- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT00054054
S0216, Combination Chemotherapy and RT in Treating Patients With Stage III or Stage IV Head and Neck Cancer
Docetaxel (NSC-628503), Cisplatin (NSC-119875), And 5-Fluorouracil (NSC-19893) Induction Chemotherapy Followed By Accelerated Fractionation/Concomitant Boost Radiation And Concurrent Single Agent Cisplatin (NSC-119875), In Patients With Advanced Squamous Cell Head And Neck Cancer
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining more than one chemotherapy drug with radiation therapy may kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy and radiation therapy in treating patients with stage III or stage IV head and neck cancer.
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Detailní popis
OBJECTIVES:
- Determine the overall survival of patients with stage III or IV squamous cell head and neck cancer treated with docetaxel, cisplatin, and fluorouracil followed by accelerated fractionation/concomitant boost radiotherapy and cisplatin.
- Determine the unconfirmed complete response rate in these patients after treatment with induction chemotherapy.
- Determine the overall complete response rate (confirmed and unconfirmed) in patients treated with this regimen.
- Determine the toxic effects of this regimen in these patients.
OUTLINE:
- Induction Chemotherapy: Patients receive docetaxel IV over 1 hour and cisplatin IV over 30-60 minutes on day 1 and fluorouracil IV continuously on days 1-4. Treatment repeats every 21 days for 2 courses in the absence of unacceptable toxicity.
- Chemoradiotherapy: Beginning within 3-4 weeks after administration of the second course of induction chemotherapy, patients receive accelerated fractionation radiotherapy once daily, 5 days per week, for 6 weeks with concomitant boost radiotherapy once daily, 5 days a week, for the last 2.5 weeks of radiotherapy. Patients also receive concurrent cisplatin IV over 30-60 minutes on days 1 and 22.
Patients are followed every 2 months for 1 year, every 3 months for 2 years, every 4 months for 1 year, and then every 6 months for 1 year.
PROJECTED ACCRUAL: A total of 60 patients will be accrued for this study within 2 years.
Typ studie
Fáze
- Fáze 2
Kontakty a umístění
Studijní místa
-
-
Ontario
-
Toronto, Ontario, Kanada, M5G 1X8
- Hospital for Sick Children
-
-
-
-
Alabama
-
Birmingham, Alabama, Spojené státy, 35294-3300
- University of Alabama at Birmingham Comprehensive Cancer Center
-
Mobile, Alabama, Spojené státy, 36607
- MBCCOP - Gulf Coast
-
-
Arizona
-
Phoenix, Arizona, Spojené státy, 85006-2726
- CCOP - Western Regional, Arizona
-
Phoenix, Arizona, Spojené státy, 85012
- Veterans Affairs Medical Center - Phoenix (Carl T. Hayden)
-
Tucson, Arizona, Spojené státy, 85723
- Veterans Affairs Medical Center - Tucson
-
Tucson, Arizona, Spojené státy, 85724
- Arizona Cancer Center at University of Arizona Health Sciences Center
-
-
Arkansas
-
Little Rock, Arkansas, Spojené státy, 72205
- Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
-
Little Rock, Arkansas, Spojené státy, 72205
- Veterans Affairs Medical Center - Little Rock (McClellan)
-
-
California
-
Duarte, California, Spojené státy, 91010-3000
- City of Hope Comprehensive Cancer Center
-
Fresno, California, Spojené státy, 93720
- California Cancer Center
-
Los Angeles, California, Spojené státy, 90033
- USC/Norris Comprehensive Cancer Center and Hospital
