Erdafitinib en el tratamiento de pacientes con tumores sólidos avanzados en recaída o refractarios, linfoma no Hodgkin o trastornos histiocíticos con mutaciones de FGFR (ensayo pediátrico de tratamiento MATCH)
MATCH pediátrico del NCI-COG (Análisis molecular para la elección de la terapia): subprotocolo de fase 2 de erdafitinib en pacientes con tumores que albergan alteraciones de FGFR1/2/3/4
This phase II Pediatric MATCH trial studies how well erdafitinib works in treating patients with solid tumors, non-Hodgkin lymphoma, or histiocytic disorders with FGFR mutations that have spread to other places in the body and have come back or do not respond to treatment. Erdafitinib may stop the growth of cancer cells with FGFR mutations by blocking some of the enzymes needed for cell growth.
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
- Meduloblastoma infantil recidivante
- Ependimoma infantil recurrente
- Neoplasia sólida maligna avanzada
- Neoplasia sólida maligna refractaria
- Hepatoblastoma recurrente
- Histiocitosis de células de Langerhans recurrente
- Glioma maligno recurrente
- Neoplasia sólida maligna recurrente
- Neuroblastoma recurrente
- Tumor rabdoide recurrente
- Ependimoma refractario
- Hepatoblastoma refractario
- Histiocitosis de células de Langerhans refractaria
- Glioma maligno refractario
- Meduloblastoma refractario
- Neuroblastoma refractario
- Linfoma no Hodgkin refractario
- Tumor rabdoide refractario
- Tumor de Wilms
- Rabdomiosarcoma infantil recurrente
- Neoplasia primaria recurrente del sistema nervioso central
- Neoplasia primaria refractaria del sistema nervioso central
- Linfoma no Hodgkin infantil recidivante
- Sarcoma de tejido blando infantil recidivante
- Sarcoma de Ewing recidivante/tumor neuroectodérmico primitivo periférico
- Sarcoma de Ewing refractario/tumor neuroectodérmico primitivo periférico
- Tumor maligno de células germinativas infantil recidivante
- Tumor maligno de células germinativas infantil refractario
- Osteosarcoma infantil recurrente
- Osteosarcoma infantil refractario
- Rabdomiosarcoma infantil refractario
- Sarcoma de tejido blando infantil refractario
Intervención / Tratamiento
Intervención / Tratamiento
- Otro: Laboratory Biomarker Analysis
- Procedimiento: Biospecimen Collection
- Procedimiento: Magnetic Resonance Imaging
- Otro: Pharmacological Study
- Droga: Erdafitinib
- Procedimiento: Bone Marrow Aspiration and Biopsy
- Procedimiento: Bone Scan
- Procedimiento: Computed Tomography
- Procedimiento: Positron Emission Tomography
- Procedimiento: Radionuclide Imaging
- Procedimiento: X-Ray Imaging
Descripción detallada
PRIMARY OBJECTIVE:
I. To determine the objective response rate (ORR; complete response + partial response) in pediatric patients treated with erdafitinib with advanced solid tumors (including central nervous system [CNS] tumors), non-Hodgkin lymphomas or histiocytic disorders that harbor genetic alterations in the FGFR1/2/3/4 pathway.
SECONDARY OBJECTIVES:
I. To estimate the progression free survival in pediatric patients treated with erdafitinib with advanced solid tumors (including CNS tumors), non-Hodgkin lymphomas or histiocytic disorders that harbor genetic alterations in the FGFR1/2/3/4.
II. To obtain information about the tolerability of erdafitinib in children with relapsed or refractory cancer.
III. To provide preliminary estimates of the pharmacokinetics of erdafitinib in children with relapsed or refractory cancer.
EXPLORATORY OBJECTIVE:
I. To explore approaches to profiling changes in tumor genomics over time through evaluation of circulating tumor deoxyribonucleic acid (DNA).
