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The Search for the Optimal cut-off Value of p53-Immunohistochemistry to Predict Prognosis of Invasive Bladder Cancer: A Multi-Center, Multi-Laboratory Analysis.
Mertens, Laura S; Claps, Francesco; Mayr, Roman; Hodgson, Anjelica; Shariat, Shahrokh F; Hippe, Katrin; Neuzillet, Yann; Sanders, Joyce; Burger, Maximilian; Pouessel, Damien; Otto, Wolfgang; van der Kwast, Theo H; Lotan, Yair; Allory, Yves; Downes, Michelle R; van Rhijn, Bas W G.
Afiliação
  • Mertens LS; Department of Surgical Oncology (Urology), Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
  • Claps F; Department of Surgical Oncology (Urology), Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
  • Mayr R; Department of Urology, Caritas St Josef Medical Center, 9147University of Regensburg, Regensburg, Germany.
  • Hodgson A; Division of Anatomic Pathology, Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
  • Shariat SF; Department of Laboratory Medicine and Pathobiology, 7938University of Toronto, Toronto, ON, Canada.
  • Hippe K; Department of Pathology, University Health Network, Princess Margaret Cancer Center, 7938University of Toronto, Toronto, ON, Canada.
  • Neuzillet Y; Department of Urology, University of Texas Southwestern Medical center, Dallas, TX, USA.
  • Sanders J; Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
  • Burger M; Department of Urology, Weill Cornell Medical College, New York, NY, USA.
  • Pouessel D; Department of Urology, Second Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Otto W; Institute for Urology and Reproductive Health, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
  • van der Kwast TH; Dept. Pathology, University Medical Center - Regensburg, Regensburg, Germany.
  • Lotan Y; Department of Surgical Oncology (Urology), Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
  • Allory Y; Institut Curie, CNRS, UMR144, Molecular Oncology team, PSL Research University, Paris, France.
  • Downes MR; Core Facility Molecular Pathology & Biobank, Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
  • van Rhijn BWG; Department of Urology, Hôpital Foch, UVSQ-Paris-Saclay University, Suresnes, France.
Int J Surg Pathol ; 31(2): 157-166, 2023 Apr.
Article em En | MEDLINE | ID: mdl-35466737
Introduction: Mutations in the TP53 gene are indicative of worse outcome in bladder cancer and are usually assessed by immunohistochemistry. To define p53-overexpression, a threshold of >10% is most commonly used (cut-off1). Recently, a novel cut-off (aberrant = 0% or ≥50%) (cut-off2) showed better correlation to clinical outcome. In this study, we evaluate the association between p53-immunohistochemistry cut-offs, clinico-pathological variables and disease-specific survival (DSS). Methods: Seven-hundred-fifty chemotherapy-naïve patients who underwent radical cystectomy were included (92% muscle-invasive bladder cancer. In addition to cut-off1 and cut-off2, a third cut-off (cut-off3) was determined based on the highest Youden-index value. Cut-off values were associated with clinico-pathological variables and FGFR3 mutation status. The Kaplan-Meier method was used to estimate DSS. Results: Aberrant p53-expression was found in 489 (65%) (cut-off1) and 466 (62%) (cut-off2) tumors. Cut-off3 was determined at 25% and aberrant p53-expression in 410 cases (55%) (cutoff3). p53-expression levels were significantly associated with higher pT-stage (cut-off1/2/3: P = 0.047, P = 0.006 and P = 0.0002, respectively), higher grade (all, P < 0.0001), and FGFR3 wild-type (cut-off1: P = 0.02, cut-offs2&3: P = 0.001). Median follow-up was 5.3 years (interquartile range, 4.0-6.0 years). p53-expression was not associated with DSS for any of the three cut-offs (cut-off1/2/3: P-log-rank = 0.566, 0.77 and 0.50, respectively). If we only considered locally advanced bladder cancer, results on DSS remained non-significant. Conclusion: This multi-center, multi-laboratory study showed that, regardless of the cut-off used, p53-immunohistochemistry did not enable selection of patients with worse outcome. Our results suggest that p53-immunohistochemistry alone is not suitable to guide clinical decision making after radical cystectomy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária / Proteína Supressora de Tumor p53 Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Int J Surg Pathol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária / Proteína Supressora de Tumor p53 Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Int J Surg Pathol Ano de publicação: 2023 Tipo de documento: Article