-
Martinez, California, Spojené státy, 94553
- Veterans Affairs Outpatient Clinic - Martinez
-
Oakland, California, Spojené státy, 94609-3305
- CCOP - Bay Area Tumor Institute
-
Orange, California, Spojené státy, 92868
- Chao Family Comprehensive Cancer Center at University of California Irvine Cancer Center
-
Sacramento, California, Spojené státy, 95817
- University of California Davis Cancer Center
-
Santa Rosa, California, Spojené státy, 95403
- CCOP - Santa Rosa Memorial Hospital
-
Travis Air Force Base, California, Spojené státy, 94535
- David Grant Medical Center
-
-
Colorado
-
Aurora, Colorado, Spojené státy, 80010
- University of Colorado Cancer Center at University of Colorado Health Sciences Center
-
Denver, Colorado, Spojené státy, 80220
- Veterans Affairs Medical Center - Denver
-
-
District of Columbia
-
Washington, District of Columbia, Spojené státy, 20060
- MBCCOP - Howard University Cancer Center
-
-
Florida
-
Tampa, Florida, Spojené státy, 33612
- Veterans Affairs Medical Center - Tampa (Haley)
-
-
Georgia
-
Atlanta, Georgia, Spojené státy, 30342-1701
- CCOP - Atlanta Regional
-
-
Hawaii
-
Honolulu, Hawaii, Spojené státy, 96813
- MBCCOP - Hawaii
-
-
Illinois
-
Chicago, Illinois, Spojené státy, 60612
- Veterans Affairs Medical Center - Chicago (Westside Hospital)
-
Chicago, Illinois, Spojené státy, 60612
- MBCCOP - University of Illinois at Chicago
-
Decatur, Illinois, Spojené státy, 62526
- CCOP - Central Illinois
-
Hines, Illinois, Spojené státy, 60141
- Veterans Affairs Medical Center - Hines (Hines Junior VA Hospital)
-
Maywood, Illinois, Spojené státy, 60153-5500
- Cardinal Bernardin Cancer Center at Loyola University Medical Center
-
-
Kansas
-
Kansas City, Kansas, Spojené státy, 66160-7353
- Kansas Masonic Cancer Research Institute at the University of Kansas Medical Center
-
Wichita, Kansas, Spojené státy, 67214-3882
- CCOP - Wichita
-
Wichita, Kansas, Spojené státy, 67218
- Veterans Affairs Medical Center - Wichita
-
-
Kentucky
-
Lexington, Kentucky, Spojené státy, 40502-2236
- Veterans Affairs Medical Center - Lexington
-
Lexington, Kentucky, Spojené státy, 40536-0084
- Markey Cancer Center at University of Kentucky Chandler Medical Center
-
-
Louisiana
-
New Orleans, Louisiana, Spojené státy, 70112
- Veterans Affairs Medical Center - New Orleans
-
New Orleans, Louisiana, Spojené státy, 70112
- MBCCOP - LSU Health Sciences Center
-
New Orleans, Louisiana, Spojené státy, 70112
- Tulane Cancer Center at Tulane University Hospital and Clinic
-
Shreveport, Louisiana, Spojené státy, 71130-3932
- Louisiana State University Health Sciences Center - Shreveport
-
Shreveport, Louisiana, Spojené státy, 71101-4295
- Veterans Affairs Medical Center - Shreveport
-
-
Massachusetts
-
Boston, Massachusetts, Spojené státy, 02118
- Cancer Research Center at Boston Medical Center
-
-
Michigan
-
Ann Arbor, Michigan, Spojené státy, 48105
- Veterans Affairs Medical Center - Ann Arbor
-
Ann Arbor, Michigan, Spojené státy, 48106
- CCOP - Michigan Cancer Research Consortium
-
Ann Arbor, Michigan, Spojené státy, 48109-0912
- University of Michigan Comprehensive Cancer Center
-
Detroit, Michigan, Spojené státy, 48202
- Josephine Ford Cancer Center at Henry Ford Hospital
-
Detroit, Michigan, Spojené státy, 48201-1379
- Barbara Ann Karmanos Cancer Institute
-
Detroit, Michigan, Spojené státy, 48201-1932
- Veterans Affairs Medical Center - Detroit
