The efficacy of immediate lymphatic reconstruction in preventing breast cancer-related lymphedema: long-term follow-up study
DOI:
https://doi.org/10.2340/jphs.v60.43738Keywords:
Lymphedema, axillary reverse mapping, lymphovenous anastomosisAbstract
Background: Immediate lymphatic reconstruction (ILR) has emerged as an effective intervention to reduce breast cancer-related lymphedema, which affects 2–30% of patients who undergo axillary lymph node dissection (ALND). Our previous research validated ILR’s effectiveness over 14 months, but the duration was short and warranted further study. This study provides long-term evidence of its benefits in a well-defined patient cohort.
Method: This retrospective cohort study included unilateral breast cancer patients who underwent ALND between November 2019 and February 2021 with ≥ 24 months of follow-up. Patients were grouped by whether ILR was attempted intraoperatively. Exclusion criteria were recurrence, prophylactic mastectomy, and pre-existing lymphedema. The primary outcome was lymphedema incidence at ≥ 24 months; the secondary was lymphedema-free survival. Outcomes were evaluated using Cox regression models.
Results: Among 73 patients, we analyzed ALND patients divided into a control group (n = 57, defined as no-try or failure) and an ILR group (n = 16). The pooled median follow-up was 37 months. (range, 26~47 months). Among the ILR group, 13 underwent end-to-end anastomosis and 3 end-to-side. Postoperative lymphedema was higher in the control group (24.6%) compared to the ILR group (6.3%). Multivariate Cox regression analysis showed a significantly lower hazard ratio for the ILR group (HR: 0.117, 95% CI: 0.014–0.965), emphasizing ILR’s effectiveness in reducing lymphedema risk post-ALND. Additionally, survival plots illustrating lymphedema-free survival showed a significant difference.
Conclusion: Our study emphasizes ILR’s efficacy over extended follow-up. The ILR group exhibited a lower rate of postoperative lymphedema, supporting ILR as an effective preventive measure against Breast Cancer-Related Lymphedema (BCRL) following ALND.
Downloads
References
Boccardo F, Campisi C, De Cian F, et al. Lymphedema microsurgical preventive healing approach: a new technique for primary prevention of arm lymphedema after mastectomy. Ann Surg Oncol. 2009; 16: 703–708. https://doi.org/10.1245/s10434-008-0270-y DOI: https://doi.org/10.1245/s10434-008-0270-y
Boccardo F, Campisi C, Friedman D, et al. Surgical prevention of arm lymphedema after breast cancer treatment. Ann Surg Oncol. 2011; 18: 2500–2505. https://doi.org/10.1245/s10434-011-1624-4 DOI: https://doi.org/10.1245/s10434-011-1624-4
Boccardo F, Campsisi C, De Cian F, et al. Lymphatic microsurgical preventing healing approach (LYMPHA) for primary surgical prevention of breast cancer-related lymphedema: over 4 years follow-up. Microsurgery. 2014; 34: 421–424. https://doi.org/10.1002/micr.22254 DOI: https://doi.org/10.1002/micr.22254
Temple-Oberle C, Fraser WK, Platt A, et al. Immediate lymphatic reconstruction during axillary node dissection for breast cancer: a systematic review and meta-analysis. Plast Reconstr Surg Glob Open. 2022; 10: e4291. https://doi.org/10.1097/GOX.0000000000004291 DOI: https://doi.org/10.1097/GOX.0000000000004291
Levy AS, Murphy AI, Ishtihar S, et al. Lymphatic microsurgical preventive healing approach for the primary prevention of lymphedema: a 4-year follow-up. Plast Reconstr Surg. 2023; 151(2): 413–420. https://doi.org/10.1097/PRS.0000000000009857
Melisa D, Singhal D, Shillue K, et al. A 4-year institutional experience of immediate lymphatic reconstruction. Plast Reconstr Surg. 2023; 152(5): 773–778. https://doi.org/10.1097/PRS.0000000000010381 DOI: https://doi.org/10.1097/PRS.0000000000010381
Chung JH, Kwon S-H, Jung S-P, et al. Assessing the preventive effect of immediate lymphatic reconstruction on the upper extremity lymphedema. Gland Surg. 2023; 12(3): 334–343. https://doi.org/10.21037/gs-22-554 DOI: https://doi.org/10.21037/gs-22-554
Disipio T, Rye S, Newman B, et al. Incidence of unilateral arm lymphoedema after breast cancer: a systematic review and meta-analysis. Lancet Oncol. 2013; 14(6): 500–501. https://doi.org/10.1016/S1470-2045(13)70076-7 DOI: https://doi.org/10.1016/S1470-2045(13)70076-7
McLaughlin SA, Wright MJ, Morris KT, et al. Prevalence of lymphedema in women with breast cancer 5 years after sentinel lymph node biopsy or axillary dissection: objective measurements. J Clin Oncol. 2008; 26(32): 5213–9. https://doi.org/10.1200/JCO.2008.16.3725 DOI: https://doi.org/10.1200/JCO.2008.16.3725
Thompson M, Korourian S, Henry-Tilman R, et al. Axillary reverse mapping (ARM): a new concept to identify and enhance lymphatic preservation. Ann Sug Oncol. 2007; 14(6): 1890–5. https://doi.org/10.1245/s10434-007-9412-x DOI: https://doi.org/10.1245/s10434-007-9412-x
