MedPath

A study to estimate improvement in quality of life, cost effectiveness of radiotherapy in patients of breast cancer with bone metastases.

Not Applicable
Conditions
Health Condition 1: null- Patients of breast cancer who have been newly diagnosed with bone metastases and who will be planned for palliative radiotherapy
Registration Number
CTRI/2018/03/012317
Lead Sponsor
Tata Memorial Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Any breast cancer patient with newly diagnosed bone metastases.

2.Histological proof of malignancy of the breast.

Exclusion Criteria

1.Unwilling to give written informed consent.

2.Patients previously treated for bone metastases.

3.Unwilling for regular physical and or telephonic follow up

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To establish a cohort of breast cancer patients with bone metastases receiving standard <br/ ><br>evidence based management to study the morbidity related to bone metastases and clinically relevant skeletal related complications <br/ ><br>Timepoint: 5 years
Secondary Outcome Measures
NameTimeMethod
1.To evaluate the severity and characteristics of pain at baseline and its response to treatment. <br/ ><br>2.Identify factors predicting 10% risk of pathological fracture at 1 year. <br/ ><br>3.Identify factors predicting 5% risk of clinical cord compression at 1 year <br/ ><br>4.Identify factors predicting an overall survival of less than 6 months in this patient population. <br/ ><br>Timepoint: 3 years
© Copyright 2025. All Rights Reserved by MedPath