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새로 진단된 골육종 환자의 화학요법에 약물 카보잔티닙 추가를 테스트하기 위한 연구

2026년 10월 24일 업데이트: National Cancer Institute (NCI)

새로 진단된 골육종에 대한 세포독성 화학요법과 병용한 VEFGR2/MET 억제제 카보잔티닙의 타당성 및 무작위 2/3상 연구

This phase II/III trial tests the safety, side effects, and best dose of the drug cabozantinib in combination with standard chemotherapy, and to compare the effect of adding cabozantinib to standard chemotherapy alone in treating patients with newly diagnosed osteosarcoma. Cabozantinib is in a class of medications called kinase inhibitors which block protein signals affecting new blood vessel formation and the ability to activate growth signaling pathways. This may help slow the growth of tumor cells. The drugs used in standard chemotherapy for this trial are methotrexate, doxorubicin, and cisplatin (MAP). Methotrexate stops cells from making DNA and may kill tumor cells. It is a type of antimetabolite. Doxorubicin is in a class of medications called anthracyclines. It works by slowing or stopping the growth of tumor cells in the body. Cisplatin is in a class of medications known as platinum-containing compounds. It works by killing, stopping or slowing the growth of tumor cells. Adding cabozantinib to standard chemotherapy may work better in treating newly diagnosed osteosarcoma.

연구 개요

상태

정지된

정황

개입 / 치료

상세 설명

PRIMARY OBJECTIVES:

I. To determine the feasibility of adding cabozantinib S-malate (cabozantinib) to standard MAP (high dose methotrexate, doxorubicin hydrochloride [doxorubicin], and cisplatin) chemotherapy in patients with newly diagnosed metastatic osteosarcoma with a resectable primary tumor.

II. To determine whether MAP chemotherapy plus cabozantinib results in more favorable event-free survival (EFS) than MAP chemotherapy alone in patients with localized, resectable osteosarcoma.

III. To determine whether MAP chemotherapy plus cabozantinib results in more favorable event-free survival (EFS) than MAP chemotherapy alone in patients with metastatic, pelvic and unresectable osteosarcoma.

SECONDARY OBJECTIVES:

I. To determine whether MAP chemotherapy plus cabozantinib results in more favorable overall survival (OS) than MAP chemotherapy alone in patients with localized, resectable osteosarcoma.

II. To determine whether MAP chemotherapy plus cabozantinib results in more favorable overall survival (OS) than MAP chemotherapy alone in patients with metastatic, pelvic and unresectable osteosarcoma.

III. To prospectively validate that elevated circulating tumor DNA (ctDNA) levels greater than or equal to 5% at the time of diagnosis are associated with increased risk of EFS-event in patients with localized, resectable osteosarcoma.

IV. To prospectively validate that elevated ctDNA levels greater than or equal to 5% at the time of diagnosis are associated with increased risk of EFS-event in patients with metastatic, pelvic and unresectable osteosarcoma.

V. To prospectively validate that elevated ctDNA levels greater than or equal to 3% after initiation of therapy and prior to definitive surgery are associated with increased risk of EFS-event in patients with localized, resectable osteosarcoma.

VI. To prospectively validate that elevated ctDNA levels greater than or equal to 3% after initiation of therapy and prior to definitive surgery are associated with increased risk of EFS-event in patients with metastatic, pelvic and unresectable osteosarcoma.

VII. To determine whether MAP chemotherapy plus cabozantinib results in increased symptom burden and decreased tolerability to patients as measured by patient reported therapy-specific acute toxicities (Patient-Reported Outcomes-Common Terminology Criteria for Adverse Events [PRO-CTCAE]).

EXPLORATORY OBJECTIVES:

I. To determine the rate of good histologic response (> 90%) of resected primary tumor specimens following neoadjuvant chemotherapy with MAP plus cabozantinib and compare with response rates for MAP chemotherapy alone.

II. To describe the toxicities of the addition of cabozantinib to MAP chemotherapy in patients with newly diagnosed osteosarcoma.

III. To compare the probability of Grade 3 or higher port site wound complications on the MAP plus cabozantinib regimen to that of MAP chemotherapy alone in patients with newly diagnosed osteosarcoma who received a port for the administration of chemotherapy.

IV. To describe frequency of application of local control methods (surgery, hypofractionated stereotactic body radiotherapy, or radiofrequency ablation) for extrapulmonary metastatic osteosarcoma.

V. To compare total cumulative delivered doses of MAP chemotherapy agents between standard and experimental arms across multiple phases of therapy.

VI. To assess the pharmacokinetics of cabozantinib when administered concomitantly with standard chemotherapy agents during feasibility.

VII. To collect pulmonary metastatic lesions, paired primary tumor tissue, and serial blood samples for tumor profiling, liquid biopsies, and future testing of correlative biology studies.

VIII. To determine whether ctDNA at diagnosis and early on-treatment, as a continuous measurement of ctDNA burden, is associated with an increased risk of EFS-event in patients with newly diagnosed osteosarcoma.

IX. To evaluate whether the magnitude of change in ctDNA levels from diagnosis to planned surgical procedure is associated with risk of EFS-event in patients with newly diagnosed osteosarcoma.

X. To determine whether ctDNA levels greater than or equal to 3% after planned surgical procedures are associated with increased risk of EFS-event.

XI. To describe the presence of specific copy-number alterations, including MYC amplifications, detected in ctDNA and matched diagnostic tumor samples in patients with newly diagnosed osteosarcoma and determine whether frequently occurring copy-number alterations are associated with increased risk of EFS-event.

XII. To determine whether ctDNA burden is predictive of response to the experimental therapy in patients with newly diagnosed osteosarcoma.

XIII. To prospectively compare the impact of combination therapy on symptom bother as measured by the Functional Assessment of Cancer Therapy-General Questionnaire (FACT-G) item GP5 in patients with osteosarcoma receiving MAP chemotherapy with or without cabozantinib, and to assess the relationship between symptom bother and number of patient-reported acute toxicities (as measured by the PRO-CTCAE).

OUTLINE: This is a dose-escalation study of cabozantinib (Feasibility Phase) followed by a randomized phase II/III study (Efficacy Phase).

FEASIBILITY PHASE (CLOSED TO ACCRUAL 05/09/2025): Patients receive cabozantinib orally (PO), methotrexate intravenously (IV), doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles. Patients are then considered for appropriate local control. Then they receive "consolidation" with methotrexate IV, doxorubicin IV, and cisplatin IV for one 35-day cycle, followed by cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV for one 35-day cycle, and cabozantinib PO, methotrexate IV, and doxorubicin IV for two 35-day cycles. Patients then receive cabozantinib PO for six 28-day "maintenance" cycles.

EFFICACY PHASE: Patients with standard risk osteosarcoma are randomized to Arm A or Arm B. Patients with high risk osteosarcoma are randomized to Arm C or Arm D.

ARM A: Standard risk patients receive methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles, followed by appropriate local control. Patients then receive "consolidation" with methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day cycles and methotrexate IV and doxorubicin IV for two additional 35-day cycles.

ARM B: Standard risk patients receive cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles, followed by appropriate local control. Patients then receive one 35-day "consolidation" cycle with methotrexate IV, doxorubicin IV, and cisplatin IV, then a second 35-day "consolidation" cycle with cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV, followed by two additional 35-day "consolidation" cycles with cabozantinib PO, methotrexate IV, and doxorubicin IV. Patients then receive cabozantinib PO for six 28-day "maintenance" cycles.

ARM C: High risk patients receive methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles, followed by appropriate local control. Patients then receive "consolidation" with methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day cycles and methotrexate IV and doxorubicin IV for two additional 35-day cycles.

ARM D: High risk patients receive cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles, followed by appropriate local control. Patients then receive one 35-day "consolidation" cycle with methotrexate IV, doxorubicin IV, and cisplatin IV, then a second 35-day "consolidation" cycle with cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV, followed by two additional 35-day "consolidation" cycles with cabozantinib PO, methotrexate IV, and doxorubicin IV. Patients then receive cabozantinib PO for six 28-day "maintenance" cycles.

All patients also undergo X-ray, computed tomography (CT), magnetic resonance imaging (MRI), and positron emission tomography (PET) or bone scintigraphy at diagnosis and additional time points throughout the trial. All patients also undergo collection of blood samples during screening and on study.

