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Exploring the Link Between Cancer Genetics and PPSP

2019년 7월 2일 업데이트: Institute of Cancer Research, United Kingdom

Exploring the Link Between Cancer Genetics and Persistent Post-surgical Pain (PPSP) Following Breast Cancer Treatment

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.

연구 개요

상세 설명

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.

연구 유형

관찰

등록 (예상)

104

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

샘플링 방법

확률 샘플

연구 인구

Although two groups of patients will be identified retrospectively:

  1. The first group will be patients who have been referred to the pain management team for persistent-post surgical pain following breast cancer treatment.
  2. 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.

Ultimately, archived paraffin-embedded tissue samples, that have previously been taken from these patients, will be requested. Samples accessed will be from patients who have previously provided consent for their samples to be used for research purposes.

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
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.

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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
The difference in the proportion of mutations of the PIK3CA gene.
기간: Within 6-8months
PIK3CA genomics will result in a binary measure (either wild-type or mutant). The difference in proportion of the PIK3CA gene mutation in those with persistent post-surgical pain compared with those without persistent post-surgical pain will be the primary outcome measure.
Within 6-8months

2차 결과 측정

결과 측정
측정값 설명
기간
Proportion of individual gene mutations in pain group compared with the no pain group.
기간: Within 6-8months
DNA analysis will determine the presence or absence of other gene mutations (binary outcome).
Within 6-8months
Difference in mean gene expression in those with pain compared with those without pain.
기간: Within 6-8months
Exploring the difference in gene expression between the two groups.
Within 6-8months
Proportion of individual DNA copy number changes (either amplification/gain or loss) in those with pain compared with those without pain.
기간: Within 6-8months
DNA copy number can either be unchanged or changed. Changes are described as either 'amplification/gain' or 'loss'. Data will be analysed as binary data (either no change or change).
Within 6-8months
Frequency of changes to DNA copy number (either amplification/gain or loss) in those with pain compared with those without pain.
기간: Within 6-8months
DNA copy number can either be unchanged or changed. Changes are described as either 'amplification/gain' or 'loss'. Data will be analysed as binary data (either no change or change).
Within 6-8months
Difference in median of magnitude of activation status of signalling pathways between those with pain and those without pain.
기간: Within 6-8months
Comparison the activation status of signalling pathways between the two groups. The magnitude of activation status will be reported as a percentage.
Within 6-8months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Matt Brown, MBBS, Royal Marsden NHS Foundation Trust

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (예상)

2019년 7월 1일

기본 완료 (예상)

2019년 12월 1일

연구 완료 (예상)

2019년 12월 1일

연구 등록 날짜

최초 제출

2019년 6월 21일

QC 기준을 충족하는 최초 제출

2019년 7월 2일

처음 게시됨 (실제)

2019년 7월 5일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2019년 7월 5일

QC 기준을 충족하는 마지막 업데이트 제출

2019년 7월 2일

마지막으로 확인됨

2019년 7월 1일

추가 정보

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기타 연구 ID 번호

  • CCR 5006

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