Predictive model for systemic recurrence following cisplatin-based neoadjuvant chemotherapy and radical nephroureterectomy for high risk upper tract urothelial carcinoma.


Journal

Urologic oncology
ISSN: 1873-2496
Titre abrégé: Urol Oncol
Pays: United States
ID NLM: 9805460

Informations de publication

Date de publication:
11 2021
Historique:
received: 07 03 2021
revised: 13 05 2021
accepted: 30 05 2021
pubmed: 1 8 2021
medline: 11 2 2022
entrez: 31 7 2021
Statut: ppublish

Résumé

Neoadjuvant chemotherapy (NAC) is increasingly used prior to radical nephroureterectomy (RNU) for upper tract urothelial carcinoma (UTUC). Systemic recurrence (SR) carries a dismal prognosis. We sought to determine risk factors associated with SR in this setting. We evaluated a multi-center database of patients with UTUC who received cisplatin-based NAC before RNU. Final pathology at RNU was dichotomized into ypT<2 vs ypT≥2. Univariable and multivariable analyses were performed to identify risk factors associated with SR. Three groups were defined based on the number of significant risk factors (groups 1, 2, 3 for 0-1, 2, 3 risk factors, respectively) and evaluated for recurrence-free survival (RFS) using the Kaplan-Meier method. 106 patients were identified between 2004 and 2018. Median age was 67.0 years [IQR = 61-73.3]; 57 (54%) and 49 (46 %) patients received MVAC and GC, respectively. Final pathological stage was ypT<2 in 57 (54%); 23% (24/106) had SR. On univariable analysis, pathological variables on final specimen including ypT≥2, lymphovascular invasion (ypLVI), and nodal involvement were associated with SR. On multivariable analysis, ypLVI OR = 4.1 (95% CI 1.2-13.6; P = 0.024) and pathological nodal involvement OR = 4.5 (95% CI 1.3-15.7; P = 0.017) were predictive of recurrence. Stratifying by the number of risk factors, the 2-year RFS was 95%, 55%, and 18% for groups 1, 2, and 3 respectively (log-rank <0.001). This model evaluates the risk of SR following NAC and RNU to guide counseling and decision-making after surgery. Adverse pathological variable including ypLVI and nodal involvement, in combination with ypT-stage, are strongly associated with SR.

Identifiants

pubmed: 34330655
pii: S1078-1439(21)00259-3
doi: 10.1016/j.urolonc.2021.05.037
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Cisplatin Q20Q21Q62J

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

788.e15-788.e21

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Rashed A Ghandour (RA)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX; Urology Institute, University Hospitals Cleveland Medical Center, Cleveland, OH. Electronic address: vitaly.margulis@utsouthwestern.edu.

Yuval Freifeld (Y)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX.

Joseph Cheaib (J)

The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD.

Nirmish Singla (N)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX; The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD.

Xiaosong Meng (X)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX.

Alexander Kenigsberg (A)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX.

Aditya Bagrodia (A)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX.

Solomon Woldu (S)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX.

Jean Hoffman-Censits (J)

The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD; Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins, Baltimore, MD.

Dmitry Enikeev (D)

Institute for Urology and Reproductive Health, Sechenov University, Moscow.

Leonid Rapoport (L)

Institute for Urology and Reproductive Health, Sechenov University, Moscow.

Firas G Petros (FG)

Department of Urology, University of Texas MD Anderson Cancer Center, Houston, TX.

Jay D Raman (JD)

Division of Urology, Penn State Health Milton S. Hershey Medical Center, Hershey, PA.

Philip M Pierorazio (PM)

The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD.

Surena F Matin (SF)

Department of Urology, University of Texas MD Anderson Cancer Center, Houston, TX.

Vitaly Margulis (V)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX; Institute for Urology and Reproductive Health, Sechenov University, Moscow.

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Classifications MeSH