Inguinal and Ilio-inguinal Lymphadenectomy in Management of Palpable Melanoma Lymph Node Metastasis: A Long-Term Prospective Evaluation of Morbidity and Quality of Life.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 30 05 2019
pubmed: 14 9 2019
medline: 16 4 2020
entrez: 14 9 2019
Statut: ppublish

Résumé

Prospective data are lacking on long-term morbidity of inguinal lymphadenectomy including the influence of extent of surgery, use of radiotherapy, and patient factors. The aim of this study is to evaluate the effects of these factors on patient outcome, quality of life (QOL), regional symptoms, and limb volumes after inguinal or ilio-inguinal lymphadenectomy for melanoma. Analysis of the subgroup of patients with inguinal lymph node field relapse of melanoma, treated by inguinal or ilio-inguinal lymphadenectomy in the ANZMTG/TROG randomized trial of adjuvant radiotherapy versus observation. Sixty-nine patients, 46 having undergone inguinal and 23 ilio-inguinal lymphadenectomy, with median follow-up of 73 months were analyzed. Mean limb volume increased rapidly after surgery (7% by 3 months) and continued to increase for at least another 18 months. Patients with body mass index (BMI) ≥ 25 kg/m Inguinal lymphadenectomy for melanoma is a potentially morbid procedure with significant increases in limb volume. Patients report reasonable QOL but may have ongoing regional symptoms. Overweight/obesity is associated with poorer QOL, increased limb volume, and regional symptoms.

Identifiants

pubmed: 31515719
doi: 10.1245/s10434-019-07810-0
pii: 10.1245/s10434-019-07810-0
doi:

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

4663-4672

Auteurs

Michael A Henderson (MA)

Division of Cancer Surgery, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia. Michael.Henderson@petermac.org.

D Gyorki (D)

Division of Cancer Surgery, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia.

B H Burmeister (BH)

Princess Alexandra Hospital, University of Queensland, Brisbane, Australia.

J Ainslie (J)

Division of Cancer Surgery, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia.

R Fisher (R)

Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.

J Di Iulio (J)

Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.

B M Smithers (BM)

Princess Alexandra Hospital, University of Queensland, Brisbane, Australia.

A Hong (A)

Melanoma Institute of Australia, University of Sydney, Sydney, Australia.

K Shannon (K)

Melanoma Institute of Australia, University of Sydney, Sydney, Australia.

R A Scolyer (RA)

Melanoma Institute of Australia, University of Sydney, Sydney, Australia.

S Carruthers (S)

Royal Adelaide Hospital, University of Adelaide, Adelaide, Australia.

B J Coventry (BJ)

Royal Adelaide Hospital, University of Adelaide, Adelaide, Australia.

S Babington (S)

Christchurch Hospital, Christchurch, New Zealand.

J Duprat (J)

Hospital Do Cancer, São Paulo, Brazil.

H J Hoekstra (HJ)

University Medical Centre Groningen, Groningen, The Netherlands.

J F Thompson (JF)

Melanoma Institute of Australia, University of Sydney, Sydney, Australia.

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Classifications MeSH