- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT00070174
Gemtuzumab Ozogamicin in Treating Young Patients With Newly Diagnosed Acute Myeloid Leukemia Undergoing Remission Induction and Intensification Therapy
Treatment of Newly Diagnosed Childhood Acute Myeloid Leukemia (AML) Using Intensive MRC-Based Therapy and Gemtuzumab Ozogamicin (GMTZ): A COG Pilot Study
RATIONALE: Giving chemotherapy before a donor bone marrow transplant helps stop the growth of cancer cells. It also helps stop the patient's immune system from rejecting the donor's stem cells. Also, monoclonal antibodies, such as gemtuzumab ozogamicin, can find cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets.
PURPOSE: This phase II trial is studying how well gemtuzumab ozogamicin works in treating young patients who are undergoing remission induction, intensification therapy, and allogeneic bone marrow transplant for newly diagnosed acute myeloid leukemia.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
- Arzneimittel: Cyclophosphamid
- Arzneimittel: Mitoxantronhydrochlorid
- Arzneimittel: Asparaginase
- Arzneimittel: Cytarabin
- Arzneimittel: Daunorubicinhydrochlorid
- Arzneimittel: Etoposid
- Arzneimittel: Methotrexat
- Verfahren: allogene Knochenmarktransplantation
- Arzneimittel: busulfan
- Arzneimittel: Cyclosporin
- Arzneimittel: gemtuzumab ozogamicin
Detaillierte Beschreibung
OBJECTIVES:
Primary
- Determine the safety of gemtuzumab ozogamicin in children with newly diagnosed acute myeloid leukemia undergoing intensive remission induction and intensification therapy.
- Determine the complete remission rate of patients treated with this regimen.
Secondary
- Determine the feasibility of performing biological studies (e.g., FLT3-ITD and MRD) for risk group stratification in these patients.
- Determine the effect of karyotypic abnormalities on survival in patients treated with this regimen.
OUTLINE: This is a multicenter study.
- Induction I: Patients receive high-dose cytarabine (ARA-C) IV twice daily on days 1-10; daunorubicin IV over 6 hours on days 1, 3, and 5; etoposide IV over 4 hours on days 1-5; and gemtuzumab ozogamicin IV over 2 hours on day 6. Patients with CNS-negative disease receive ARA-C intrathecally (IT) on day 1. Patients with CNS-positive disease receive ARA-C IT twice weekly for 2-3 weeks. Between days 28-35, patients are evaluated. Patients achieving remission or who have no more than 20% blasts proceed to induction II.
- Induction II: Patients receive ARA-C IV twice daily on days 1-8; ARA-C IT on day 1; and daunorubicin IV and etoposide IV as in induction I. Between days 28-35 patients are evaluated. Patients achieving complete remission proceed to intensification course I.
- Intensification course I: Patients receive ARA-C IV over 1 hour twice daily on days 1-5; ARA-C IT as in induction II; and etoposide IV over 1 hour on days 1-5. Patients are evaluated at day 28. Patients with a 5/6 or 6/6 matched family donor proceed to allogeneic bone marrow transplantation. All other patients in complete remission proceed to intensification course II.
- Intensification course II: Patients receive ARA-C IV over 2 hours twice daily on days 1-4; ARA-C IT as in induction II; mitoxantrone IV over 1 hour on days 3-6; and gemtuzumab ozogamicin IV over 2 hours on day 7. Patients are evaluated on day 28 and then proceed to intensification course III.
- Intensification course III: Patients receive ARA-C IV over 3 hours twice daily on days 1, 2, 8, and 9 and asparaginase intramuscularly on days 2 and 9.
- Allogeneic bone marrow transplantation: Patients receive a preparative regimen comprising busulfan IV over 2 hours 4 times daily on days -9 to -6 and cyclophosphamide IV over 1 hour once daily on days -5 to -2. Allogeneic stem cells are infused on day 0.
- Graft-versus-host disease prophylaxis: Patients receive oral or IV cyclosporine twice daily on days -1 to 50 and methotrexate IV once daily on days 1, 3, 6, and 11.
In all courses, treatment continues in the absence of disease progression or unacceptable toxicity.
Patients are followed monthly for 6 months, every 2 months for 6 months, every 4 months for 1 year, every 6 months for 1 year, and then annually thereafter.
