Abstract

IntroductionLymphedema is a frequent consequence of lymph node excision during breast cancer surgery. Current treatment options are limited mainly to external compression therapies to limit edema development. We investigated previously, postsurgical lymphedema in a sheep model following the removal of a single lymph node and determined that autologous lymph node transplantation has the potential to reduce or prevent edema development. In this report, we examine the potential of lymphangiogenic therapy to restore lymphatic function and reduce postsurgical lymphedema.MethodsLymphangiogenic growth factors (vascular endothelial growth factor C (VEGF-C)) and angiopoietin-2 (ANG-2) were loaded into a gel-based drug delivery system (HAMC; a blend of hyaluronan and methylcellulose). Drug release rates and lymphangiogenic signaling in target endothelial cells were assessed in vitro and vascular permeability biocompatibility tests were examined in vivo. Following, the removal of a single popliteal lymph node, HAMC with the growth factors was injected into the excision site. Six weeks later, lymphatic functionality was assessed by injecting 125Iodine radiolabeled bovine serum albumin (125I-BSA) into prenodal vessels and measuring its recovery in plasma. Circumferential leg measurements were plotted over time and areas under the curves used to quantify edema formation.ResultsThe growth factors were released over a two-week period in vitro by diffusion from HAMC, with 50% being released in the first 24 hr. The system induced lymphangiogenic signaling in target endothelial cells, while inducing only a minimal inflammatory response in sheep. Removal of the node significantly reduced lymphatic functionality (nodectomy 1.9 ± 0.9, HAMC alone 1.7 ± 0.8) compared with intact groups (3.2 ± 0.7). In contrast, there was no significant difference between the growth factor treatment group (2.3 ± 0.73) and the intact group indicating improved function with the molecular factors. An increase in the number of regenerated lymphatic vessels at treatment sites was observed with fluoroscopy. Groups receiving HAMC plus growth factors displayed significantly reduced edema (107.4 ± 51.3) compared with nontreated groups (nodectomy 219.8 ± 118.7 and HAMC alone 162.6 ± 141).ConclusionsGrowth factor therapy has the potential to increase lymphatic function and reduce edema magnitude in an animal model of lymphedema. The application of this concept to lymphedema patients warrants further examination.

Highlights

  • Lymphedema is a frequent consequence of lymph node excision during breast cancer surgery

  • We report that the delivery of vascular endothelial growth factor C (VEGF-C) and ANG-2 from HAMC into the nodal excision site has a positive impact on lymphatic function and reduces the magnitude of edema

  • In this study, we report that the addition of two lymphangiogenic growth factors to a nodal excision site enhances lymphatic transport function and reduces the edema burden in a sheep model of lymphedema

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Summary

Introduction

Lymphedema is a frequent consequence of lymph node excision during breast cancer surgery. Current treatment options are limited mainly to external compression therapies to limit edema development. Postsurgical lymphedema in a sheep model following the removal of a single lymph node and determined that autologous lymph node transplantation has the potential to reduce or prevent edema development. We examine the potential of lymphangiogenic therapy to restore lymphatic function and reduce postsurgical lymphedema. Most affected individuals are offered some form of nonsurgical external compression therapies to limit edema development, but there is great interest in developing more effective treatment options. We argued that the lymph node itself may have an important role in tissue fluid balance and observed that vascularized autologous lymph node transplantation could enhance lymphatic function and reduce edema significantly [2]. While lymphatics normally have an impressive capacity to regenerate following injury, it is possible that this process fails to compensate fully and that nonoptimal lymph transport conditions predispose the patient to edema formation

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