Experimental assessment of pro-lymphangiogenic growth factors in the treatment of post-surgical lymphedema following lymphadenectomy

The formulation and sterilization of HAMC was modified from Gupta's description [11]. To prepare the HAMC components, a 0.5 wt/vol solution of methylcellulose (MC; M7140) in distilled water was created using a dispersion technique. Briefly, MC was added to one third of distilled water at boiling, and once completely wetted, the remaining two thirds of distilled water (cold) were added. The solution was placed in 4°C until completely dissolved. Sodium hyaluronate (HA; molecular weight 1500 kDa, NovaMatrix, Akershus, Norway) was dissolved in distilled water to obtain a 0.1 wt/vol solution. Both solutions were sterile filtered through a 0.22-μm polyethersulfone membrane filtration system (Nalgene, New York, USA) and lyophilized under sterile conditions. To produce growth factor-supplemented HAMC, 3 μg/ml of VEGF-C (R&D Systems, Ontario, Canada) and ANG-2 (R&D Systems) were combined with sterile filtered phosphate-buffered saline (PBS) in a laminar flow hood and mixed to ensure homogeneous dispersion of proteins within the polymer matrix. Methylcellulose was then added, and the mixture was vortexed to dissolve the MC. Last, hyaluronan was added and the solution was vortexed and incubated overnight at 4°C to allow HA to dissolve into the MC solution. Final concentrations of either 1 or 3 μg/ml of growth factors were used throughout the study as indicated.

To determine the release profile of the growth factors from HAMC, 1 ml of growth factor-infused HAMC (1 or 3 μg/ml) was loaded manually into a 3-ml tuberculin syringe. The gel solution was then injected into 9 ml of Dulbecco's modified Eagle's medium (DMEM) supplemented with 0.5% fetal bovine serum (FBS) in a 15-ml Falcon tube. Growth factor release was assessed at 37°C over a 256-hr time period. At each time point, all media were removed and stored at -20°C for further analysis by enzyme-linked immunosorbent assay (ELISA; R&D Systems). Fresh media were then added to each tube, and the experiment was continued. As an internal control, 1 μg/ml and 3 μg/ml samples of each growth factor (in 0.5% FBS-supplemented media) were kept at 37°C for 256 hr.

The above release rate experiment was repeated in the presence of the hyaluronan degrading enzyme hyaluronidase (0.5 U/ml to 50 U/ml) in PBS at pH 5.5, the optimum pH for this enzyme (HAase; bovine testicular hyaluronidase).

The primary bovine lymphatic endothelial cells utilized in this study were generously provided by Dr. Dumont (Sunnybrook Health Science Center, Ontario, Canada). Cultures were maintained in 10% FBS in DMEM on uncoated plates at 37°C and 5% CO₂. Cultures were supplemented with 10 n/g of VEGF-C to stimulate cell growth. Once cultures reached 70% confluency, they were used in bioactivity experiments.

To ensure that the concentrations of VEGF-C and Ang-2 introduced into the drug delivery system were capable of activating target receptors in lymphatic endothelial cells (LEC), we performed the following experiments. Bovine LEC cultures were serum-starved overnight in DMEM supplement with 0.5% FBS to minimize signaling through the lymphangiogenic pathways of interest. Following the starvation period, cultures were stimulated in one of two ways. In the case of Western blot analysis of VEGFR-3, HAMC (containing 3 μg/mL of both VEGF-C and ANG-2) was added directly onto the bovine plates, and cultures were stimulated for 24 hr. To further reduce background signaling through the Tie-2 receptor, cultures were incubated with release media for 10 min. To form this release media, VEGF-C and ANG-2 (loaded at 3 μg/mL) were released from HAMC for 8 hr, and then the resultant supernatant was centrifuged to remove HAMC. As controls, cultures were also treated with VEGF-C (200 ng/ml) and ANG-2 (800 ng/ml) in 5 ml of 0.5% FBS in DMEM to determine the baseline signaling levels through each receptor. Furthermore, 1 ml of HAMC not loaded with growth factors was included as a vehicle control. Following treatment, cells were lysed for 30 min in phospholipase C-γ lysis buffer (50 mM HEPES (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid) pH 7.5, 150 mM sodium chloride, 10% glycerol, 1% Triton X-100, 1 mM ethylene glycol tetraacetic acid, 1.5 mM magnesium chloride, 10 mM sodium fluoride, 10 mM sodium pyrophosphate, 1 mM sodium orthovanadate and protease inhibitor cocktail (Roche Diagnostics, DE, USA) for 30 min on ice, centrifuged, and the supernatants of each sample were collected and then immunoprecipitated for VEGFR-3 (C-20, SC-321, rabbit polyclonal antibody; Santa Cruz Biotechnology, Santa Cruz, CA, USA) and Tie-2 (C-20, SC-324, rabbit polyclonal antibody; Santa Cruz Biotechnology) overnight at 4°C. Samples were resolved on 8% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) gels and transferred to a polyvinylidene fluoride membrane (GE Healthcare, Ontario, Canada). Blots were blocked in either 5% BSA or 3% milk overnight. The following day samples were incubated in primary antibody (1:1000 anti-phosphotyrosine 4G10; Millipore, Ontario, Canada), Tie-2 and VEGFR3 at 4°C overnight. Blots were then incubated in a horseradish peroxidase-linked secondary (1:10,000, Bio-Rad, Ontario, Canada) for 45 min at room temperature and developed using a chemiluminescence kit (Supersignal West Pico; Thermo Scientific, Ontario, Canada).

