Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06889623

Immediate Chemotherapy Following Resection for High-Risk Non-Muscle-Invasive Bladder Cancer

Residual tumors after transurethral resection of bladder tumors (TURBT) range from 17-70%, and floating tumor cells from traditional segmental resection may lead to recurrence if they re-implant in the bladder wall. Immediate systemic chemotherapy post-surgery aims to eliminate microlesions promptly and minimize recurrence risk, yet its safety and efficacy require further exploration. This prospective, single-arm study delves into evaluating the efficacy and safety of immediate postoperative systemic chemotherapy in patients with suspected high-risk non-muscle-invasive bladder cancer.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Shanghai Changhai Hospital

Shanghai, Shanghai Municipality, 200000, China

Location status: Recruiting

Location contact

Shuxiong Zeng, M.D. Ph.D

CONTACT

[email protected]

+8618930568759 ext. +8618930568759

About this study

Bladder cancer ranks as the ninth most prevalent cancer globally, with urothelial carcinoma being the primary form, leading to over 220,000 deaths annually. While 70-75% of bladder cancer cases initially present as non-muscle invasive bladder cancer (NMIBC) with favorable prognoses, the recurrence rate can reach 78% within five years post-standard treatment. The primary objective of transurethral resection of bladder tumors (TURBT) is to accurately diagnose and completely eliminate all visible lesions, as the quality of resection significantly impacts prognosis. However, a systematic review reveals a notable risk of residual tumor post-initial resection. For individuals with high-risk non-muscle invasive bladder cancer (NMIBC), EAU guidelines recommend a follow-up resection 2-6 weeks later. Clinical trials have demonstrated that administering a single chemotherapy session within 24 hours of the initial resection can lower recurrence rates. This approach may work by eradicating floating tumor cells, ablating residual tumor cells, and addressing overlooked small tumors. Gemcitabine and cisplatin (GC) have good efficacy and tolerance in patients with bladder cancer and have become the most commonly used regimen in the neoadjuvant treatment of bladder cancer. There is currently a lack of strong evidence that GC chemotherapy 24 hours after surgery can safely and effectively reduce the risk of recurrence in suspected high-risk NMIBC cases. Our goal is to conduct a prospective clinical trial to investigate the feasibility of this treatment method by evaluating the incidence of adverse events and recurrence-free survival in this group of patients by administering systemic chemotherapy 24 hours after TURBT for patients with suspected high-recurrence bladder cancer.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with a history and cystoscopy results indicating high-risk NMIBC:
  • High-grade T1
  • Any recurrent high-grade Ta
  • High-grade Ta & Tumor diameter greater than 3 cm or multifocal
  • Any CIS
  • Any BCG failure in patients with high-grade disease
  • Any variant histology
  • Any LVI
  • Any high-grade prostatic urethral involvement
  • Patients in generally good condition with a follow-up period of 2 years

Exclusion criteria

  • Bladder cancer other than UC
  • MIBC or benign diseases
  • Incomplete tumor resection
  • Active infection
  • Concurrent upper urinary tract or prostatic urethral UC
  • Previous systemic chemotherapy, immunotherapy, or radiotherapy
  • Leukopenia/thrombocytopenia
  • Serum creatinine greater than twice the normal level
  • Uncontrollable urinary tract infection

Treatment and study plan

Immediate postoperative chemotherapy

Procedure

Systemic chemotherapy with cisplatin/gemcitabine intravenous infusion within 24 hours after TURBT

Primary outcomes

  1. One-year recurrence-free survival rate

    Time frame: About two years after the first immediate chemotherapy

    The percentage of patients who remain cancer-free for one year after treatment.

Secondary outcomes

  1. Pathological downstaging rate

    Time frame: About 2-6 weeks after the first immediate chemotherapy

    The percentage of patients whose cancer has decreased in stage following treatment.

  2. The incidence of grade ≥ 3 adverse events(AEs)

    Time frame: About two years after the first immediate chemotherapy

    The frequency of severe or serious side effects experienced by patients during a clinical trial or medical treatment(CTCAE V5.0 ).

  3. UroCAD.MRD Index

    Time frame: TURBT perioperative period, about 15 days

    Body fluid samples were collected from patients before and after TUBRT and chemotherapy for chromosomal instability testing, and the residual tumor status of patients was analyzed by analyzing the changes in the UroCAD.MRD index.

Study contacts

Contact information is provided by the study sponsor or research team.

Shuxiong Zeng, M.D. Ph.D

CONTACT

[email protected]

+8618930568759 ext. +8618930568759

Sponsors and collaborators

Lead sponsor

Changhai Hospital

Other

Registry information

Official study title

Impact of Immediate Cisplatin/Gemcitabine Chemotherapy Following Resection for High-Risk Non-Muscle-Invasive Bladder Cancer: an Open-label, Single-arm, Prospective Trial

Acronym: HIGCrecur

Important dates

Study start
2024
Primary completion
2026
Study completion
2028
First posted
Mar 21, 2025
Registry last updated
Mar 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.