Prevention of Secondary Lymphedema after Complete Lymph Node Dissection in Melanoma Patients: The Role of Preventive Multiple Lymphatic–Venous Anastomosis in Observational Era
Abstract
:1. Introduction
2. Methods
- -
- Group 1: Patients underwent CLND in any case of report of positive-SLNB;
- -
- Group 2: Patients underwent CLND only in the case of clinical detectable lymphatic metastasis.
3. Results
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
- Dummer, R.; Hauschild, A.; Lindenblatt, N.; Pentheroudakis, G.; Keilholz, U. Cutaneous melanoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2015, 26, v126–v132. [Google Scholar] [CrossRef] [PubMed]
- Keung, E.Z.; Gershenwald, J.E. The eighth edition American Joint Committee on Cancer (AJCC) melanoma staging system: Implications for melanoma treatment and care. Expert Rev. Anticancer Ther. 2018, 18, 775–784. [Google Scholar] [CrossRef] [PubMed]
- Morton, D.L.; Thompson, J.F.; Cochran, A.J.; Mozzillo, N.; Nieweg, O.E.; Roses, D.F.; Hoekstra, H.J.; Karakousis, C.P.; Puleo, C.A.; Coventry, B.J.; et al. Final trial report of sentinel-node biopsy versus nodal observation in melanoma. N. Engl. J. Med. 2014, 370, 599–609. [Google Scholar] [CrossRef] [Green Version]
- Michielin, O.; Van Akkooi, A.C.J.; Ascierto, P.A.; Dummer, R.; Keilholz, U.; ESMO Guidelines Committee. Cutaneous melanoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2019, 30, 1884–1901. [Google Scholar] [CrossRef] [Green Version]
- Leiter, U.; Stadler, R.; Mauch, C.; Hohenberger, W.; Brockmeyer, N.; Berking, C.; Sunderkötter, C.; Kaatz, M.; Schulte, K.W.; Lehmann, P.; et al. Complete lymph node dissection versus no dissection in patients with sentinel lymph node biopsy positive melanoma (DeCOG-SLT): A multicentre, randomised, phase 3 trial. Lancet Oncol. 2016, 17, 757–767. [Google Scholar] [CrossRef]
- Faries, M.B.; Thompson, J.F.; Cochran, A.J.; Andtbacka, R.H.; Mozzillo, N.; Zager, J.S.; Jahkola, T.; Bowles, T.L.; Testori, A.; Beitsch, P.D.; et al. Completion dissection or observation for sentinel-node metastasis in melanoma. N. Engl. J. Med. 2017, 376, 2211–2222. [Google Scholar] [CrossRef]
- Ingvar, C.; Erichsen, C.; Jönsson, P.-E. Morbidity following Prophylactic and Therapeutic Lymph Node Dissection for Melanoma—A Comparison. Tumori J. 1984, 70, 529–533. [Google Scholar] [CrossRef]
- Madu, M.F.; Franke, V.; Bruin, M.M.; Berger, D.M.; Bierman, C.; Jóźwiak, K.; Klop, W.M.; Wouters, M.W.; van Akkooi, A.C.; Van de Wiel, B.A. Immediate completion lymph node dissection in stage IIIA melanoma does not provide significant additional staging information beyond EORTC SN tumour burden criteria. Eur. J. Cancer 2017, 87, 212–215. [Google Scholar] [CrossRef]
- Verver, D.; van Klaveren, D.; van Akkooi, A.C.J.; Rutkowski, P.; Powell, B.W.E.M.; Robert, C.; Testori, A.; van Leeuwen, B.L.; van der Veldt, A.A.M.; Keilholz, U.; et al. Risk stratification of sentinel node-positive melanoma patients defines surgical management and adjuvant therapy treatment considerations. Eur. J Cancer. 2018, 96, 25–33. [Google Scholar] [CrossRef]