Sheep were fasted 24 hr prior to anesthesia induction. The animals were anesthetized initially by 15-ml intravenous injection of sodium pentothal. Subsequently, 2.0-3.5% isofluorane was delivered through an endotracheal tube via a Moduflex Dispomed machine with Hallowell respirator for surgical maintenance. The dorsal surface of each animal was shaved, washed with soap and water and prepped with alcohol to remove all existing contaminants from skin. Intradermal injections of 100 μl of HAMC and HAMC dually infused with VEGF-C and ANG-2 were administered through 25-gauge needles. Equal volumes of saline and bradykinin (1 mg/ml) served, respectively, as the negative and positive controls. Injections were administered in duplicate once hourly for the first 3 hr (255, 195, 135, 75 min) and then at 45, 30 and 15 min. Following injections at 15 min, 100 μL of ¹²⁵I bovine serum albumin (¹²⁵I-BSA) (0.364 mg/ml; Perkin Elmer, Ontario, Canada) and 25 ml of Evans blue dye (EB) were introduced through a catheter in the cephalic vein, following which the catheter was flushed with 5 ml of heparinized saline. A 15-min time period was then allowed to elapse to allow radioactivity and dye to accumulate at points of inflammation, at which point the animal was killed. Skin encompassing the injection points was removed and photographed with a Nikon digital camera (model CoolPix 4500). Each injection area was then punched out individually using a 2.54-cm cork borer, placed in 10% formalin and measured for radioactivity in a gamma counter (1282 Compugamma CS Universal gamma counter; LLK Wallas, Turku, Finland) to quantify ¹²⁵I-BSA accumulation. Hematoxylin and eosin staining was performed on 7-μm paraffin-embedded cross-sections of the injection areas to determine neutrophil infiltration. On the basis of preliminary results, it became necessary to assess inflammation induction over a longer period of time, and as a result intradermal injections of HAMC (with and without growth factors) were introduced into nonanesthetized sheep at time points corresponding to 24 and 128 hr prior to being killed.

Lymphedema induction was conducted as previously described by Tobbia et al. [2, 7]. Fasting and anesthesia induction were performed as described in the previous section. Surgical areas were shaved, washed with soap and water and disinfected with 70% alcohol. A vertical incision (6-8 cm) was made over the lateral aspect of the popliteal region in the hindlimb and the popliteal fossa was exposed. Following identification of the popliteal node in its surrounding fat pad, the pre- and postnodal lymphatics were ligated and the node was excised. At this time, growth factor therapy was introduced. Pre-prepared HAMC (1 ml preloaded into a 3-ml syringe with a blunted 18-gauge needle) was introduced into the area of nodal excision. To increase the retention of HAMC at this site, the fat pad pocket was then carefully sealed with absorbable suture. In the case of sham surgeries, the popliteal fat pad was exposed but undisturbed. A piece of saline-soaked gauze was applied to the area for 10 min to duplicate the length of time needed to perform the growth factor treatment surgery. The animals were returned to their holding pens after recovery from the anesthetic.