PROJECTED ACCRUAL: A total of 330 patients will be accrued for this study.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Phase 2
Kontakte und Standorte
Studienorte
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New South Wales
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Westmead, New South Wales, Australien, 2145
- Westmead Hospital
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Queensland
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Herston, Brisbane, Queensland, Australien, 4029
- Office of S. David Lang
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Western Australia
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Perth, Western Australia, Australien, 6001
- Princess Margaret Hospital for Children
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Alberta
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Calgary, Alberta, Kanada, T2T 5C7
- Alberta Children's Hospital
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British Columbia
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Vancouver, British Columbia, Kanada, V6H 3V4
- Children's & Women's Hospital of British Columbia
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Manitoba
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Winnipeg, Manitoba, Kanada, R3E 0V9
- CancerCare Manitoba
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Newfoundland and Labrador
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St. John's, Newfoundland and Labrador, Kanada, A1B 3V6
- Janeway Children's Health and Rehabilitation Centre
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Nova Scotia
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Halifax, Nova Scotia, Kanada, B3K 6R8
- IWK Health Centre
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Ontario
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Hamilton, Ontario, Kanada, L8N 3Z5
- McMaster Children's Hospital at Hamilton Health Sciences
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Quebec
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Montreal, Quebec, Kanada, H3T 1C5
- Hôpital Sainte Justine
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Montreal, Quebec, Kanada, H3H 1P3
- McGill Cancer Centre at McGill University
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Ste-Foy, Quebec, Kanada, G1V 4G2
- Centre Hospitalier Universitaire de Quebec
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-
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Santurce, Puerto Rico, 00912
- San Jorge Children's Hospital
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-
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Chihuahua
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Bern, Chihuahua, Schweiz, 3010
- Swiss Pediatric Oncology Group Bern
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Alabama
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Birmingham, Alabama, Vereinigte Staaten, 35294
- Comprehensive Cancer Center at University of Alabama at Birmingham
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Arizona
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Phoenix, Arizona, Vereinigte Staaten, 85016-7710
- Phoenix Children's Hospital
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Arkansas
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Little Rock, Arkansas, Vereinigte Staaten, 72205
- Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
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California
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Downey, California, Vereinigte Staaten, 90242-2814
- Southern California Permanente Medical Group
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Loma Linda, California, Vereinigte Staaten, 92354-2870
- Loma Linda University Cancer Institute at Loma Linda University Medical Center
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Long Beach, California, Vereinigte Staaten, 90801
- Jonathan Jaques Children's Cancer Center at Miller Children's Hospital
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Los Angeles, California, Vereinigte Staaten, 90027
- Children's Hospital Los Angeles
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Los Angeles, California, Vereinigte Staaten, 90048-1865
- Samuel Oschin Comprehensive Cancer Institute at Cedars-Sinai Medical Center
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Madera, California, Vereinigte Staaten, 93638-8762
- Children's Hospital Central California
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Oakland, California, Vereinigte Staaten, 94609-1809
- Children's Hospital and Research Center - Oakland
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Orange, California, Vereinigte Staaten, 92668
- Children's Hospital of Orange County
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Sacramento, California, Vereinigte Staaten, 95817
- University of California Davis Cancer Center
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Sacramento, California, Vereinigte Staaten, 95825
- Kaiser Permanente Medical Center - Oakland
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Sacramento, California, Vereinigte Staaten, 95819
- Sutter Cancer Center
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San Diego, California, Vereinigte Staaten, 92123-4282
- Children's Hospital and Health Center - San Diego
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Colorado
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Denver, Colorado, Vereinigte Staaten, 80218-1088
- Children's Hospital Cancer Center
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Connecticut
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Hartford, Connecticut, Vereinigte Staaten, 06106
- Carole and Ray Neag Comprehensive Cancer Center at the University of Connecticut Health Center
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Delaware
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Wilmington, Delaware, Vereinigte Staaten, 19899
- Alfred I. DuPont Hospital for Children
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District of Columbia
