2024
DOI: 10.3390/cancers16071366
|View full text |Cite
|
Sign up to set email alerts
|

Revolutionizing Treatment: Breakthrough Approaches for BCG-Unresponsive Non-Muscle-Invasive Bladder Cancer

Maciej Jaromin,
Tomasz Konecki,
Piotr Kutwin

Abstract: Bladder cancer is the 10th most popular cancer in the world, and non-muscle-invasive bladder cancer (NMIBC) is diagnosed in ~80% of all cases. Treatments for NMIBC include transurethral resection of the bladder tumor (TURBT) and intravesical instillations of Bacillus Calmette-Guérin (BCG). Treatment of BCG-unresponsive tumors is scarce and usually leads to Radical Cystectomy. In this paper, we review recent advancements in conservative treatment of BCG-unresponsive tumors. The main focus of the paper is FDA-ap… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 69 publications
(72 reference statements)
0
1
0
Order By: Relevance
“…Thus, we anticipate our gene therapy strategy could be swiftly adopted into clinical practice to address critical gaps that limit the application of gene therapy: The problem of practicality: As far as we know, there are currently no methods in the clinic that allow the delivery of gene therapy vectors to specific target cells in tissue. FDA-approved in situ gene therapies either expose the patient to vector systemically (e.g., Elevidys® for Duchenne Muscular Dystrophy 25 ) or inject vector directly into a confined space, such as the bladder (Adstiladrin® 26 ), the spinal canal (Qalsody® for amyotrophic lateral sclerosis 27 ) or the eyeball (Luxturna® for retinal disease 28 ). In the latter three treatments, the vector has little opportunity to leak and thus is able to unload its DNA cargo into a maximum number of target cells.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, we anticipate our gene therapy strategy could be swiftly adopted into clinical practice to address critical gaps that limit the application of gene therapy: The problem of practicality: As far as we know, there are currently no methods in the clinic that allow the delivery of gene therapy vectors to specific target cells in tissue. FDA-approved in situ gene therapies either expose the patient to vector systemically (e.g., Elevidys® for Duchenne Muscular Dystrophy 25 ) or inject vector directly into a confined space, such as the bladder (Adstiladrin® 26 ), the spinal canal (Qalsody® for amyotrophic lateral sclerosis 27 ) or the eyeball (Luxturna® for retinal disease 28 ). In the latter three treatments, the vector has little opportunity to leak and thus is able to unload its DNA cargo into a maximum number of target cells.…”
Section: Discussionmentioning
confidence: 99%