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- Klinische proef NCT00012363
S0101 Gemcitabine and Irinotecan in Treating Patients With Metastatic or Recurrent Cancer of the Esophagus
Gemcitabine Plus Irinotecan in Patients With Esophageal Cancer, Phase II
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.
PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy in treating patients who have metastatic or recurrent cancer of the esophagus.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
OBJECTIVES:
- Determine the 6-month survival rate of patients with metastatic or recurrent carcinoma of the esophagus or gastroesophageal junction treated with gemcitabine and irinotecan.
- Determine the qualitative and quantitative toxic effects of this regimen in these patients.
OUTLINE: Patients receive gemcitabine IV over 30 minutes and irinotecan IV over 90 minutes on days 1 and 8. Treatment repeats every 21 days for at least 6 courses in the absence of disease progression or unacceptable toxicity.
Patients are followed every 3 months for 1 year and then every 6 months for 2 years.
PROJECTED ACCRUAL: A total of 30-55 patients will be accrued for this study.
Studietype
Inschrijving (Werkelijk)
Fase
- Fase 2
Contacten en locaties
Studie Locaties
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Alabama
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Mobile, Alabama, Verenigde Staten, 36688
- MBCCOP - Gulf Coast
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Arizona
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Phoenix, Arizona, Verenigde Staten, 85006-2726
- CCOP - Greater Phoenix
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Phoenix, Arizona, Verenigde Staten, 85012
- Veterans Affairs Medical Center - Phoenix (Carl T. Hayden)
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Tucson, Arizona, Verenigde Staten, 85724
- Arizona Cancer Center
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Tucson, Arizona, Verenigde Staten, 85723
- Veterans Affairs Medical Center - Tucson
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Arkansas
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Little Rock, Arkansas, Verenigde Staten, 72205
- University of Arkansas for Medical Sciences
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Little Rock, Arkansas, Verenigde Staten, 72205
- Veterans Affairs Medical Center - Little Rock (McClellan)
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California
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Duarte, California, Verenigde Staten, 91010
- City of Hope Comprehensive Cancer Center
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Los Angeles, California, Verenigde Staten, 90095-1781
- Jonsson Comprehensive Cancer Center, UCLA
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Los Angeles, California, Verenigde Staten, 90033-0804
- USC/Norris Comprehensive Cancer Center and Hospital
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Los Angeles, California, Verenigde Staten, 90073
- Veterans Affairs Medical Center - West Los Angeles
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Martinez, California, Verenigde Staten, 94553
- Veterans Affairs Outpatient Clinic - Martinez
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Oakland, California, Verenigde Staten, 94609-3305
- CCOP - Bay Area Tumor Institute
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Orange, California, Verenigde Staten, 92868
- Chao Family Comprehensive Cancer Center
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Sacramento, California, Verenigde Staten, 95817
- University of California Davis Medical Center
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Santa Rosa, California, Verenigde Staten, 95403
- CCOP - Santa Rosa Memorial Hospital
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Travis Air Force Base, California, Verenigde Staten, 94535
- David Grant Medical Center
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Colorado
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Denver, Colorado, Verenigde Staten, 80220
- Veterans Affairs Medical Center - Denver
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Denver, Colorado, Verenigde Staten, 80010
- University of Colorado Cancer Center
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District of Columbia
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Washington, District of Columbia, Verenigde Staten, 20060
- MBCCOP-Howard University Cancer Center
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Georgia
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Atlanta, Georgia, Verenigde Staten, 30342-1701
- CCOP - Atlanta Regional
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Fort Gordon, Georgia, Verenigde Staten, 30905-5650
- Dwight David Eisenhower Army Medical Center
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Hawaii
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Honolulu, Hawaii, Verenigde Staten, 96859-5000
- Tripler Army Medical Center
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Honolulu, Hawaii, Verenigde Staten, 96813-2424
- Cancer Research Center of Hawaii
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Illinois
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Chicago, Illinois, Verenigde Staten, 60612-7323
- MBCCOP - University of Illinois at Chicago
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Chicago, Illinois, Verenigde Staten, 60612
- Veterans Affairs Medical Center - Chicago (Westside Hospital)
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Decatur, Illinois, Verenigde Staten, 62526
- CCOP - Central Illinois
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Hines, Illinois, Verenigde Staten, 60141
- Veterans Affairs Medical Center - Hines (Hines Junior VA Hospital)
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Maywood, Illinois, Verenigde Staten, 60153
- Loyola University Medical Center
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Kansas
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Kansas City, Kansas, Verenigde Staten, 66160-7353
- University of Kansas Medical Center
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Wichita, Kansas, Verenigde Staten, 67214-3882
- CCOP - Wichita
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Wichita, Kansas, Verenigde Staten, 67218
- Veterans Affairs Medical Center - Wichita
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Kentucky
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Lexington, Kentucky, Verenigde Staten, 40536-0084
- Albert B. Chandler Medical Center, University of Kentucky
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Lexington, Kentucky, Verenigde Staten, 40502-2236
- Veterans Affairs Medical Center - Lexington
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Louisiana
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New Orleans, Louisiana, Verenigde Staten, 70112
- Tulane University School of Medicine
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New Orleans, Louisiana, Verenigde Staten, 70112
- MBCCOP - LSU Health Sciences Center
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Shreveport, Louisiana, Verenigde Staten, 71130-3932
- Louisiana State University Health Sciences Center - Shreveport
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Shreveport, Louisiana, Verenigde Staten, 71130
- Veterans Affairs Medical Center - Shreveport
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Massachusetts
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Boston, Massachusetts, Verenigde Staten, 02118
- Boston Medical Center
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Jamaica Plain, Massachusetts, Verenigde Staten, 02130
- Veterans Affairs Medical Center - Boston (Jamaica Plain)
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Michigan
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Ann Arbor, Michigan, Verenigde Staten, 48105
- Veterans Affairs Medical Center - Ann Arbor
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Ann Arbor, Michigan, Verenigde Staten, 48106
- CCOP - Ann Arbor Regional
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Ann Arbor, Michigan, Verenigde Staten, 48109-0912
- University Of Michigan Comprehensive Cancer Center
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Detroit, Michigan, Verenigde Staten, 48202
- Henry Ford Hospital
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Detroit, Michigan, Verenigde Staten, 48201-1379
- Barbara Ann Karmanos Cancer Institute
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Detroit, Michigan, Verenigde Staten, 48201-1932
- Veterans Affairs Medical Center - Detroit
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Grand Rapids, Michigan, Verenigde Staten, 49503
- CCOP - Grand Rapids Clinical Oncology Program
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Royal Oak, Michigan, Verenigde Staten, 48073-6769
- CCOP - Beaumont
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Southfield, Michigan, Verenigde Staten, 48075-9975
- Providence Hospital - Southfield
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Minnesota
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Duluth, Minnesota, Verenigde Staten, 55805
- CCOP - Duluth
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Mississippi
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Biloxi, Mississippi, Verenigde Staten, 39531-2410
- Veterans Affairs Medical Center - Biloxi
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Jackson, Mississippi, Verenigde Staten, 39216-4505
- University of Mississippi Medical Center
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Jackson, Mississippi, Verenigde Staten, 39216
- Veterans Affairs Medical Center - Jackson
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Keesler AFB, Mississippi, Verenigde Staten, 39534-2576
- Keesler Medical Center - Keesler AFB
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Missouri
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Kansas City, Missouri, Verenigde Staten, 64128
- Veterans Affairs Medical Center - Kansas City
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Kansas City, Missouri, Verenigde Staten, 64131
- CCOP - Kansas City
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Saint Louis, Missouri, Verenigde Staten, 63141
- CCOP - St. Louis-Cape Girardeau
