Conditional analyses of recurrence and progression in patients with TaG1 non-muscle-invasive bladder cancer

Standard

Conditional analyses of recurrence and progression in patients with TaG1 non-muscle-invasive bladder cancer. / von Landenberg, Nicolas; Aziz, Atiqullah; von Rundstedt, Friedrich C; Dobruch, Jakub; Kluth, Luis A; Necchi, Andrea; Noon, Aidan; Rink, Michael; Hendricksen, Kees; Decaestecker, Karel P J; Seiler, Roland; Poyet, Cédric; Fajkovic, Harun; Shariat, Shahrokh F; Xylinas, Evanguelos; Roghmann, Florian; Young Academic Urologists′ Working Group on Urothelial Cancer of the European Association of Urology.

in: UROL ONCOL-SEMIN ORI, Jahrgang 36, Nr. 5, 05.2018, S. 238.e19-238.e27.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

von Landenberg, N, Aziz, A, von Rundstedt, FC, Dobruch, J, Kluth, LA, Necchi, A, Noon, A, Rink, M, Hendricksen, K, Decaestecker, KPJ, Seiler, R, Poyet, C, Fajkovic, H, Shariat, SF, Xylinas, E, Roghmann, F & Young Academic Urologists′ Working Group on Urothelial Cancer of the European Association of Urology 2018, 'Conditional analyses of recurrence and progression in patients with TaG1 non-muscle-invasive bladder cancer', UROL ONCOL-SEMIN ORI, Jg. 36, Nr. 5, S. 238.e19-238.e27. https://doi.org/10.1016/j.urolonc.2018.01.017

APA

von Landenberg, N., Aziz, A., von Rundstedt, F. C., Dobruch, J., Kluth, L. A., Necchi, A., Noon, A., Rink, M., Hendricksen, K., Decaestecker, K. P. J., Seiler, R., Poyet, C., Fajkovic, H., Shariat, S. F., Xylinas, E., Roghmann, F., & Young Academic Urologists′ Working Group on Urothelial Cancer of the European Association of Urology (2018). Conditional analyses of recurrence and progression in patients with TaG1 non-muscle-invasive bladder cancer. UROL ONCOL-SEMIN ORI, 36(5), 238.e19-238.e27. https://doi.org/10.1016/j.urolonc.2018.01.017

Vancouver

von Landenberg N, Aziz A, von Rundstedt FC, Dobruch J, Kluth LA, Necchi A et al. Conditional analyses of recurrence and progression in patients with TaG1 non-muscle-invasive bladder cancer. UROL ONCOL-SEMIN ORI. 2018 Mai;36(5):238.e19-238.e27. https://doi.org/10.1016/j.urolonc.2018.01.017

Bibtex

@article{2a5d3b3556644dc8a9594db8ccf1e3cc,
title = "Conditional analyses of recurrence and progression in patients with TaG1 non-muscle-invasive bladder cancer",
abstract = "OBJECTIVE: To determine conditional recurrence-free survival (RFS) and progression-free survival (PFS) and improve decision-making toward surveillance protocols and scheduling. Furthermore, evaluating the evolution of predictors for disease recurrence over time, because TaG1 non-muscle-invasive bladder cancer harbors a risk of disease recurrence and progression.MATERIAL AND METHODS: The retrospective multicenter design study includes 1,245 TaG1 bladder cancer patients with median follow-up of 62.7 (interquartile range: 34.3-91.1) months. Conditional RFS and PFS estimates were calculated using the Kaplan-Meier method. Multivariable Cox regression model was calculated proportional for the prediction of recurrence and progression (covariables: age, tumor size, multiple tumors, prior recurrence, and immediate postoperative instillation of chemotherapy).RESULTS: After 3 months without event, the conditional RFS and PFS (to ≥pT2) rates for 5 additional years without event were 57.5% and 93.4%, respectively. Given a 1-, 2-, 3-, and 5-year survival, the conditional RFS rates for 5 additional years without event improved by +9.8 (67.3%), +5.2 (72.5%), +6.5 (79.0%), +2.0 (81.0%), and +1.0% (82.0%), respectively. In contrast, the 5-year conditional PFS rates were more or less stable with 94.3% after 1 year to 94.1% after 5 years. Multivariable analyses showed decreasing impact of risk parameters on RFS estimates over time. Based on these findings, we suggest a risk stratification to individualize follow-up for intermediate risk TaG1. Main limitation was the retrospective design.CONCLUSIONS: Conditional-survival analyses demonstrates that the patient risk profile changes over time. RFS rates rise with increasing survival whereas PFS rates were stable. The impact of prognostic features decreases over time. Our findings can be used for patient counseling and planning of personalized follow-up.",
keywords = "Aged, Disease Progression, Female, Follow-Up Studies, Humans, Male, Middle Aged, Neoplasm Invasiveness, Neoplasm Recurrence, Local, Neoplasm Staging, Retrospective Studies, Risk Factors, Survival Rate, Urinary Bladder Neoplasms, Journal Article, Multicenter Study",
author = "{von Landenberg}, Nicolas and Atiqullah Aziz and {von Rundstedt}, {Friedrich C} and Jakub Dobruch and Kluth, {Luis A} and Andrea Necchi and Aidan Noon and Michael Rink and Kees Hendricksen and Decaestecker, {Karel P J} and Roland Seiler and C{\'e}dric Poyet and Harun Fajkovic and Shariat, {Shahrokh F} and Evanguelos Xylinas and Florian Roghmann and {Young Academic Urologists′ Working Group on Urothelial Cancer of the European Association of Urology}",
note = "Copyright {\textcopyright} 2018 Elsevier Inc. All rights reserved.",
year = "2018",
month = may,
doi = "10.1016/j.urolonc.2018.01.017",
language = "English",
volume = "36",
pages = "238.e19--238.e27",
journal = "UROL ONCOL-SEMIN ORI",
issn = "1078-1439",
publisher = "Elsevier Inc.",
number = "5",