OUTLINE:
Patients receive erdafitinib orally (PO) once daily (QD) on days 1-28 of each cycle. Treatment repeats every 28 days for up to 26 cycles (2 years) in the absence of disease progression or unacceptable toxicity. Patients undergo an x-ray, computed tomography (CT) scan, magnetic resonance imaging (MRI), positron emission tomography (PET) scan, radionuclide imaging, and/or bone scan, as well as a bone marrow aspiration and/or biopsy during screening and on study. Patients also undergo blood sample collection on study.
After completion of study treatment, patients are followed up periodically.
Tipo de estudio
Tipo de estudio
Inscripción (Actual)
Inscripción
Fase
Fase
- Fase 2
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Alabama
-
Birmingham, Alabama, Estados Unidos, 35233
- Children's Hospital of Alabama
-
-
Alaska
-
Anchorage, Alaska, Estados Unidos, 99508
- Providence Alaska Medical Center
-
-
Arizona
-
Mesa, Arizona, Estados Unidos, 85202
- Banner Children's at Desert
-
Tucson, Arizona, Estados Unidos, 85719
- Banner University Medical Center - Tucson
-
-
Arkansas
-
Little Rock, Arkansas, Estados Unidos, 72202-3591
- Arkansas Children's Hospital
-
-
California
-
Downey, California, Estados Unidos, 90242
- Kaiser Permanente Downey Medical Center
-
Loma Linda, California, Estados Unidos, 92354
- Loma Linda University Medical Center
-
Long Beach, California, Estados Unidos, 90806
- Miller Children's and Women's Hospital Long Beach
-
Los Angeles, California, Estados Unidos, 90048
- Cedars-Sinai Medical Center
-
Los Angeles, California, Estados Unidos, 90027
- Children's Hospital Los Angeles
-
Madera, California, Estados Unidos, 93636
- Valley Children's Hospital
-
Oakland, California, Estados Unidos, 94609
- UCSF Benioff Children's Hospital Oakland
-
Oakland, California, Estados Unidos, 94611
- Kaiser Permanente-Oakland
-
Sacramento, California, Estados Unidos, 95817
- University of California Davis Comprehensive Cancer Center
-
San Francisco, California, Estados Unidos, 94158
- UCSF Medical Center-Mission Bay
-
-
Colorado
-
Aurora, Colorado, Estados Unidos, 80045
- Children's Hospital Colorado
-
Denver, Colorado, Estados Unidos, 80218
- Rocky Mountain Hospital for Children-Presbyterian Saint Luke's Medical Center
-
-
Connecticut
-
New Haven, Connecticut, Estados Unidos, 06520
- Yale University
-
-
Delaware
-
Wilmington, Delaware, Estados Unidos, 19803
- Alfred I duPont Hospital for Children
-
-
District of Columbia
-
Washington D.C., District of Columbia, Estados Unidos, 20010
- Children's National Medical Center
-
-
Florida
-
Gainesville, Florida, Estados Unidos, 32610
- UF Health Cancer Institute - Gainesville
-
Hollywood, Florida, Estados Unidos, 33021
- Memorial Regional Hospital/Joe DiMaggio Children's Hospital
-
Jacksonville, Florida, Estados Unidos, 32207
- Nemours Children's Clinic-Jacksonville
-
Miami, Florida, Estados Unidos, 33155
- Nicklaus Children's Hospital
-
Miami, Florida, Estados Unidos, 33136
- University of Miami Miller School of Medicine-Sylvester Cancer Center
-
Orlando, Florida, Estados Unidos, 32827
- Nemours Children's Hospital
-
Orlando, Florida, Estados Unidos, 32803
- AdventHealth Orlando
-
Orlando, Florida, Estados Unidos, 32806
- Arnold Palmer Hospital for Children
-
St. Petersburg, Florida, Estados Unidos, 33701
- Johns Hopkins All Children's Hospital
-
Tampa, Florida, Estados Unidos, 33607
- Saint Joseph's Hospital/Children's Hospital-Tampa
-
West Palm Beach, Florida, Estados Unidos, 33407
- Saint Mary's Medical Center
-
-
Georgia
-
Atlanta, Georgia, Estados Unidos, 30329
- Children's Healthcare of Atlanta - Arthur M Blank Hospital
-
-
Idaho
-
Boise, Idaho, Estados Unidos, 83712
- Saint Luke's Cancer Institute - Boise
-
-
Illinois
-
Chicago, Illinois, Estados Unidos, 60637
- University of Chicago Comprehensive Cancer Center