Johnson AR, Fleishman A, Granoff SD, et al. Evaluating the impact of immediate lymphatic reconstruction for the surgical prevention of lymphedema. Plast Reconstr Surg. 2021; 147(3): 373–381. https://doi.org/10.1097/PRS.0000000000007636 DOI: https://doi.org/10.1097/PRS.0000000000007636
Pressman PI. Surgical treatment and lymphedema. Cancer. 1998; 83(12 Suppl American): 2782–2787. https://doi.org/10.1002/(SICI)1097-0142(19981215)83:12B+%3C2782::AID-CNCR26%3E3.0.CO;2-2 DOI: https://doi.org/10.1002/(SICI)1097-0142(19981215)83:12B+<2782::AID-CNCR26>3.0.CO;2-2
Levy AS, Rhode CH, et al. Lymphatic microsurgical preventive healing approach for primary prevention of lymphedema : a 4-year follow up. Plast Reconstr Surg. 2023; 151(2): 413–420. https://doi.org/10.1097/PRS.0000000000009857 DOI: https://doi.org/10.1097/PRS.0000000000009857
Weinstein B, Le NK, Robertson E, et al. Reverse lymphatic mapping and immediate microsurgical lymphatic reconstruction reduced early risk of breast cancer-related lymphedema. Plast Reconstr Surg. 2022; 149(5): 1061–1069. https://doi.org/10.1097/PRS.0000000000008986 DOI: https://doi.org/10.1097/PRS.0000000000008986
Magnus J, Saeg F, Meade A, et al. Immediate lymphatic reconstruction for prevention of secondary lymphedema: a meta-analysis. J Plast Reconstr Aesthet Surg. 2022; 75(3): 1130–1141. https://doi.org/10.1016/j.bjps.2021.11.094 DOI: https://doi.org/10.1016/j.bjps.2021.11.094
Feldman S, Bansil H, Ascherman J, et al. Single institution experience with lymphatic microsurgical preventive healing approach (LYMPHA) for the primary prevention of lymphedema. Ann Surg Oncol. 2015; 22(10): 3296–3301. https://doi.org/10.1245/s10434-015-4721-y DOI: https://doi.org/10.1245/s10434-015-4721-y
Mohamed A, Mohamed E, Sherif M, et al. Breast lymphedema after conservative breast surgery: an up-to-date systematic review. Clin Breast Cancer. 2020; 21(3): 156–161. https://doi.org/10.1016/j.clbc.2020.11.017 DOI: https://doi.org/10.1016/j.clbc.2020.11.017
Inger-Lise N, Dahl AA, Løkkevik E, et al. Arm and Shoulder morbidity in breast cancer patients after breast-conserving therapy versus mastectomy. Acta Oncol. 2008;47;835–42. https://doi.org/10.1080/02841860801961257 DOI: https://doi.org/10.1080/02841860801961257
Freitas-Silva R, Conde DM, De Freitas-Júnior R, et al. Comparison of quality of life, satisfaction with surgery and shoulder-arm morbidity in breast cancer survivors submitted to breast-conserving therpay or mastectomy followed by immediate breast reconstruction. Clinical Science. 2010; 65(8): 781–787. https://doi.org/10.1590/S1807-59322010000800009 DOI: https://doi.org/10.1590/S1807-59322010000800009
Pafitanis G, Narushima M, Yamamoto T, et al. Insights to establish early learning curve in clinical supermicrosurgery. Microsurgery. 2019; 39(1): 100–101. https://doi.org/10.1002/micr.30401 DOI: https://doi.org/10.1002/micr.30401
Ishiura R, Yamamoto T, Saito T, et al. Comparison of lymphovenous shunt methods in a rat model: supermicrosurgical lymphaticovenular anastomosis versus microsurgical lymphaticovenous implantation. Plast Reconstr Surg. 2017; 139(6): 1407–1413. https://doi.org/10.1097/PRS.0000000000003354 DOI: https://doi.org/10.1097/PRS.0000000000003354
Brahma B, Yamamoto T, Panigoro SS, et al. Supermicrosurgery lymphaticovenous and lymphaticolymphatic anastomosis: technical detail and short-term follow-up for immediate lymphatic reconstruction in breast cancer treatment-related lymphedema prevention. J Vasc Surg Venous Lymphat Disord. 2024; 12(4): 101863. https://doi.org/10.1016/j.jvsv.2024.101863 DOI: https://doi.org/10.1016/j.jvsv.2024.101863
Nicole K, Weinstein B, Parikh J, et al. Immediate lymphatic reconstruction in 77 consecutive breast cancer patients: 2-year follow up. J Reconstr Microsrug. 2024; 40(04); 262–267. https://doi.org/10.1055/a-2153-2203 DOI: https://doi.org/10.1055/a-2153-2203
Corridi M, Mehrara B, Dayan J, Bloomfield E, et al. Efficacy of immediate lymphatic reconstruction to decrease incidence of breast cancer-related lymphedema. Ann Surg. 2023; 278(4): 630–637. https://doi.org/10.1097/SLA.0000000000005952 DOI: https://doi.org/10.1097/SLA.0000000000005952
Hahamoff M, Gupta N, Munoz D, et al. A lymphedema surveillance program for breast cancer patients reveals the promise of surgical prevention. J Surg Res. 2019; 244; 604–611. https://doi.org/10.1016/j.jss.2017.10.008 DOI: https://doi.org/10.1016/j.jss.2017.10.008
Additional Files
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Ki-Jae Kim, Sun-Hyeok Kim, Seung-Pil Jung, Eul-Sik Yoon, Jae-Ho Chung

This work is licensed under a Creative Commons Attribution 4.0 International License.
Acta Chirurgica Scandinavica Society owns the copyright for all material published until Volume 57 (2023) unless otherwise specified. As from 2024 all published articles, unless otherwise specified, are published under CC-BY licences, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, with the condition of proper attribution to the original work.