연구 유형

중재적

등록 (추정된)

1122

단계

  • 2 단계
  • 3단계

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  • 뉴질랜드
      • Christchurch, 뉴질랜드, 8011
        • Christchurch Hospital
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      • Grafton, Auckland, 뉴질랜드, 1145
        • Starship Children's Hospital
  • 미국
    • Alabama
      • Birmingham, Alabama, 미국, 35233
        • Children's Hospital of Alabama
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      • Mesa, Arizona, 미국, 85202
        • Banner Children's at Desert
      • Phoenix, Arizona, 미국, 85054
        • Mayo Clinic Hospital in Arizona
      • Phoenix, Arizona, 미국, 85016
        • Phoenix Childrens Hospital
      • Tucson, Arizona, 미국, 85719
        • Banner University Medical Center - Tucson
    • Arkansas
      • Little Rock, Arkansas, 미국, 72202-3591
        • Arkansas Children's Hospital
    • California
      • Downey, California, 미국, 90242
        • Kaiser Permanente Downey Medical Center
      • Duarte, California, 미국, 91010
        • City of Hope Comprehensive Cancer Center
      • Loma Linda, California, 미국, 92354
        • Loma Linda University Medical Center
      • Long Beach, California, 미국, 90806
        • Miller Children's and Women's Hospital Long Beach
      • Los Angeles, California, 미국, 90048
        • Cedars-Sinai Medical Center
      • Los Angeles, California, 미국, 90027
        • Children's Hospital Los Angeles
      • Los Angeles, California, 미국, 90095
        • Mattel Children's Hospital UCLA
      • Madera, California, 미국, 93636
        • Valley Children's Hospital
      • Oakland, California, 미국, 94609
        • UCSF Benioff Children's Hospital Oakland
      • Oakland, California, 미국, 94611
        • Kaiser Permanente-Oakland
      • Orange, California, 미국, 92868
        • Children's Hospital of Orange County
      • Palo Alto, California, 미국, 94304
        • Lucile Packard Children's Hospital Stanford University
      • Sacramento, California, 미국, 95817
        • University of California Davis Comprehensive Cancer Center
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        • Rady Children's Hospital - San Diego
      • San Francisco, California, 미국, 94158
        • UCSF Medical Center-Mission Bay
    • Colorado
      • Aurora, Colorado, 미국, 80045
        • Children's Hospital Colorado
      • Denver, Colorado, 미국, 80218
        • Rocky Mountain Hospital for Children-Presbyterian Saint Luke's Medical Center
    • Connecticut
      • Hartford, Connecticut, 미국, 06106
        • Connecticut Children's Medical Center
      • New Haven, Connecticut, 미국, 06520
        • Yale University
    • Delaware
      • Wilmington, Delaware, 미국, 19803
        • Alfred I duPont Hospital for Children
    • District of Columbia
      • Washington D.C., District of Columbia, 미국, 20010
        • Children's National Medical Center
      • Washington D.C., District of Columbia, 미국, 20007
        • MedStar Georgetown University Hospital
    • Florida
      • Fort Myers, Florida, 미국, 33908
        • Golisano Children's Hospital of Southwest Florida
      • Gainesville, Florida, 미국, 32610
        • UF Health Cancer Institute - Gainesville
      • Hollywood, Florida, 미국, 33021
        • Memorial Regional Hospital/Joe DiMaggio Children's Hospital
      • Jacksonville, Florida, 미국, 32207
        • Nemours Children's Clinic-Jacksonville
      • Miami, Florida, 미국, 33155
        • Nicklaus Children's Hospital
      • Miami, Florida, 미국, 33136
        • University of Miami Miller School of Medicine-Sylvester Cancer Center
      • Miami, Florida, 미국, 33176
        • Miami Cancer Institute
      • Orlando, Florida, 미국, 32827
        • Nemours Children's Hospital
      • Orlando, Florida, 미국, 32803
        • AdventHealth Orlando
      • Orlando, Florida, 미국, 32806
        • Arnold Palmer Hospital for Children
      • Pensacola, Florida, 미국, 32504
        • Nemours Children's Clinic - Pensacola
      • St. Petersburg, Florida, 미국, 33701
        • Johns Hopkins All Children's Hospital
      • Tampa, Florida, 미국, 33607
        • Saint Joseph's Hospital/Children's Hospital-Tampa
    • Georgia
      • Atlanta, Georgia, 미국, 30329
        • Children's Healthcare of Atlanta - Arthur M Blank Hospital
      • Augusta, Georgia, 미국, 30912
        • Augusta University Medical Center
      • Savannah, Georgia, 미국, 31404
        • Memorial Health University Medical Center
    • Hawaii
      • Honolulu, Hawaii, 미국, 96826
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    • Idaho
      • Boise, Idaho, 미국, 83712
        • Saint Luke's Cancer Institute - Boise
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      • Chicago, Illinois, 미국, 60611
        • Northwestern University
      • Chicago, Illinois, 미국, 60637
        • University of Chicago Comprehensive Cancer Center
      • Chicago, Illinois, 미국, 60612
        • University of Illinois
      • Chicago, Illinois, 미국, 60611
        • Lurie Children's Hospital-Chicago
      • Peoria, Illinois, 미국, 61637
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      • Springfield, Illinois, 미국, 62702
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    • Indiana
      • Indianapolis, Indiana, 미국, 46202
        • Riley Hospital for Children
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      • Des Moines, Iowa, 미국, 50309
        • Blank Children's Hospital
      • Iowa City, Iowa, 미국, 52242
        • University of Iowa/Holden Comprehensive Cancer Center
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      • Lexington, Kentucky, 미국, 40536
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      • Louisville, Kentucky, 미국, 40202
        • Norton Children's Hospital
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      • New Orleans, Louisiana, 미국, 70121
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      • New Orleans, Louisiana, 미국, 70118
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      • Bangor, Maine, 미국, 04401
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      • Scarborough, Maine, 미국, 04074
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      • Baltimore, Maryland, 미국, 21215
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      • Bethesda, Maryland, 미국, 20889-5600
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    • Massachusetts
      • Boston, Massachusetts, 미국, 02215
        • Dana-Farber Cancer Institute
      • Boston, Massachusetts, 미국, 02114
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      • Worcester, Massachusetts, 미국, 01655
        • UMass Memorial Medical Center - University Campus
    • Michigan
      • Ann Arbor, Michigan, 미국, 48109
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      • Ann Arbor, Michigan, 미국, 48109
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        • Henry Ford Cancer Institute-Downriver
      • Clinton Township, Michigan, 미국, 48038
        • Henry Ford Macomb Hospital-Clinton Township
      • Dearborn, Michigan, 미국, 48126
        • Henry Ford Medical Center-Fairlane
      • Detroit, Michigan, 미국, 48202
        • Henry Ford Hospital
      • Detroit, Michigan, 미국, 48201
        • Children's Hospital of Michigan
      • Grand Rapids, Michigan, 미국, 49503
        • Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital
      • Jackson, Michigan, 미국, 49201
        • Allegiance Health
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      • Novi, Michigan, 미국, 48377
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        • Henry Ford West Bloomfield Hospital
      • Wyandotte, Michigan, 미국, 48192
        • Henry Ford Wyandotte Hospital
    • Minnesota
      • Minneapolis, Minnesota, 미국, 55404
        • Children's Hospitals and Clinics of Minnesota - Minneapolis
      • Minneapolis, Minnesota, 미국, 55455
        • University of Minnesota/Masonic Cancer Center
      • Rochester, Minnesota, 미국, 55905
        • Mayo Clinic in Rochester
    • Mississippi
      • Jackson, Mississippi, 미국, 39216
        • University of Mississippi Medical Center
    • Missouri
      • Columbia, Missouri, 미국, 65212
        • University of Missouri Children's Hospital
      • Kansas City, Missouri, 미국, 64108
        • Children's Mercy Hospitals and Clinics
      • St Louis, Missouri, 미국, 63110
        • Washington University School of Medicine
      • St Louis, Missouri, 미국, 63141
        • Mercy Hospital Saint Louis
      • St Louis, Missouri, 미국, 63104
        • Cardinal Glennon Children's Medical Center
    • Nebraska
      • Omaha, Nebraska, 미국, 68198
        • University of Nebraska Medical Center
      • Omaha, Nebraska, 미국, 68114
        • Children's Hospital and Medical Center of Omaha
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      • Las Vegas, Nevada, 미국, 89144
        • Summerlin Hospital Medical Center
      • Las Vegas, Nevada, 미국, 89135
        • Alliance for Childhood Diseases/Cure 4 the Kids Foundation
    • New Hampshire
      • Lebanon, New Hampshire, 미국, 03756
        • Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center
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      • Hackensack, New Jersey, 미국, 07601
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      • Morristown, New Jersey, 미국, 07960