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Washington, District of Columbia, Vereinigte Staaten, 20010-2970
- Children's National Medical Center
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Washington, District of Columbia, Vereinigte Staaten, 20007-2197
- Lombardi Cancer Center at Georgetown University Medical Center
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Florida
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Ft. Lauderdale, Florida, Vereinigte Staaten, 33316
- Broward General Medical Center Cancer Center
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Ft. Myers, Florida, Vereinigte Staaten, 33908
- Lee Cancer Care of Lee Memorial Health System
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Gainesville, Florida, Vereinigte Staaten, 32610
- University of Florida Shands Cancer Center
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Hollywood, Florida, Vereinigte Staaten, 33021
- Memorial Cancer Institute at Memorial Regional Hospital
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Jacksonville, Florida, Vereinigte Staaten, 32207
- Nemours Children's Clinic
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Miami, Florida, Vereinigte Staaten, 33155
- Miami Children's Hospital
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Miami, Florida, Vereinigte Staaten, 33176
- Baptist-South Miami Regional Cancer Program
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Miami, Florida, Vereinigte Staaten, 33101
- University of Miami Sylvester Comprehensive Cancer Center
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Orlando, Florida, Vereinigte Staaten, 32806
- M.D. Anderson Cancer Center - Orlando
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Orlando, Florida, Vereinigte Staaten, 32804
- Florida Hospital Cancer Institute at Florida Hospital Orlando
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Pensacola, Florida, Vereinigte Staaten, 32504
- Sacred Heart Cancer Center at Sacred Heart Hospital
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St. Petersburg, Florida, Vereinigte Staaten, 33701
- All Children's Hospital
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Tampa, Florida, Vereinigte Staaten, 33607
- St. Joseph's Cancer Institute at St. Joseph's Hospital
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West Palm Beach, Florida, Vereinigte Staaten, 33407
- Kaplan Cancer Center at St. Mary's Medical Center
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Georgia
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Atlanta, Georgia, Vereinigte Staaten, 30322
- Emory University Hospital - Atlanta
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Savannah, Georgia, Vereinigte Staaten, 31404-6283
- Curtis & Elizabeth Anderson Cancer Institute at Memorial Health University Medical Center
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Hawaii
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Honolulu, Hawaii, Vereinigte Staaten, 95813
- Cancer Research Center of Hawaii
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Idaho
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Boise, Idaho, Vereinigte Staaten, 83712-6297
- St. Luke's Mountain States Tumor Institute - Boise
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Illinois
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Chicago, Illinois, Vereinigte Staaten, 60614
- Children's Memorial Hospital - Chicago
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Chicago, Illinois, Vereinigte Staaten, 60637-1463
- University of Chicago Cancer Research Center
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Park Ridge, Illinois, Vereinigte Staaten, 60068-1174
- Lutheran General Cancer Care Center
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Springfield, Illinois, Vereinigte Staaten, 62794-9230
- Southern Illinois University School of Medicine
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Indiana
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Indianapolis, Indiana, Vereinigte Staaten, 46260
- St. Vincent Indianapolis Hospital
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Indianapolis, Indiana, Vereinigte Staaten, 46202-5225
- Indiana University Cancer Center
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Iowa
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Iowa City, Iowa, Vereinigte Staaten, 52242-1083
- Holden Comprehensive Cancer Center at University of Iowa
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Kansas
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Wichita, Kansas, Vereinigte Staaten, 67214
- Wesley Medical Center
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Wichita, Kansas, Vereinigte Staaten, 67214
- Via Christi Cancer Center at Via Christi Regional Medical Center
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Kentucky
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Lexington, Kentucky, Vereinigte Staaten, 40506
- Markey Cancer Center at University of Kentucky Chandler Medical Center
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Louisville, Kentucky, Vereinigte Staaten, 40202-1822
- Kosair Children's Hospital
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Maine
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Bangor, Maine, Vereinigte Staaten, 04401
- CancerCare of Maine at Eastern Maine Medial Center
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Scarborough, Maine, Vereinigte Staaten, 04074-9308
- Maine Children's Cancer Program
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Maryland
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Baltimore, Maryland, Vereinigte Staaten, 21215
- Alvin and Lois Lapidus Cancer Institute at Sinai Hospital
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Baltimore, Maryland, Vereinigte Staaten, 21287-5001
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
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Massachusetts
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Boston, Massachusetts, Vereinigte Staaten, 02111
- Floating Hospital for Children
