A systematic review of gene-mediated therapy in BCG-unresponsive NMIBC: emerging evidence and future perspectives.
[OBJECTIVE] BCG-unresponsive non-muscle-invasive bladder cancer (NMIBC) represents a major therapeutic challenge, given the high risk of disease progression and the absence of validated bladder-sparin
- 연구 설계 systematic review
APA
Bertrand C, Ouzaid I, et al. (2025). A systematic review of gene-mediated therapy in BCG-unresponsive NMIBC: emerging evidence and future perspectives.. World journal of urology, 44(1), 44. https://doi.org/10.1007/s00345-025-06151-w
MLA
Bertrand C, et al.. "A systematic review of gene-mediated therapy in BCG-unresponsive NMIBC: emerging evidence and future perspectives.." World journal of urology, vol. 44, no. 1, 2025, pp. 44.
PMID
41396440
Abstract
[OBJECTIVE] BCG-unresponsive non-muscle-invasive bladder cancer (NMIBC) represents a major therapeutic challenge, given the high risk of disease progression and the absence of validated bladder-sparing strategies. In this context, gene-mediated therapy has emerged as a promising bladder-sparing approach.
[METHODS] A systematic review of the literature available on Medline and Google Scholar was conducted to report the main oncological evidence, safety profile and future perspectives on gene therapies in BCG-unresponsive NMIBC. A total of 3157 records were screened and 13 references were included in our result section, including 8 articles from PubMed and 5 unpublished studies presented at conferences between 2023 and 2025.
[RESULTS] Gene-mediated therapies are emerging as a promising therapeutic strategy, with complete responses rates ranging from 53.4% to 82.9% at 3 months and from 24.4% to 57.1% at 12 months. Median duration of response rate ranging from 9,7 to 28 months. The safety profile is promising, with overall adverse events ranging from 47% to 91%, including grade ≥ 3 adverse events in 4% to 14% of cases, and no treatment-related deaths. The recent Food and Drug Administration approval of Nadofaragene firadenovec, is expected to provide relevant real-world clinical data. However, precise patient selection, the lack of predictive biomarkers for response or monitoring, and the cost-related challenges of these treatments remain major limitations.
[CONCLUSIONS] Gene therapies represent a novel and promising therapeutic approach for BCG-unresponsive NMIBC, with significant oncological efficacy and a favorable safety profile.
[METHODS] A systematic review of the literature available on Medline and Google Scholar was conducted to report the main oncological evidence, safety profile and future perspectives on gene therapies in BCG-unresponsive NMIBC. A total of 3157 records were screened and 13 references were included in our result section, including 8 articles from PubMed and 5 unpublished studies presented at conferences between 2023 and 2025.
[RESULTS] Gene-mediated therapies are emerging as a promising therapeutic strategy, with complete responses rates ranging from 53.4% to 82.9% at 3 months and from 24.4% to 57.1% at 12 months. Median duration of response rate ranging from 9,7 to 28 months. The safety profile is promising, with overall adverse events ranging from 47% to 91%, including grade ≥ 3 adverse events in 4% to 14% of cases, and no treatment-related deaths. The recent Food and Drug Administration approval of Nadofaragene firadenovec, is expected to provide relevant real-world clinical data. However, precise patient selection, the lack of predictive biomarkers for response or monitoring, and the cost-related challenges of these treatments remain major limitations.
[CONCLUSIONS] Gene therapies represent a novel and promising therapeutic approach for BCG-unresponsive NMIBC, with significant oncological efficacy and a favorable safety profile.
MeSH Terms
Humans; BCG Vaccine; Urinary Bladder Neoplasms; Genetic Therapy; Forecasting; Adjuvants, Immunologic; Non-Muscle Invasive Bladder Neoplasms