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        • Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital
      • Newark, New Jersey, 미국, 07112
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      • Paterson, New Jersey, 미국, 07503
        • Saint Joseph's Regional Medical Center
    • New York
      • Albany, New York, 미국, 12208
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      • Buffalo, New York, 미국, 14263
        • Roswell Park Cancer Institute
      • Mineola, New York, 미국, 11501
        • NYU Langone Hospital - Long Island
      • New Hyde Park, New York, 미국, 11040
        • The Steven and Alexandra Cohen Children's Medical Center of New York
      • New York, New York, 미국, 10065
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      • New York, New York, 미국, 10032
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      • New York, New York, 미국, 10065
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      • New York, New York, 미국, 10016
        • Laura and Isaac Perlmutter Cancer Center at NYU Langone
      • Rochester, New York, 미국, 14642
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      • Syracuse, New York, 미국, 13210
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      • The Bronx, New York, 미국, 10467
        • Montefiore Medical Center - Moses Campus
      • Valhalla, New York, 미국, 10595
        • New York Medical College
    • North Carolina
      • Chapel Hill, North Carolina, 미국, 27599
        • UNC Lineberger Comprehensive Cancer Center
      • Charlotte, North Carolina, 미국, 28203
        • Carolinas Medical Center/Levine Cancer Institute
      • Charlotte, North Carolina, 미국, 28204
        • Novant Health Presbyterian Medical Center
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    • North Dakota
      • Fargo, North Dakota, 미국, 58122
        • Sanford Broadway Medical Center
    • Ohio
      • Akron, Ohio, 미국, 44308
        • Children's Hospital Medical Center of Akron
      • Cincinnati, Ohio, 미국, 45229
        • Cincinnati Children's Hospital Medical Center
      • Cleveland, Ohio, 미국, 44195
        • Cleveland Clinic Foundation
      • Cleveland, Ohio, 미국, 44106
        • Rainbow Babies and Childrens Hospital
      • Columbus, Ohio, 미국, 43205
        • Nationwide Children's Hospital
      • Columbus, Ohio, 미국, 43210
        • Ohio State University Comprehensive Cancer Center
      • Dayton, Ohio, 미국, 45404
        • Dayton Children's Hospital
      • Toledo, Ohio, 미국, 43606
        • ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital
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      • Oklahoma City, Oklahoma, 미국, 73104
        • University of Oklahoma Health Sciences Center
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      • Portland, Oregon, 미국, 97239
        • Oregon Health and Science University
      • Portland, Oregon, 미국, 97227
        • Legacy Emanuel Children's Hospital
    • Pennsylvania
      • Danville, Pennsylvania, 미국, 17822
        • Geisinger Medical Center
      • Hershey, Pennsylvania, 미국, 17033
        • Penn State Children's Hospital
      • Philadelphia, Pennsylvania, 미국, 19104
        • Children's Hospital of Philadelphia
      • Philadelphia, Pennsylvania, 미국, 19107
        • Thomas Jefferson University Hospital
      • Philadelphia, Pennsylvania, 미국, 19134
        • Saint Christopher's Hospital for Children
      • Pittsburgh, Pennsylvania, 미국, 15232
        • UPMC Hillman Cancer Center
      • Pittsburgh, Pennsylvania, 미국, 15224
        • Children's Hospital of Pittsburgh of UPMC
    • South Carolina
      • Charleston, South Carolina, 미국, 29425
        • Medical University of South Carolina
      • Columbia, South Carolina, 미국, 29203
        • Prisma Health Richland Hospital
      • Gaffney, South Carolina, 미국, 29341
        • Gibbs Cancer Center-Gaffney
      • Greenville, South Carolina, 미국, 29607
        • Saint Francis Cancer Center
      • Greenville, South Carolina, 미국, 29601
        • Saint Francis Hospital
      • Greenville, South Carolina, 미국, 29605
        • BI-LO Charities Children's Cancer Center
      • Greer, South Carolina, 미국, 29651
        • Gibbs Cancer Center-Pelham
      • Spartanburg, South Carolina, 미국, 29303
        • Spartanburg Medical Center
    • South Dakota
      • Sioux Falls, South Dakota, 미국, 57117-5134
        • Sanford USD Medical Center - Sioux Falls
    • Tennessee
      • Knoxville, Tennessee, 미국, 37916
        • East Tennessee Childrens Hospital
      • Memphis, Tennessee, 미국, 38105
        • Saint Jude Children's Research Hospital
      • Nashville, Tennessee, 미국, 37232
        • Vanderbilt University/Ingram Cancer Center
      • Nashville, Tennessee, 미국, 37203
        • The Children's Hospital at TriStar Centennial
    • Texas
      • Austin, Texas, 미국, 78723
        • Dell Children's Medical Center of Central Texas
      • Corpus Christi, Texas, 미국, 78411
        • Driscoll Children's Hospital
      • Dallas, Texas, 미국, 75390
        • UT Southwestern/Simmons Cancer Center-Dallas
      • Dallas, Texas, 미국, 75230
        • Medical City Dallas Hospital
      • El Paso, Texas, 미국, 79905
        • El Paso Children's Hospital
      • Fort Worth, Texas, 미국, 76104
        • Cook Children's Medical Center
      • Houston, Texas, 미국, 77030
        • UT MD Anderson Cancer Center
      • Houston, Texas, 미국, 77030
        • Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center
      • Lubbock, Texas, 미국, 79410
        • Covenant Children's Hospital
      • Lubbock, Texas, 미국, 79415
        • UMC Cancer Center / UMC Health System
      • San Antonio, Texas, 미국, 78229
        • University of Texas Health Science Center at San Antonio
      • San Antonio, Texas, 미국, 78207
        • Children's Hospital of San Antonio
      • San Antonio, Texas, 미국, 78229
        • Methodist Children's Hospital of South Texas
      • Temple, Texas, 미국, 76508
        • Scott and White Memorial Hospital
    • Utah
      • Salt Lake City, Utah, 미국, 84113
        • Primary Children's Hospital
    • Virginia
      • Charlottesville, Virginia, 미국, 22908
        • University of Virginia Cancer Center
      • Norfolk, Virginia, 미국, 23507
        • Children's Hospital of The King's Daughters
      • Richmond, Virginia, 미국, 23235
        • VCU Massey Cancer Center at Stony Point
      • Richmond, Virginia, 미국, 23298
        • VCU Massey Comprehensive Cancer Center
    • Washington
      • Seattle, Washington, 미국, 98105
        • Seattle Children's Hospital
      • Spokane, Washington, 미국, 99204
        • Providence Sacred Heart Medical Center and Children's Hospital
      • Tacoma, Washington, 미국, 98405
        • Mary Bridge Children's Hospital and Health Center
      • Tacoma, Washington, 미국, 98431
        • Madigan Army Medical Center
    • West Virginia
      • Charleston, West Virginia, 미국, 25304
        • Vandalia Health/CAMC Institute for Academic Medicine
    • Wisconsin
      • Green Bay, Wisconsin, 미국, 54301
        • Saint Vincent Hospital Cancer Center Green Bay
      • Madison, Wisconsin, 미국, 53792
        • University of Wisconsin Carbone Cancer Center - University Hospital
      • Marshfield, Wisconsin, 미국, 54449
        • Marshfield Medical Center-Marshfield
      • Milwaukee, Wisconsin, 미국, 53226
        • Children's Hospital of Wisconsin
  • 캐나다
      • Québec, 캐나다, G1V 4G2
        • CHU de Quebec-Centre Hospitalier de l'Universite Laval (CHUL)
    • Alberta
      • Calgary, Alberta, 캐나다, T3B 6A8
        • Alberta Children's Hospital
      • Edmonton, Alberta, 캐나다, T6G 2B7
        • University of Alberta Hospital
    • Manitoba
      • Winnipeg, Manitoba, 캐나다, R3E 0V9
        • CancerCare Manitoba
    • Nova Scotia
      • Halifax, Nova Scotia, 캐나다, B3K 6R8
        • IWK Health Centre
    • Ontario
      • London, Ontario, 캐나다, N6A 5W9
        • Children's Hospital
      • Ottawa, Ontario, 캐나다, K1H 8L1
        • Children's Hospital of Eastern Ontario
      • Toronto, Ontario, 캐나다, M5G 1X8
        • Hospital for Sick Children
    • Quebec
      • Montreal, Quebec, 캐나다, H3H 1P3
        • The Montreal Children's Hospital of the MUHC
      • Montreal, Quebec, 캐나다, H3T 1C5
        • Centre Hospitalier Universitaire Sainte-Justine
      • Sherbrooke, Quebec, 캐나다, J1H 5N4
        • Centre Hospitalier Universitaire de Sherbrooke-Fleurimont
    • Saskatchewan
      • Saskatoon, Saskatchewan, 캐나다, S7N 0W8
        • Jim Pattison Children's Hospital
  • 호주
    • New South Wales
      • Randwick, New South Wales, 호주, 2031
        • Sydney Children's Hospital
      • Westmead, New South Wales, 호주, 2145
        • The Children's Hospital at Westmead
    • Queensland
      • South Brisbane, Queensland, 호주, 4101
        • Queensland Children's Hospital
    • South Australia
      • North Adelaide, South Australia, 호주, 5006
        • Women's and Children's Hospital-Adelaide
    • Victoria
      • Clayton, Victoria, 호주, 3168
        • Monash Medical Center-Clayton Campus
      • Parkville, Victoria, 호주, 3052
        • Royal Children's Hospital
    • Western Australia
      • Perth, Western Australia, 호주, 6009
        • Perth Children's Hospital