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Michigan
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Ann Arbor, Michigan, Vereinigte Staaten, 48109-0238
- C.S. Mott Children's Hospital at University of Michigan
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Detroit, Michigan, Vereinigte Staaten, 48201
- Barbara Ann Karmanos Cancer Institute
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East Lansing, Michigan, Vereinigte Staaten, 48824-1313
- Breslin Cancer Center at Ingham Regional Medical Center
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Grand Rapids, Michigan, Vereinigte Staaten, 49503-2560
- Spectrum Health Cancer Care - Butterworth Campus
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Grosse Point Woods, Michigan, Vereinigte Staaten, 48236
- Van Elslander Cancer Center at St. John Hospital and Medical Center
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Kalamazoo, Michigan, Vereinigte Staaten, 49007-5341
- CCOP - Kalamazoo
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Minnesota
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Minneapolis, Minnesota, Vereinigte Staaten, 55404
- Children's Hospitals and Clinics - Minneapolis/St. Paul
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Minneapolis, Minnesota, Vereinigte Staaten, 55455-0392
- Fairview University Medical Center - University Campus
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Rochester, Minnesota, Vereinigte Staaten, 55905-0001
- Mayo Clinic Cancer Center
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Mississippi
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Jackson, Mississippi, Vereinigte Staaten, 39216-4505
- University of Mississippi Medical Center
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Keesler AFB, Mississippi, Vereinigte Staaten, 39534-2511
- Keesler Medical Center - Keesler Air Force Base
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Missouri
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Kansas City, Missouri, Vereinigte Staaten, 64108
- Children's Mercy Hospital
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St. Louis, Missouri, Vereinigte Staaten, 63110
- Siteman Cancer Center at Barnes-Jewish Hospital
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St. Louis, Missouri, Vereinigte Staaten, 63104
- Cardinal Glennon Children's Hospital
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Nebraska
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Omaha, Nebraska, Vereinigte Staaten, 68114-4113
- Children's Hospital of Omaha
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Nevada
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Las Vegas, Nevada, Vereinigte Staaten, 89109-2306
- Sunrise Hospital and Medical Center
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New Jersey
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Hackensack, New Jersey, Vereinigte Staaten, 07601
- Hackensack University Medical Center
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Livingston, New Jersey, Vereinigte Staaten, 07039
- St. Barnabas Medical Center
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New Brunswick, New Jersey, Vereinigte Staaten, 08901
- Cancer Institute of New Jersey at UMDNJ - Robert Wood Johnson Medical School
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Newark, New Jersey, Vereinigte Staaten, 07112-2094
- Newark Beth Israel Medical Center
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Paterson, New Jersey, Vereinigte Staaten, 07503
- St. Joseph's Hospital and Medical Center
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New Mexico
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Albuquerque, New Mexico, Vereinigte Staaten, 87131-0001
- University of New Mexico Cancer Research and Treatment Center
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New York
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Bronx, New York, Vereinigte Staaten, 10467
- Albert Einstein Cancer Center at Albert Einstein College of Medicine
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Brooklyn, New York, Vereinigte Staaten, 11219
- Maimonides Medical Center
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Brooklyn, New York, Vereinigte Staaten, 11201-5493
- Brooklyn Hospital Center
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Buffalo, New York, Vereinigte Staaten, 14263
- Roswell Park Cancer Institute
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Mineola, New York, Vereinigte Staaten, 11501
- Winthrop University Hospital
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New Hyde Park, New York, Vereinigte Staaten, 11040
- Schneider Children's Hospital
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New York, New York, Vereinigte Staaten, 10032-1537
- Herbert Irving Comprehensive Cancer Center at Columbia University
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Syracuse, New York, Vereinigte Staaten, 13210
- SUNY Upstate Medical University Hospital
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Valhalla, New York, Vereinigte Staaten, 10595
- New York Medical College
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North Carolina
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Asheville, North Carolina, Vereinigte Staaten, 28801-4690
- Mission Hospitals - Memorial Campus
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Chapel Hill, North Carolina, Vereinigte Staaten, 27599-7220
- Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill
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Charlotte, North Carolina, Vereinigte Staaten, 28233
- Presbyterian Cancer Center at Presbyterian Hospital
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Charlotte, North Carolina, Vereinigte Staaten, 28232
- Blumenthal Cancer Center at Carolinas Medical Center
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Greenville, North Carolina, Vereinigte Staaten, 27834
- Leo W. Jenkins Cancer Center at Pitt County Memorial Hospital
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Winston-Salem, North Carolina, Vereinigte Staaten, 27157-1081