-
Chicago, Illinois, Estados Unidos, 60611
- Lurie Children's Hospital-Chicago
-
Peoria, Illinois, Estados Unidos, 61637
- OSF Children's Hospital of Illinois
-
Springfield, Illinois, Estados Unidos, 62702
- Southern Illinois University School of Medicine
-
-
Indiana
-
Indianapolis, Indiana, Estados Unidos, 46202
- Riley Hospital for Children
-
Indianapolis, Indiana, Estados Unidos, 46260
- Ascension Saint Vincent Indianapolis Hospital
-
-
Iowa
-
Des Moines, Iowa, Estados Unidos, 50309
- Blank Children's Hospital
-
Iowa City, Iowa, Estados Unidos, 52242
- University of Iowa/Holden Comprehensive Cancer Center
-
-
Kentucky
-
Lexington, Kentucky, Estados Unidos, 40536
- University of Kentucky/Markey Cancer Center
-
Louisville, Kentucky, Estados Unidos, 40202
- Norton Children's Hospital
-
-
Louisiana
-
New Orleans, Louisiana, Estados Unidos, 70121
- Ochsner Medical Center Jefferson
-
New Orleans, Louisiana, Estados Unidos, 70118
- Children's Hospital New Orleans
-
-
Maine
-
Bangor, Maine, Estados Unidos, 04401
- Eastern Maine Medical Center
-
-
Maryland
-
Baltimore, Maryland, Estados Unidos, 21287
- Johns Hopkins University/Sidney Kimmel Cancer Center
-
Baltimore, Maryland, Estados Unidos, 21215
- Sinai Hospital of Baltimore
-
-
Michigan
-
Ann Arbor, Michigan, Estados Unidos, 48109
- C S Mott Children's Hospital
-
East Lansing, Michigan, Estados Unidos, 48823
- Michigan State University
-
Grand Rapids, Michigan, Estados Unidos, 49503
- Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital
-
Kalamazoo, Michigan, Estados Unidos, 49007
- Bronson Methodist Hospital
-
-
Minnesota
-
Minneapolis, Minnesota, Estados Unidos, 55404
- Children's Hospitals and Clinics of Minnesota - Minneapolis
-
Minneapolis, Minnesota, Estados Unidos, 55455
- University of Minnesota/Masonic Cancer Center
-
-
Mississippi
-
Jackson, Mississippi, Estados Unidos, 39216
- University of Mississippi Medical Center
-
-
Missouri
-
Kansas City, Missouri, Estados Unidos, 64108
- Children's Mercy Hospitals and Clinics
-
St Louis, Missouri, Estados Unidos, 63110
- Washington University School of Medicine
-
St Louis, Missouri, Estados Unidos, 63141
- Mercy Hospital Saint Louis
-
St Louis, Missouri, Estados Unidos, 63104
- Cardinal Glennon Children's Medical Center
-
-
Nebraska
-
Omaha, Nebraska, Estados Unidos, 68198
- University of Nebraska Medical Center
-
Omaha, Nebraska, Estados Unidos, 68114
- Children's Hospital and Medical Center of Omaha
-
-
New Jersey
-
Hackensack, New Jersey, Estados Unidos, 07601
- Hackensack University Medical Center
-
Morristown, New Jersey, Estados Unidos, 07960
- Morristown Medical Center
-
New Brunswick, New Jersey, Estados Unidos, 08901
- Saint Peter's University Hospital
-
-
New York
-
Albany, New York, Estados Unidos, 12208
- Albany Medical Center
-
Buffalo, New York, Estados Unidos, 14263
- Roswell Park Cancer Institute
-
New Hyde Park, New York, Estados Unidos, 11040
- The Steven and Alexandra Cohen Children's Medical Center of New York
-
New York, New York, Estados Unidos, 10065
- Memorial Sloan Kettering Cancer Center
-
New York, New York, Estados Unidos, 10032
- NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center
-
New York, New York, Estados Unidos, 10065
- NYP/Weill Cornell Medical Center
-
Rochester, New York, Estados Unidos, 14642
- University of Rochester
-
Syracuse, New York, Estados Unidos, 13210
- State University of New York Upstate Medical University
-
The Bronx, New York, Estados Unidos, 10467
- Montefiore Medical Center - Moses Campus
-
-
North Carolina
-
Asheville, North Carolina, Estados Unidos, 28801
- Mission Hospital
-
Charlotte, North Carolina, Estados Unidos, 28203
- Carolinas Medical Center/Levine Cancer Institute
-
Durham, North Carolina, Estados Unidos, 27710
- Duke University Medical Center
-
-
North Dakota
-
Fargo, North Dakota, Estados Unidos, 58122