}

RIS

TY - JOUR

T1 - Conditional analyses of recurrence and progression in patients with TaG1 non-muscle-invasive bladder cancer

AU - von Landenberg, Nicolas

AU - Aziz, Atiqullah

AU - von Rundstedt, Friedrich C

AU - Dobruch, Jakub

AU - Kluth, Luis A

AU - Necchi, Andrea

AU - Noon, Aidan

AU - Rink, Michael

AU - Hendricksen, Kees

AU - Decaestecker, Karel P J

AU - Seiler, Roland

AU - Poyet, Cédric

AU - Fajkovic, Harun

AU - Shariat, Shahrokh F

AU - Xylinas, Evanguelos

AU - Roghmann, Florian

AU - Young Academic Urologists′ Working Group on Urothelial Cancer of the European Association of Urology

N1 - Copyright © 2018 Elsevier Inc. All rights reserved.

PY - 2018/5

Y1 - 2018/5

N2 - OBJECTIVE: To determine conditional recurrence-free survival (RFS) and progression-free survival (PFS) and improve decision-making toward surveillance protocols and scheduling. Furthermore, evaluating the evolution of predictors for disease recurrence over time, because TaG1 non-muscle-invasive bladder cancer harbors a risk of disease recurrence and progression.MATERIAL AND METHODS: The retrospective multicenter design study includes 1,245 TaG1 bladder cancer patients with median follow-up of 62.7 (interquartile range: 34.3-91.1) months. Conditional RFS and PFS estimates were calculated using the Kaplan-Meier method. Multivariable Cox regression model was calculated proportional for the prediction of recurrence and progression (covariables: age, tumor size, multiple tumors, prior recurrence, and immediate postoperative instillation of chemotherapy).RESULTS: After 3 months without event, the conditional RFS and PFS (to ≥pT2) rates for 5 additional years without event were 57.5% and 93.4%, respectively. Given a 1-, 2-, 3-, and 5-year survival, the conditional RFS rates for 5 additional years without event improved by +9.8 (67.3%), +5.2 (72.5%), +6.5 (79.0%), +2.0 (81.0%), and +1.0% (82.0%), respectively. In contrast, the 5-year conditional PFS rates were more or less stable with 94.3% after 1 year to 94.1% after 5 years. Multivariable analyses showed decreasing impact of risk parameters on RFS estimates over time. Based on these findings, we suggest a risk stratification to individualize follow-up for intermediate risk TaG1. Main limitation was the retrospective design.CONCLUSIONS: Conditional-survival analyses demonstrates that the patient risk profile changes over time. RFS rates rise with increasing survival whereas PFS rates were stable. The impact of prognostic features decreases over time. Our findings can be used for patient counseling and planning of personalized follow-up.

AB - OBJECTIVE: To determine conditional recurrence-free survival (RFS) and progression-free survival (PFS) and improve decision-making toward surveillance protocols and scheduling. Furthermore, evaluating the evolution of predictors for disease recurrence over time, because TaG1 non-muscle-invasive bladder cancer harbors a risk of disease recurrence and progression.MATERIAL AND METHODS: The retrospective multicenter design study includes 1,245 TaG1 bladder cancer patients with median follow-up of 62.7 (interquartile range: 34.3-91.1) months. Conditional RFS and PFS estimates were calculated using the Kaplan-Meier method. Multivariable Cox regression model was calculated proportional for the prediction of recurrence and progression (covariables: age, tumor size, multiple tumors, prior recurrence, and immediate postoperative instillation of chemotherapy).RESULTS: After 3 months without event, the conditional RFS and PFS (to ≥pT2) rates for 5 additional years without event were 57.5% and 93.4%, respectively. Given a 1-, 2-, 3-, and 5-year survival, the conditional RFS rates for 5 additional years without event improved by +9.8 (67.3%), +5.2 (72.5%), +6.5 (79.0%), +2.0 (81.0%), and +1.0% (82.0%), respectively. In contrast, the 5-year conditional PFS rates were more or less stable with 94.3% after 1 year to 94.1% after 5 years. Multivariable analyses showed decreasing impact of risk parameters on RFS estimates over time. Based on these findings, we suggest a risk stratification to individualize follow-up for intermediate risk TaG1. Main limitation was the retrospective design.CONCLUSIONS: Conditional-survival analyses demonstrates that the patient risk profile changes over time. RFS rates rise with increasing survival whereas PFS rates were stable. The impact of prognostic features decreases over time. Our findings can be used for patient counseling and planning of personalized follow-up.

KW - Aged

KW - Disease Progression

KW - Female

KW - Follow-Up Studies

KW - Humans

KW - Male

KW - Middle Aged

KW - Neoplasm Invasiveness

KW - Neoplasm Recurrence, Local

KW - Neoplasm Staging

KW - Retrospective Studies

KW - Risk Factors

KW - Survival Rate

KW - Urinary Bladder Neoplasms

KW - Journal Article

KW - Multicenter Study

U2 - 10.1016/j.urolonc.2018.01.017

DO - 10.1016/j.urolonc.2018.01.017

M3 - SCORING: Journal article

C2 - 29506940

VL - 36

SP - 238.e19-238.e27

JO - UROL ONCOL-SEMIN ORI

JF - UROL ONCOL-SEMIN ORI

SN - 1078-1439

IS - 5

ER -