RETROSPECTIVE

Study Groups

Patients with pain

This will be the group of patients in whom pain is a significant enough problem, that they have been referred to the specialist Pain Management Team. These patients will be identified retrospectively.

Patients seen in Pain Management Clinics between 1st of January 2016 and 31st of December 2018, who have consented to be included in the Pain Management database and have a clinician specified pain diagnosis of pain persistent post-surgical pain following breast cancer treatment will be identified. If these patients have an unclear pain diagnosis, they will not be included.

No interventions assigned to this group

Patients without pain

This will be the group of patients in whom pain is deemed not to be a significant problem.

Once again, these patients will be identified retrospectively. Appropriately matched patients to the 52 patients in the "patients with pain" will be identified using records of hospital operating lists by the peri-operative medicine team.

Patients will be matched based upon the following details:

• Age (within 5 years of matched case)
• Surgical procedure (matched for the following elements:

• Surgery to breast tissue (biopsy, lumpectomy, wide-local excision or mastectomy)
• +/- Sentinal lymph node biopsy or axillary dissection
• +/- Reconstruction
• Surgical procedure within 3-months of matched case.

Provided these individuals have not had an appointment with or referral to the Pain Management Team, they will be included in the matched controls.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Patients receiving treatment at the Royal Marsden Hospital.
• Patients with a diagnosis of primary breast cancer.
• Patients who have had surgical resection of their breast tumour.
• Paraffin-embedded tissue samples available from Royal Marsden Tissue Banks.

Exclusion Criteria

• Under 18 years of age.
• Lack of adequate tissue sample available from the Tissue Bank.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Institute of Cancer Research, United Kingdom

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Matt Brown, MBBS

Role: PRINCIPAL_INVESTIGATOR

Royal Marsden NHS Foundation Trust

Central Contacts

David Magee, BMBS

Role: CONTACT

davidmagee@nhs.net

020 7808 2771

Matt Brown, MBBS

Role: CONTACT

matthew.brown@rmh.nhs.uk

020 7808 2771

Other Identifiers

CCR 5006

Identifier Type: -

Identifier Source: org_study_id