Mayo Adhesive Probability Score Does Not Have Prognostic Ability in Locally Advanced Renal Cell Carcinoma.

body composition kidney cancer mayo adhesive probability renal cell carcinoma survival

Journal

Journal of kidney cancer and VHL
ISSN: 2203-5826
Titre abrégé: J Kidney Cancer VHL
Pays: Australia
ID NLM: 101695919

Informations de publication

Date de publication:
2023
Historique:
received: 09 01 2023
accepted: 12 03 2023
entrez: 27 3 2023
pubmed: 28 3 2023
medline: 28 3 2023
Statut: epublish

Résumé

Nephrectomy remains standard treatment for renal cell carcinoma (RCC). The Mayo Adhesive Probability (MAP) score is predictive of adherent perinephric fat and associated surgical complexity, and is determined by assessing perinephric fat and stranding. MAP has additionally predicted progression-free survival (PFS), though primarily reported in stage T1-T2 RCC. Here, we examine MAP's ability to predict overall survival (OS) and PFS in T3-T4 RCC. From our prospectively maintained RCC database, patients that underwent radical nephrectomy (2009-2016) with available abdominal imaging (<90 days preop) and T3/T4 RCC underwent MAP scoring. Survival analyses were conducted with MAP scores as individual (0-5) and dichotomized (0-3 vs 4-5) using Kaplan-Meier method. Multivariable Cox proportional hazard regression models for PFS and OS were built with backward elimination. 141 patients were included. 134 (95%) and 7 (5%) had pT3 and pT4 disease, respectively. 46.1% of patients had an inferior vena cava thrombus. Mean MAP score was 3.22±1.52, with 75 (53%) patients having a score between 0-3 and 66 (47%) having a score of 4-5. Both male gender (p=0.006) and clear cell histology (p=0.012) were associated with increased MAP scores. On Kaplan-Meier and multivariable analysis, no significant associations were identified between MAP and PFS (HR=1.01, 95% CI 0.85-1.20, p=0.93) or OS (HR=1.01, 95% CI 0.84-1.21, p=0.917). In this cohort of patients with locally advanced RCC, high MAP scores were not predictive of worse PFS or OS.

Identifiants

pubmed: 36969300
doi: 10.15586/jkcvhl.v10i1.269
pii: JKCVHL-10-019
pmc: PMC10036918
doi:

Types de publication

Journal Article

Langues

eng

Pagination

19-25

Subventions

Organisme : NCI NIH HHS
ID : P30 CA138292
Pays : United States

Informations de copyright

Copyright: Schmeusser BN, et al.

Déclaration de conflit d'intérêts

All of the authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Benjamin N Schmeusser (BN)

Department of Urology, Emory University School of Medicine, Atlanta, GA, USA.

Tad A Manalo (TA)

Department of Urology, University of Colorado School of Medicine, Denver, CO, USA.

Yuan Liu (Y)

Department of Biostatistics and Bioinformatics, Emory University School of Medicine, Atlanta, GA, USA.

Yash B Shah (YB)

Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.

Adil Ali (A)

Department of Urology, Emory University School of Medicine, Atlanta, GA, USA.

Manuel Armas-Phan (M)

Department of Urology, Emory University School of Medicine, Atlanta, GA, USA.

Dattatraya H Patil (DH)

Department of Urology, Emory University School of Medicine, Atlanta, GA, USA.

Reza Nabavizadeh (R)

Department of Urology, Emory University School of Medicine, Atlanta, GA, USA.

Kenneth Ogan (K)

Department of Urology, Emory University School of Medicine, Atlanta, GA, USA.
Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.

Viraj A Master (VA)

Department of Urology, Emory University School of Medicine, Atlanta, GA, USA.
Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.

Classifications MeSH