The hind legs were shaved and leg circumference measurements were taken at a point 10 cm distal to the hock (tarsus). This landmark was highlighted with a skin marker for subsequent measurements postoperatively at the same location. The limb circumferences were divided by the original (presurgical value) and expressed as percentage change over time. To compare the edema outcomes in the various groups, the percentage change in limb circumference was plotted against time, and graphical integration of the area under the curves was calculated using the trapezoidal rule.

The primary role of the lymphatic system is to transport protein and fluid from the interstitium back to the venous system. Therefore, the ability to monitor the transport of a radiolabeled protein through the lymphatic system and its accumulation in blood is a measure of lymphatic functionality. This method has been used in several previous studies by our group [2, 7]. All animals were fasted, and anesthetic was induced as described above. Evans blue dye (1% in saline) was injected subcutaneously above the hind leg hoof to enhance visualization of the prenodal lymphatic vessels. An incision was made through the skin and subcutaneous tissues over the lower lateral aspect of the hindlimb, and a single vessel was cannulated with a 26-gauge angiocatheter. Saline (100 μl) was injected into the cannula over 30 seconds to check for leaks. Radiolabeled BSA (¹²⁵I-BSA, 0.364 mg/ml, in a 100-μl volume) was then injected over a 60-second period into the prenodal lymphatic vessel and flushed with 100 μl of saline. Blood samples were taken from a neckline inserted into the jugular vein at time 0, and every 5 min up to 1 hr and then every 30 min up to 2 hr. Fluoroscopic imaging was then conducted and the animals were killed (20 ml euthanyl, 240 mg/ml, administered intravenously). It was determined that our radiolabeled tracer was undergoing some breakdown upon introduction into the animal. To determine the extent of the breakdown, trichloroacetic acid precipitations were performed on 2-hr plasma samples from each animal. Supernatant and pellet samples were compared to equivalent volumes of unprecipitated plasma to determine the amount of bound iodine. Plasma samples (1 ml) were then placed in the external gamma counter to determine ¹²⁵I-BSA accumulations in blood over time. These values were expressed as a percentage of the total value of radioactivity (counts per minute) injected and corrected to reflect only BSA still bound to its radiolabel. These values were then plotted versus time. To allow comparison between the experimental groups, the graphical integration of the area under each curve was calculated using the trapezoidal rule.

Immediately following the lymphatic function studies, imaging was performed. Approximately 1 mL of lipiodol (Ultrafluid; E-Z-EM Canada, Inc., Anjou, Quebec, Canada) was injected into the angiocatheter placed in the upstream popliteal prenodal vessel and the lymphatics/nodes were visualized using a mobile fluoroscopy system (BV Pulsera; Philips Healthcare, Andover, MA, USA).

All data are expressed as means ± SEM unless otherwise stated. The data were analyzed with linear regression or one-way ANOVA followed by a one-sided Dunnett's t-test where indicated. We considered P < 0.05 to be significant.

Previous studies have shown that HAMC attenuates the inflammatory response and promotes healing of the dura when injected into the intrathecal space in either control or spinal cord injury rats [11]. We felt it necessary to determine whether similar results could be expected upon introduction of growth factor-infused HAMC in our sheep model.

The average tracer accumulation in blood is illustrated for all groups in Figure 5a. The black line (intact limbs) provides the reference point for the various interventions. At the other extreme (orange line), very little BSA enters the blood immediately after lymph node excision, because the lymphatics have been disrupted. It is clear that sham surgical procedures impact lymphatic function negatively, presumably because some of the fragile vessels have been damaged (red line). By 6 wk after excision, the normal lymphatic regeneration has improved lymph transport somewhat (gray line) and this is similar to that observed with HAMC alone (green line). Some improvement in lymphatic function was noted in the group receiving HAMC plus growth factors (blue line).

To determine whether the functionality changes were significant, the areas under the curves were compared. Lymph node removal was found to significantly reduce functionality in the nontreated groups (nodectomy 1.9 ± 0.9 or HAMC alone 1.7 ± 0.8) in comparison to intact controls (3.2 ± 0.7) (Figure 5b). Alternatively, values for the growth factor-treated groups (2.3 ± 0.7) were not significantly different from the values observed in both sham and control groups. This indicates similar lymphatic functionality across all three groups (growth factor-treated, sham and intact). Growth factor-treated limbs did not return completely to the functionality levels measured in intact limbs over the 6-wk period.

