Personalized treatment with PARP inhibitors in advanced urothelial carcinoma: a case report and literature review.
Noura AbbasLaudy ChehadeAli ShamseddinePublished in: Therapeutic advances in medical oncology (2024)
Bladder cancer (BC) poses a significant health challenge, particularly in metastatic cases, where the prognosis is unfavorable and therapeutic options are limited. Poly ADP-ribose polymerase (PARP) inhibitors have gained approval for use in various cancer types, but their application in BC remains controversial, despite the notable prevalence of DNA damage response alterations in advanced or metastatic urothelial carcinomas. In this report, we describe a 66-year-old heavy-smoking female diagnosed with muscle-invasive BC. She underwent multiple rounds of chemotherapy and radiation, yet her disease remained poorly controlled, leading to metastasis in the left obturator internus muscle. Comprehensive genomic profiling through FoundationOne ® Liquid CDx, examining a 324-gene panel using circulating tumor DNA from blood samples, revealed a pathogenic ATM gene alteration (p.Q654fs*10, c.1960delC), suggesting potential eligibility for PARP inhibitor therapy. Remarkably, the patient achieved a complete response to talazoparib, prompting an optimal investigation into BC candidates for this promising therapy.
Keyphrases
- dna repair
- circulating tumor
- dna damage response
- dna damage
- copy number
- small cell lung cancer
- cell free
- squamous cell carcinoma
- circulating tumor cells
- skeletal muscle
- high grade
- genome wide
- healthcare
- public health
- deep brain stimulation
- mental health
- risk factors
- genome wide identification
- locally advanced
- case report
- dna methylation
- single molecule
- squamous cell
- combination therapy
- stem cells
- gene expression
- ionic liquid
- radiation induced
- replacement therapy
- mesenchymal stem cells
- radiation therapy
- health promotion
- urinary tract
- young adults
- transcription factor