- Comprehensive Cancer Center at Wake Forest University
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North Dakota
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Fargo, North Dakota, Vereinigte Staaten, 58122
- CCOP - MeritCare Hospital
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Ohio
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Akron, Ohio, Vereinigte Staaten, 44308-1062
- Children's Hospital Medical Center of Akron
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Cincinnati, Ohio, Vereinigte Staaten, 45229-3039
- Cincinnati Children's Hospital Medical Center
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Cleveland, Ohio, Vereinigte Staaten, 44106-5000
- Rainbow Babies and Children's Hospital
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Cleveland, Ohio, Vereinigte Staaten, 44195-5217
- Cleveland Clinic Taussig Cancer Center
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Columbus, Ohio, Vereinigte Staaten, 43205-2696
- Columbus Children's Hospital
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Dayton, Ohio, Vereinigte Staaten, 45404-1815
- Children's Medical Center - Dayton
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Toledo, Ohio, Vereinigte Staaten, 43606
- Toledo Hospital
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Toledo, Ohio, Vereinigte Staaten, 43608
- Medical College of Ohio Cancer Institute
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Oklahoma
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Oklahoma City, Oklahoma, Vereinigte Staaten, 73104
- Oklahoma University Medical Center
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Oregon
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Portland, Oregon, Vereinigte Staaten, 97201-3098
- Cancer Institute at Oregon Health and Science University
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Pennsylvania
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Danville, Pennsylvania, Vereinigte Staaten, 17822-1320
- Geisinger Medical Center
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Hershey, Pennsylvania, Vereinigte Staaten, 17033-0850
- Penn State Cancer Institute at Milton S. Hershey Medical Center
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Philadelphia, Pennsylvania, Vereinigte Staaten, 19104-9786
- Children's Hospital of Philadelphia
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Philadelphia, Pennsylvania, Vereinigte Staaten, 19134
- St. Christopher's Hospital for Children
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Pittsburgh, Pennsylvania, Vereinigte Staaten, 15213-2583
- Children's Hospital of Pittsburgh
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South Carolina
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Charleston, South Carolina, Vereinigte Staaten, 29425
- Hollings Cancer Center at Medical University of South Carolina
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Columbia, South Carolina, Vereinigte Staaten, 29203-6897
- Palmetto Health South Carolina Cancer Center
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South Dakota
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Sioux Falls, South Dakota, Vereinigte Staaten, 57117-5039
- Sioux Valley Hospital and University of South Dakota Medical Center
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Tennessee
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Nashville, Tennessee, Vereinigte Staaten, 37232-6310
- Vanderbilt-Ingram Cancer Center
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Texas
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Amarillo, Texas, Vereinigte Staaten, 79106
- Texas Tech University Health Sciences Center School of Medicine
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Austin, Texas, Vereinigte Staaten, 78701
- Children's Hospital of Austin
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Corpus Christi, Texas, Vereinigte Staaten, 78411-1721
- Driscoll Children's Hospital
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Dallas, Texas, Vereinigte Staaten, 75390-9063
- Simmons Comprehensive Cancer Center at University of Texas Southwestern Medical Center - Dallas
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Lubbock, Texas, Vereinigte Staaten, 79410
- Covenant Children's Hospital
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San Antonio, Texas, Vereinigte Staaten, 78229-3993
- Methodist Children's Hospital of South Texas
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San Antonio, Texas, Vereinigte Staaten, 78207
- University of Texas Health Science Center at San Antonio
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Temple, Texas, Vereinigte Staaten, 76508
- CCOP - Scott and White Hospital
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-
Utah
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Salt Lake City, Utah, Vereinigte Staaten, 84113-1100
- Primary Children's Medical Center
-
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Vermont
-
Burlington, Vermont, Vereinigte Staaten, 05405
- Fletcher Allen Health Care - University Health Center Campus
-
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Virginia
-
Fairfax, Virginia, Vereinigte Staaten, 22031
- Inova Fairfax Hospital
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Richmond, Virginia, Vereinigte Staaten, 23298-0121
- Massey Cancer Center at Virginia Commonwealth University
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Roanoke, Virginia, Vereinigte Staaten, 24029
- Carilion Cancer Center of Western Virginia
-
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Washington
-
Seattle, Washington, Vereinigte Staaten, 98105
- Children's Hospital and Regional Medical Center - Seattle
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Spokane, Washington, Vereinigte Staaten, 99220-2555
- Providence Cancer Center at Sacred Heart Medical Center
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Tacoma, Washington, Vereinigte Staaten, 98431
- Madigan Army Medical Center
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Tacoma, Washington, Vereinigte Staaten, 98405
- Mary Bridge Children's Hospital and Health Center - Tacoma
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West Virginia
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Charleston, West Virginia, Vereinigte Staaten, 25302
- West Virginia University - Robert C. Byrd Health Sciences Center - Charleston Division
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Huntington, West Virginia, Vereinigte Staaten, 25701
- Cabell Huntington Hospital
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Wisconsin
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Green Bay, Wisconsin, Vereinigte Staaten, 54301
- St. Vincent Hospital
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La Crosse, Wisconsin, Vereinigte Staaten, 54601-5429
- Gundersen Lutheran Cancer Center at Gundersen Lutheran Medical Center
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Madison, Wisconsin, Vereinigte Staaten, 53792-0001
- University of Wisconsin Comprehensive Cancer Center
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Milwaukee, Wisconsin, Vereinigte Staaten, 53226
- Midwest Children's Cancer Center
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Kind
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
DISEASE CHARACTERISTICS:
Newly diagnosed primary acute myeloid leukemia (AML)
- At least 20% bone marrow blasts
Meets the customary FAB criteria for AML
- Patients with cytopenias and bone marrow blasts who do not meet the FAB criteria are eligible provided they have a karyotypic abnormality characteristic of de novo AML (e.g., t[8;21], inv16, or t[16;16]) OR they have the unequivocal presence of megakaryoblasts
- Isolated granulocytic sarcoma (myeloblastoma) allowed regardless of the results outlined above
- Previously untreated disease
- No promyelocytic leukemia (FAB M3)
- No documented myelodysplastic syndromes (preleukemia) (e.g., chronic myelomonocytic leukemia, refractory anemia [RA], RA with excess blasts, or RA with ringed sideroblasts)
- No juvenile myelomonocytic leukemia
- No Fanconi's anemia, Kostmann syndrome, Shwachman syndrome, or any other known bone marrow failure syndrome
- No Down syndrome
PATIENT CHARACTERISTICS:
Age
- 1 month to 21 years* NOTE: *Children under 1 month of age who have progressive disease are allowed
Performance status
- Karnofsky 50-100% (over 16 years of age) OR
- Lansky 50-100% (ages 1 to 16)* NOTE: Children under 1 year of age do not require a performance status
Life expectancy
- Not specified
Hematopoietic
- Not specified
Hepatic
- No inadequate liver function
Renal
- No inadequate renal function
- No hyperuricemia (greater than 8.0 mg/dL)
- Creatinine clearance or radioisotope glomerular filtration rate (GFR) at least 70 mL/min OR an equivalent normal GFR OR
- Creatinine no greater than 1.5 times normal
Cardiovascular
- Shortening fraction at least 27% by echocardiogram OR
- Ejection fraction at least 50% by MUGA
Pulmonary
- No proven or suspected pneumonia
Other
- Not pregnant or nursing
- No proven or suspected sepsis or meningitis
PRIOR CONCURRENT THERAPY:
Biologic therapy
- Not specified
Chemotherapy
- No prior chemotherapy except intrathecal cytarabine administered that was administered at diagnosis
Endocrine therapy
- Prior topical and inhalation steroids allowed
- No concurrent steroids as antiemetics
Radiotherapy
- No prior radiotherapy
Surgery
- Not specified
Other
- No prior antileukemic therapy
- No concurrent pressor agent or ventilatory support unless approved by the study chair
- No concurrent participation in another COG therapeutic study
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Maskierung: Keine (Offenes Etikett)
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
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Sicherheit
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Vollständige Remissionsrate
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
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Durchführbarkeit
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Effect of karyotypic abnormalities
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Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Studienstuhl: Janet Franklin, MD, MPH, Children's Hospital Los Angeles
Publikationen und hilfreiche Links
Allgemeine Veröffentlichungen
- Ho PA, Kopecky KJ, Alonzo TA, Gerbing RB, Miller KL, Kuhn J, Zeng R, Ries RE, Raimondi SC, Hirsch BA, Oehler V, Hurwitz CA, Franklin JL, Gamis AS, Petersdorf SH, Anderson JE, Godwin JE, Reaman GH, Willman CL, Bernstein ID, Radich JP, Appelbaum FR, Stirewalt DL, Meshinchi S. Prognostic implications of the IDH1 synonymous SNP rs11554137 in pediatric and adult AML: a report from the Children's Oncology Group and SWOG. Blood. 2011 Oct 27;118(17):4561-6. doi: 10.1182/blood-2011-04-348888. Epub 2011 Aug 26.
- Pollard JA, Alonzo TA, Loken M, Gerbing RB, Ho PA, Bernstein ID, Raimondi SC, Hirsch B, Franklin J, Walter RB, Gamis A, Meshinchi S. Correlation of CD33 expression level with disease characteristics and response to gemtuzumab ozogamicin containing chemotherapy in childhood AML. Blood. 2012 Apr 19;119(16):3705-11. doi: 10.1182/blood-2011-12-398370. Epub 2012 Feb 29.
- Vujkovic M, Attiyeh EF, Ries RE, Goodman EK, Ding Y, Kavcic M, Alonzo TA, Wang YC, Gerbing RB, Sung L, Hirsch B, Raimondi S, Gamis AS, Meshinchi S, Aplenc R. Genomic architecture and treatment outcome in pediatric acute myeloid leukemia: a Children's Oncology Group report. Blood. 2017 Jun 8;129(23):3051-3058. doi: 10.1182/blood-2017-03-772384. Epub 2017 Apr 14.
- Ho PA, Kuhn J, Gerbing RB, Pollard JA, Zeng R, Miller KL, Heerema NA, Raimondi SC, Hirsch BA, Franklin JL, Lange B, Gamis AS, Alonzo TA, Meshinchi S. WT1 synonymous single nucleotide polymorphism rs16754 correlates with higher mRNA expression and predicts significantly improved outcome in favorable-risk pediatric acute myeloid leukemia: a report from the children's oncology group. J Clin Oncol. 2011 Feb 20;29(6):704-11. doi: 10.1200/JCO.2010.31.9327. Epub 2010 Dec 28.
