Timing of sentinel node biopsy independently predicts disease-free and overall survival in clinical stage I-II melanoma patients: A multicentre study of the Italian Melanoma Intergroup (IMI).

Melanoma Prognosis Sentinel lymph node

Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
09 2020
Historique:
received: 28 04 2020
revised: 26 06 2020
accepted: 01 07 2020
pubmed: 3 8 2020
medline: 3 8 2020
entrez: 3 8 2020
Statut: ppublish

Résumé

Sentinel lymph node biopsy (SNB) still remains a key procedure to appropriately stage melanoma patients and to select those who are candidate to novel treatments with immunotherapy and targeted therapy in the adjuvant setting. The impact of timing of SNB on disease-free survival (DFS) and overall survival (OS) is still unclear. The study was conducted at 6 Italian Melanoma Intergroup (IMI) centres and included 8953 consecutive clinical stage I-II melanoma patients who were diagnosed, treated, and followed up between November 1997 and March 2018. All patients were prospectively included in dedicated IMI database. Multivariable Cox regression analyses were performed to investigate how baseline characteristics and time interval until SNB are related to DFS and OS. Considering the whole population, at multivariable analysis, after adjusting for age, gender, Breslow thickness, site, ulceration, and the SNB status, a delay in the timing of SNB was associated with a better DFS (adjusted hazard ratio [aHR, delayed versus early SNB] 0.98, 95% confidence interval [CI] 0.97-0.99, p < 0.001) and OS (aHR 0.98, 95% CI 0.97-0.99, p = 0.001). Specifically, in patients with a negative SNB status, a beneficial impact of delayed SNB (i.e. at least 32 days after primary excision) was confirmed for DFS (aHR 0.70, 95%CI 0.63-0.79, p < 0.001) and OS (aHR 0.69, 95%CI 0.61-0.78, p < 0.001), whereas in those with a positive SNB status, DFS (aHR 0.96, 95%CI 0.84-1.09, p = 0.534) and OS (aHR 0.94 95%CI 0.81-1.08, p = 0.374) were not significantly different in patients with early or delayed SNB. Our study does not support a strict time interval for SNB. These results may be useful for national guidelines, for counselling patients and reducing the number of high urgency referrals.

Sections du résumé

BACKGROUND
Sentinel lymph node biopsy (SNB) still remains a key procedure to appropriately stage melanoma patients and to select those who are candidate to novel treatments with immunotherapy and targeted therapy in the adjuvant setting. The impact of timing of SNB on disease-free survival (DFS) and overall survival (OS) is still unclear.
MATERIAL AND METHODS
The study was conducted at 6 Italian Melanoma Intergroup (IMI) centres and included 8953 consecutive clinical stage I-II melanoma patients who were diagnosed, treated, and followed up between November 1997 and March 2018. All patients were prospectively included in dedicated IMI database. Multivariable Cox regression analyses were performed to investigate how baseline characteristics and time interval until SNB are related to DFS and OS.
RESULTS
Considering the whole population, at multivariable analysis, after adjusting for age, gender, Breslow thickness, site, ulceration, and the SNB status, a delay in the timing of SNB was associated with a better DFS (adjusted hazard ratio [aHR, delayed versus early SNB] 0.98, 95% confidence interval [CI] 0.97-0.99, p < 0.001) and OS (aHR 0.98, 95% CI 0.97-0.99, p = 0.001). Specifically, in patients with a negative SNB status, a beneficial impact of delayed SNB (i.e. at least 32 days after primary excision) was confirmed for DFS (aHR 0.70, 95%CI 0.63-0.79, p < 0.001) and OS (aHR 0.69, 95%CI 0.61-0.78, p < 0.001), whereas in those with a positive SNB status, DFS (aHR 0.96, 95%CI 0.84-1.09, p = 0.534) and OS (aHR 0.94 95%CI 0.81-1.08, p = 0.374) were not significantly different in patients with early or delayed SNB.
CONCLUSIONS
Our study does not support a strict time interval for SNB. These results may be useful for national guidelines, for counselling patients and reducing the number of high urgency referrals.

Identifiants

pubmed: 32739767
pii: S0959-8049(20)30370-1
doi: 10.1016/j.ejca.2020.07.001
pmc: PMC7391020
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

30-39

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement The authors declare no conflict of interest.

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Auteurs

Mario Mandalà (M)

Unit of Medical Oncology, Papa Giovanni XXIII Hospital, Bergamo, Italy. Electronic address: mmandala@asst-pg23.it.

Francesca Galli (F)

Methodology for Clinical Research Laboratory, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Roberto Patuzzo (R)

Melanoma and Sarcoma Unit, Department of Surgery, IRCCS Fondazione Istituto Nazionale dei Tumori, Milan, Italy.

Andrea Maurichi (A)

Melanoma and Sarcoma Unit, Department of Surgery, IRCCS Fondazione Istituto Nazionale dei Tumori, Milan, Italy.

Simone Mocellin (S)

Unit of Surgery, Veneto Institute of Oncology - IOV.

Carlo R Rossi (CR)

University of Padua, Italy.

Eliana Rulli (E)

Methodology for Clinical Research Laboratory, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Maria Montesco (M)

Pathological Anatomy and Histology, Veneto Institute of Oncology - IOV, Istituto di Ricovero e Cura a Carattere Scientifico, Padua, Italy.

Pietro Quaglino (P)

Dermatologic Clinic, Department of Medical Sciences, University of Turin Medical School, Turin, Italy.

Virginia Caliendo (V)

Department of Surgery, University of Turin Madical Scholl.

Vincenzo De Giorgi (V)

Department of Dermatology, University of Florence, Italy.

Barbara Merelli (B)

Unit of Medical Oncology, Papa Giovanni XXIII Hospital, Bergamo, Italy.

Corrado Caracò (C)

Istituto Nazionale Tumori IRCCS Fondazione 'G. Pascale', Naples, Italy.

Dario Piazzalunga (D)

Unit of Surgery, Papa Giovanni XXIII Hospital, Bergamo, Italy.

Alice Labianca (A)

Unit of Medical Oncology, Papa Giovanni XXIII Hospital, Bergamo, Italy.

Simone Ribero (S)

Dermatologic Clinic, Department of Medical Sciences, University of Turin Medical School, Turin, Italy.

Rebecca Senetta (R)

Pathology Division, 'Città della Salute e della Scienza di Torino' University Hospital, Turin, Italy.

Andrea Gianatti (A)

Unit of Pathology, Papa Giovanni XXIII Hospital, Bergamo, Italy.

Barbara Valeri (B)

Department of Pathology and Laboratory Medicine, IRCCS Fondazione Istituto Nazionale dei Tumori di Milano, Milan, Italy.

Daniela Massi (D)

Histopatology and Molecular Diagnostics, Careggi University Hospital, Florence, Italy.

Paolo A Ascierto (PA)

Unit Melanoma, Cancer Immunotherapy and Innovative Therapies, Istituto Nazionale Tumori IRCCS Fondazione 'G. Pascale', Naples, Italy.

Mario Santinami (M)

Melanoma and Sarcoma Unit, Department of Surgery, IRCCS Fondazione Istituto Nazionale dei Tumori, Milan, Italy.

Classifications MeSH