- Sanford Broadway Medical Center
-
-
Ohio
-
Cincinnati, Ohio, Estados Unidos, 45229
- Cincinnati Children's Hospital Medical Center
-
Cleveland, Ohio, Estados Unidos, 44106
- Rainbow Babies and Childrens Hospital
-
Columbus, Ohio, Estados Unidos, 43205
- Nationwide Children's Hospital
-
Dayton, Ohio, Estados Unidos, 45404
- Dayton Children's Hospital
-
Toledo, Ohio, Estados Unidos, 43606
- ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital
-
-
Oklahoma
-
Oklahoma City, Oklahoma, Estados Unidos, 73104
- University of Oklahoma Health Sciences Center
-
-
Oregon
-
Portland, Oregon, Estados Unidos, 97239
- Oregon Health and Science University
-
Portland, Oregon, Estados Unidos, 97227
- Legacy Emanuel Children's Hospital
-
-
Pennsylvania
-
Danville, Pennsylvania, Estados Unidos, 17822
- Geisinger Medical Center
-
Philadelphia, Pennsylvania, Estados Unidos, 19104
- Children's Hospital of Philadelphia
-
Pittsburgh, Pennsylvania, Estados Unidos, 15224
- Children's Hospital of Pittsburgh of UPMC
-
-
South Carolina
-
Columbia, South Carolina, Estados Unidos, 29203
- Prisma Health Richland Hospital
-
Greenville, South Carolina, Estados Unidos, 29605
- BI-LO Charities Children's Cancer Center
-
-
South Dakota
-
Sioux Falls, South Dakota, Estados Unidos, 57117-5134
- Sanford USD Medical Center - Sioux Falls
-
-
Tennessee
-
Knoxville, Tennessee, Estados Unidos, 37916
- East Tennessee Childrens Hospital
-
Memphis, Tennessee, Estados Unidos, 38105
- Saint Jude Children's Research Hospital
-
Nashville, Tennessee, Estados Unidos, 37232
- Vanderbilt University/Ingram Cancer Center
-
Nashville, Tennessee, Estados Unidos, 37203
- The Children's Hospital at TriStar Centennial
-
-
Texas
-
Austin, Texas, Estados Unidos, 78723
- Dell Children's Medical Center of Central Texas
-
Dallas, Texas, Estados Unidos, 75390
- UT Southwestern/Simmons Cancer Center-Dallas
-
Dallas, Texas, Estados Unidos, 75230
- Medical City Dallas Hospital
-
Fort Worth, Texas, Estados Unidos, 76104
- Cook Children's Medical Center
-
Houston, Texas, Estados Unidos, 77030
- UT MD Anderson Cancer Center
-
Houston, Texas, Estados Unidos, 77030
- Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center
-
San Antonio, Texas, Estados Unidos, 78207
- Children's Hospital of San Antonio
-
San Antonio, Texas, Estados Unidos, 78229
- Methodist Children's Hospital of South Texas
-
Temple, Texas, Estados Unidos, 76508
- Scott and White Memorial Hospital
-
-
Utah
-
Salt Lake City, Utah, Estados Unidos, 84113
- Primary Children's Hospital
-
-
Vermont
-
Burlington, Vermont, Estados Unidos, 05405
- University of Vermont and State Agricultural College
-
-
Virginia
-
Norfolk, Virginia, Estados Unidos, 23507
- Children's Hospital of The King's Daughters
-
Richmond, Virginia, Estados Unidos, 23298
- VCU Massey Comprehensive Cancer Center
-
-
Washington
-
Seattle, Washington, Estados Unidos, 98105
- Seattle Children's Hospital
-
Spokane, Washington, Estados Unidos, 99204
- Providence Sacred Heart Medical Center and Children's Hospital
-
Tacoma, Washington, Estados Unidos, 98431
- Madigan Army Medical Center
-
-
West Virginia
-
Morgantown, West Virginia, Estados Unidos, 26506
- West Virginia University Healthcare
-
-
Wisconsin
-
Madison, Wisconsin, Estados Unidos, 53792
- University of Wisconsin Carbone Cancer Center - University Hospital
-
Milwaukee, Wisconsin, Estados Unidos, 53226
- Children's Hospital of Wisconsin
-
-
-
-
-
San Juan, Puerto Rico, 00926
- University Pediatric Hospital
-
San Juan, Puerto Rico, 00912
- San Jorge Children's Hospital
-
-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
-
Patient must have enrolled onto APEC1621SC and must have been given a treatment assignment to molecular analysis for therapy choice (MATCH) to APEC1621B based on the presence of an actionable mutation as defined in APEC1621SC