- de Vries, M.; Hoekstra, H.J.; Hoekstra-Weebers, J.E. Quality of Life After Axillary or Groin Sentinel Lymph Node Biopsy, With or Without Completion Lymph Node Dissection, in Patients With Cutaneous Melanoma. Ann. Surg. Oncol. 2009, 16, 2840–2847. [Google Scholar] [CrossRef] [Green Version]
- Faries, M.B.; The MSLT Cooperative Group; Thompson, J.F.; Cochran, A.; Elashoff, R.; Glass, E.C.; Mozzillo, N.; Nieweg, O.E.; Roses, D.F.; Hoekstra, H.J.; et al. The Impact on Morbidity and Length of Stay of Early Versus Delayed Complete Lymphadenectomy in Melanoma: Results of the Multicenter Selective Lymphadenectomy Trial (I). Ann. Surg. Oncol. 2010, 17, 3324–3329. [Google Scholar] [CrossRef] [Green Version]
- Giudice, G.; Vestita, M.; Robusto, F.; Annoscia, P.; Ciancio, F.; Nacchiero, E. Breast cancer cutaneous metastases mimicking Papilloma Cutis Lymphostatica. Biopsy to avoid pitfalls. Int. J. Surg. Case Rep. 2018, 46, 31–33. [Google Scholar] [CrossRef]
- Nacchiero, E.; Maruccia, M.; Vestita, M.; Elia, R.; Marannino, P.; Giudice, G. Multiple lymphatic-venous anastomoses in reducing the risk of lymphedema in melanoma patients undergoing complete lymph node dissection. A retrospective case-control study. J. Plast. Reconstr. Aesthetic Surg. 2019, 72, 642–648. [Google Scholar] [CrossRef]
- Giudice, G.; Robusto, F.; Vestita, M.; Annoscia, P.; Elia, R.; Nacchiero, E. Single-stage excision and sentinel lymph node biopsy in cutaneous melanoma in selected patients: A retrospective case–control study. Melanoma Res. 2017, 27, 573–579. [Google Scholar] [CrossRef] [PubMed]
- Nacchiero, E.; Vestita, M.; Robusto, F.; Maruccia, M.; Annoscia, P.; Giudice, G. Surgical management of tumor-positive interval node in melanoma patients. Medicine 2018, 97, e0584. [Google Scholar] [CrossRef] [PubMed]
- Chakera, A.H.; Hesse, B.; Burak, Z.; Ballinger, J.R.; Britten, A.; Caracò, C.; Cochran, A.J.; Cook, M.G.; Drzewiecki, K.T.; Essner, R.; et al. EANM-EORTC general recommendations for sentinel node diagnostics in melanoma. Eur. J. Nucl. Med. Mol. Imaging 2009, 36, 1713–1742. [Google Scholar] [CrossRef]
- Giudice, G.; Nacchiero, E.; Robusto, F.; Campisi, C. Optimizing the Staging of Melanoma Patients for Their Best Surgical Management. Lymphology 2015, 48, 163–174. [Google Scholar] [PubMed]
- Giudice, G.; Robusto, F.; Nacchiero, E. The surgical treatment of a melanoma patient with macroscopic metastasis in peri and retrocaval lymph nodes and with a positive sentinel lymph node in the groin. Ann. Ital. Chir. 2016, 87, S2239253X16024762. [Google Scholar] [PubMed]
- Hidding, J.T.; Viehoff, P.; Beurskens, C.H.; Van Laarhoven, H.W.; Der Sanden, M.W.N.-V.; Van Der Wees, P.J. Measurement Properties of Instruments for Measuring of Lymphedema: Systematic Review. Phys. Ther. 2016, 96, 1965–1981. [Google Scholar] [CrossRef]