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

40년 이하 (어린이, 성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • Patients must be < 40 years of age at the time of enrollment.
  • Patients must have a body surface area of >= 0.8 m^2 at the time of enrollment.
  • Patients must have histologic diagnosis (by institutional pathologist) of newly diagnosed high grade osteosarcoma. Primary tumors of all extremity and axial sites are eligible as long as diagnosis of high-grade osteosarcoma is established. Osteosarcoma as a second malignancy is eligible if no prior exposure to systemic chemotherapies.
  • Feasibility Phase (NOTE: as of Amendment #2B, the feasibility phase has been completed) Patients must have metastatic disease and a resectable primary tumor. Designation of a primary tumor as resectable will be determined at the time of diagnosis by the institutional multidisciplinary team.

For this study, metastatic disease is defined as one or more of the following:

  • Lesions which are discontinuous from the primary tumor, are not regional lymph nodes, and do not share a bone or body cavity with the primary tumor. Skip lesions in the same bone as the primary tumor do not constitute metastatic disease. Skip lesions in an adjacent bone are considered bone metastases.

  • Lung metastases: defined as biopsy-proven metastasis or the presence of one or more pulmonary lesions >= 5 mm, OR multiple pulmonary lesions >= 3 mm or greater in size.

  • Bone metastases: Areas suspicious for bone metastasis based on fludeoxyglucose F-18 (18F-FDG)-positron emission tomography (PET) scan (or whole body technetium-99 bone scan if 18F-FDG-PET is unavailable at the treating institution) require confirmatory biopsy or supportive anatomic imaging of at least one suspicious site with either magnetic resonance imaging (MRI) or computed tomography (CT) (whole body 18F-FDG-PET/CT or 18F-FDG-PET/MR scans are acceptable).

    • Efficacy Phases (Phase 2/3) NOTE: as of Amendment #2B, the efficacy phase is open for enrollment.

Patients with both localized and metastatic disease are eligible for the efficacy phase, regardless of resectability. Patients will be enrolled to two separate cohorts:

  • Cohort 1 (Standard Risk): Patients with non-pelvic primary osteosarcoma deemed to be resectable at the time of diagnosis by the institutional multidisciplinary team, without evidence of metastatic lesions.

  • Cohort 2 (High-Risk): Patients with a primary pelvic tumor, a primary tumor designated as unresectable by the institutional multidisciplinary team, AND/OR radiographic evidence of metastatic lesions.

    • A serum creatinine based on age/sex as follows (within 7 days prior to enrollment unless otherwise indicated):

  • (Age: Maximum Serum Creatinine [mg/dL]; Sex)

    • 1 month to < 6 months: 0.4 (male); 0.4 (female)
    • 6 months to < 1 year: 0.5 (male); 0.5 (female)
    • 1 to < 2 years: 0.6 (male); 0.6 (female)
    • 2 to < 6 years: 0.8 (male); 0.8 (female)
    • 6 to < 10 years: 1 (male); 1 (female)
    • 10 to < 13 years: 1.2 (male); 1.2 (female)
    • 13 to < 16 years: 1.5 (male); 1.4 (female)
    • >= 16 years: 1.7 (male); 1.4 (female)

  • OR - a 24 hour urine creatinine clearance >= 70 mL/min/1.73 m^2

  • OR - a glomerular filtration rate (GFR) >= 70 mL/min/1.73 m^2. GFR must be performed using direct measurement with a nuclear blood sampling method OR direct small molecule clearance method (iothalamate or other molecule per institutional standard).

    • Note: Estimated GFR (eGFR) from serum creatinine, cystatin C or other estimates are not acceptable for determining eligibility.

      • Total bilirubin =< 1.5 x upper limit of normal (ULN) for age (within 7 days prior to enrollment unless otherwise indicated)
      • Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase [ALT]) =< 135 U/L (within 7 days prior to enrollment unless otherwise indicated)

  • Note: For the purpose of this study, the ULN for SGPT (ALT) has been set to the value of 45 U/L

    • No history of congenital prolonged corrected QT (QTc) syndrome, New York Heart Association (NYHA) Class III or IV congestive heart failure, unstable angina pectoris, serious cardiac arrhythmias

  • Shortening fraction of >= 27%, or

  • Ejection fraction of >= 50%

  • Corrected QT interval by Fridericia (QTcF) < 480 msec on electrocardiogram. Patients with Grade 1 prolonged QTc (450-480 msec) at time of study enrollment should have correctable causes of prolonged QTc addressed if possible (i.e., electrolytes, medications).

    • Peripheral absolute neutrophil count (ANC) >= 1000/uL (within 7 days prior to enrollment unless otherwise indicated)
    • Platelet count >= 100,000/uL (transfusion independent, defined as not receiving platelet transfusions within a 7-day period prior to enrollment) (within 7 days prior to enrollment unless otherwise indicated)
    • Hemoglobin >= 8.0 g/dL (within 7 days prior to enrollment unless otherwise indicated)
    • International normalized ratio (INR) =< 1.5 (within 7 days prior to enrollment unless otherwise indicated)
    • Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible as long as they are NOT receiving anti-retroviral agents that are strong inhibitors or inducers of CYP3A4, CYP2D6, and/or MRP2 transporter protein.
    • All patients and/or their parents or legal guardians must sign a written informed consent.
    • All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met.

Exclusion Criteria:

  • Patients who have received previous systemic therapy for osteosarcoma or a prior oncologic diagnosis.
  • Patients who have central nervous system metastases.
  • Patients with central cavitating pulmonary lesions invading or encasing any major blood vessels in the lung.
  • Patients who are unable to swallow tablets. Tablets cannot be crushed or chewed.
  • Patients with gastrointestinal disorders including active disorders associated with a high risk of perforation or fistula formation. Specifically, no clinically significant gastrointestinal (GI) bleeding, GI perforation, bowel obstruction, intra-abdominal abscess or fistula for 6 months prior to enrollment, no hemoptysis or other signs of pulmonary hemorrhage for 3 months prior to enrollment.
  • Patients with active bleeding or bleeding diathesis. No clinically significant hematuria, hematemesis, or hemoptysis or other history of significant bleeding within 3 months prior to enrollment.
  • Patients with uncompensated or symptomatic hypothyroidism. Patients who have hypothyroidism controlled with thyroid replacement hormone are eligible.
  • Patients with moderate to severe hepatic impairment (Child-Pugh B or C).
  • Patients who have had primary tumor resection or attempted curative resection of metastases prior to enrollment.
  • Patients who have undergone other major surgical procedure (eg, laparotomy) within 14 days prior to enrollment. Thoracoscopic procedures for diagnostic purposes (biopsy of lung nodule) and central access such as port-a-cath placement are allowed.
  • Patients with a history of serious or non-healing wound or bone fracture (pathologic fracture of primary tumor is not considered exclusion).
  • Patients with any medical or surgical conditions that would interfere with gastrointestinal absorption of cabozantinib.
  • Patients with previously identify allergy or hypersensitivity to components of the study treatment formulations.
  • Patients who are receiving any other investigational agent not defined within this protocol are not eligible.
  • Patients who in the opinion of the investigator may not be able to comply with the safety monitoring requirements of the study are not eligible.
  • Patients who received enzyme-inducing anticonvulsants within 14 days prior to enrollment.
  • Patients with a prior history of hypertension (> 95th percentile for age, height, and sex for patients < 18 years and > 140/90 mmHg for patients >= 18 years requiring medication for blood pressure control.
  • Patients who are receiving drugs that prolong QTc.
  • Patients receiving anticoagulation with oral coumarin agents (eg warfarin), direct thrombin inhibitors (eg dabigatran), direct factor Xa inhibitor betrixaban, or platelet inhibitors (eg, clopidogrel). Low dose aspirin for cardioprotection (per local applicable guidelines) and low dose, low molecular weight heparins (LMWH) are permitted. Anticoagulation with therapeutic doses of LMWH and direct factor Xa inhibitors rivaroxaban or apixaban are allowed in subjects who are on a stable dose for at least 6 weeks before the first dose of study treatment, and who have had no complications from a thromboembolic event or the anticoagulation regimen.
  • Patients receiving strong CYP3A4 inducers or strong CYP3A4 inhibitors.
  • Female patients who are pregnant since fetal toxicities and teratogenic effects have been noted for several of the study drugs. A pregnancy test is required for female patients of childbearing potential.
  • Lactating females who plan to breastfeed their infants.
  • Sexually active patients of reproductive potential who have not agreed to use an effective contraceptive method for the duration of protocol therapy.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 순차적 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
활성 비교기: Efficacy Phase Arm A (MAP)

Standard risk patients receive methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles, followed by appropriate local control. Patients then receive "consolidation" with methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day cycles and methotrexate IV and doxorubicin IV for two additional 35-day cycles. Patients also undergo X-ray, CT, MRI, and PET or bone scintigraphy at diagnosis and additional time points throughout the trial. All patients also undergo collection of blood samples during screening and on study.
의약품: Doxorubicin Hydrochloride

Given IV

다른 이름들:
  • 아드리아마이신
  • 5,12-나프타세네디온, 10-[(3-아미노-2,3,6-트리데옥시-알파-L-릭소-헥소피라노실)옥시]-7,8,9,10-테트라히드로-6,8,11-트리히드록시 -8-(히드록시아세틸)-1-메톡시-, 염산염, (8S-cis)-(9CI)
  • ADM
  • 아드리아신
  • 아드리아마이신 염산염
  • 아드리아마이신 PFS
  • 아드리아마이신 RDF
  • 아드리아마이신, 염화수소
  • 아드리블라스티나
  • 아드리블라스틴
  • 아드리메닥
  • 클로리드라토 데 독소루비시나
  • DOX
  • 독소셀
  • 독소렘
  • 독소루비신 HCl
  • 독소루비신.HCl
  • 독소루빈
  • 파미블라스티나
  • FI 106
  • FI-106
  • 하이드록시다우노루비신
  • 루벡스
  • FI106
의약품: Cisplatin

Given IV

다른 이름들:
  • CDDP
  • 시스-디암민디클로리도백금
  • 시스마플라트
  • 시스플라티넘
  • 네오플라틴
  • 플라티놀
  • 아비플라틴
  • 블라스톨렘
  • 브리플라틴
  • 시스-디아민-디클로로백금
  • 시스-디아민디클로로 백금(II)
  • 시스-디아민디클로로백금
  • 시스-디클로로암민 백금(II)
  • 시스-백금 디아민 디클로라이드
  • 시스-백금
  • 시스-백금 II
  • 시스-백금 II 디아민 디클로라이드
  • 시스플라티나
  • 시스플라틸
  • 치토플라티노
  • 시토신
  • DDP
  • 레더플라틴
  • 메타플라틴
  • Peyrone의 염화물
  • 페이론의 소금
  • 플라시스
  • 플라스티스틸
  • 플라타민
  • 플라티블라스틴
  • 플라티블라스틴-S
  • 플래티넥스
  • 플라티놀-AQ
  • 플라티놀-AQ VHA 플러스
  • 플라티녹산
  • 백금
  • 백금 디암미노디클로라이드
  • 플라티란
  • 플라티스틴
  • 플라토신
의약품: Methotrexate

Given IV

다른 이름들:
  • 아비트렉세이트
  • 폴렉스
  • 멕세이트
  • MTX
  • 알파-메토프테린
  • 아메토프테린
  • 브라멕세이트
  • CL 14377
  • CL-14377
  • Emtexate
  • Emthexat
  • Emthexate
  • 파미트렉사트
  • 폴덱사토
  • 폴렉스 PFS
  • 란타렐
  • 레더트렉세이트
  • 루멕슨
  • 맥스렉스
  • 메드사트렉세이트
  • 메텍스
  • 메토블라스틴
  • 메토트렉세이트 LPF
  • 메토트렉세이트 메틸아미노프테린
  • 메토트렉사툼
  • 메토트렉사토
  • 메트로텍스
  • 멕세이트-AQ
  • 노바트렉스
  • 류마트렉스
  • 텍세이트
  • 트레메텍스
  • 트렉세론
  • 트리실렘
  • WR-19039
  • 질람보
절차: Computed Tomography

Undergo CT

다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
절차: Magnetic Resonance Imaging

Undergo MRI

다른 이름들:
  • MRI
  • 자기 공명
  • 자기공명영상 스캔
  • 의료영상, 자기공명 / 핵자기공명
  • 씨
  • MR 이미징
  • MRI 검사
  • NMR 이미징
  • NMRI
  • 핵자기공명영상
  • 자기공명영상(MRI)
  • SMRI
  • 자기공명영상(시술)
  • 구조적 MRI
절차: Surgical Procedure

Undergo surgery

다른 이름들:
  • 작업
  • 수술
  • 수술 종류
  • 외과
  • 외과 개입
  • 수술 절차
  • 수술의 종류
  • 수술, NOS
절차: Bone Scan

Undergo bone scintography

다른 이름들:
  • 뼈 신티그래피
절차: X-Ray Imaging

Undergo X-ray

다른 이름들:
  • 기존 엑스레이
  • 진단 방사선과
  • 의료 영상, 엑스레이
  • 방사선 촬영
  • RG
  • 정적 엑스레이
  • 엑스레이
  • 일반 필름 방사선 사진
  • 방사선 촬영 절차(시술)
실험적: Efficacy Phase Arm B (cabozantinib, MAP)

Standard risk patients receive cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles, followed by appropriate local control. Patients then receive one 35-day "consolidation" cycle with methotrexate IV, doxorubicin IV, and cisplatin IV, then a second 35-day "consolidation" cycle with cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV, followed by two additional 35-day "consolidation" cycles with cabozantinib PO, methotrexate IV, and doxorubicin IV. Patients then receive cabozantinib PO for six 28-day "maintenance" cycles. Patients also undergo X-ray, CT, MRI, and PET or bone scintigraphy at diagnosis and additional time points throughout the trial. All patients also undergo collection of blood samples during screening and on study.
의약품: Doxorubicin Hydrochloride

Given IV

다른 이름들:
  • 아드리아마이신
  • 5,12-나프타세네디온, 10-[(3-아미노-2,3,6-트리데옥시-알파-L-릭소-헥소피라노실)옥시]-7,8,9,10-테트라히드로-6,8,11-트리히드록시 -8-(히드록시아세틸)-1-메톡시-, 염산염, (8S-cis)-(9CI)
  • ADM
  • 아드리아신
  • 아드리아마이신 염산염
  • 아드리아마이신 PFS
  • 아드리아마이신 RDF
  • 아드리아마이신, 염화수소
  • 아드리블라스티나
  • 아드리블라스틴
  • 아드리메닥
  • 클로리드라토 데 독소루비시나
  • DOX
  • 독소셀
  • 독소렘
  • 독소루비신 HCl
  • 독소루비신.HCl
  • 독소루빈
  • 파미블라스티나
  • FI 106
  • FI-106
  • 하이드록시다우노루비신
  • 루벡스
  • FI106
의약품: Cisplatin