- Ho PA, Alonzo TA, Kopecky KJ, Miller KL, Kuhn J, Zeng R, Gerbing RB, Raimondi SC, Hirsch BA, Oehler V, Hurwitz CA, Franklin JL, Gamis AS, Petersdorf SH, Anderson JE, Reaman GH, Baker LH, Willman CL, Bernstein ID, Radich JP, Appelbaum FR, Stirewalt DL, Meshinchi S. Molecular alterations of the IDH1 gene in AML: a Children's Oncology Group and Southwest Oncology Group study. Leukemia. 2010 May;24(5):909-13. doi: 10.1038/leu.2010.56. Epub 2010 Apr 8.
- Ho PA, Zeng R, Alonzo TA, Gerbing RB, Miller KL, Pollard JA, Stirewalt DL, Heerema NA, Raimondi SC, Hirsch B, Franklin JL, Lange B, Meshinchi S. Prevalence and prognostic implications of WT1 mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group. Blood. 2010 Aug 5;116(5):702-10. doi: 10.1182/blood-2010-02-268953. Epub 2010 Apr 22.
- Phillips CL, Gerbing R, Alonzo T, Perentesis JP, Harley IT, Meshinchi S, Bhatla D, Radloff G, Davies SM. MDM2 polymorphism increases susceptibility to childhood acute myeloid leukemia: a report from the Children's Oncology Group. Pediatr Blood Cancer. 2010 Aug;55(2):248-53. doi: 10.1002/pbc.22519.
- Pollard JA, Alonzo TA, Gerbing RB, Ho PA, Zeng R, Ravindranath Y, Dahl G, Lacayo NJ, Becton D, Chang M, Weinstein HJ, Hirsch B, Raimondi SC, Heerema NA, Woods WG, Lange BJ, Hurwitz C, Arceci RJ, Radich JP, Bernstein ID, Heinrich MC, Meshinchi S. Prevalence and prognostic significance of KIT mutations in pediatric patients with core binding factor AML enrolled on serial pediatric cooperative trials for de novo AML. Blood. 2010 Mar 25;115(12):2372-9. doi: 10.1182/blood-2009-09-241075. Epub 2010 Jan 7.
- Berman JN, Gerbing RB, Sung L, et al.: Prevalence and clinical implications of N-RAS mutations in childhood AML - A report from the Children's Oncology Group. [Abstract] Blood 114 (22): A-3115, 2009.
- Ho PA, Alonzo TA, Gerbing RB, Pollard J, Stirewalt DL, Hurwitz C, Heerema NA, Hirsch B, Raimondi SC, Lange B, Franklin JL, Radich JP, Meshinchi S. Prevalence and prognostic implications of CEBPA mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group. Blood. 2009 Jun 25;113(26):6558-66. doi: 10.1182/blood-2008-10-184747. Epub 2009 Mar 20.
- Sung L, Alonzo TA, Gerbing RB, Aplenc R, Lange BJ, Woods WG, Feusner J, Franklin J, Patterson MJ, Gamis AS; Children's Oncology Group. Respiratory syncytial virus infections in children with acute myeloid leukemia: a report from the Children's Oncology Group. Pediatr Blood Cancer. 2008 Dec;51(6):784-6. doi: 10.1002/pbc.21710.
- Pollard J, Alonzo T, Gerbing R, et al.: Prevalence and prognostic significance of c-KIT mutations in pediatric CBF AML patients enrolled on serial CCG/COG protocols. [Abstract] Blood 110 (11): A-1442, 2007.
- Cooper TM, Franklin J, Gerbing RB, Alonzo TA, Hurwitz C, Raimondi SC, Hirsch B, Smith FO, Mathew P, Arceci RJ, Feusner J, Iannone R, Lavey RS, Meshinchi S, Gamis A. AAML03P1, a pilot study of the safety of gemtuzumab ozogamicin in combination with chemotherapy for newly diagnosed childhood acute myeloid leukemia: a report from the Children's Oncology Group. Cancer. 2012 Feb 1;118(3):761-9. doi: 10.1002/cncr.26190. Epub 2011 Jul 15.
- Gudgeon CJ, Harrington KH, Laszlo GS, Alonzo TA, Gerbing RB, Gamis AS, Raimondi SC, Hirsch BA, Meshinchi S, Walter RB. High expression of neutrophil elastase predicts improved survival in pediatric acute myeloid leukemia: a report from the Children's Oncology Group. Leuk Lymphoma. 2013 Jan;54(1):202-4. doi: 10.3109/10428194.2012.700480. Epub 2012 Jul 9. No abstract available.