- Starritt, E.C.; Joseph, D.; McKinnon, J.G.; Lo, S.K.; de Wilt, J.H.; Thompson, J.F. Lymphedema after complete axillary node dissection for melanoma: Assessment using a new, objective definition. Ann Surg. 2004, 240, 866–874. [Google Scholar] [CrossRef]
- Spillane, A.J.; Saw, R.P.M.; Tucker, M.; Byth, K.; Thompson, J. Defining Lower Limb Lymphedema After Inguinal or Ilio-Inguinal Dissection in Patients With Melanoma Using Classification and Regression Tree Analysis. Ann. Surg. 2008, 248, 286–293. [Google Scholar] [CrossRef]
- Rossi, C.R.; Mozzillo, N.; Maurichi, A.; Pasquali, S.; Macripò, G.; Borgognoni, L.; Solari, N.; Piazzalunga, D.; Mascheroni, L.; Giudice, G.; et al. Number of Excised Lymph Nodes as a Quality Assurance Measure for Lymphadenectomy in Melanoma. JAMA Surg. 2014, 149, 700–706. [Google Scholar] [CrossRef] [Green Version]
- Sabel, M.S.; Griffith, K.A.; Arora, A.; Shargorodsky, J.; Blazer, D.G.; Rees, R.; Wong, S.L.; Cimmino, V.M.; Chang, A.E. Inguinal node dissection for melanoma in the era of sentinel lymph node biopsy. Surgery 2007, 141, 728–735. [Google Scholar] [CrossRef]
- Ciudad, P.; Maruccia, M.; Socas, J.; Lee, M.H.; Chung, K.P.; Constantinescu, T.; Kiranantawat, K.; Nicoli, F.; Sapountzis, S.; Yeo, M.S.; et al. The laparoscopic righ gastroepiploic lymph node flap transfer for upper and lower limb lymphedema: Technique and outcomes. Microsurgery 2017, 37, 197–205. [Google Scholar] [CrossRef]
- Lawton, G.; Rasque, H.; Ariyan, S. Preservation of muscle fascia to decrease lymphedema after complete axillary and ilioinguinofemoral lymphadenectomy for melanoma. J. Am. Coll. Surg. 2002, 195, 339–351. [Google Scholar] [CrossRef]
- Delman, K.A.; Kooby, D.A.; Ogan, K.; Hsiao, W.; Master, V. Feasibility of a Novel Approach to Inguinal Lymphadenectomy: Minimally Invasive Groin Dissection for Melanoma. Ann. Surg. Oncol. 2009, 17, 731–737. [Google Scholar] [CrossRef]
- Cigna, E.; Pierazzi, D.M.; Sereni, S.; Marcasciano, M.; Losco, L.; Bolletta, A. Lymphatico-venous anastomosis in chronic ulcer with venous insufficiency: A case report. Microsurgery 2021, 41, 574–578. [Google Scholar] [CrossRef] [PubMed]
- Bolletta, A.; Di Taranto, G.; Chen, S.; Elia, R.; Amorosi, V.; Chan, J.C.; Chen, H. Surgical treatment of Milroy disease. J. Surg. Oncol. 2019, 121, 175–181. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Lo Torto, F.; Kaciulyte, J.; Mori, F.L.; Frattaroli, J.M.; Marcasciano, M.; Casella, D.; Cigna, E.; Losco, L.; Manrique, O.J.; Nicoli, F.; et al. Microsurgical lymphedema treatment: An objective evaluation of the quality of online information. J. Plast. Reconstr. Aesthet. Surg. 2021, 74, 637–640. [Google Scholar] [CrossRef] [PubMed]
- Kaciulyte, J.; Garutti, L.; Spadoni, D.; Velazquez-Mujica, J.; Losco, L.; Ciudad, P.; Marcasciano, M.; Torto, F.L.; Casella, D.; Ribuffo, D.; et al. Genital Lymphedema and How to Deal with It: Pearls and Pitfalls from over 38 Years of Experience with Unusual Lymphatic System Impairment. Medicina 2021, 57, 1175. [Google Scholar] [CrossRef] [PubMed]