Given IV

다른 이름들:
  • CDDP
  • 시스-디암민디클로리도백금
  • 시스마플라트
  • 시스플라티넘
  • 네오플라틴
  • 플라티놀
  • 아비플라틴
  • 블라스톨렘
  • 브리플라틴
  • 시스-디아민-디클로로백금
  • 시스-디아민디클로로 백금(II)
  • 시스-디아민디클로로백금
  • 시스-디클로로암민 백금(II)
  • 시스-백금 디아민 디클로라이드
  • 시스-백금
  • 시스-백금 II
  • 시스-백금 II 디아민 디클로라이드
  • 시스플라티나
  • 시스플라틸
  • 치토플라티노
  • 시토신
  • DDP
  • 레더플라틴
  • 메타플라틴
  • Peyrone의 염화물
  • 페이론의 소금
  • 플라시스
  • 플라스티스틸
  • 플라타민
  • 플라티블라스틴
  • 플라티블라스틴-S
  • 플래티넥스
  • 플라티놀-AQ
  • 플라티놀-AQ VHA 플러스
  • 플라티녹산
  • 백금
  • 백금 디암미노디클로라이드
  • 플라티란
  • 플라티스틴
  • 플라토신
의약품: Methotrexate

Given IV

다른 이름들:
  • 아비트렉세이트
  • 폴렉스
  • 멕세이트
  • MTX
  • 알파-메토프테린
  • 아메토프테린
  • 브라멕세이트
  • CL 14377
  • CL-14377
  • Emtexate
  • Emthexat
  • Emthexate
  • 파미트렉사트
  • 폴덱사토
  • 폴렉스 PFS
  • 란타렐
  • 레더트렉세이트
  • 루멕슨
  • 맥스렉스
  • 메드사트렉세이트
  • 메텍스
  • 메토블라스틴
  • 메토트렉세이트 LPF
  • 메토트렉세이트 메틸아미노프테린
  • 메토트렉사툼
  • 메토트렉사토
  • 메트로텍스
  • 멕세이트-AQ
  • 노바트렉스
  • 류마트렉스
  • 텍세이트
  • 트레메텍스
  • 트렉세론
  • 트리실렘
  • WR-19039
  • 질람보
절차: Computed Tomography

Undergo CT

다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
절차: Magnetic Resonance Imaging

Undergo MRI

다른 이름들:
  • MRI
  • 자기 공명
  • 자기공명영상 스캔
  • 의료영상, 자기공명 / 핵자기공명
  • 씨
  • MR 이미징
  • MRI 검사
  • NMR 이미징
  • NMRI
  • 핵자기공명영상
  • 자기공명영상(MRI)
  • SMRI
  • 자기공명영상(시술)
  • 구조적 MRI
의약품: Cabozantinib S-malate

Given PO

다른 이름들:
  • BMS-907351
  • 카보메틱스
  • 코메트릭
  • XL-184
  • XL184
  • 특대형 184
절차: Surgical Procedure

Undergo surgery

다른 이름들:
  • 작업
  • 수술
  • 수술 종류
  • 외과
  • 외과 개입
  • 수술 절차
  • 수술의 종류
  • 수술, NOS
절차: Bone Scan

Undergo bone scintography

다른 이름들:
  • 뼈 신티그래피
절차: X-Ray Imaging

Undergo X-ray

다른 이름들:
  • 기존 엑스레이
  • 진단 방사선과
  • 의료 영상, 엑스레이
  • 방사선 촬영
  • RG
  • 정적 엑스레이
  • 엑스레이
  • 일반 필름 방사선 사진
  • 방사선 촬영 절차(시술)
활성 비교기: Efficacy Phase Arm C (MAP)

High risk patients receive methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles, followed by appropriate local control. Patients then receive "consolidation" with methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day cycles and methotrexate IV and doxorubicin IV for two additional 35-day cycles. Patients also undergo X-ray, CT, MRI, and PET or bone scintigraphy at diagnosis and additional time points throughout the trial. All patients also undergo collection of blood samples during screening and on study.
의약품: Doxorubicin Hydrochloride

Given IV

다른 이름들:
  • 아드리아마이신
  • 5,12-나프타세네디온, 10-[(3-아미노-2,3,6-트리데옥시-알파-L-릭소-헥소피라노실)옥시]-7,8,9,10-테트라히드로-6,8,11-트리히드록시 -8-(히드록시아세틸)-1-메톡시-, 염산염, (8S-cis)-(9CI)
  • ADM
  • 아드리아신
  • 아드리아마이신 염산염
  • 아드리아마이신 PFS
  • 아드리아마이신 RDF
  • 아드리아마이신, 염화수소
  • 아드리블라스티나
  • 아드리블라스틴
  • 아드리메닥
  • 클로리드라토 데 독소루비시나
  • DOX
  • 독소셀
  • 독소렘
  • 독소루비신 HCl
  • 독소루비신.HCl
  • 독소루빈
  • 파미블라스티나
  • FI 106
  • FI-106
  • 하이드록시다우노루비신
  • 루벡스
  • FI106
의약품: Cisplatin

Given IV

다른 이름들:
  • CDDP
  • 시스-디암민디클로리도백금
  • 시스마플라트
  • 시스플라티넘
  • 네오플라틴
  • 플라티놀
  • 아비플라틴
  • 블라스톨렘
  • 브리플라틴
  • 시스-디아민-디클로로백금
  • 시스-디아민디클로로 백금(II)
  • 시스-디아민디클로로백금
  • 시스-디클로로암민 백금(II)
  • 시스-백금 디아민 디클로라이드
  • 시스-백금
  • 시스-백금 II
  • 시스-백금 II 디아민 디클로라이드
  • 시스플라티나
  • 시스플라틸
  • 치토플라티노
  • 시토신
  • DDP
  • 레더플라틴
  • 메타플라틴
  • Peyrone의 염화물
  • 페이론의 소금
  • 플라시스
  • 플라스티스틸
  • 플라타민
  • 플라티블라스틴
  • 플라티블라스틴-S
  • 플래티넥스
  • 플라티놀-AQ
  • 플라티놀-AQ VHA 플러스
  • 플라티녹산
  • 백금
  • 백금 디암미노디클로라이드
  • 플라티란
  • 플라티스틴
  • 플라토신
의약품: Methotrexate

Given IV

다른 이름들:
  • 아비트렉세이트
  • 폴렉스
  • 멕세이트
  • MTX
  • 알파-메토프테린
  • 아메토프테린
  • 브라멕세이트
  • CL 14377
  • CL-14377
  • Emtexate
  • Emthexat
  • Emthexate
  • 파미트렉사트
  • 폴덱사토
  • 폴렉스 PFS
  • 란타렐
  • 레더트렉세이트
  • 루멕슨
  • 맥스렉스
  • 메드사트렉세이트
  • 메텍스
  • 메토블라스틴
  • 메토트렉세이트 LPF
  • 메토트렉세이트 메틸아미노프테린
  • 메토트렉사툼
  • 메토트렉사토
  • 메트로텍스
  • 멕세이트-AQ
  • 노바트렉스
  • 류마트렉스
  • 텍세이트
  • 트레메텍스
  • 트렉세론
  • 트리실렘
  • WR-19039
  • 질람보
절차: Computed Tomography

Undergo CT

다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
절차: Magnetic Resonance Imaging

Undergo MRI

다른 이름들:
  • MRI
  • 자기 공명
  • 자기공명영상 스캔
  • 의료영상, 자기공명 / 핵자기공명
  • 씨
  • MR 이미징
  • MRI 검사
  • NMR 이미징
  • NMRI
  • 핵자기공명영상
  • 자기공명영상(MRI)
  • SMRI
  • 자기공명영상(시술)
  • 구조적 MRI
절차: Surgical Procedure

Undergo surgery

다른 이름들:
  • 작업
  • 수술
  • 수술 종류
  • 외과
  • 외과 개입
  • 수술 절차
  • 수술의 종류
  • 수술, NOS
절차: Bone Scan