-
Patients must be >/= 12 months and =/< 21 years of age at the time of study enrollment
-
Patients must have a body surface area >/= 0.53 m^2 at enrollment
-
Patients must have radiographically measurable disease at the time of study enrollment; patients with neuroblastoma who do not have measurable disease but have metaiodobenzylguanidine (MIBG) positive (+) evaluable disease are eligible; measurable disease in patients with CNS involvement is defined as lesion that is at minimum 10 mm in one dimension on standard MRI or CT
-
Note: The following do not qualify as measurable disease:
- Malignant fluid collections (e.g., ascites, pleural effusions)
- Bone marrow infiltration except that detected by MIBG scan for neuroblastoma
- Lesions only detected by nuclear medicine studies (e.g., bone, gallium or positron emission tomography [PET] scans) except as noted for neuroblastoma
- Elevated tumor markers in plasma or cerebrospinal fluid (CSF)
- Previously radiated lesions that have not demonstrated clear progression post radiation
- Leptomeningeal lesions that do not meet the measurement requirements for Response Evaluation Criteria in Solid Tumors (RECIST) 1.1
-
-
Karnofsky >/= 50% for patients > 16 years of age and Lansky >/= 50 for patients =/< 16 years of age; Note: neurologic deficits in patients with CNS tumors must have been relatively stable for at least 7 days prior to study enrollment; patients who are unable to walk because of paralysis, but who are up in a wheelchair, will be considered ambulatory for the purpose of assessing the performance score
-
Patients must have fully recovered from the acute toxic effects of all prior anti-cancer therapy and must meet the following minimum duration from prior anti-cancer directed therapy prior to enrollment; if after the required timeframe, the numerical eligibility criteria are met, e.g. blood count criteria, the patient is considered to have recovered adequately
-
Cytotoxic chemotherapy or other anti-cancer agents known to be myelosuppressive; >/= 21 days after the last dose of cytotoxic or myelosuppressive chemotherapy (42 days if prior nitrosourea)
-
Anti-cancer agents not known to be myelosuppressive (e.g. not associated with reduced platelet or absolute neutrophil count [ANC] counts): >/= 7 days after the last dose of agent
-
Antibodies: >/= 21 days must have elapsed from infusion of last dose of antibody, and toxicity related to prior antibody therapy must be recovered to grade =/< 1
-
Corticosteroids: if used to modify immune adverse events related to prior therapy, >/= 14 days must have elapsed since last dose of corticosteroid
-
Hematopoietic growth factors: >/= 14 days after the last dose of a long-acting growth factor (e.g. pegfilgrastim) or 7 days for short-acting growth factor; for growth factors that have known adverse events occurring beyond 7 days after administration, this period must be extended beyond the time during which adverse events are known to occur; the duration of this interval must be discussed with the study chair and the study-assigned research coordinator
-
Interleukins, interferons and cytokines (other than hematopoietic growth factors): >/= 21 days after the completion of interleukins, interferon or cytokines (other than hematopoietic growth factors)
-
Stem cell infusions (with or without total body irradiation [TBI]):
- Allogeneic (non-autologous) bone marrow or stem cell transplant, or any stem cell infusion including donor lymphocyte infusion (DLI) or boost infusion: >/= 84 days after infusion and no evidence of graft versus host disease (GVHD)
- Autologous stem cell infusion including boost infusion: >/= 42 days
-
Cellular therapy: >/= 42 days after the completion of any type of cellular therapy (e.g. modified T cells, natural killer [NK] cells, dendritic cells, etc.)