-
Grand Rapids, Michigan, Spojené státy, 49503
- CCOP - Grand Rapids
-
Royal Oak, Michigan, Spojené státy, 48073-6769
- CCOP - Beaumont
-
Southfield, Michigan, Spojené státy, 48075
- Providence Cancer Institute at Providence Hospital
-
-
Mississippi
-
Jackson, Mississippi, Spojené státy, 39216-4505
- University of Mississippi Medical Center
-
Jackson, Mississippi, Spojené státy, 39216
- Veterans Affairs Medical Center - Jackson
-
-
Missouri
-
Kansas City, Missouri, Spojené státy, 64131
- CCOP - Kansas City
-
Saint Louis, Missouri, Spojené státy, 63141
- CCOP - St. Louis-Cape Girardeau
-
Saint Louis, Missouri, Spojené státy, 63110
- St. Louis University Hospital Cancer Center
-
Springfield, Missouri, Spojené státy, 65807
- CCOP - Cancer Research for the Ozarks
-
-
Montana
-
Billings, Montana, Spojené státy, 59101
- CCOP - Montana Cancer Consortium
-
-
New Jersey
-
East Orange, New Jersey, Spojené státy, 07018-1095
- Veterans Affairs Medical Center - East Orange
-
-
New Mexico
-
Albuquerque, New Mexico, Spojené státy, 87108-5138
- Veterans Affairs Medical Center - Albuquerque
-
Albuquerque, New Mexico, Spojené státy, 87131
- MBCCOP - University of New Mexico HSC
-
-
New York
-
New York, New York, Spojené státy, 10016
- NYU School of Medicine's Kaplan Comprehensive Cancer Center
-
New York, New York, Spojené státy, 10032
- Herbert Irving Comprehensive Cancer Center at Columbia University
-
Rochester, New York, Spojené státy, 14642
- James P. Wilmot Cancer Center at University of Rochester Medical Center
-
-
North Carolina
-
Salisbury, North Carolina, Spojené státy, 28144
- Veterans Affairs Medical Center - Salisbury
-
Winston-Salem, North Carolina, Spojené státy, 27104-4241
- CCOP - Southeast Cancer Control Consortium
-
-
Ohio
-
Cincinnati, Ohio, Spojené státy, 45220-2288
- Veterans Affairs Medical Center - Cincinnati
-
Cincinnati, Ohio, Spojené státy, 45267-0501
- Charles M. Barrett Cancer Center at University Hospital
-
Cleveland, Ohio, Spojené státy, 44195-9001
- Cleveland Clinic Taussig Cancer Center
-
Columbus, Ohio, Spojené státy, 43206
- CCOP - Columbus
-
Dayton, Ohio, Spojené státy, 45429
- CCOP - Dayton
-
Dayton, Ohio, Spojené státy, 45428-1002
- Veterans Affairs Medical Center - Dayton
-
-
Oregon
-
Portland, Oregon, Spojené státy, 97207
- Veterans Affairs Medical Center - Portland
-
Portland, Oregon, Spojené státy, 97225
- CCOP - Columbia River Oncology Program
-
Portland, Oregon, Spojené státy, 97201-3098
- Cancer Institute at Oregon Health and Science University
-
-
South Carolina
-
Charleston, South Carolina, Spojené státy, 29425
- Hollings Cancer Center at Medical University of South Carolina
-
Charleston, South Carolina, Spojené státy, 29401-5799
- Veterans Affairs Medical Center - Charleston
-
Greenville, South Carolina, Spojené státy, 29615
- CCOP - Greenville
-
Spartanburg, South Carolina, Spojené státy, 29303
- CCOP - Upstate Carolina
-
-
Tennessee
-
Memphis, Tennessee, Spojené státy, 38104
- University of Tennessee Cancer Institute
-
-
Texas
-
Amarillo, Texas, Spojené státy, 79106
- Harrington Cancer Center
-
Amarillo, Texas, Spojené státy, 79106
- Veterans Affairs Medical Center - Amarillo
-
Fort Sam Houston, Texas, Spojené státy, 78234-6200
- Brooke Army Medical Center
-
Galveston, Texas, Spojené státy, 77555-0565
- University of Texas Medical Branch
-
Houston, Texas, Spojené státy, 77030
- Veterans Affairs Medical Center - Houston