Undergo bone scintography

다른 이름들:
  • 뼈 신티그래피
절차: X-Ray Imaging

Undergo X-ray

다른 이름들:
  • 기존 엑스레이
  • 진단 방사선과
  • 의료 영상, 엑스레이
  • 방사선 촬영
  • RG
  • 정적 엑스레이
  • 엑스레이
  • 일반 필름 방사선 사진
  • 방사선 촬영 절차(시술)
실험적: Efficacy Phase Arm D (cabozantinib, MAP)

High risk patients receive cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles, followed by appropriate local control. Patients then receive one 35-day "consolidation" cycle with methotrexate IV, doxorubicin IV, and cisplatin IV, then a second 35-day "consolidation" cycle with cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV, followed by two additional 35-day "consolidation" cycles with cabozantinib PO, methotrexate IV, and doxorubicin IV. Patients then receive cabozantinib PO for six 28-day "maintenance" cycles. Patients also undergo X-ray, CT, MRI, and PET or bone scintigraphy at diagnosis and additional time points throughout the trial. All patients also undergo collection of blood samples during screening and on study.
의약품: Doxorubicin Hydrochloride

Given IV

다른 이름들:
  • 아드리아마이신
  • 5,12-나프타세네디온, 10-[(3-아미노-2,3,6-트리데옥시-알파-L-릭소-헥소피라노실)옥시]-7,8,9,10-테트라히드로-6,8,11-트리히드록시 -8-(히드록시아세틸)-1-메톡시-, 염산염, (8S-cis)-(9CI)
  • ADM
  • 아드리아신
  • 아드리아마이신 염산염
  • 아드리아마이신 PFS
  • 아드리아마이신 RDF
  • 아드리아마이신, 염화수소
  • 아드리블라스티나
  • 아드리블라스틴
  • 아드리메닥
  • 클로리드라토 데 독소루비시나
  • DOX
  • 독소셀
  • 독소렘
  • 독소루비신 HCl
  • 독소루비신.HCl
  • 독소루빈
  • 파미블라스티나
  • FI 106
  • FI-106
  • 하이드록시다우노루비신
  • 루벡스
  • FI106
의약품: Cisplatin

Given IV

다른 이름들:
  • CDDP
  • 시스-디암민디클로리도백금
  • 시스마플라트
  • 시스플라티넘
  • 네오플라틴
  • 플라티놀
  • 아비플라틴
  • 블라스톨렘
  • 브리플라틴
  • 시스-디아민-디클로로백금
  • 시스-디아민디클로로 백금(II)
  • 시스-디아민디클로로백금
  • 시스-디클로로암민 백금(II)
  • 시스-백금 디아민 디클로라이드
  • 시스-백금
  • 시스-백금 II
  • 시스-백금 II 디아민 디클로라이드
  • 시스플라티나
  • 시스플라틸
  • 치토플라티노
  • 시토신
  • DDP
  • 레더플라틴
  • 메타플라틴
  • Peyrone의 염화물
  • 페이론의 소금
  • 플라시스
  • 플라스티스틸
  • 플라타민
  • 플라티블라스틴
  • 플라티블라스틴-S
  • 플래티넥스
  • 플라티놀-AQ
  • 플라티놀-AQ VHA 플러스
  • 플라티녹산
  • 백금
  • 백금 디암미노디클로라이드
  • 플라티란
  • 플라티스틴
  • 플라토신
의약품: Methotrexate

Given IV

다른 이름들:
  • 아비트렉세이트
  • 폴렉스
  • 멕세이트
  • MTX
  • 알파-메토프테린
  • 아메토프테린
  • 브라멕세이트
  • CL 14377
  • CL-14377
  • Emtexate
  • Emthexat
  • Emthexate
  • 파미트렉사트
  • 폴덱사토
  • 폴렉스 PFS
  • 란타렐
  • 레더트렉세이트
  • 루멕슨
  • 맥스렉스
  • 메드사트렉세이트
  • 메텍스
  • 메토블라스틴
  • 메토트렉세이트 LPF
  • 메토트렉세이트 메틸아미노프테린
  • 메토트렉사툼
  • 메토트렉사토
  • 메트로텍스
  • 멕세이트-AQ
  • 노바트렉스
  • 류마트렉스
  • 텍세이트
  • 트레메텍스
  • 트렉세론
  • 트리실렘
  • WR-19039
  • 질람보
절차: Computed Tomography

Undergo CT

다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
절차: Magnetic Resonance Imaging

Undergo MRI

다른 이름들:
  • MRI
  • 자기 공명
  • 자기공명영상 스캔
  • 의료영상, 자기공명 / 핵자기공명
  • 씨
  • MR 이미징
  • MRI 검사
  • NMR 이미징
  • NMRI
  • 핵자기공명영상
  • 자기공명영상(MRI)
  • SMRI
  • 자기공명영상(시술)
  • 구조적 MRI
의약품: Cabozantinib S-malate

Given PO

다른 이름들:
  • BMS-907351
  • 카보메틱스
  • 코메트릭
  • XL-184
  • XL184
  • 특대형 184
절차: Bone Scan

Undergo bone scintography

다른 이름들:
  • 뼈 신티그래피
절차: X-Ray Imaging

Undergo X-ray

다른 이름들:
  • 기존 엑스레이
  • 진단 방사선과
  • 의료 영상, 엑스레이
  • 방사선 촬영
  • RG
  • 정적 엑스레이
  • 엑스레이
  • 일반 필름 방사선 사진
  • 방사선 촬영 절차(시술)
실험적: Feasibility phase (cabozantinib, MAP)

(CLOSED TO ACCRUAL 05/09/2025): Patients receive cabozantinib orally (PO), methotrexate intravenously (IV), doxorubicin IV, and cisplatin IV for two 35-day "induction" cycles. Patients are then considered for appropriate local control. Then they receive "consolidation" with methotrexate IV, doxorubicin IV, and cisplatin IV for one 35-day cycle, followed by cabozantinib PO, methotrexate IV, doxorubicin IV, and cisplatin IV for one 35-day cycle, and cabozantinib PO, methotrexate IV, and doxorubicin IV for two 35-day cycles. Patients then receive cabozantinib PO for six 28-day "maintenance" cycles.
의약품: Doxorubicin Hydrochloride

Given IV

다른 이름들:
  • 아드리아마이신
  • 5,12-나프타세네디온, 10-[(3-아미노-2,3,6-트리데옥시-알파-L-릭소-헥소피라노실)옥시]-7,8,9,10-테트라히드로-6,8,11-트리히드록시 -8-(히드록시아세틸)-1-메톡시-, 염산염, (8S-cis)-(9CI)
  • ADM
  • 아드리아신
  • 아드리아마이신 염산염
  • 아드리아마이신 PFS
  • 아드리아마이신 RDF
  • 아드리아마이신, 염화수소
  • 아드리블라스티나
  • 아드리블라스틴
  • 아드리메닥
  • 클로리드라토 데 독소루비시나
  • DOX
  • 독소셀
  • 독소렘
  • 독소루비신 HCl
  • 독소루비신.HCl
  • 독소루빈
  • 파미블라스티나
  • FI 106
  • FI-106
  • 하이드록시다우노루비신
  • 루벡스
  • FI106
의약품: Cisplatin

Given IV

다른 이름들:
  • CDDP
  • 시스-디암민디클로리도백금
  • 시스마플라트
  • 시스플라티넘
  • 네오플라틴
  • 플라티놀
  • 아비플라틴
  • 블라스톨렘
  • 브리플라틴
  • 시스-디아민-디클로로백금
  • 시스-디아민디클로로 백금(II)
  • 시스-디아민디클로로백금
  • 시스-디클로로암민 백금(II)
  • 시스-백금 디아민 디클로라이드
  • 시스-백금
  • 시스-백금 II
  • 시스-백금 II 디아민 디클로라이드
  • 시스플라티나
  • 시스플라틸
  • 치토플라티노
  • 시토신
  • DDP
  • 레더플라틴
  • 메타플라틴
  • Peyrone의 염화물
  • 페이론의 소금
  • 플라시스
  • 플라스티스틸
  • 플라타민
  • 플라티블라스틴
  • 플라티블라스틴-S
  • 플래티넥스
  • 플라티놀-AQ
  • 플라티놀-AQ VHA 플러스
  • 플라티녹산
  • 백금
  • 백금 디암미노디클로라이드
  • 플라티란
  • 플라티스틴
  • 플라토신
의약품: Methotrexate

