Surveillance Recommendations in Reducing Risk of and Optimally Managing Breast Cancer-Related Lymphedema
Abstract
:1. Introduction
1.1. Definition
1.2. Incidence
1.3. Symptoms
Clinical Stage | Description |
---|---|
0 | A subclinical stage where swelling is not seen despite underlying changes in the lymphatic system |
I | The initial stage of swelling which can be transient and where simple elevation can alleviate swelling |
II | Swelling is constant and pitting without resolution using elevation |
III | The tissue has become hard and fibrotic with associated skin changes |
Severity | Based on volume differences between affected and contralateral limb in unilateral presentation |
Mild ≤ 20% increase; Moderate = 20%–38% increase, Severe ≥ 38% increase |
2. Assessment and Management of LE
2.1. Assessment
2.2. Treatment
2.2.1. Non-Invasive Components of Care
2.2.2. Surgical Treatment
2.2.3. Nodal Status Determination
3. Adjunct Therapies
3.1. Pneumatic Compression Therapy
3.2. Aqua Lymphatic Therapy
3.3. Complementary and Alternative Medicine
3.4. Low-Level-Laser Therapy
4. Predisposing Factors
4.1. Exercise
4.2. Breast Cancer Surgery and Radiation Therapy
4.3. Comorbidities
4.4. Genetic Predisposition
5. Risk-Reduction Strategies and Preventive Interventions
5.1. Self-Management
Exercise and Weight-Lifting
5.2. Surgical Prevention
7. Supportive Care
7.1. Adherence to Self-Management of BCRL
7.2. Health Care Provider Knowledge
7.3. Palliative Care
8. Interdisciplinary Surveillance
8.1. Measures for Surveillance
8.1.1. Lymphedema Breast Cancer Questionnaire (LBCQ)
8.1.2. Functional Assessment of Cancer Therapy (FACT-B+4)
8.2. Innovation in Qualitative Measures
9. Clinical Research
Aims | (1) To determine if rigorous surveillance with web-based questionnaires in conjunction with arm volume measurements demonstrates earlier detection of BCRL compared to standard care. (2) To determine if earlier detection of BCRL using web-based HRQOL questionnaires in conjunction with arm volume measures improves QOL and functional outcomes. (3) To assess the cost and efficiency of nursing time in completing and evaluating questionnaires |
Methods | Longitudinal, prospective, mixed-method study which will recruit women with newly-diagnosed breast cancer to complete a comprehensive symptom and quality of life assessment (LBCQ) and undergo arm volume measures pre-operatively, post-operatively, and quarterly. Preoperatively and at 12-month follow-up, patients will complete the FACT-B+4 questionnaire. Descriptive statistics and correlations will be used to examine relationships between actual measured arm volumes and subjective web-based questionnaire responses to determine if early symptoms correlate with limb volume changes. This study has been approved by the University of Missouri Health Sciences Institutional Review Board. |
Results | Currently recruiting (n = 25 currently have given informed, written consent; up to 100 will be recruited) |
Conclusion | Early diagnosis and intervention for BCRL is reported to improve the patients’ quality of life and functional outcomes. By utilizing a novel electronic tool developed in our institution (LBCQ) as a component of rigorous surveillance, we hope to show lymphedema is diagnosed earlier than with standard care, resulting in improved HRQOL and functional outcomes for our patients. |
Clinical Trial Organization | Clinical Trial Number | Name of Trial | Principal Investigator(s) |
---|---|---|---|
Alliance (CALGB) | 70305 | A randomized education/exercise intervention study to reduce risk of lymphedema in women treated for breast cancer | Electra Paskett, Jane Armer, Lisa Yee, Michele Naughton, et al. |
Alliance (ACOSOG) | Z1070 Successor Trial | Axillary management of T0-T3 node positive breast cancer receiving neoadjuvant chemotherapy | Judy C. Boughey MD, Tom Buchholz MD, Bruce Haffty MD, Vera Suman PhD, Janice Cormier, MD, MPH, Jane Armer, RN, PhD |
Gynecologic Oncology Group (GOG) | The Lymphedema and Gynecologic Cancer (LEG) Study: Incidence, Risk Factors, and Impact | Richard Barakat, MD, MSKCC, NCI R01 |
10. Conclusions
10.1. Prospective Surveillance Model
10.2. Costs Associated with Traditional and Prospective Models
Pre-op assessment with every woman who will undergo breast cancer surgery and/or RT. | H&P; height, weight, BMI, baseline bilateral limb (arm) volume measures with certified lymphedema therapist, functional assessment; provision of educational and resource information (predisposing factors, risk-reduction activities, signs and symptoms of early BCRL, support group information, team contact information; physical activity assessment and program information; nutritional information); introduction to team members and Q & A opportunities |
Post-operative visit by team nurse and lymphedema therapist | Bilateral LV measure and assessment; supportive-educative visit; Ongoing: assess eligibility for clinical trials |
Interval visits @ 1, 3, 6, 9, 12 months | Weight; BMI; bilateral LV measures; functional assessment; physical activity assessment; skin assessment. Ongoing: physical exercise program options, unless contraindicated; weight management program options; nutritional support and referral with dietician; support group information; virtual support group/blogs; contact with patient by team member monthly the first year post-breast cancer treatment; psychological/psychosocial assessment/Family assessment with a trained counselor. |
Semi-Annual visits for 1–3 years | Same as above with team contact every 2 months to discuss status and evaluate need for resource referral. |
Annual visits, if no BCRL is diagnosed | Team contact quarterly to discuss status and evaluate need for resource referral. |
If BCRL is diagnosed: | Imaging: (lymphoscintigraphy/lymphangioscintigraphy, lymphography, MRI, ultrasound) to assess and/or rule out problems with lymphatic structures and flow and venous circulation, if indicated. Ongoing: Visits per treatment plan prescribed by lymphedema therapist for initial CDT. |
Ongoing: support of self-management: Team contact every month or more often initially if necessary, treatment information, clinical trial information if available, support group information/other media information, new product information, Online LBCQ q 3 months or per institutional protocol, Fact-B+4 annually or per institutional protocol | |
Ongoing throughout survivorship: | Celebration events at least annually |
10.3. Future Research
Acknowledgments
Author Contributions
Conflicts of Interest
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Ostby, P.L.; Armer, J.M.; Dale, P.S.; Van Loo, M.J.; Wilbanks, C.L.; Stewart, B.R. Surveillance Recommendations in Reducing Risk of and Optimally Managing Breast Cancer-Related Lymphedema. J. Pers. Med. 2014, 4, 424-447. https://doi.org/10.3390/jpm4030424
Ostby PL, Armer JM, Dale PS, Van Loo MJ, Wilbanks CL, Stewart BR. Surveillance Recommendations in Reducing Risk of and Optimally Managing Breast Cancer-Related Lymphedema. Journal of Personalized Medicine. 2014; 4(3):424-447. https://doi.org/10.3390/jpm4030424
Chicago/Turabian StyleOstby, Pamela L., Jane M. Armer, Paul S. Dale, Margaret J. Van Loo, Cassie L. Wilbanks, and Bob R. Stewart. 2014. "Surveillance Recommendations in Reducing Risk of and Optimally Managing Breast Cancer-Related Lymphedema" Journal of Personalized Medicine 4, no. 3: 424-447. https://doi.org/10.3390/jpm4030424
APA StyleOstby, P. L., Armer, J. M., Dale, P. S., Van Loo, M. J., Wilbanks, C. L., & Stewart, B. R. (2014). Surveillance Recommendations in Reducing Risk of and Optimally Managing Breast Cancer-Related Lymphedema. Journal of Personalized Medicine, 4(3), 424-447. https://doi.org/10.3390/jpm4030424