-
Houston, Texas, Spojené státy, 77030-4095
- University of Texas - MD Anderson Cancer Center
-
San Antonio, Texas, Spojené státy, 78229-3900
- University of Texas Health Science Center at San Antonio
-
San Antonio, Texas, Spojené státy, 78229
- Veterans Affairs Medical Center - San Antonio (Murphy)
-
Temple, Texas, Spojené státy, 76504
- Veterans Affairs Medical Center - Temple
-
Temple, Texas, Spojené státy, 76508
- CCOP - Scott and White Hospital
-
-
Utah
-
Salt Lake City, Utah, Spojené státy, 84148
- Veterans Affairs Medical Center - Salt Lake City
-
Salt Lake City, Utah, Spojené státy, 84112-5550
- Huntsman Cancer Institute
-
-
Washington
-
Seattle, Washington, Spojené státy, 98101
- CCOP - Virginia Mason Research Center
-
Seattle, Washington, Spojené státy, 98108
- Veterans Affairs Medical Center - Seattle
-
Seattle, Washington, Spojené státy, 98109
- Puget Sound Oncology Consortium
-
Tacoma, Washington, Spojené státy, 98431-5000
- Madigan Army Medical Center
-
Tacoma, Washington, Spojené státy, 98405-0986
- CCOP - Northwest
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
DISEASE CHARACTERISTICS:
Histologically confirmed squamous cell carcinoma of the head and neck (excluding lip, nasopharynx, paranasal sinus, and salivary gland) by biopsy or fine needle aspirate of the primary lesion or neck mass
- Stage III or IV disease
No evidence of distant metastases
- Negative chest x-ray
Primary site in the head and neck region must be identified
- No unknown primary site
- Considered to be appropriate for definitive radiotherapy with curative intent
PATIENT CHARACTERISTICS:
Age
- 18 and over
Performance status
- Zubrod 0-1
Life expectancy
- Not specified
Hematopoietic
- Granulocyte count greater than 1,500/mm^3
- Platelet count greater than 100,000/mm^3
Hepatic
- Bilirubin no greater than upper limit of normal (ULN)
- Alkaline phosphatase less than 2 times ULN
- ALT or AST less than 1.5 times ULN
Renal
- Creatinine less than 1.5 mg/dL
Cardiovascular
- No myocardial infarction within the past 3 months
- No unstable or uncontrolled angina
Other
- Not pregnant or nursing
- Fertile patients must use effective contraception
- 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 currently in complete remission
- No evidence of pre-existing peripheral neuropathy
- No active systemic infection
- No history of hypersensitivity reaction to products containing polysorbate 80
PRIOR CONCURRENT THERAPY:
Biologic therapy
- Not specified
Chemotherapy
- No prior chemotherapy
Endocrine therapy
- Not specified
Radiotherapy
- See Disease Characteristics
- No prior radiotherapy
Surgery
- No prior surgery for head or neck cancer
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Publikace a užitečné odkazy
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Primární dokončení (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Novotvary
- Novotvary podle místa
- Novotvary hlavy a krku
- Fyziologické účinky léků
- Molekulární mechanismy farmakologického působení
- Antimetabolity, Antineoplastika
- Antimetabolity
- Antineoplastická činidla
- Imunosupresivní látky
- Imunologické faktory
- Tubulinové modulátory
- Antimitotické látky
- Modulátory mitózy
- Docetaxel
- Fluorouracil
Další identifikační čísla studie
- CDR0000269781
- U10CA032102 (Grant/smlouva NIH USA)
- S0216 (Jiný identifikátor: SWOG)
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .