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Recruiting
NCT07762586
Luminal Bladder Cancer Effective Response to Neoadjuvant Chemotherapy (LUMBER-NAC)
Conditions: Bladder Cancer
Sex: All
Ages: 18 Years – 90 Years
Healthy volunteers: No
Phase: PHASE2
Enrollment: 60
Sponsor: Rutgers, The State University of New Jersey
Location: Rutgers Cancer Institute New Brunswick New Jersey
Summary
This study is a two-arm phase II randomized trial investigating patients with luminal subtype muscle-invasive bladder cancer (MIBC) receiving neoadjuvant therapy (NAT) followed by cystectomy compared to those receiving upfront cystectomy.
Eligibility Criteria
Inclusion Criteria:
* ▪ Inclusion Criteria
* Willing and able to provide informed consent
* Age ≥18 years old
* Eligible to receive standard of care systemic neoadjuvant therapy
* Eastern Cooperative Group (ECOG) performance status of 0-1
* Documented histologically confirmed urothelial muscle-invasive bladder cancer
* cT2N0M0 bladder cancer based on pre-TURBT bimanual exam and cross-sectional imaging performed within 8 weeks of surgery or initiation of NAT.
* Willing to undergo RC with urinary diversion
* No signs of extravesical disease on pre-TURBT conventional imaging
* Variant histology is allowed so long as the tumor is predominantly urothelial carcinoma.
* No presence of LVI on TURBT
* Decipher Bladder GSC test result
* Ineligible for or refusing TMT
* No cN+
* The population is adult men or women of any ethnicity diagnosed with muscle-invasive bladder cancer.
Exclusion Criteria:
* Patients under 18 years old. Considering the minimal incidence of bladder cancer among the pediatric population, children are not eligible for this study.
* Not willing or unable to give informed consent.
* Clinical or pathological evidence of metastatic disease, including, non-regional lymph nodes, visceral lesions, and bone lesions.
* Significant hepatic impairment (Serum bilirubin \> 1.5x upper limit of normal).
* Significant renal impairment (creatinine clearance \
Source: ClinicalTrials.gov (NCT07762586). StuddyBuddy aggregates publicly available trial information.