Fibronectin urothelial gene expression as a new reliable biomarker for early detection of local toxicity secondary to adjuvant intravesical therapy for non-muscle invasive bladder cancer.

Bacillus Calmette–Guerin biomarker bladder washing fibronectin non-muscle invasive bladder cancer toxicity

Journal

Therapeutic advances in urology
ISSN: 1756-2872
Titre abrégé: Ther Adv Urol
Pays: England
ID NLM: 101487328

Informations de publication

Date de publication:
Historique:
received: 19 09 2020
accepted: 16 01 2021
entrez: 15 3 2021
pubmed: 16 3 2021
medline: 16 3 2021
Statut: epublish

Résumé

A marker of urothelial damage could be helpful for early detection and monitoring of local toxicity due to intravesical therapy for non-muscle invasive bladder cancer (NMIBC). The aim of the study was to investigate the correlation between fibronectin (FN) gene expression in bladder washings and local toxicity secondary to adjuvant intravesical therapy. Patients undergoing adjuvant intravesical therapy for NMIBC and age-matched healthy patients were enrolled. Real time polymerase chain reaction was performed to analyze FN expression in bladder washings. Local toxicity was classified as: 0-1 mild (no medical therapy), 2 moderate (medical therapy and/or instillation postponed), 3 severe (discontinuation of therapy). Seventy-two patients and 21 controls entered the study. A useful pellet was obtained in 58 patients and 18 controls. Intravesical Bacillus Calmette-Guerin (BCG), Epirubicin and Mitomycin C was offered to 69%, 13.8% and 17.2% of patients respectively. Compared with healthy controls (FN = 1.0 fold), overall median FN expression before adjuvant intravesical therapy was 1.73 fold [interquartile range (IQR) 0.8-2.3], while during therapy median FN expression increased to 3.41 (IQR: 1.6-6.1) fold. Considering 40 intermediate and high-risk patients undergoing intravesical BCG, median FN expression before adjuvant treatment was 1.92 [(IQR: 1.0-2.7) fold, increasing up to 4.1 (IQR: 1.9-6.6) during therapy. In more detail, FN increased during BCG therapy, showing a median expression of 4.22 (IQR: 2.2-5.5) and 6.16 (IQR: 2.6-8.7) fold in presence of grade 2 and 3 toxicity respectively, while remaining more or less stable in asymptomatic patients. After receiver operating characteristic curve analysis, FN value of 3.6 fold resulted, corresponding to 75% sensitivity and 69% specificity to predict grade 2-3 toxicity events (area under the curve 0.74, 95% confidence interval 0.63-0.85, Our study validated the correlation between FN expression and urothelial damage. BCG seems to induce a urothelial activation with FN overexpression during adjuvant intravesical therapy. Grade of toxicity was related to FN expression.

Sections du résumé

BACKGROUND BACKGROUND
A marker of urothelial damage could be helpful for early detection and monitoring of local toxicity due to intravesical therapy for non-muscle invasive bladder cancer (NMIBC). The aim of the study was to investigate the correlation between fibronectin (FN) gene expression in bladder washings and local toxicity secondary to adjuvant intravesical therapy.
MATERIALS AND METHODS METHODS
Patients undergoing adjuvant intravesical therapy for NMIBC and age-matched healthy patients were enrolled. Real time polymerase chain reaction was performed to analyze FN expression in bladder washings. Local toxicity was classified as: 0-1 mild (no medical therapy), 2 moderate (medical therapy and/or instillation postponed), 3 severe (discontinuation of therapy).
RESULTS RESULTS
Seventy-two patients and 21 controls entered the study. A useful pellet was obtained in 58 patients and 18 controls. Intravesical Bacillus Calmette-Guerin (BCG), Epirubicin and Mitomycin C was offered to 69%, 13.8% and 17.2% of patients respectively. Compared with healthy controls (FN = 1.0 fold), overall median FN expression before adjuvant intravesical therapy was 1.73 fold [interquartile range (IQR) 0.8-2.3], while during therapy median FN expression increased to 3.41 (IQR: 1.6-6.1) fold. Considering 40 intermediate and high-risk patients undergoing intravesical BCG, median FN expression before adjuvant treatment was 1.92 [(IQR: 1.0-2.7) fold, increasing up to 4.1 (IQR: 1.9-6.6) during therapy. In more detail, FN increased during BCG therapy, showing a median expression of 4.22 (IQR: 2.2-5.5) and 6.16 (IQR: 2.6-8.7) fold in presence of grade 2 and 3 toxicity respectively, while remaining more or less stable in asymptomatic patients. After receiver operating characteristic curve analysis, FN value of 3.6 fold resulted, corresponding to 75% sensitivity and 69% specificity to predict grade 2-3 toxicity events (area under the curve 0.74, 95% confidence interval 0.63-0.85,
CONCLUSION CONCLUSIONS
Our study validated the correlation between FN expression and urothelial damage. BCG seems to induce a urothelial activation with FN overexpression during adjuvant intravesical therapy. Grade of toxicity was related to FN expression.

Identifiants

pubmed: 33717214
doi: 10.1177/1756287221995683
pii: 10.1177_1756287221995683
pmc: PMC7923969
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1756287221995683

Informations de copyright

© The Author(s), 2021.

Déclaration de conflit d'intérêts

Conflict of interest statement: The authors declare that there is no conflict of interest.

Références

Urol Oncol. 2018 Jan;36(1):8.e17-8.e24
pubmed: 28947304
Clin Genitourin Cancer. 2019 Aug;17(4):e751-e758
pubmed: 31126772
J Vis Exp. 2010 Nov 22;(45):
pubmed: 21189466
Urol Oncol. 2006 Jul-Aug;24(4):322-3
pubmed: 16818185
Urology. 2006 Jun;67(6):1216-23
pubmed: 16765182
World J Surg Oncol. 2018 Mar 21;16(1):61
pubmed: 29562940
Clin Cancer Res. 2000 Sep;6(9):3585-94
pubmed: 10999749
Eur Urol Focus. 2018 Jul;4(4):464-467
pubmed: 30473130
Urology. 2005 Feb;65(2):284-9
pubmed: 15708039
BJU Int. 2005 Mar;95(4):655-9
pubmed: 15705098
Eur Urol. 2009 Aug;56(2):247-56
pubmed: 19409692
Eur Urol. 2009 Aug;56(2):260-5
pubmed: 19395154
Eur Urol. 2017 Mar;71(3):447-461
pubmed: 27324428
Bioconjug Chem. 2017 May 17;28(5):1481-1490
pubmed: 28475311
Nat Rev Genet. 2010 Jan;11(1):31-46
pubmed: 19997069
Can Urol Assoc J. 2009 Dec;3(6 Suppl 4):S199-205
pubmed: 20019985
Urol Oncol. 2016 Jul;34(7):292.e9-292.e16
pubmed: 27005925
Int J Cancer. 2000 Apr 1;86(1):83-8
pubmed: 10728599
Urol Oncol. 2018 May;36(5):239.e1-239.e7
pubmed: 29506941
BJU Int. 2019 Jan;123(1):11-21
pubmed: 29807387
Clin Biochem. 2013 Oct;46(15):1377-82
pubmed: 23735602
J Urol. 2002 Nov;168(5):1964-70
pubmed: 12394686
Int J Biochem Cell Biol. 1997 Jul;29(7):939-43
pubmed: 9375374
Urol Oncol. 2020 Jun;38(6):603.e1-603.e7
pubmed: 32081560
Clin Exp Metastasis. 2016 Jan;33(1):29-44
pubmed: 26456754
J Exp Clin Cancer Res. 2017 May 18;36(1):70
pubmed: 28521777

Auteurs

Fabrizio Di Maida (F)

Department of Experimental and Clinical Medicine, University of Florence - Unit of Oncologic Minimally-Invasive Urology and Andrology, Careggi Hospital, Largo Brambilla 3, San Luca Nuovo, Firenze 50134, Italy.

Cristina Scalici Gesolfo (C)

Department of Surgical, Oncological and Oral Sciences, Section of Urology, University of Palermo, Palermo, Sicilia, Italy.

Riccardo Tellini (R)

Department of Experimental and Clinical Medicine, University of Florence - Unit of Oncologic Minimally-Invasive Urology and Andrology, Careggi Hospital, Florence, Italy.

Andrea Mari (A)

Department of Experimental and Clinical Medicine, University of Florence - Unit of Oncologic Minimally-Invasive Urology and Andrology, Careggi Hospital, Florence, Italy.

Chiara Sanfilippo (C)

Department of Statistics, University of Palermo, Palermo, Italy.

Luca Lambertini (L)

Department of Experimental and Clinical Medicine, University of Florence - Unit of Oncologic Minimally-Invasive Urology and Andrology, Careggi Hospital, Florence, Italy.

Antonio Andrea Grosso (AA)

Department of Experimental and Clinical Medicine, University of Florence - Unit of Oncologic Minimally-Invasive Urology and Andrology, Careggi Hospital, Florence, Italy.

Marco Carini (M)

Department of Experimental and Clinical Medicine, University of Florence - Unit of Oncologic Minimally-Invasive Urology and Andrology, Careggi Hospital, Florence, Italy.

Andrea Minervini (A)

Department of Experimental and Clinical Medicine, University of Florence - Unit of Oncologic Minimally-Invasive Urology and Andrology, Careggi Hospital, Florence, Italy.

Vincenzo Serretta (V)

Department of Surgical, Oncological and Oral Sciences, Section of Urology, University of Palermo, Palermo, Sicilia, Italy.

Classifications MeSH