-
X-ray therapy (XRT)/external beam irradiation including protons: >/= 14 days after local XRT; >/= 150 days after TBI, craniospinal XRT or if radiation to >/= 50% of the pelvis; >/= 42 days if other substantial bone marrow (BM) radiation
- Note: radiation may not be delivered to "measurable disease" tumor site(s) being used to follow response to subprotocol treatment
-
Radiopharmaceutical therapy (e.g., radiolabeled antibody, iobenguane I-131 [131I-MIBG]): >/= 42 days after systemically administered radiopharmaceutical therapy
-
Patients must not have received prior exposure to erdafitinib or another FGFR inhibitor such as (but not limited to) AZD4547, BGJ398, BAY1163877, LY2874455
-
-
For patients with solid tumors without known bone marrow involvement:
- Peripheral absolute neutrophil count (ANC) >/= 1000/mm^3 (performed within 7 days prior to enrollment)
- Platelet count >/= 100,000/mm^3 (transfusion independent, defined as not receiving platelet transfusions for at least 7 days prior to enrollment) (performed within 7 days prior to enrollment)
- Hemoglobin >/= 8.0 g/dL at baseline (may receive red blood cell [RBC] transfusions) (performed within 7 days prior to enrollment)
-
Patients with known bone marrow metastatic disease will be eligible for study provided they meet the blood counts (may receive platelet or packed [p]RBC transfusions provided they are not known to be refractory to red cell or platelet transfusions); these patients will not be evaluable for hematologic toxicity
-
Creatinine clearance or radioisotope glomerular filtration rate (GFR) >/= 70 ml/min/1.73 m^2 or a serum creatinine based on age/gender as follows (performed within 7 days prior to enrollment):
- Age: 1 to < 2 years; maximum serum creatinine (mg/dL): male 0.6; female 0.6
- Age: 2 to < 6 years; maximum serum creatinine (mg/dL): male 0.8; female 0.8
- Age: 6 to < 10 years; maximum serum creatinine (mg/dL): male 1; female 1
- Age: 10 to < 13 years; maximum serum creatinine (mg/dL): male 1.2; female 1.2
- Age: 13 to < 16 years; maximum serum creatinine (mg/dL): male 1.5; female 1.4
- Age: >/= 16 years; maximum serum creatinine (mg/dL): male 1.7; female 1.4
-
Bilirubin (sum of conjugated + unconjugated) =/< 1.5 x upper limit of normal (ULN) for age (performed within 7 days prior to enrollment)
-
Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase [ALT]) =/< 135 U/L; (for the purpose of this study, the ULN for SGPT is 45 U/L) (performed within 7 days prior to enrollment)
-
Serum albumin >/= 2 g/dL (performed within 7 days prior to enrollment)
-
Corrected QT (QTc) interval =/< 480 milliseconds
-
Pulse oximetry > 94% on room air if there is clinical indication for determination (e.g. dyspnea at rest)
-
Patients must be able to swallow intact tablets
-
All patients and/or their parents or legally authorized representatives must sign a written informed consent; assent, when appropriate, will be obtained according to institutional guidelines
Exclusion Criteria:
-
Pregnant or breast-feeding women will not be entered on this study due to risks of fetal and teratogenic adverse events as seen in animal studies; pregnancy tests must be obtained in girls who are post-menarchal; males or females of reproductive potential may not participate unless they have agreed to use an effective contraceptive method, while receiving study treatment and for 3 months after the last dose of erdafitinib; male subjects (with a partner of child-bearing potential) must use a condom with spermicide when sexually active and must not donate sperm from the first dose of study drug until 3 months after the last dose of study drug
-
Concomitant medications
- Corticosteroids: patients receiving corticosteroids who have not been on a stable or decreasing dose of corticosteroid for at least 7 days prior to enrollment are not eligible; if used to modify immune adverse events related to prior therapy, >/= 14 days must have elapsed since last dose of corticosteroid
- Investigational drugs: patients who are currently receiving another investigational drug are not eligible
