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Keyhole Limpet Hemocyanin Compared With Doxorubicin in Treating Patients With Bladder Cancer

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ClinicalTrials.gov Identifier: NCT00006034
Recruitment Status : Completed
First Posted : October 7, 2003
Last Update Posted : May 15, 2013
Sponsor:
Information provided by:
National Cancer Institute (NCI)

July 5, 2000
October 7, 2003
May 15, 2013
June 1998
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Complete list of historical versions of study NCT00006034 on ClinicalTrials.gov Archive Site
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Keyhole Limpet Hemocyanin Compared With Doxorubicin in Treating Patients With Bladder Cancer
A Randomized, Multicenter Phase III Trial Evaluating the Efficacy and Safety of BCI-ImmuneActivator Versus Adriamycin in BCG Refractory or Intolerant Patients With Carcinoma in Situ With or Without Resected Superficial Papillary Bladder Cancer

RATIONALE: Biological therapies use different ways to stimulate the immune system and stop cancer cells from growing. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. It is not yet known whether keyhole limpet hemocyanin is more effective than doxorubicin for bladder cancer.

PURPOSE: Randomized phase III trial to compare the effectiveness of keyhole limpet hemocyanin with that of doxorubicin in treating patients who have bladder cancer that has not responded to BCG or in those patients who cannot tolerate BCG.

OBJECTIVES:

  • Compare the efficacy of BCI-ImmuneActivator™ (keyhole limpet hemocyanin) versus doxorubicin in BCG refractory or intolerant patients with carcinoma in situ with or without resected superficial papillary bladder cancer.
  • Compare the toxicity and safety of these treatments in these patients.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center and prior BCG response (refractory vs intolerant). Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive a sensitizing dose of keyhole limpet hemocyanin (KLH) intradermally at week -2 followed by induction KLH IV once weekly at weeks 1-6. Patients with partial or no response receive IV KLH reinduction therapy once weekly at weeks 13-18. Patients with complete response receive IV KLH maintenance therapy monthly at weeks 13, 17, and 21, and then at months 6-12.
  • Arm II: Patients receive doxorubicin IV once weekly at weeks 1-6. Patients with complete response receive maintenance therapy comprising doxorubicin IV at weeks 13, 17, and 21 and months 6-12.

Treatment continues in the absence of disease progression or unacceptable toxicity.

Patients are followed every 3 months for 1.5 years, and then every 6 months for 1 year. (Patient total participation in this study may last as long as 42 months.)

PROJECTED ACCRUAL: A total of 150 patients (75 per treatment arm) will be accrued for this study.

Interventional
Phase 3
Allocation: Randomized
Primary Purpose: Treatment
Bladder Cancer
  • Biological: keyhole limpet hemocyanin
    Given intradermally and IV
  • Drug: doxorubicin hydrochloride
    Given IV
  • Experimental: Arm I
    Patients receive a sensitizing dose of keyhole limpet hemocyanin (KLH) intradermally in week 2 followed by induction KLH IV once weekly in weeks 1-6. Patients with partial or no response receive IV KLH reinduction therapy once weekly in weeks 13-18. Patients with complete response receive IV KLH maintenance therapy monthly in weeks 13, 17, and 21, and then in months 6-12.
    Intervention: Biological: keyhole limpet hemocyanin
  • Active Comparator: Arm II
    Patients receive doxorubicin IV once weekly in weeks 1-6.
    Intervention: Drug: doxorubicin hydrochloride
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
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March 2004
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DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed carcinoma in situ of the bladder with or without resected superficial papillary tumor

    • Biopsy within 3 months of study with or without positive urinary cytology within 6 weeks of study
  • Cystoscopy within 3 months of study
  • Negative imaging study of the ureters and kidneys within 6 months of study
  • BCG refractory disease

    • Received and failed at least 1 prior induction course consisting of BCG weekly for 6 weeks OR
  • BCG intolerant

    • Unable to receive an adequate course of intravesical BCG due to extreme toxicity
  • Opted against or medically contraindicated to cystectomy

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Performance status

  • ECOG 0-2 OR
  • Karnofsky 60-100%

Life expectancy

  • Not specified

Hematopoietic

  • WBC greater than 4,000/mm^3
  • Platelet count greater than 100,000/mm^3
  • Hemoglobin greater than 11 g/dL

Hepatic

  • Bilirubin normal
  • SGOT/SGPT normal

Renal

  • Creatinine no greater than 1.5 times upper limit of normal

Cardiovascular

  • No severe cardiovascular disease

Other

  • No other severe disease
  • No other malignancy within the past 5 years except basal or squamous cell skin cancer or noninvasive cancer of the cervix
  • No evidence of autoimmune disease, known immune deficiency, or immunosuppression
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • See Disease Characteristics
  • No prior keyhole limpet hemocyanin immune activator

Chemotherapy

  • No prior doxorubicin
  • At least 3 months since prior mitomycin
  • No other concurrent chemotherapy

Endocrine therapy

  • No concurrent steroids

Radiotherapy

  • At least 4 months since prior radiotherapy

Surgery

  • See Disease Characteristics

Other

  • At least 4 weeks since prior intravesical therapy
  • At least 3 months since prior investigational agents
  • No concurrent cytotoxic immunosuppressive agents
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00006034
INTRACEL-BCI-9804-04
CDR0000068047 ( Registry Identifier: PDQ (Physician Data Query) )
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Intracel
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Study Chair: Michael G Hanna Jr., PhD Intracel
National Cancer Institute (NCI)
January 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP