Promoter Mutation as a Potential Predictive Biomarker in BCG-Treated Bladder Cancer Patients.

Int J Mol Sci

Instituto de Investigação e Inovação em Saúde (i3S), 4200-135 Porto, Portugal.

Published: January 2020

AI Article Synopsis

  • Telomerase reverse transcriptase (TERT) promoter mutations are common in bladder cancer, particularly in patients treated with Bacillus Calmette-Guérin (BCG) therapy.
  • In a study of 125 non-muscle invasive bladder cancer cases treated with BCG, TERT mutations were present in 56% of tumors, but these mutations did not correlate with tumor stage or grade.
  • The specific c.1-146G>A mutation emerged as a significant predictor for nonrecurrence of cancer post-BCG therapy, suggesting its importance for assessing treatment response and recurrence-free survival.

Article Abstract

Telomerase reverse transcriptase gene promoter () mutations are recognized as one of the most frequent genetic events in bladder cancer (BC). No studies have focused on the relevance of TERTp mutations in the specific group of tumors treated with Bacillus Calmette-Guérin (BCG) intravesical therapy. Methods - 125 non muscle invasive BC treated with BCG therapy (BCG-NMIBC) were screened for mutations, rs2853669 single nucleotide polymorphism, and Fibroblast Growth Factor Receptor 3 () hotspot mutations. Results - mutations were found in 56.0% of BCG-NMIBC and were not associated with tumor stage or grade. mutations were found in 44.9% of the cases and were not associated with tumor stage or grade nor with mutations. The rs2853669 single nucleotide polymorphism was associated with tumors of higher grade. The specific c.1-146G>A mutation was an independent predictor of nonrecurrence after BCG therapy (hazard ratio-0.382; 95% confidence interval-0.150-0.971, = 0.048). Conclusions - mutations are frequent in BCG-NMIBC and -146G>A appears to be an independent predictive marker of response to BCG treatment with an impact in recurrence-free survival.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037401PMC
http://dx.doi.org/10.3390/ijms21030947DOI Listing

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