- Di Taranto, G.; Chen, S.H.; Elia, R.; Bolletta, A.; Amorosi, V.; Sitpahul, N.; Chan, J.C.; Ribuffo, D.; Chen, H.C. Free gastroepiploic lymph nodes and omentum flap for treatment of lower limb ulcers in severe lymphedema: Killing two birds with one stone. J. Surg. Oncol. 2020, 121, 168–174. [Google Scholar] [CrossRef] [Green Version]
- Di Taranto, G.; Bolletta, A.; Chen, S.H.; Losco, L.; Elia, R.; Cigna, E.; Rubino, C.; Ribuffo, D.; Chen, H.C. A prospective study on combined lymphedema surgery: Gastroepiploic vascularized lymph nodes transfer and lymphaticovenous anastomosis followed by suction lipectomy. Microsurgery 2021, 41, 34–43. [Google Scholar] [CrossRef]
- Nacchiero, E.; Maruccia, M.; Elia, R.; Robusto, F.; Giudice, G.; Manrique, O.; Campisi, C. Lymphovenous Anastomosis for the Treatment of Lymphedema: A Systematic Review of the Literature and Meta-Analysis. Lymphology 2020, 53, 172–194. [Google Scholar] [CrossRef]
- Maruccia, M.; Pezzolla, A.; Nacchiero, E.; DiCillo, P.; Macchia, L.; Fiore, P.; Giudice, G.; Elia, R. Efficacy and early results after combining laparoscopic harvest of double gastroepiploic lymph node flap and active physiotherapy for lower extremity lymphedema. Microsurgery 2019, 39, 679–687. [Google Scholar] [CrossRef] [PubMed]
- Maruccia, M.; Elia, R.; Ciudad, P.; Nacchiero, E.; Nicoli, F.; Vestita, M.; Chen, H.C.; Giudice, G. Postmastectomy upper limb lymphedema: Combined vascularized lymph node transfer and scar release with fat graft expedites surgical and patients’ related outcomes. A retrospective comparative study. J. Plast. Reconstr. Aesthet. Surg. 2019, 72, 892–901. [Google Scholar] [CrossRef]
- Ciudad, P.; Manrique, O.J.; Bustos, S.; Coca, J.J.P.; Chang, C.; Shih, P.; Nicoli, F.; Torto, F.L.; Agko, M.; Huang, T.C.; et al. Comparisons in long-term clinical outcomes among patients with upper or lower extremity lymphedema treated with diverse vascularized lymph node transfer. Microsurgery 2019, 40, 130–136. [Google Scholar] [CrossRef] [PubMed]
- Baumann, F.T.; Reike, A.; Hallek, M.; Wiskemann, J.; Reimer, V. Does Exercise Have a Preventive Effect on Secondary Lymphedema in Breast Cancer Patients Following Local Treatment—A Systematic Review. Breast Care 2018, 13, 380–385. [Google Scholar] [CrossRef] [PubMed]
- Boccardo, F.M.; De Cian, F.; Campisi, C.C.; Molinari, L.; Spinaci, S.; Dessalvi, S.; Talamo, G.; Villa, G.; Bellini, C.; Parodi, A.; et al. Surgical prevention and treatment of lymphedema after lymph node dissection in patients with cutaneous melanoma. Lymphology 2013, 46, 20–26. [Google Scholar]
- Hayashida, K.; Yoshida, S.; Yoshimoto, H.; Fujioka, M.; Saijo, H.; Migita, K.; Kumaya, M.; Akita, S. Adipose-Derived Stem Cells and Vascularized Lymph Node Transfers Successfully Treat Mouse Hindlimb Secondary Lymphedema by Early Reconnection of the Lymphatic System and Lymphangiogenesis. Plast. Reconstr. Surg. 2017, 139, 639–651. [Google Scholar] [CrossRef]
- Wrone, D.A.; Tanabe, K.K.; Cosimi, A.B.; Gadd, M.A.; Souba, W.W.; Sober, A.J. Lymphedema After Sentinel Lymph Node Biopsy for Cutaneous Melanoma. Arch. Dermatol. 2000, 136, 511–514. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Characteristics | Control Group | Group 1 | Group 2 | p |