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Saint Louis, Missouri, Verenigde Staten, 63110
- St. Louis University Health Sciences Center
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Springfield, Missouri, Verenigde Staten, 65807
- CCOP - Cancer Research for the Ozarks
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Montana
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Billings, Montana, Verenigde Staten, 59101
- CCOP - Montana Cancer Consortium
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New Mexico
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Albuquerque, New Mexico, Verenigde Staten, 87108-5138
- Veterans Affairs Medical Center - Albuquerque
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Albuquerque, New Mexico, Verenigde Staten, 87131
- MBCCOP - University of New Mexico HSC
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New York
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Albany, New York, Verenigde Staten, 12208
- Veterans Affairs Medical Center - Albany
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New York, New York, Verenigde Staten, 10032
- Herbert Irving Comprehensive Cancer Center
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Rochester, New York, Verenigde Staten, 14642
- University of Rochester Medical Center
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North Carolina
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Winston-Salem, North Carolina, Verenigde Staten, 27104-4241
- CCOP - Southeast Cancer Control Consortium
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Ohio
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Cincinnati, Ohio, Verenigde Staten, 45220-2288
- Veterans Affairs Medical Center - Cincinnati
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Cincinnati, Ohio, Verenigde Staten, 45267-0501
- Barrett Cancer Center, The University Hospital
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Cleveland, Ohio, Verenigde Staten, 44195-9001
- Cleveland Clinic Taussig Cancer Center
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Columbus, Ohio, Verenigde Staten, 43206
- CCOP - Columbus
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Dayton, Ohio, Verenigde Staten, 45428
- Veterans Affairs Medical Center - Dayton
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Kettering, Ohio, Verenigde Staten, 45429
- CCOP - Dayton
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Oklahoma
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Oklahoma City, Oklahoma, Verenigde Staten, 73104
- Oklahoma Medical Research Foundation
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Oklahoma City, Oklahoma, Verenigde Staten, 73104
- Veterans Affairs Medical Center - Oklahoma City
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Oregon
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Portland, Oregon, Verenigde Staten, 97207
- Veterans Affairs Medical Center - Portland
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Portland, Oregon, Verenigde Staten, 97225
- CCOP - Columbia River Program
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Portland, Oregon, Verenigde Staten, 97239
- OHSU Cancer Institute
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South Carolina
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Charleston, South Carolina, Verenigde Staten, 29425-0721
- Medical University of South Carolina
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Charleston, South Carolina, Verenigde Staten, 29401-5799
- Veterans Affairs Medical Center - Charleston
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Greenville, South Carolina, Verenigde Staten, 29615
- CCOP - Greenville
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Spartanburg, South Carolina, Verenigde Staten, 29303
- CCOP - Upstate Carolina
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Texas
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Fort Sam Houston, Texas, Verenigde Staten, 78234-6200
- Brooke Army Medical Center
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Galveston, Texas, Verenigde Staten, 77555-0565
- University of Texas Medical Branch
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Houston, Texas, Verenigde Staten, 77030
- Veterans Affairs Medical Center - Houston
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Houston, Texas, Verenigde Staten, 77030-4095
- University of Texas - MD Anderson Cancer Center
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San Antonio, Texas, Verenigde Staten, 78284
- Veterans Affairs Medical Center - San Antonio (Murphy)
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San Antonio, Texas, Verenigde Staten, 78284-7845
- University of Texas Health Science Center at San Antonio
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Temple, Texas, Verenigde Staten, 76504
- Veterans Affairs Medical Center - Temple
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Temple, Texas, Verenigde Staten, 76508
- CCOP - Scott and White Hospital
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Utah
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Salt Lake City, Utah, Verenigde Staten, 84148
