Hyperthermic Intravesical Perfusion for Muscle-invasive Bladder Urothelial Carcinoma

Launched by HENAN CANCER HOSPITAL · Mar 2, 2022

Keywords

ClinConnect Summary

This clinical trial is studying a treatment called hyperthermic intravesical perfusion for patients with a specific type of bladder cancer known as muscle-invasive bladder urothelial carcinoma. The goal is to see if this treatment can reduce the risk of cancer spreading during surgery and to evaluate its safety. The trial is currently recruiting participants who are between 18 and 75 years old, have been diagnosed with this type of bladder cancer, and are planning to undergo surgery as part of their treatment.

To join the trial, participants need to be in good health overall and able to give their written consent. They should not have any other serious health issues or be pregnant or breastfeeding. If someone decides to participate, they can expect to receive the hyperthermic treatment as part of their care plan. The trial aims to find out if this approach can help improve outcomes for individuals facing this challenging diagnosis.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Be willing and able to provide written informed consent for the trial.
• • 18-75 years of age on day of signing informed consent.
• • Have histologically confirmed muscle invasive disease of the urinary bladder.
• • Histology must be urothelial carcinoma (transitional cell carcinoma) or urothelial carcinoma with mixed histology/features.
• • Clinical stage II-III and Have a surgical evaluation that documents the plan for multimodality therapy with a consolidative radical cystectomy.
• • Eastern Cooperative Oncology Group 0-1 and good organ function.
• Exclusion Criteria:
• • A non-surgical approach recommended by the treating urologist due to any reason.
• • Is currently participating in or has participated in a study of an investigational agent or using an investigational device within 28 days prior to study registration.
• • Has a diagnosis of immunodeficiency or received systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to study registration.
• • Has a known additional malignancy that is progressing or required treatment ≤ 48 months of study registration. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin, in situ cervical cancer.
• • Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
• • Has an active autoimmune disease requiring systemic treatment.
• • Has known evidence of interstitial lung disease or active, non-infectious pneumonitis.
• • Has an active infection requiring systemic therapy.
• • Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator
• • Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
• • Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 120 days after the last dose of trial treatment.
• • Has received prior therapy with an anti-programmed cell death 1, anti-programmed cell death-Ligand 1 antibody.
• • Has a known history of Human Immunodeficiency Virus.
• • Has known active Hepatitis B or Hepatitis C.