Improving Quality of Life for Patients With Breast Cancer Invading the Chest Wall: A Prospective Registry For Patients Undergoing Full Thickness Chest Wall Resection

NCT ID: NCT03265379

Last Updated: 2025-12-03

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 104 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2017-08-22
• Study Completion Date: 2030-08-22

Brief Summary

Although chest wall recurrence of breast cancer is uncommon, it represents a difficult clinical scenario. The role of full thickness chest wall resection (FTCWR) for breast cancer recurrence in the chest wall is controversial and is complicated by the fact that no prospective evidence exists evaluating the utility of FTCWR in prolonging survival or improving health related quality of life (HRQOL) and thus, there is a lack of evidence to guide treatment decisions. Gathering HRQOL, local-regional recurrence (LRR) and survival data in a prospective fashion is thus critical in this population. Therefore, we designed a prospective trial to evaluate the outcomes for FTCWR in terms of LRC and HRQOL, and short-term morbidity and mortality, with secondary focus on potential long-term overall survival benefit.

Detailed Description

This study is a prospective, non-randomized cohort study for patients with chest wall-recurrent/invasive breast cancer treated with full thickness chest wall resection (FTCWR), chemotherapy and/or radiation. The design of this study was created using the framework for surgical trials set out by the IDEAL collaboration (Idea, Development, Exploration, Assessment, Long-Term follow up), 14 after a systematic evaluation of the current literature had been completed. Given that no prospective evidence exists in this patient population and based on the IDEAL framework, this study is designed to create a prospective registry.

Data on the efficacy of the standard interventions (surgery, chemotherapy, radiation) will be evaluated using 'global criteria', that is, the data that will be collected via the scores on the FACT-B, the Brief Pain Inventory, and the specific cancer outcomes as outlined previously (local regional recurrence (LRC), overall survival, short term morbidity and mortality as well as disease-free survival).

The primary objective is to measure the differences in Functional Assessment of Cancer Therapy - Breast (FACT-B) scale scores from baseline to 6 month evaluation.

In addition to measuring health related quality of life (HRQOL) at 6 months, differences in the FACT-B scale at 1-month, 3-months and 1-year postoperatively will be examined. Rates of LRC, defined as local recurrence in the ipsilateral chest wall, axilla, infra- or supraclavicular region at 1, 2, 3 and 5-years postoperatively will be measured, as well as thirty and ninety-day morbidity and mortality (to be classified using the Thoracic Morbidity and Mortality (TM and M) classification system). As well, data will be collected on overall survival, measured as the proportion of patients surviving to at 1-year, 2-years, 3-years and 5 years postoperatively. Lastly, data will be collected on disease-free survival, defined as any evidence of systemic recurrence plus LRR at 1-year, 2-years, 3-years and 5-years postoperatively.

Conditions

Breast Cancer

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

patients with an isolated recurrence in the chest wall

FACT-B and Brief Pain Inventory

Intervention Type: OTHER

Quality of Life Questionnaires

distant metastatic disease is present but who undergo FTCWR

FACT-B and Brief Pain Inventory

Intervention Type: OTHER

Quality of Life Questionnaires

patient with primary tumor, no distant ds, failed conventional

FACT-B and Brief Pain Inventory

Intervention Type: OTHER

Quality of Life Questionnaires

patients refusing to undergo surgery

FACT-B and Brief Pain Inventory

Intervention Type: OTHER

Quality of Life Questionnaires

Interventions

FACT-B and Brief Pain Inventory

Quality of Life Questionnaires

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. >18 years of age

2. Breast cancer with invasion of the chest wall (ribs, para-costal soft tissue, intercostal muscle or soft-tissue) that is:

1. Radiologically proven on cross-sectional imaging

2. Histologically proven

3. Medically fit for surgery

4. >1 year disease-free interval (between initial treatment and recurrence) for patients with local recurrence

Exclusion Criteria

1. Medically inoperable due to co-morbidity or other contraindication to surgery

2. Technically unresectable disease

3. Ineligible for chemotherapy

4. ECOG performance status >2

5. Patient refusal

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

Sponsors

University Health Network, Toronto

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Shaf Keshavjee

Role: PRINCIPAL_INVESTIGATOR

University Health Network, Toronto

Locations

University Health Network (Toronto General Hospital and Princess Margaret Cancer Centre)

Toronto, Ontario, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

Jennifer Lister, BSc CCRP

Role: CONTACT

Jennifer.Lister@uhn.ca

416-340-4857

Facility Contacts

Jennifer Lister, BSc CCRP

Role: primary

Jennifer.Lister@uhn.ca

416-340-4857

Other Identifiers

17-5560

Identifier Type: -

Identifier Source: org_study_id