- Loken MR, Alonzo TA, Pardo L, Gerbing RB, Raimondi SC, Hirsch BA, Ho PA, Franklin J, Cooper TM, Gamis AS, Meshinchi S. Residual disease detected by multidimensional flow cytometry signifies high relapse risk in patients with de novo acute myeloid leukemia: a report from Children's Oncology Group. Blood. 2012 Aug 23;120(8):1581-8. doi: 10.1182/blood-2012-02-408336. Epub 2012 May 30.
- Ho PA, Kutny MA, Alonzo TA, Gerbing RB, Joaquin J, Raimondi SC, Gamis AS, Meshinchi S. Leukemic mutations in the methylation-associated genes DNMT3A and IDH2 are rare events in pediatric AML: a report from the Children's Oncology Group. Pediatr Blood Cancer. 2011 Aug;57(2):204-9. doi: 10.1002/pbc.23179. Epub 2011 Apr 18.
- Walter RB, Alonzo TA, Gerbing RB, Ho PA, Smith FO, Raimondi SC, Hirsch BA, Gamis AS, Franklin JL, Hurwitz CA, Loken MR, Meshinchi S. High expression of the very late antigen-4 integrin independently predicts reduced risk of relapse and improved outcome in pediatric acute myeloid leukemia: a report from the children's oncology group. J Clin Oncol. 2010 Jun 10;28(17):2831-8. doi: 10.1200/JCO.2009.27.5693. Epub 2010 Apr 26.
- Walter RB, Alonzo TA, Gerbing RB, et al.: High expression of the very late antigen (VLA)-4 (CD49d) integrin predicts for reduced risk of relapse and better outcome in pediatric acute myeloid leukemia (AML): A report from the Children's Oncology Group. [Abstract] Blood 114 (22): A-1592, 2009.
- Franklin J, Alonzo T, Hurwitz CA, et al.: COG AAML03P1: efficacy and safety in a pilot study of intensive chemotherapy including gemtuzumab in children newly diagnosed with acute myeloid leukemia (AML). [Abstract] Blood 112 (11): A- 136, 2008.
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
- Akute Erythroleukämie im Kindesalter (M6)
- Akute megakaryozytische Leukämie im Kindesalter (M7)
- akute minimal differenzierte myeloische Leukämie im Kindesalter (M0)
- unbehandelte akute myeloische Leukämie im Kindesalter und andere myeloische Malignome
- Akute myeloische Leukämie im Kindesalter ohne Reifung (M1)
- Akute myeloische Leukämie im Kindesalter mit Reifung (M2)
- Akute myelomonozytäre Leukämie im Kindesalter (M4)
- Akute monoblastische Leukämie im Kindesalter (M5a)
- Akute Monozytenleukämie im Kindesalter (M5b)
Zusätzliche relevante MeSH-Bedingungen
- Neubildungen nach histologischem Typ
- Neubildungen
- Leukämie
- Leukämie, Myeloid
- Leukämie, myeloisch, akut
- Physiologische Wirkungen von Arzneimitteln
- Molekulare Mechanismen der pharmakologischen Wirkung
- Antiinfektiva
- Agenten des peripheren Nervensystems
- Antivirale Mittel
- Inhibitoren der Nukleinsäuresynthese
- Enzym-Inhibitoren
- Analgetika
- Agenten des sensorischen Systems
- Antirheumatika
- Antimetaboliten, antineoplastisch
- Antimetaboliten
- Antineoplastische Mittel
- Immunsuppressive Mittel
- Immunologische Faktoren
- Antineoplastische Mittel, alkylierend
- Alkylierungsmittel
- Myeloablative Agonisten
- Antineoplastische Mittel, Phytogen
- Topoisomerase-II-Inhibitoren
- Topoisomerase-Inhibitoren
- Antineoplastische Mittel, immunologische
- Dermatologische Wirkstoffe
- Antibiotika, antineoplastische
- Antimykotika
- Reproduktionskontrollmittel
- Abtreibungsmittel, nichtsteroidal
- Abtreibungsmittel
- Folsäure-Antagonisten
- Calcineurin-Inhibitoren
- Cyclophosphamid
- Etoposid
- Cytarabin
- Methotrexat
- Daunorubicin
- Asparaginase
- Mitoxantron
- Busulfan
- Cyclosporin
- Cyclosporine
- Gemtuzumab
Andere Studien-ID-Nummern
- AAML03P1
- CDR0000330133 (Andere Kennung: Clinical Trials.gov)
- COG-AAML03P1 (Andere Kennung: Children's Oncology Group)
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