---|---|---|---|---|
Total, n (%) | 120 | 23 | 29 | / |
Gender (M), n (%) | 64 (53.3) | 12 (52.2) | 14 (48.3) | 0.89 |
Age (y) | ||||
Median | 53.3 | 54.8 | 54.2 | 0.43 |
Range | 18.9–74.2 | 18.0–68.9 | 19.8–81.1 | |
Breslow thickness, n (%) | ||||
<1 mm | 24 (20.0) | 5 (21.7) | 5 (17.2) | 0.99 |
1–2 mm | 53 (44.2) | 10 (43.5) | 11 (37.9) | |
2–4 mm | 26 (21.7) | 5 (21.7) | 8 (27.6) | |
>4 mm | 17 (14.2) | 3 (13.0) | 5 (17.2) | |
Ulceration, n (%) | 27 (22.5) | 5 (21.7) | 8 (27.6) | 0.83 |
>1 mitosis/mm, n(%) | 17 (14.2) | 5 (21.7) | 7 (24.1) | 0.35 |
Obesity (BMI > 30 kg/m2) | 16 (13.3) | 5 (21.7) | 6 (20.7) | 0.43 |
Duration of surgical procedure (hours) | ||||
Median | 0.50 | 1.75 | 2.00 | <0.01 |
Range | 0.25–1.00 | 0.50–2.50 | 0.75–2.75 | |
Length of stay (days) | ||||
Median | 10 | 10 | 10 | 0.90 |
Range | 8–14 | 8–14 | 8–14 |
CLND Site | Control Group | Group 1 | Group 2 | ||
---|---|---|---|---|---|
N | N | p | N | p | |
Axilla | 7/51 (13.7%) | 0/8 (0.0%) | / | 0/11 (0.0%) | / |
Groin | 22/69 (31.9%) | 1/15 (7.7%) | 0.05 | 1/18 (5.6%) | 0.02 |
TOT | 29/120 (24.2%) | 1/23 (4.3%) | 0.03 | 1/29 (3.5%) | 0.01 |
Characteristics | Group 1 | Group 2 | ||
---|---|---|---|---|
HR | 95% CI | HR | 95% CI | |
Age | 1.001 | 0.982 1.019 | 1.006 | 0.989 1.013 |
Sex (M) | 1.503 | 0.603 3.743 | 1.180 | 0.477 2.919 |
Obesity | 1.738 | 0.588 5.138 | 2.028 | 0.673 6.115 |
Lymphatic Basin (groin) | 2.542 | 0.952 6.787 | 2.796 | 1.051 7.440 |
PMLVA | 0.123 | 0.015 0.980 | 0.319 | 0.114 0.890 |
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Nacchiero, E.; Maruccia, M.; Robusto, F.; Elia, R.; De Cosmo, A.; Giudice, G. Prevention of Secondary Lymphedema after Complete Lymph Node Dissection in Melanoma Patients: The Role of Preventive Multiple Lymphatic–Venous Anastomosis in Observational Era. Medicina 2022, 58, 117. https://doi.org/10.3390/medicina58010117
Nacchiero E, Maruccia M, Robusto F, Elia R, De Cosmo A, Giudice G. Prevention of Secondary Lymphedema after Complete Lymph Node Dissection in Melanoma Patients: The Role of Preventive Multiple Lymphatic–Venous Anastomosis in Observational Era. Medicina. 2022; 58(1):117. https://doi.org/10.3390/medicina58010117
Chicago/Turabian StyleNacchiero, Eleonora, Michele Maruccia, Fabio Robusto, Rossella Elia, Alessio De Cosmo, and Giuseppe Giudice. 2022. "Prevention of Secondary Lymphedema after Complete Lymph Node Dissection in Melanoma Patients: The Role of Preventive Multiple Lymphatic–Venous Anastomosis in Observational Era" Medicina 58, no. 1: 117. https://doi.org/10.3390/medicina58010117
APA StyleNacchiero, E., Maruccia, M., Robusto, F., Elia, R., De Cosmo, A., & Giudice, G. (2022). Prevention of Secondary Lymphedema after Complete Lymph Node Dissection in Melanoma Patients: The Role of Preventive Multiple Lymphatic–Venous Anastomosis in Observational Era. Medicina, 58(1), 117. https://doi.org/10.3390/medicina58010117