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The goal of this observational study is to learn if participants agree to take part in the study, if the methods we are using for the study are feasible for the participants and the researchers, and to study how well two tools (tissue dielectric constant and ultrasound) measure breast edema after breast conserving surgery for breast cancer.
Participants who agree to be in the study will be asked to come in for one appointment of approximately two hours. All data will be collected during this one visit. Participants will be asked to fill out two questionnaires regarding their symptoms, and one questionnaire regarding their surgical scar. The research staff will conduct a clinical examination, measure breast edema using ultrasound and tissue dielectric constant, measure arm volume with the perometer and fluid with the SOZO, and take photographs of both breasts.
The goal of this observational study is to learn if the study protocol is feasible, if we can accrue participants easily, and to determine how well two tools (tissue dielectric constant and ultrasound) identify breast edema after breast conserving surgery for breast cancer.
Participants will be asked to attend one appointment in which all data will be collected. This will include questionnaires regarding symptoms, clinical examination, measurement of breast edema using two tools (ultrasound and tissue dielectric constant), measurement with the perometer and SOZO, and clinical photographs.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Participants with breast edema: N=15 | This group will contain women who report breast edema and have been diagnosed with breast edema through clinical examination | ||
| Participants without breast edema: N=15 | These participants do not report a history of breast edema and do not have a history of breast edema. |
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| Measure | Description | Time Frame |
|---|---|---|
| Tissue Dielectric Constant | A TDC interbreast ratio ≥ 1.28 in any quadrant will be used as an indicator of breast lymphedema | Baseline |
| Breast Ultrasound | Skin thickness >1.60 mm in superior and lateral quadrants, >2.0 mm in the medial and inferior quadrants will be used as an indicator of breast lymphedema. | Baseline |
| Measure | Description | Time Frame |
|---|---|---|
| Patient-Reported Outcome Measures | Breast Cancer Treatment Outcome Scale (BCTOS-12) Minimum Score = 12, Maximum Score = 48 Higher score indicates worse outcome | Baseline |
| Patient-Reported Outcome Measures |
| Measure | Description | Time Frame |
|---|---|---|
| Perometry | Perometry will be undertaken per clinical protocol to screen for arm lymphedema | Baseline |
| Bioimpedance Spectroscopy (SOZO) | Bioimpedance Spectroscopy will be undertaken per clinical protocol |
All participants must meet the following inclusion criteria:
EXCLUSION CRITERIA
Participants will be excluded if they:
Have bilateral BC
Have metastatic or inflammatory BC
Will be excluded from the SOZO measurement of the study if they have implanted cardiac devices or neurostimulators
Have any medical condition that may result in breast swelling;
Be pregnant or currently breast feeding.
Have a known over-active thyroid or known benign thyroid tumour
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Women screened for lymphedema in the MGH Lymphedema Research Program Prospective Screening Program; and/or women treated in physical or occupational therapy for breast cancer-related conditions after breast conserving surgery.
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| Name | Affiliation | Role |
|---|---|---|
| Cheryl Brunelle, MScPT | Massachusetts General Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | United States |
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| ID | Term |
|---|---|
| D000072656 | Breast Cancer Lymphedema |
| D008209 | Lymphedema |
| ID | Term |
|---|---|
| D008206 | Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
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Breast-Q Version 2.0 Breast Conserving Therapy Module, Postoperative Scales i. Psychosocial Well-Being (min score 10, max score 50), higher score indicating better outcome
| Baseline |
| Scar Assessment Tool | Patient and Observer Scar Scale Linear Scar Version 3.0 | Baseline |
| Clinical Examination of Lymphedema of the Upper Extremity Clinical Exam Tool | This is a validated measure used to administer clinical examination of the breast, trunk and upper extremity for lymphedema | Baseline |
| Clinical Examination - Pitting Edema | The following will be assessed:
| Baseline |
| Clinical Examination - Peau d'orange | The following will be assessed:
| Baseline |
| Clinical Examination - Tissue fibrosis | The following will be assessed:
| Baseline |
| Clinical Examination - Tenderness to palpation | The following will be assessed:
| Baseline |
| Clinical Examination - Erythema | The following will be assessed: - Each breast quadrant: Presence or absence of erythema (redness of the skin) | Baseline |
| Clinical Examination - Scar localization | The following will be assessed: - Scar measurements for the breast and axillary scars, including location (quadrant, distance from the center of the nipple to the center of the scar), scar length, width and orientation (vertical, horizontal, oblique or radial). | Baseline |
| Clinical Examination - Visual fullness | The following will be assessed: - Lateral chest wall and inframammary tissue: The examiner will record presence or absence of visual fullness | Baseline |
| Clinical Examination - Stemmer sign | The following will be assessed: - Lateral chest wall and inframammary tissue: Presence or absence of the Stemmer sign. The Stemmer sign is a physical examination finding used to diagnose lymphedema. If the examiner cannot pinch the skin then this positive finding is associated with lymphedema. The Stemmer sign has been found to be a sensitive predictor for primary and secondary lymphedema with moderate specificity (Goss JA, Greene AK. Sensitivity and Specificity of the Stemmer Sign for Lymphedema: A Clinical Lymphoscintigraphic Study. Plast Reconstr Surg Glob Open. 2019 Jun 25;7(6):e2295. doi: 10.1097/GOX.0000000000002295. PMID: 31624689; PMCID: PMC6635205) | Baseline |
| Clinical Examination - Tissue thickening | The following will be assessed by the examiner: - Nipple and nipple-areolar complex: Tissue thickening on the side of surgery as compared to the unaffected side | Baseline |
| Clinical Examination - Skin color changes | The following will be assessed by the examiner: - Nipple and nipple-areolar complex: Skin color changes as compared to the unaffected side (lighter, darker, same) | Baseline |
| Patient-Reported Outcome Measures | Breast-Q Version 2.0 Breast Conserving Therapy Module, Postoperative Scales ii. Sexual Well-Being (min score 6, max score 30), higher score indicating better outcome | Baseline |
| Patient-Reported Outcome Measures | Breast-Q Version 2.0 Breast Conserving Therapy Module, Postoperative Scales iii. Satisfaction with Breasts (min score 11, max score 44), higher score indicating better outcome | Baseline |
| Patient-Reported Outcome Measures | Breast-Q Version 2.0 Breast Conserving Therapy Module, Postoperative Scales iv. Physical Well-Being: Chest (min score 10, max score 30), higher score indicating better outcome | Baseline |
| Patient-Reported Outcome Measures | Breast-Q Version 2.0 Breast Conserving Therapy Module, Postoperative Scales v. Adverse Effects of Radiation (min score 6, max score 18), higher score indicating better outcome | Baseline |
| Patient-Reported Outcome Measures | Breast-Q Version 2.0 Breast Conserving Therapy Module, Postoperative Scales vi. Satisfaction with Information - Breast Surgeon (min score 12, max score 48), higher score indicating better outcome | Baseline |
| Baseline |
| Clinical Photographs | Clinical photographs of each breast, repeated for the right and then the left breast, taken per study protocol 5 positions each side, including a close up photo of the breast and surgical scar. | Baseline |
| D013568 | Pathological Conditions, Signs and Symptoms |