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A single-center trial for using chemoradiation therapy to keep bladder after bladder urothelial carcinoma resection treatment

A single-center trial for using chemoradiation therapy to keep bladder after bladder urothelial carcinoma resection treatment

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029504
Enrollment
Unknown
Registered
2020-02-03
Start date
2020-03-01
Completion date
Unknown
Last updated
2020-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

bladder urothelial carcinoma

Interventions

Case series:trimodal therapy

Sponsors

Department of Urology, Chongqing University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 78 Years

Inclusion criteria

Inclusion criteria: (1) Aged 20 to 78 years; (2) ECOG 0-2; (3) Bladder urothelial carcinoma diagnosed by the pathological histology ,and needed the radical resection; (4) Patients with strong retain bladder will and good compliance; (5) Tumor can be treated by excision of transurethral resection or bladder part; (6) Normal bladder function; (7) Laboratory examination must be in accordance with the following indicators: Hb > 90 g/L, WBC > 3.5 * 10^9/L, platelets > 90 * 10^9/L; Transaminase and total bilirubin is less than 1.5 UNL; Creatinine < 144 umol/L; (8) Voluntary participation, the participants himself or his legal representative sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Pathology results for the carcinoma was not the urinary tract, such as squamous cell carcinoma, adenocarcinoma and small cell carcinoma and sarcoma, etc; (2) CT found positive pelvic lymph nodes (multiple, length to diameter is greater than 1 cm); (3) Confirmed by pathology or researchers identified with lymph node metastasis; (4) CT or MRI imaging found distant metastases (visceral metastasis, bone metastasis, etc.); (5) Activity or have symptoms of viral hepatitis or other chronic liver diseases; (6) allergies by paclitaxel, gemcitabine,cisplatin,and other platinum-based preparations; (7) Pregnancy and lactation; (8) Once had treatment by other chemotherapy or radiation therapy; (9) Chickenpox, herpes zoster, gout and high uric acid hematic disease, peripheral neuritis; (10) The clinical significance of heart disease, including: in the past six months have myocardial infarction, or arterial thrombosis; Severe or unstable angina; New York heart association class III or IV heart disease; Atrial fibrillation or other need treatment of arrhythmia; (11) Has a history of kidney disease, hematopoietic function is not complete, the auditory nerve dysfunction; (12) With other malignant tumor in the past five years; (13) The other condition that is not suitable to participate in this study by the researchers.

Design outcomes

Primary

MeasureTime frame
complete response rate of disease after 2 years;

Secondary

MeasureTime frame
FACT-P;ECOG;Disease progression-free surial;OS;

Countries

China

Contacts

Public ContactNan Liu

Department of Urology, Chongqing University Cancer Hospital

51346199@qq.com+86 13350340658

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026