Breast
non-CME
Brian Diskin, MD (he/him/his)
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center
New York, United States
Disclosure information not submitted.
Brian Diskin, MD (he/him/his)
Breast Service, Department of Surgery
Memorial Sloan Kettering Cancer Center
New York, United States
Disclosure information not submitted.
Bayley Axelrod, BS
Sloan Kettering Institute
Memorial Sloan Kettering Cancer Center, United States
Disclosure information not submitted.
Varadan Sevilimedu, MBBS, DrPH
Biostatistics Service, Department of Epidemiology and Biostatistics
Memorial Sloan Kettering Cancer Center, United States
Disclosure information not submitted.
Monica Morrow, MD, FACS
Chief, Breast Surgical Service; Anne Burnet Windfohr Chair of Clinical Oncology, Memorial Sloan Kettering Cancer Center; Professor of Surgery Weill Cornell Medical College
Memorial Sloan Kettering Cancer Center
New York, New York, United States
Disclosure(s): No financial relationships to disclose
Babak J. Mehrara, MD
Plastic and Reconstructive Surgical Service, Department of Surgery
Memorial Sloan Kettering Cancer Center, United States
Disclosure information not submitted.
Andrea Barrio, MD
Associate Attending
Memorial Sloan Kettering Cancer Center
Disclosure information not submitted.
From 11/2016 to 03/2020, 304 patients treated with ALND were enrolled; 281 had at least 6 months of follow-up and are included. At a median follow-up of 2.3 years, 175 patients had an abnormal L-Dex (increase in ≥6.5 from baseline), and 18 patients developed lymphedema without a prior L-Dex abnormality. Of the 175 abnormal L-Dex patients, only 49 subsequently developed lymphedema, for a total of 67 patients with lymphedema (23.8%). As a predictor of future lymphedema, positive predictive value of L-Dex was 28% (49/175), with a false-positive rate of 59%. When lymphedema was present, L-Dex and TM were abnormal in 94% (63/67) and 99% (66/67) of patients, respectively. Overall, 281 patients had 1188 L-Dex and 1178 TM measurements. Correlating all measurements, sensitivity and specificity of L-Dex compared with perometer were 93% and 68%, respectively, and of TM with perometer were 78% and 89%, respectively. Correlation of perometer with L-Dex (r=0.66, p< 0.001) and volume changes by TM (r=0.67, p< 0.001) was moderate (Figure).
Conclusions:
In a prospective cohort of patients treated with ALND undergoing lymphedema screening, L-Dex and TM accurately diagnosed lymphedema identified by perometer over 90% of the time. More than 60% of patients had an abnormal L-Dex, and few developed lymphedema. The high false-positive rate of L-Dex results in overdiagnosis and precludes its use as a sole diagnostic method for lymphedema.