In intact and sham surgical groups, there were clearly visible popliteal lymph nodes with identifiable prenodal and postnodal vessels (Figure 6a). Six weeks after lymph node excision, some fluid continuity had been reestablished, because both the afferent and efferent vessels were visible and connected by an entanglement of newly regenerated vessels (example in Figure 6b). These newly formed vessels appeared to be fragile as indicated by the frequent leaks in this area upon contrast agent infusion. The irregular regeneration pattern and what appeared to be partial filling of some of the vessels precluded meaningful quantitative analysis between groups. However, general trends were noted. In the HAMC alone group, the regeneration pattern was similar to that observed in the nodectomy group (example in Figure 6c). In the limbs receiving HAMC plus growth factors, there appeared to be an increase in the number of regenerated vessels (Figure 6d).

As expected, limb circumferences did not change over time in the sham-treated animals. In contrast, the removal of a popliteal lymph node resulted in edema formation in 100% of animals. The presence of HAMC plus growth factors appeared to produce the best results in terms of reducing edema levels. Typical examples from each group are illustrated in Figure 7a.

Similar to the lymphatic functionality experiment, the areas under the curves were used to conduct quantitative comparisons between groups (Figure 7b). Growth factor-treated groups displayed edema magnitudes slightly greater than but not significantly different to sham levels (107.4 ± 51.3 and 59.2 ± 62.5, respectively). Nontreated groups displayed significantly greater edema levels in comparison to the sham group (nodectomy 219.8 ± 118.7 and HAMC 162.6 ± 141). This result suggests that growth factor treatment has the ability to reduce edema magnitude following lymph node removal.

When we plotted all of the individual lymphatic function data versus their corresponding edema measurements at 6 wk for all groups, we observed a significant negative correlation (P = 0.001) (Figure 8). That is, the highest levels of lymphatic function correlated with the lowest levels of edema, supporting the notion that improvement in lymph transport capacity with growth factors has potential for lymphedema treatment.

It is clear that new animal models need to be developed to understand more fully the pathogenesis of lymphedema and to develop new therapeutic approaches [18]. The use of small animals, especially the mouse, has been very beneficial in helping to elucidate the molecules that play a role in lymphangiogenesis. However, a major advantage of utilizing a larger animal, such as the sheep, for lymphedema studies is that lymphatic function can be measured, something that is extremely difficult to achieve in a small species. In sheep, the pre- and postnodal popliteal ducts are easy to identify, and some of these are of sufficient size for cannulation. In this regard, the ability to transport a known mass of radiolabeled albumin to plasma provides a useful measure of the lymph transport effectiveness of a given lymphatic network. Therefore, following the injection of ¹²⁵I-BSA into prenodal lymphatic vessels, one would expect that the mass transport rate of this protein tracer to plasma would reflect the integrity of the lymphatic network in question, a notion that is supported by the data in this report.

In humans, lymph-venous anastomoses can form with long-term lymphatic obstruction [19, 20]. If such connections were to exist in our sheep experiments, the labeled BSA would be diverted into the limb vasculature and would not pass through the nodal excision site. However, over the many years we have used the sheep model, we have never observed these connections in the popliteal region. Presumably, the level of impediment caused by nodal excision in the animal model is relatively benign compared to that which occurs in humans with cancer. In the human case, the surgical procedures related to the removal of the cancer and lymph nodes are much more extensive and likely provide a significantly greater insult to the lymphatic system than that occurring in our experiments. In the latter case, relatively robust lymphangiogenesis occurs and some degree of fluid continuity is restored relatively quickly so that the stimulus for lymph-venous connections in the leg may not be as great as is the case with some lymphedema patients.

In cancer patients, the removal of one or more lymph nodes often gives rise to acute edema which resolves successfully. It is, of course, the chronic form of edema that occurs in a subgroup of patients that is most problematic. The exact conditions that drive the formation of this subgroup are unknown. It has been suggested that women with greater than average peripheral lymph flow are more likely to develop lymphedema following breast cancer surgery [21]. The authors postulated that this predisposing factor might explain why lymphedema develops in patients in which only a few nodes have been removed. In all likelihood, lymphedema is the result of a complex interplay between many factors (surgery, lymph node removal, radiation, injury and predisposing characteristics) that lead to the development of this condition. It should be noted that we are not attempting to replicate the complex conditions experienced by cancer patients in our model. Instead, our model permits us to examine the properties of a single lymphatic network in order to develop basic therapeutic principles that could be applicable to the human condition.