- Veterans Affairs Medical Center - Salt Lake City
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Salt Lake City, Utah, Verenigde Staten, 84112-5550
- Huntsman Cancer Institute
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Washington
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Seattle, Washington, Verenigde Staten, 98101
- CCOP - Virginia Mason Research Center
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Seattle, Washington, Verenigde Staten, 98104
- Swedish Cancer Institute
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Seattle, Washington, Verenigde Staten, 98108
- Veterans Affairs Medical Center - Seattle
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Tacoma, Washington, Verenigde Staten, 98431-5000
- Madigan Army Medical Center
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Tacoma, Washington, Verenigde Staten, 98405-0986
- CCOP - Northwest
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
DISEASE CHARACTERISTICS:
Histologically confirmed metastatic or recurrent carcinoma of the esophagus or gastroesophageal junction
- Squamous cell carcinoma OR
- Adenocarcinoma
- No known brain metastases
PATIENT CHARACTERISTICS:
Age:
- 18 to 100
Performance status:
- Zubrod 0-2
Life expectancy:
- Not specified
Hematopoietic:
- Granulocyte count at least 1,500/mm^3
- Platelet count at least 100,000/mm^3
Hepatic:
- Not specified
Renal:
- Creatinine no greater than 1.5 times upper limit of normal
Cardiovascular:
- No uncontrolled hypertension
- No unstable angina
- No symptomatic congestive heart failure
- No myocardial infarction within the past 6 months
- No serious uncontrolled cardiac arrhythmia
Gastrointestinal:
- No active inflammatory bowel disease
- No significant bowel obstruction
- No chronic diarrhea
Other:
- Not pregnant or nursing
- Fertile patients must use effective contraception
- No active infection requiring systemic therapy
- No other prior malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or adequately treated stage I or II cancer in complete remission
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- At least 28 days since prior biologic therapy
- No prior biologic therapy for metastatic or recurrent disease
- No concurrent sargramostim (GM-CSF)
- No concurrent immunotherapy for tumor
Chemotherapy:
- At least 28 days since prior chemotherapy
- No prior chemotherapy for metastatic or recurrent disease
- No prior gemcitabine or irinotecan
- Prior adjuvant or neoadjuvant chemotherapy at time of initial diagnosis of localized disease allowed
- No other concurrent chemotherapy for tumor
Endocrine therapy:
- See Disease Characteristics
- At least 28 days since prior endocrine therapy
- No prior endocrine therapy for metastatic or recurrent disease
- No concurrent hormonal therapy for tumor
Radiotherapy:
- At least 28 days since prior radiotherapy
- No prior radiotherapy for metastatic or recurrent disease
- Prior adjuvant or neoadjuvant radiotherapy at time of initial diagnosis of localized disease allowed
- No concurrent radiotherapy for tumor
Surgery:
- Prior thoraco-abdominal surgery allowed
- At least 3 weeks since prior surgery and recovered
Other:
- No other concurrent anti-cancer therapy for tumor
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Gemcitabine + Irinotecan
Gemcitabine 1000mg/m2 IV over 30 min on Days 1,8 q21days; Irinotecan 100mg/m2 IV over 90 min on Days 1,8 q21days
|
1,000mg/m2, IV over 30 min, days 1 & 8, q 21 days
Andere namen:
100 mg/m2, IV over 90 min, days 1 & 8, q 21days
Andere namen:
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
6-month survival rate
Tijdsspanne: 6 months after registration
|
To assess the six-month survival rate in patients with esophageal cancer treated with a gemcitabine-irinotecan combination chemotherapy regimen.
|
6 months after registration
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Toxicities
Tijdsspanne: Week 1 and Week 2 of each cycle
|
To assess the qualitative and quantitative toxicities associated with this regimen in a Phase II study.
|
Week 1 and Week 2 of each cycle
|
Medewerkers en onderzoekers
Sponsor
Medewerkers
Onderzoekers
- Studie stoel: Stephen K. Williamson, MD, University of Kansas
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Schatting)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Ziekten van het spijsverteringsstelsel
- Neoplasmata
- Neoplasmata per site
- Gastro-intestinale neoplasmata
- Neoplasmata van het spijsverteringsstelsel
- Gastro-intestinale aandoeningen
- Maag Ziekten
- Hoofd- en nekneoplasmata
- Slokdarmaandoeningen
- Maagneoplasmata
- Slokdarmneoplasmata
- Fysiologische effecten van medicijnen
- Moleculaire mechanismen van farmacologische werking
- Anti-infectieuze middelen
- Antivirale middelen
- Enzymremmers
- Antimetabolieten, antineoplastische
- Antimetabolieten
- Antineoplastische middelen
- Immunosuppressieve middelen
- Immunologische factoren
- Topoisomeraseremmers
- Topoisomerase I-remmers
- Gemcitabine
- Irinotecan
Andere studie-ID-nummers
- CDR0000068515
- U10CA032102 (Subsidie/contract van de Amerikaanse NIH)
- S0101 (Andere identificatie: SWOG)
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