42 Transitional Lymphedema: Understanding the Temporal Dynamics Post-Axillary Surgery

Publication
Article
Miami Breast Cancer Conference® Abstracts Supplement41st Annual Miami Breast Cancer Conference® - Abstracts
Volume 38
Issue 4
Pages: 49

Background

Lymphedema poses a significant challenge for patients with breast cancer who have undergone axillary lymph node dissection (ALND). Traditional techniques for lymphedema assessment, such as arm circumference measurement and bioimpedance spectroscopy (Lymphedema Index [L-Dex]), have been useful but limited in scope. One underexamined facet of this condition is its temporal characteristics—specifically, the period between surgery and the onset of lymphedema symptoms. Our study aims to elucidate the concept of transitional lymphedema, a term we propose to describe lymphedema occurring between 3 to 6 months after axillary surgery that would be resolved with longer follow-up.

Methods

A retrospective cohort study included patients with breast cancer undergoing ALND with Simplified Lymphatic Microsurgical Preventing Healing Approach (SLYMPHA) between January 2019 and June 2022 at a single institution. Patient demographics and treatment characteristics were collected. An L-Dex score outside the normal range (±10 L-Dex unit) or an increase of at least 10 L-Dex units above the patient’s baseline was considered abnormal.

Results

L-Dex Score at Each Postoperative Visit

L-Dex Score at Each Postoperative Visit

A total of 51 patients met the inclusion criteria, with a mean (SD) age of 56.8 (12.6) years and a mean (SD) body mass index (BMI) of 29.5 (7.2) kg/m2. A total of 41 patients (80.4%) received adjuvant radiation, and 41 patients (80.4%) received neoadjuvant chemotherapy. Of the 18 patients with abnormal L-Dex scores, an abnormal L-Dex developed in 5 patients (27.7%) at 3 months, 6 patients (33.3%) at 6 months, 3 patients (16.6%) at 9 months, and 4 patients (22.2%) at 12 months. There was a decrease in the mean absolute L-Dex score at each postoperative visit. When comparing the L-Dex difference from the baseline, it was lower at 12 months (4.67) compared with the 3-month (10.12) postoperative visit (CI, 0.1086-9.968; P = .0432). Additionally, 88.2% of patients who developed an abnormal L-Dex score at some time had adjuvant radiation compared with 76.4% of patients who never had an abnormal L-Dex reading; however, it was not significant. Of note, 52.17% of patients with BMI of at least 30 kg/m2 developed abnormal L-Dex scores compared with 22.2% of patients with a BMI below 30 kg/m2 (P = .02). From patients with at least 20 axillary lymph nodes removed, 45% developed abnormal L-Dex, whereas it was 28.5% when fewer than 20 lymph nodes were removed (P = .04).

Conclusions

Most increases in L-Dex scores seen in the first 6 postoperative months showed resolution after a follow-up of more than 12 months. Higher BMI (≥ 30 kg/m2) and removal of at least 20 axillary lymph nodes were associated with higher L-Dex measurements during postoperative follow-up visits.

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1 Centrally Located Breast Cancer Is More Aggressive in Bahraini Patients
1 Centrally Located Breast Cancer Is More Aggressive in Bahraini Patients
2 Is Laterality in Breast Cancer Still Worth Studying? Local Experience in Bahrain
2 Is Laterality in Breast Cancer Still Worth Studying? Local Experience in Bahrain
3 Gender Disparities in the  National Institutes of Health  Funding for Breast Cancer
3 Gender Disparities in the National Institutes of Health Funding for Breast Cancer
4 Bacopaside: Exploring Its Potential in Addressing Chemoresistance and Modulating Doxorubicin Accumulation in Triple-Negative Breast Cancer Cells
4 Bacopaside: Exploring Its Potential in Addressing Chemoresistance and Modulating Doxorubicin Accumulation in Triple-Negative Breast Cancer Cells
5 Predictors of Axillary Complete Pathologic Response in Hormone Receptor–Positive, HER2-Negative, Clinically Node-Positive Breast Cancer
5 Predictors of Axillary Complete Pathologic Response in Hormone Receptor–Positive, HER2-Negative, Clinically Node-Positive Breast Cancer
6 Treatment Outcomes of the KEYNOTE-522 Regimen in an Ethnically Diverse Patient Population
6 Treatment Outcomes of the KEYNOTE-522 Regimen in an Ethnically Diverse Patient Population
7 Real-World Efficacy and Adverse Events of Neoadjuvant Immunotherapy in Early-Stage Triple-Negative Breast Cancer Patients: A Multicenter Experience
7 Real-World Efficacy and Adverse Events of Neoadjuvant Immunotherapy in Early-Stage Triple-Negative Breast Cancer Patients: A Multicenter Experience
8 Using a Liquid Biopsy Mediated Approach for Determination of HER2 Amplification Status in Patient Samples
8 Using a Liquid Biopsy Mediated Approach for Determination of HER2 Amplification Status in Patient Samples
9 Elacestrant (ELA) vs Standard-of-Care (SOC) in ER+/HER2–Advanced (adv) or Metastatic Breast Cancer (mBC) with ESR1 Mutation (ESR1-mut): Key Biomarkers and Clinical Subgroup Analyses From the Phase 3 EMERALD Trial
9 Elacestrant (ELA) vs Standard-of-Care (SOC) in ER+/HER2–Advanced (adv) or Metastatic Breast Cancer (mBC) with ESR1 Mutation (ESR1-mut): Key Biomarkers and Clinical Subgroup Analyses From the Phase 3 EMERALD Trial
10 Real-World Effectiveness of Palbociclib (PAL) Plus Aromatase Inhibitors (AI) in Patients With Metastatic Breast Cancer (MBC) and Cardiovascular Diseases (CVD)
10 Real-World Effectiveness of Palbociclib (PAL) Plus Aromatase Inhibitors (AI) in Patients With Metastatic Breast Cancer (MBC) and Cardiovascular Diseases (CVD)
11 Phase 3 Study of Neoadjuvant Pembrolizumab or Placebo Plus Chemotherapy, Followed by Adjuvant Pembrolizumab or Placebo Plus Endocrine Therapy for Early-Stage High-Risk ER+/HER2– Breast Cancer: KEYNOTE-756
11 Phase 3 Study of Neoadjuvant Pembrolizumab or Placebo Plus Chemotherapy, Followed by Adjuvant Pembrolizumab or Placebo Plus Endocrine Therapy for Early-Stage High-Risk ER+/HER2– Breast Cancer: KEYNOTE-756
12 EMERALD Trial Analysis of Patient-Reported Outcomes (PROs) in Patients (pts) With ER+/HER2- Advanced or Metastatic Breast  Cancer (mBC) Comparing Oral Elacestrant vs Standard-of-Care (SoC) Endocrine Therapy
12 EMERALD Trial Analysis of Patient-Reported Outcomes (PROs) in Patients (pts) With ER+/HER2- Advanced or Metastatic Breast Cancer (mBC) Comparing Oral Elacestrant vs Standard-of-Care (SoC) Endocrine Therapy
13 The Cause and Eradication of Breast Cancer
13 The Cause and Eradication of Breast Cancer
14 Outcomes With First-Line (1L) Ribociclib (RIB) + Endocrine Therapy (ET) vs Physician’s Choice Combination Chemotherapy (combo CT) by Age in Pre/Perimenopausal Patients (pts) With Aggressive HR+/HER2– Advanced Breast Cancer (ABC): A Subgroup Analysis of the RIGHT Choice Trial
14 Outcomes With First-Line (1L) Ribociclib (RIB) + Endocrine Therapy (ET) vs Physician’s Choice Combination Chemotherapy (combo CT) by Age in Pre/Perimenopausal Patients (pts) With Aggressive HR+/HER2– Advanced Breast Cancer (ABC): A Subgroup Analysis of the RIGHT Choice Trial
15 Concurrent Use of Abemaciclib and Radiation Therapy (RT) Among Patients With HR+, HER2– Metastatic Breast Cancer (MBC): Real-World Utilization and Safety
15 Concurrent Use of Abemaciclib and Radiation Therapy (RT) Among Patients With HR+, HER2– Metastatic Breast Cancer (MBC): Real-World Utilization and Safety
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