Skip to main content
OpenTrials
Completed

NCT Number: NCT00045630

S0219, Combination Chemotherapy Followed By Observation or Surgery in Patients With Stage II or Stage III Cancer of the Urothelium

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells and decrease the need for surgery.

PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy followed by observation or surgery to remove the bladder (cystectomy) in treating patients who have stage II or stage III cancer of the urothelium.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Cancer Center at Providence Alaska Medical Center, Anchorage, Alaska, United States

Loading trial locations.

About this study

OBJECTIVES:

  • Determine the pathologic complete response of patients with stage II or III transitional cell cancer of the urothelium treated with neoadjuvant gemcitabine, paclitaxel, and carboplatin followed by observation or immediate cystectomy.
  • Determine, preliminarily, if molecular markers predict response, survival, and tumor recurrence in patients treated with these regimens.
  • Determine recurrence rates and cystectomy-free survival of patients who choose observation after an initial response to neoadjuvant chemotherapy.
  • Compare the survival of patients treated with neoadjuvant chemotherapy followed by cystectomy vs observation.
  • Determine the feasibility, tolerability, and toxicity of these regimens in these patients.

OUTLINE: This is a multicenter study.

Patients receive gemcitabine IV over 30 minutes and paclitaxel IV over 30 minutes on days 1 and 8 and carboplatin IV over 30 minutes on day 1. Treatment repeats every 3 weeks for 3 courses in the absence of disease progression or unacceptable toxicity.

Within 4-8 weeks after completion of neoadjuvant chemotherapy, patients undergo a third transurethral resection of bladder tumor.

Patients with T0 disease after neoadjuvant chemotherapy may choose to undergo observation. These patients undergo cystoscopies with biopsies every 3 months for 1 year, every 4 months for 1 year, and then every 6 months until disease progression.

Patients with T1 disease or greater after neoadjuvant chemotherapy undergo immediate cystectomy. Patients with T0 disease may also choose this option. Patients undergoing immediate cystectomy are followed every 6 months for 2 years and then annually for 3 years.

PROJECTED ACCRUAL: A total of 95 patients will be accrued for this study within 2 years.

Who can participate

Healthy volunteers accepted: No

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

DISEASE CHARACTERISTICS:

  • Histologically confirmed muscle-invasive (T2-T4a), node-negative (N0) urothelial transitional cell cancer (TCC) of the bladder
  • Focal squamous and/or adenocarcinoma differentiation, defined as ≤ 10% of tumor volume allowed
  • The following diagnoses are not allowed:
  • Small cell carcinoma
  • Sarcomatoid components
  • Disease diagnosed with an initial transurethral resection of bladder tumor (TURBT) and a second TURBT performed within 8 weeks of first with attempt to remove all tumor present
  • Residual disease after second TURBT allowed
  • No more than 14-56 days after second TURBT
  • No metastatic disease by chest x-ray and CT scan or MRI of the abdomen and pelvis
  • Fresh tumor tissue, paraffin tumor tissue, unstained slides, or cell block specimen from one or both TURBTs available

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Performance status

  • Zubrod 0-2

Life expectancy

  • Not specified

Hematopoietic

  • White blood cell count (WBC) at least 3,500/mm^3
  • Absolute granulocyte count at least 1,500/mm^3
  • Platelet count at least lower limit of normal

Hepatic

  • Bilirubin no greater than 1.5 mg/dL
  • Aspartate aminotransferase (SGOT) no greater than 2 times upper limit of normal

Renal

  • Creatinine no greater than 2.0 mg/dL AND/OR
  • Creatinine clearance at least 60 mL/min

Other

  • No prohibitive medical risk that would preclude radical cystectomy
  • No other serious concurrent systemic disorder that would preclude study compliance
  • No other malignancy except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, adequately treated stage I or II cancer in complete remission, or any other cancer for which patient has been disease-free for 5 years
  • Not pregnant or nursing
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • Prior intravesical immunotherapy allowed

Chemotherapy

  • No prior systemic chemotherapy for TCC of the urothelium
  • Prior intravesical chemotherapy allowed

Endocrine therapy

  • Not specified

Radiotherapy

  • No prior radiotherapy for TCC of the urothelium
  • No concurrent radiotherapy

Surgery

  • See Disease Characteristics

Treatment and study plan

carboplatin

Drug

Gemcitabine

Drug

Other names: gemcitabine hydrochloride

paclitaxel

Drug

Other names: Taxol

Surgery

Procedure

Primary outcomes

  1. Pathologic Complete Response Rate by Transurethral Resection of Bladder Tumor (TURBT) and Imaging Studies After Chemotherapy

    Time frame: up to 12 weeks after registration (assessed within 8 weeks after completion of 3 cycles of chemotherapy )

    Pathologic complete response (CR) is defined as absence of viable tumor in the TURBT specimen. Stable/No Response is defined as at least some disease evaluation tests were done (same tests as baseline) and status does not qualify for CR or Progression. Progression is defined as one or more of the following must occur: unequivocal progression of disease in the opinion of the treating physician. Appearance of any new lesion/site. Death due to disease without documented progression or symptomatic deterioration.

Secondary outcomes

  1. Overall Survival (OS)

    Time frame: 0-2 years

    Overall survival is defined from the date of registration to date of death from any cause

  2. Number of Patients With Grade 3 Through Grade 5 Adverse Events That Are Related to Study Drug

    Time frame: Patients were assessed for adverse events at weeks 1, 2, 4, 5, 7, 8, and following surgery

    Adverse Events (AEs) are reported by the NCI Common Terminology Criteria for Adverse Events (CTCAE) version 2.0. For each patient, worst grade of each event type is reported. Grade 3 = Severe, Grade 4 = Life-threatening, Grade 5 = Fatal.

Sponsors and collaborators

Lead sponsor

SWOG Cancer Research Network

Network

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

A Sequential Approach to the Treatment of Muscle Invasive, Non-Metastatic Urothelial Carcinoma of the Bladder: A Phase II Trial of Neoadjuvant Gemcitabine, Paclitaxel and Carboplatin With Molecular Correlates

Important dates

Study start
2003
Primary completion
2008
Study completion
2011
First posted
Jan 27, 2003
Registry last updated
May 27, 2013

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.