There is no agreed-upon time beyond which one considers edema to be chronic. For practical reasons, we did not follow the animals beyond a 6-wk period. Nonetheless, we feel that our sheep model is suitable for the measurement of lymphatic-related physiological changes over time and can provide a realistic framework for the development of therapeutic measures and methods of administration that are human-sized in perspective.

There are many potential drug delivery approaches that could be used to introduce lymphangiogenic growth factors. The HAMC system offers several advantages in this regard. A hydrogel represents a network of water-swollen polymer chains in which water is the dispersion medium. When HAMC is placed within the body, it absorbs water from the surrounding environment, the pore sizes within the matrix expand and proteins are released [22]. This characteristic property of hydrogels accounts for the rapid burst release of growth factors at the beginning of each release study. In the case of our system, following this initial rapid release, rates appeared to slow until HAMC had undergone dissolution. This suggests that growth factors incorporated into the outer regions of HAMC could readily diffuse into media, but the diffusion distance may have been too great for those incorporated into the core of HAMC, causing release to plateau. Degradation of HAMC then allows for the release of remaining factors.

Previous HAMC studies saw almost complete diffusion-mediated release of a single growth factor from this system over a 16-hr period [13], but in these experiments the volume of HAMC used was 1000-fold less than the volumes utilized in our report.

Hyaluronan is metabolized by hyaluronidase in vivo, and it has already been shown that this enzyme can affect the degradation of HAMC [11]. As anticipated, increasing activity levels of HAase in our study were associated with increasing release rates of both growth factors. This result suggests that endogenous HAase activity in the popliteal fossa may result in more rapid release of lymphangiogenic factors in vivo than predicted from the in vitro experiments. While we do not know the release profiles of VEGF-C and ANG-2 in vivo, we expect that the release rates will depend upon consumption of the factors (maintaining a concentration gradient favoring release) in the popliteal fossa and the presence of degrading enzymes, such as hyaluronidase. We anticipate that the bioactivity of released factors will be maintained over the course of the release, owing to their incorporation into HAMC. The half-life of VEGF-C in the circulation is less than 15 min; thus HAMC will likely provide some protection to the growth factors by controlling its release over time [23].

The HAMC drug delivery system contains numerous components that could potentially invoke a reaction from the host: the methylcellulose is synthetically manufactured, hyaluronan is produced in bacteria and the growth factors are all human derived. Nonetheless, the evidence presented in this report, including assessments of vascular permeability and leukocyte infiltration, indicates that any host response is minimal. This is supported by the literature where HA has been shown to attenuate the inflammatory response in several tissues [24].

One of the most important questions in devising a molecular strategy for lymphedema treatment is the selection of the lymphangiogenic growth factor. In this regard, VEGF-C seemed an obvious choice. VEGF-C is required for the development of the lymphatic system as well as for proliferation, migration and survival of LECs [9]. It is also known that blocking signaling through its receptor, VEGFR-3, results in regression of preexisting lymphatic vessels. Recent studies in mice have revealed that VEGF-C introduction increases the rate of damaged vessel reconnection in comparison to controls [25]. After lymph node excision and transplantation, VEGF-C was observed to facilitate vessel connection to the transplanted tissue [26]. Furthermore, evidence has been found that directly links VEGF-C signaling and lymphedema. Point mutations identified in VEGFR-3 lead to a hereditary form of lymphedema, known as Milroy's disease that presents with edema of the lower extremities [27, 28].

Another factor we decided to introduce into the lesion site is angiopoietin-2. ANG-2 has been implicated in the organization of the lymphatic system through the activation of the Tie-2 receptor. ANG-2-knockout mice display abnormal lymphatic patterning, disrupted lymphatic endothelial-smooth muscle cell interactions as well as subcutaneous edema and chylous ascites, indicting an obligatory role for ANG-2 in lymphatic system development [10, 17].

Overall, this study revealed that both growth factors appear to be protected from inactivation while incorporated in HAMC until their release, when they can in turn bind and activate target receptors involved in lymphangiogenic signaling. Owing to close homology between both bovine and ovine ligands and receptors, these results suggest that similar results would likely be obtained with ovine cells, which was supported by new vessel growth in the fluoroscopic images.

