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Management and prognosis of breast cancer through FDG PET/CT

Not Applicable
Conditions
Health Condition 1: null- Breast Cancer (Retrospective data of Breast Cancer Patients will be collected)
Registration Number
CTRI/2012/09/002966
Lead Sponsor
ot applicable Thesis Protocol
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
500
Inclusion Criteria

Female breast cancer patients referred for 18[F] FDGPET/CT scan in the Nuclear Medicine Department of Max Super Speciality Hospital.

Exclusion Criteria

Patient clinical data not available.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the indication for 18[F] FDG PET/CT for breast cancer patients, used by Oncologist in Max Super Speciality Hospital: <br/ ><br>a)Diagnosis <br/ ><br>b)Staging <br/ ><br>c)Recurrence/Metastasis (Restaging) <br/ ><br>d)Treatment response evaluation <br/ ><br>e)Radiation treatment response <br/ ><br>Timepoint: Indication of 18[F] FDG PET/CT for breast cancer patients: <br/ ><br>a)Diagnosis <br/ ><br>b)Staging <br/ ><br>c)Recurrence/Metastasis (Restaging) <br/ ><br>d)Treatment response evaluation <br/ ><br>e)Radiation treatment response <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
1.To determine 18[F] FDG PET/CT effectiveness in the evaluation of chemotherapy response by calculating the percentage decrease in SUV value from the baseline value (Pre-therapy scan). <br/ ><br>2. To determine the impact of 18[F] FDG PET/CT on the treatment management plan, whether altered or supported. <br/ ><br>3. To determine the most common metastatic site in the metastatic breast cancer patients. <br/ ><br>Timepoint: 1.Percentage decrease in SUV value (post-therapy scan) from the baseline value (Pre-therapy scan). <br/ ><br>2.Change in the treatment management plan. <br/ ><br>3. Most common metastatic site in the metastatic breast cancer patients. <br/ ><br>
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