Given IV

다른 이름들:
  • 아비트렉세이트
  • 폴렉스
  • 멕세이트
  • MTX
  • 알파-메토프테린
  • 아메토프테린
  • 브라멕세이트
  • CL 14377
  • CL-14377
  • Emtexate
  • Emthexat
  • Emthexate
  • 파미트렉사트
  • 폴덱사토
  • 폴렉스 PFS
  • 란타렐
  • 레더트렉세이트
  • 루멕슨
  • 맥스렉스
  • 메드사트렉세이트
  • 메텍스
  • 메토블라스틴
  • 메토트렉세이트 LPF
  • 메토트렉세이트 메틸아미노프테린
  • 메토트렉사툼
  • 메토트렉사토
  • 메트로텍스
  • 멕세이트-AQ
  • 노바트렉스
  • 류마트렉스
  • 텍세이트
  • 트레메텍스
  • 트렉세론
  • 트리실렘
  • WR-19039
  • 질람보
절차: Computed Tomography

Undergo CT

다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
절차: Magnetic Resonance Imaging

Undergo MRI

다른 이름들:
  • MRI
  • 자기 공명
  • 자기공명영상 스캔
  • 의료영상, 자기공명 / 핵자기공명
  • 씨
  • MR 이미징
  • MRI 검사
  • NMR 이미징
  • NMRI
  • 핵자기공명영상
  • 자기공명영상(MRI)
  • SMRI
  • 자기공명영상(시술)
  • 구조적 MRI
의약품: Cabozantinib S-malate

Given PO

다른 이름들:
  • BMS-907351
  • 카보메틱스
  • 코메트릭
  • XL-184
  • XL184
  • 특대형 184
절차: Surgical Procedure

Undergo surgery

다른 이름들:
  • 작업
  • 수술
  • 수술 종류
  • 외과
  • 외과 개입
  • 수술 절차
  • 수술의 종류
  • 수술, NOS
절차: Bone Scan

Undergo bone scintography

다른 이름들:
  • 뼈 신티그래피
절차: X-Ray Imaging

Undergo X-ray

다른 이름들:
  • 기존 엑스레이
  • 진단 방사선과
  • 의료 영상, 엑스레이
  • 방사선 촬영
  • RG
  • 정적 엑스레이
  • 엑스레이
  • 일반 필름 방사선 사진
  • 방사선 촬영 절차(시술)

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Occurrence of dose-limiting toxicity (Feasibility)
기간: Baseline up to 6 weeks

Only patients with high risk osteosarcoma who have a primary tumor considered resectable at the time of enrollment will be enrolled to this part of the trial. If a feasible dose cannot be established, the study committee will consult with Children's Oncology Group leadership and National Cancer Institute Cancer Therapy Evaluation Program regarding possible modifications of the regimen and subsequent protocol amendment.
Baseline up to 6 weeks
Event-free survival (EFS) (Phase II)
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

The randomization and analysis will be stratified according to risk group. An assessment of the reduction in risk for EFS-event at the designated landmark time will be used to determine whether the trial continues to part 3. If the study proceeds to part 3, patients enrolled to part 2 of the trial will contribute to the primary analyses for part 3 of the study. If the interim criterion for continuation is not obtained, accrual will be closed with the conclusion that cabozantinib does not reduce sufficiently the risk for EFS-event for patients with newly-diagnosed osteosarcoma.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
EFS (Phase III)
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will consist of two randomized phase 3 sub-studies ('Phase 3'). One will be conducted in standard risk patients and one will be conducted in high risk patients.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
Overall survival
기간: From randomization until death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

The one-sided logrank test will be the primary statistical methodology for assessing the null statistical hypothesis. The assessment of the reduction in risk of EFS-event will be conducted in standard risk patients and high risk patients separately.
From randomization until death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

2차 결과 측정

결과 측정
측정값 설명
기간
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will validate whether elevated circulating tumor deoxyribonucleic acid (ctDNA) levels greater than or equal to 5% at the time of diagnosis are associated with increased risk of EFS-event in patients with localized, resectable osteosarcoma.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will validate whether elevated ctDNA levels greater than or equal to 5% at the time of diagnosis are associated with increased risk of EFS-event in patients with metastatic, pelvic and unresectable osteosarcoma.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will validate whether elevated ctDNA levels greater than or equal to 3% after initiation of therapy and prior to definitive surgery are associated with increased risk of EFS-event in patients with localized, resectable osteosarcoma.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will validate whether elevated ctDNA levels greater than or equal to 3% after initiation of therapy and prior to definitive surgery are associated with increased risk of EFS-event in patients with metastatic, pelvic and unresectable osteosarcoma.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
Change in symptom burden and tolerability
기간: Up to 5 years after completion of study treatment

Will determine whether methotrexate, doxorubicin, and cisplatin (MAP) chemotherapy plus cabozantinib results in increased symptom burden and decreased tolerability to patients as measured by patient reported therapy-specific acute toxicities (Patient-Reported Outcomes-Common Terminology Criteria for Adverse Events [PRO-CTCAE]).
Up to 5 years after completion of study treatment

기타 결과 측정

결과 측정
측정값 설명
기간
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will determine whether ctDNA at diagnosis and early on-treatment, as a continuous measurement of ctDNA burden, is associated with an increased risk of EFS-event in patients with newly diagnosed osteosarcoma.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will evaluate whether the magnitude of change in ctDNA levels from diagnosis to planned surgical procedure is associated with risk of EFS-event in patients with newly diagnosed osteosarcoma.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will determine whether ctDNA levels greater than or equal to 3% after planned surgical procedures are associated with increased risk of EFS-event.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment

Will describe the presence of specific copy-number alterations, including MYC amplifications, detected in ctDNA and matched diagnostic tumor samples in patients with newly diagnosed osteosarcoma and determine whether frequently occurring copy-number alterations are associated with increased risk of EFS-event.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 5 years after completion of study treatment
ctDNA burden
기간: Up to 5 years after completion of study treatment

Will determine whether ctDNA burden is predictive of response to the experimental therapy in patients with newly diagnosed osteosarcoma.
Up to 5 years after completion of study treatment
Impact of combination therapy on symptom bother
기간: Up to 5 years after completion of study treatment

Will prospectively compare the impact of combination therapy on symptom bother as measured by the Functional Assessment of Cancer Therapy-General Questionnaire item GP5 in patients with osteosarcoma receiving MAP chemotherapy with or without cabozantinib, and to assess the relationship between symptom bother and number of patient-reported acute toxicities (as measured by the PRO-CTCAE).
Up to 5 years after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 1 year after completion of study treatment

Estimates of 1-year EFS for standard risk (SR) and high risk (HR) patients on each Arm MAP and Arm cabozantinib (CABO)-MAP and the corresponding 95% confidence intervals (CIs) by sex.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 1 year after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 1 year after completion of study treatment

Estimates of 1-year EFS for SR and HR patients on each Arm MAP and Arm CABO-MAP and the corresponding 95% CIs by race.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 1 year after completion of study treatment
EFS
기간: From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 1 year after completion of study treatment

Estimates of 1-year EFS for SR and HR patients on each Arm MAP and Arm CABO-MAP and the corresponding 95% CIs by ethnicity.
From randomization until disease progression, relapse, diagnosis of a second malignant neoplasm, death or last contact, whichever occurs first, assessed up to 1 year after completion of study treatment

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

National Cancer Institute (NCI)

수사관

  • 수석 연구원: Michael W Bishop, Children's Oncology Group

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2023년 3월 3일

기본 완료 (추정된)

2030년 3월 20일

연구 완료 (추정된)

2030년 3월 20일

연구 등록 날짜

최초 제출

2023년 1월 18일

QC 기준을 충족하는 최초 제출

2023년 1월 18일

처음 게시됨 (실제)

2023년 1월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 27일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 10월 24일

마지막으로 확인됨

2026년 8월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • NCI-2022-08567
  • U10CA180886 (미국 NIH 보조금/계약)
  • AOST2032 (기타 식별자: CTEP)
  • NCI-2022-08567 (레지스트리 식별자: CTRP (Clinical Trial Reporting Program))
  • AOST2032 (기타 식별자: Children's Oncology Group)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

NCI is committed to sharing data in accordance with NIH policy. For more details on how clinical trial data is shared, access the link to the NIH data sharing policy page.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

미국에서 제조되어 미국에서 수출되는 제품

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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