Additionally, we found that HAMC appears to potentiate Tie-2 phosphorylation by ANG-2. Specifically, there appears to be an increase in Tie-2-ANG-2 association demonstrated by the increased presence of a second band in these cultures. As HAMC undergoes dissolution, the viscosity of media surrounding the cells increases, which may alter the interaction of Tie-2 with ANG-2 dimers (which form spontaneously in solution), perhaps increasing their association time, explaining the above result.

This study also indicated that HAMC may possess the surprising ability to activate the receptor tyrosine kinase (RTK) Tie-2. It is well known that low molecular weight hylauronan fragments play a role in endothelial cell proliferation and migration through activation of particular RTKs [29]. Typically, these fragments range from 3 to 16 oligosaccharides in length [30]. However, the hylauronan utilized was initially 1500 kDa, and while small amounts of random cleavage may occur, this seems like an unlikely cause of receptor activation. A second, more plausible theory is that through an association with CD44, hyaluronan indirectly influences Tie-2 signaling. Hylauronan can directly bind CD44, causing the cell surface receptor to cross link [31]. This cross linking has been shown to influence integrin signaling [31], which in turn can influence Tie-2 activation [32]. All three are common receptors found on the surface of endothelial cells, and therefore association with CD44 could indirectly affect Tie-2 signaling. The ability of HAMC to independently activate a RTK such as Tie-2 may provide an additional advantage to the lymphangiogenic process, working synergistically with the ligand ANG-2 to improve functionality.

Our results suggest that prolymphangiogenic growth factors can have a positive impact on lymphatic function and improve edema outcomes. However, there are several conceptual issues that may need refinement in future investigations. First, there is evidence that lymphangiogenesis is a two-phase process. The initial phase involves activation of endothelial cells and sprouting, while the second phase involves maturation of these vessels. Maturation includes smooth muscle cell recruitment, which appears to play an important role in the orientation of newly formed vessels [10]. With this in mind, it may be possible to build a system to control the temporal release of the growth factors to mimic more closely the endogenous realities. It should be noted, however, that the dual factor approach and the doses we utilized in this study had a significant impact on lymphatic function and edema resolution. This information provides a useful framework on which to optimize lymphangiogenic therapeutic approaches in future studies.

A second issue involves the signaling ability of VEGFC156S (utilized here) versus its wild-type counterpart. The wild-type ligand has the ability to bind both VEGFR2 and VEGFR3 receptors, while VEGFC156S is an agonist only to VEGFR3. Signaling through VEGFR2, which is found predominantly on vascular endothelium, causes increased permeability, an event that we wanted to minimize in our study. However, upon initial characterization, it was noted that VEGFC156S signaling in LECs was different from VEGF-C [16]. It was postulated that activation of VEGFR2 on LECs might be needed to induce maximal lymphangiogenic signaling. In any event, it is clear that manipulation of lymphangiogenesis in vivo is a complex issue and that optimal conditions (choice of factor, dosage and timing of application) require further investigation.

The appeal of lymphangiogenic-based therapies for the treatment of lymphedema is easy to understand. This type of treatment has the potential to reverse the disease state by facilitating naturally occurring processes. However, processes such as lymphangiogenesis are complex and not fully understood yet. Furthermore, while molecular therapies have shown benefits in breast cancer-related lymphedema, the exact nature of the defect that causes lymphedema is still unknown, and therefore the most appropriate approach to the treatment method for this disease must still be determined.

Autologous lymph node transplantation is an alternative experimental treatment for lymphedema. It is well documented that removal of the lymph nodes greatly increases the chance of developing lymphedema, especially if this is combined with radiotherapy [33]. In a previous report, we demonstrated that a successful vascularized popliteal node transplant in sheep could effectively restore lymphatic function and limit or prevent edema development when applied at the time of nodal excision [2]. Indeed, Becker and colleagues [34] transplanted femoral nodes into the axillary region of 24 postmastectomy lymphedema patients using microsurgical procedures followed by manual drainage (physiotherapy) during the first 3 months. Overall, edema resolution was good, especially in those individuals in whom the lymphedema was of the shortest duration. Surgical complexities and potential donor site morbidity issues complicate the application of lymph node transplantation in clinical practice.