Early Diagnosis of Breast Cancer-related Lymphedema

Sponsor
Kaohsiung Veterans General Hospital. (Other)
Overall Status
Recruiting
CT.gov ID
NCT06046365
Collaborator
(none)
100
1
35
2.9

Study Details

Study Description

Brief Summary

This study will conduct clinical trials to explore the mechanisms behind the development of upper limb lymphedema following breast cancer surgery. The investigators will recruit patients who have undergone breast cancer surgery and utilize Indocyanine Green (ICG) lymphography and Lymphoscintigraphy to identify the locations of lymphatic blockages. Shear Wave Elastography (SWE) will be used to detect changes in tissue limb compliance. DXA body composition analysis will measure the differences in the composition ratios between edematous and normal limbs. In addition, diffusion correlation spectrometry will be employed to monitor changes in deep tissue blood flow, complemented by continuous measurements of limb circumference and other physiological parameters. The study aims to explore the interrelationships among lymphatic circulation, limb circumference, tissue compliance, and tissue blood flow rates.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: lymphoscintigraphy
  • Diagnostic Test: circumference measurement
  • Diagnostic Test: sonography
  • Diagnostic Test: DXA body composition analysis

Detailed Description

Breast cancer ranks as the most common cancer among women in Taiwan. According to the cancer registry data of Taiwan's Ministry of Health and Welfare, there were 16,325 new cases of breast cancer in 2016. Approximately one in 12 women will develop breast cancer in her lifetime. Although the incidence rate is high, the survival rate after clinical treatment is also quite high. The five-year survival rate for early-stage breast cancer patients exceeds 90%, making it a highly manageable disease at present.

The incidence rate of breast cancer-related lymphedema is around 21.4%, and is expected to become increasingly common as the survival rate of patients improves. Aside from causing psychological distress, it also impairs a patient's work and daily life capabilities. Patients also have to bear additional medical expenses, which brings a significant financial burden to families. Current research supports that early detection and treatment are key to controlling breast cancer-related lymphedema. However, there is still a need for a clearer understanding of the risk factors causing lymphedema and the physiological changes that occur when it manifests, in order to achieve the goal of early detection.

This study will conduct clinical trials to investigate the mechanisms of upper limb lymphedema after breast cancer surgery. The investigators will recruit post-operative breast cancer patients and use Indocyanine Green (ICG) lymphography and Lymphoscintigraphy to detect lymphatic blockage locations; Shear Wave Elastography (SWE) to detect changes in tissue limb compliance; DXA body composition analysis to measure the differences in edema and normal limb composition ratios; and diffusion correlation spectrometry to measure deep tissue blood flow changes, along with continuous measurements of limb circumference and other physiological parameters. The study aims to explore the interrelationship among lymphatic circulation, limb circumference, tissue compliance, and tissue blood flow.

The expected results of this study can help the investigators understand the risk factors causing lymphedema and the physiological changes that occur when it manifests, overcome the current difficulties in early lymphedema detection, and develop effective monitoring methods and equipment. This will provide more possibilities for the early detection and treatment of future patients with breast cancer-related lymphedema.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Early Diagnosis of Breast Cancer-related Lymphedema
Actual Study Start Date :
Jan 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
mastectomy

Expected to include female patients who are undergoing breast cancer resection surgery or those who have already undergone breast resection surgery for breast cancer.

Diagnostic Test: lymphoscintigraphy
lymphoscintigraphy

Diagnostic Test: circumference measurement
circumference measurement

Diagnostic Test: sonography
B-mode sono and elastography

Diagnostic Test: DXA body composition analysis
DXA body composition analysis

Outcome Measures

Primary Outcome Measures

  1. circumference [everyday, through study completion, an average of 1 year]

    Circumference measurements are taken and recorded at 2 cm intervals from the wrist crease to the armpit on both upper limbs

  2. Tissue compliance [every 1 week, through study completion, an average of 1 year]

    Measurements are taken every 5 cm from the wrist crease to the armpit on both upper limbs using ShearWave Elastography

  3. Lymphoscintigraphy [Once at the beginning of the study, and another assessment will be conducted six months later if there is a deterioration in lymphedema]

    Golden Standard for diagnosing lymphedema, used for detecting the location of lymphatic circulation blockage

  4. Indocyanine green (ICG) lymphography [Once at the beginning of the study, and another assessment will be conducted 3 months later if there is a deterioration in lymphedema]

    Routine examination, used for detecting the type of lymphatic blockage

  5. DXA body composition analysis [Once at the beginning of the study, and another assessment will be conducted 3 months later if there is a deterioration in lymphedema]

    Using DXA to detect and compare the composition of both limbs at different stages after the onset of lymphedema, including changes in protein, fat, and mineral density

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 80 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Female patients who are expected to undergo breast cancer resection surgery or have already undergone breast resection surgery for breast cancer.

  • Absence of unhealed open wounds or other conditions unsuitable for tactile measurements within the measurement area.

  • No severe cognitive or emotional impairments.

  • No substance abuse (alcohol or drugs).

  • Females aged between 20 and 80, capable of fully complying with the requirements of this study plan.

Exclusion Criteria:
  • Presence of unhealed open wounds or other conditions unsuitable for tactile measurements within the measurement area.

  • Upper limb abnormalities in function (including joint mobility and muscle strength).

  • Significant cognitive, auditory, or expressive language issues that hinder comprehension and compliance with instructions.

  • Lack of assistance for daily measurements.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kaohsiung Veterans General Hospital Kaohsiung Taiwan 81362

Sponsors and Collaborators

  • Kaohsiung Veterans General Hospital.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zheng-Yu Hoe, MD., PhD., Chairperson, Kaohsiung Veterans General Hospital.
ClinicalTrials.gov Identifier:
NCT06046365
Other Study ID Numbers:
  • 22-CT2-15(211230-3)
First Posted:
Sep 21, 2023
Last Update Posted:
Sep 21, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Zheng-Yu Hoe, MD., PhD., Chairperson, Kaohsiung Veterans General Hospital.
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 21, 2023