Sentinel lymph node biopsy versus observation in high-risk cutaneous squamous cell carcinoma in immunosuppressed and immunocompetent patients: An inverse probability of treatment weighting study.


Journal

Journal of the European Academy of Dermatology and Venereology : JEADV
ISSN: 1468-3083
Titre abrégé: J Eur Acad Dermatol Venereol
Pays: England
ID NLM: 9216037

Informations de publication

Date de publication:
13 May 2024
Historique:
received: 28 10 2023
accepted: 28 02 2024
medline: 13 5 2024
pubmed: 13 5 2024
entrez: 13 5 2024
Statut: aheadofprint

Résumé

The survival benefit of sentinel lymph node biopsy (SLNB) in immunocompetent and immunosuppressed patients with high-risk cutaneous squamous cell carcinoma (cSCC) has not been established. To determine whether SLNB improves disease-specific survival (DSS) in high-risk cSCC. Secondary objectives were to analyse disease-free survival, nodal recurrence-free survival and overall survival (OS). Multicentre, retrospective, observational cohort study comparing survival outcomes in immunosuppressed and immunocompetent patients treated with SLNB or watchful waiting. Inverse probability of treatment weighting was used to adjust for possible confounding effects. We studied 638 tumours in immunocompetent patients (SLNB n = 42, observation n = 596) and 173 tumours in immunosuppressed patients (SLNB n = 28, observation n = 145). Overall, SLNB was positive in 15.7% of tumours. SLNB was associated with a reduced risk of nodal recurrence (NR) (hazard ratio [HR], 0.05 [95% CI, 0.01-0.43]; p = 0.006), disease specific mortality (HR, 0.17 [95% CI, 0.04-0.72]; p = 0.016) and all-cause mortality (HR, 0.33 [95% CI, 0.15-0.71]; p = 0.004) only in immunocompetent patients. SLNB was associated with improvements in NR, DSS and OS in immunocompetent but not in immunosuppressed patients with high-risk cSCC.

Sections du résumé

BACKGROUND BACKGROUND
The survival benefit of sentinel lymph node biopsy (SLNB) in immunocompetent and immunosuppressed patients with high-risk cutaneous squamous cell carcinoma (cSCC) has not been established.
OBJECTIVE OBJECTIVE
To determine whether SLNB improves disease-specific survival (DSS) in high-risk cSCC. Secondary objectives were to analyse disease-free survival, nodal recurrence-free survival and overall survival (OS).
METHODS METHODS
Multicentre, retrospective, observational cohort study comparing survival outcomes in immunosuppressed and immunocompetent patients treated with SLNB or watchful waiting. Inverse probability of treatment weighting was used to adjust for possible confounding effects.
RESULTS RESULTS
We studied 638 tumours in immunocompetent patients (SLNB n = 42, observation n = 596) and 173 tumours in immunosuppressed patients (SLNB n = 28, observation n = 145). Overall, SLNB was positive in 15.7% of tumours. SLNB was associated with a reduced risk of nodal recurrence (NR) (hazard ratio [HR], 0.05 [95% CI, 0.01-0.43]; p = 0.006), disease specific mortality (HR, 0.17 [95% CI, 0.04-0.72]; p = 0.016) and all-cause mortality (HR, 0.33 [95% CI, 0.15-0.71]; p = 0.004) only in immunocompetent patients.
CONCLUSIONS CONCLUSIONS
SLNB was associated with improvements in NR, DSS and OS in immunocompetent but not in immunosuppressed patients with high-risk cSCC.

Identifiants

pubmed: 38738666
doi: 10.1111/jdv.20051
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fundación Piel Sana de la Academia Española de Dermatología y Venereología

Informations de copyright

© 2024 European Academy of Dermatology and Venereology.

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Auteurs

Antonio Tejera-Vaquerizo (A)

Cutaneous Oncology Unit, Hospital San Juan de Dios, Córdoba, Spain.
Dermatology Department, Instituto Dermatológico GlobalDerm, Palma del Río, Córdoba, Spain.

Álvaro Gómez-Tomás (Á)

Dermatology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Facultat de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain.

Ane Jaka (A)

Dermatology Department, Hospital Universitari Germans Trials i Pujol, Institut d'Investigació GermansTrias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.

Agustín Toll (A)

Dermatology Department, Hospital Clínic de Barcelona, Universidad de Barcelona, Barcelona, Spain.

María Del Río (M)

Plastic Surgery Department, Hospital Universitari Germans Trials i Pujol, Institut d'Investigació GermansTrias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.

Carla Ferrándiz-Pulido (C)

Dermatology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Facultat de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain.

María J Fuente (MJ)

Dermatology Department, Hospital Universitari Germans Trials i Pujol, Institut d'Investigació GermansTrias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.

Cristian Carrasco (C)

Plastic Surgery Department, Hospital Universitari Germans Trials i Pujol, Institut d'Investigació GermansTrias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.

Francisco M Almazán-Fernández (FM)

Dermatology Department, Hospital Universitario Clinico San Cecilio (PTS), Granada, Spain.

Tomás Toledo-Pastrana (T)

Dermatology Department, Hospital Quirón Salud Infanta Luisa, Hospital Quirón Salud Sagrado Corazón, Sevilla, Spain.

Ada Ferrer-Fuertes (A)

Maxillofacial Department, Hospital Clínic, Barcelona, Spain.

Simone Ribero (S)

Section of Dermatology, Medical Sciences Department, University of Turin, Turin, Italy.

Gianluca Avallone (G)

Section of Dermatology, Medical Sciences Department, University of Turin, Turin, Italy.

Javier Cañueto (J)

Dermatology Department, Complejo Asistencial Universitario de Salamanca, Salamanca, Spain.

Jorge Santos-Juanes (J)

Dermatology Department, Central Universitary Hospital of Asturias and Instituto de Investigación Sanitaria of Principado de Asturias, IUOPA, Oviedo University, Oviedo, Spain.

Onofre Sanmartín (O)

Dermatology Department, Instituto Valenciano de Oncología, Valencia, Spain.

Classifications MeSH