Literature DB >> 30120861

FOXM1 overexpression is associated with adverse outcome and predicts response to intravesical instillation therapy in stage pT1 non-muscle-invasive bladder cancer.

Johannes Breyer1, Ralph M Wirtz2,3, Philipp Erben4, Sebastien Rinaldetti5, Thomas S Worst4, Robert Stoehr6, Markus Eckstein6, Danijel Sikic7, Stefan Denzinger1, Maximilian Burger1, Arndt Hartmann6, Wolfgang Otto1.   

Abstract

OBJECTIVE: To investigate the role of forkhead box protein M1 (FOXM1) mRNA expression and its prognostic value in stage pT1 non-muscle-invasive bladder cancer (NMIBC). PATIENTS AND METHODS: Clinical data and formalin-fixed paraffin-embedded tissues from transurethral resection of the bladder from patients with stage pT1 NMIBC, treated with an organ-preserving approach, were analysed retrospectively. Total RNA was isolated using commercial RNA extraction kits, and mRNA expression of FOXM1, MKI67, KRT20 and KRT5 was measured by single-step quantitative RT-PCR using RNA-specific TaqMan Assays. Statistical analysis was performed using Spearman's Rho, Wilcoxon or Kruskal-Wallis tests, Kaplan-Meier estimates of recurrence-free (RFS), progression-free (PFS) and cancer-specific survival (CSS) and Cox regression analysis.
RESULTS: Data from 296 patients (79.4% men, median age 72 years) were available for the final evaluation. Spearman correlation analysis showed that mRNA expression of FOXM1 was significantly correlated with MKI67 (ρ: 0.6530, P < 0.001) and with the luminal subtype, reflected by the positive correlation with KRT20 (ρ: 0.2113, P < 0.001). Furthermore, there was also a strong correlation of FOXM1 expression with adverse clinical and pathological variables, such as concomitant carcinoma in situ (P = 0.05), multifocal tumours (P = 0.005) and World Health Organization 1973 grade 3 disease (P < 0.001). Kaplan-Meier analysis showed overexpression of FOMX1 to be associated with worse PFS (P = 0.028) and worse CSS (P = 0.015). FOXM1 overexpression was also shown to be a predictive risk factor for CSS (hazard ratio 1.61 [1.13-2.34], L-R chi-squared: 7.19, P = 0.007). FOXM1 overexpression identified a subgroup of patients within the luminal subtype with worse RFS (P = 0.017), PFS (P < 0.001) and CSS (P = 0.015). Patients with low FOXM1 expression had better outcomes, irrespective of instillation therapy, whereas patients with high FOXM1 expression benefitted from intravesical chemotherapy with mitomycin C.
CONCLUSION: High FOXM1 expression was associated with adverse clinical and pathological features and worse outcomes, and predicted response to intravesical instillation therapy in patients with stage pT1 NMIBC.
© 2018 The Authors BJU International © 2018 BJU International Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  FOXM1; instillation therapy; non-muscle-invasive bladder cancer; pT1; prognosis

Mesh:

Substances:

Year:  2018        PMID: 30120861     DOI: 10.1111/bju.14525

Source DB:  PubMed          Journal:  BJU Int        ISSN: 1464-4096            Impact factor:   5.588


  7 in total

1.  Intravesical gemcitabine as bladder-preserving treatment for BCG unresponsive non-muscle-invasive bladder cancer. Results from a single-arm, open-label study.

Authors:  Rodolfo Hurle; Paolo Casale; Emanuela Morenghi; Alberto Saita; Nicolòmaria Buffi; Giovanni Lughezzani; Piergiuseppe Colombo; Roberto Contieri; Nicola Frego; Giorgio Guazzoni; Massimo Lazzeri
Journal:  BJUI Compass       Date:  2020-07-01

2.  Identification of 9 key genes and small molecule drugs in clear cell renal cell carcinoma.

Authors:  Yongwen Luo; Dexin Shen; Liang Chen; Gang Wang; Xuefeng Liu; Kaiyu Qian; Yu Xiao; Xinghuan Wang; Lingao Ju
Journal:  Aging (Albany NY)       Date:  2019-08-18       Impact factor: 5.682

3.  RNA Expression of DNA Damage Response Genes in Muscle-Invasive Bladder Cancer: Influence on Outcome and Response to Adjuvant Cisplatin-Based Chemotherapy.

Authors:  Jonas Herrmann; Helena Schmidt; Katja Nitschke; Cleo-Aron Weis; Philipp Nuhn; Jost von Hardenberg; Maurice Stephan Michel; Philipp Erben; Thomas Stefan Worst
Journal:  Int J Mol Sci       Date:  2021-04-18       Impact factor: 5.923

4.  Identification of Key Genes Associated with Progression and Prognosis of Bladder Cancer through Integrated Bioinformatics Analysis.

Authors:  Shiv Verma; Eswar Shankar; Spencer Lin; Vaibhav Singh; E Ricky Chan; Shufen Cao; Pingfu Fu; Gregory T MacLennan; Lee E Ponsky; Sanjay Gupta
Journal:  Cancers (Basel)       Date:  2021-11-25       Impact factor: 6.639

5.  Identification of a 13‑mRNA signature for predicting disease progression and prognosis in patients with bladder cancer.

Authors:  Hubin Yin; Chen Zhang; Xin Gou; Weiyang He; Daoju Gan
Journal:  Oncol Rep       Date:  2019-12-12       Impact factor: 3.906

6.  Prognostic Role of Survivin and Macrophage Infiltration Quantified on Protein and mRNA Level in Molecular Subtypes Determined by RT-qPCR of KRT5, KRT20, and ERBB2 in Muscle-Invasive Bladder Cancer Treated by Adjuvant Chemotherapy.

Authors:  Thorsten H Ecke; Adisch Kiani; Thorsten Schlomm; Frank Friedersdorff; Anja Rabien; Klaus Jung; Ergin Kilic; Peter Boström; Minna Tervahartiala; Pekka Taimen; Jan Gleichenhagen; Georg Johnen; Thomas Brüning; Stefan Koch; Jenny Roggisch; Ralph M Wirtz
Journal:  Int J Mol Sci       Date:  2020-10-08       Impact factor: 5.923

Review 7.  Treatment Outcomes of High-Risk Non-Muscle Invasive Bladder Cancer (HR-NMIBC) in Real-World Evidence (RWE) Studies: Systematic Literature Review (SLR).

Authors:  Mihaela Georgiana Musat; Christina Soeun Kwon; Elizabeth Masters; Slaven Sikirica; Debduth B Pijush; Anna Forsythe
Journal:  Clinicoecon Outcomes Res       Date:  2022-01-10
  7 in total

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