- Anti-cancer agents: patients who are currently receiving other anti-cancer agents are not eligible
- Anti-GVHD agents post-transplant: patients who are receiving cyclosporine, tacrolimus or other agents to prevent graft-versus-host disease post bone marrow transplant are not eligible for this trial
- CYP3A4 agents: patients who are currently receiving drugs that are strong inducers or inhibitors of CYP3A4 are not eligible; Note: CYP3A4 inducing anti-epileptic drugs and dexamethasone for CNS tumors or metastases, on a stable dose, are allowed
- CYP2C9 agents: patients who are currently receiving drugs that are strong inducers or moderate inhibitors of CYP2C9 are not eligible
-
Patients who have an uncontrolled infection are not eligible
-
Patients who have received a prior solid organ transplantation 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
-
A history of cardiovascular diseases: unstable angina, myocardial infarction, or known congestive heart failure class II-IV within the preceding 12 months; cerebrovascular accident or transient ischemic attack within the preceding 3 months, pulmonary embolism within the preceding 2 months
-
A history of any of the following: sustained ventricular tachycardia, ventricular fibrillation, torsades de pointes, cardiac arrest, Mobitz II second degree heart block or third degree heart block; known presence of dilated, hypertrophic, or restrictive cardiomyopathy
-
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
-
Patients with significant ophthalmologic conditions (uncontrolled glaucoma, central serous retinopathy, history of retinal vein occlusion or retinal detachment, excluding patients with longstanding findings secondary to existing conditions) are not eligible, to be confirmed with baseline ophthalmologic exam; all patients must have a baseline ophthalmologic exam, including fundoscopy to confirm no significant ophthalmologic conditions are present
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
|
Experimental: Treatment (erdafitinib)
Patients receive erdafitinib PO QD on days 1-28 of each cycle. Treatment repeats every 28 days for up to 26 cycles (2 years) in the absence of disease progression or unacceptable toxicity. Patients undergo an x-ray, CT scan, MRI, PET scan, radionuclide imaging, and/or bone scan, as well as a bone marrow aspiration and/or biopsy during screening and on study. Patients also undergo blood sample collection on study. |
Correlative studies Undergo blood sample collection
Otros nombres:
Undergo MRI
Otros nombres:
Correlative studies Given PO
Otros nombres:
Undergo a bone marrow aspiration and/or biopsy Undergo a bone scan
Otros nombres:
Undergo a CT scan
Otros nombres:
Undergo a PET scan
Otros nombres:
Undergo radionuclide imaging
Otros nombres:
Undergo an x-ray
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Objective Response Rate
Periodo de tiempo: Up to 2 years from study entry
|
A responder is defined as a patient who achieves a best response of partial response or complete response on the study. Response rates will be calculated as the percent of evaluable patients who are responders. The revised Response Evaluation Criteria in Solid Tumors (RECIST) guideline (version 1.1) was used to determine response and progression in this study, with specific criteria outlined for the different subtypes of tumors (e.g., 2-dimensional measurements for central nervous system (CNS) tumors). |
Up to 2 years from study entry
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Percentage of Patients Experiencing Grade 3 or Higher Adverse Events
Periodo de tiempo: Up to 2 years from study entry
|
Percentage of patients experiencing grade 3 or higher adverse events will be evaluated according to National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 |
Up to 2 years from study entry
|
|
Progression Free Survival (PFS)
Periodo de tiempo: Up to 6 months from study entry
|
The Kaplan-Meier method will be used to estimate the 6 month PFS. PFS is defined as time from initiation of protocol treatment to disease progression, recurrence, death from any cause, or date of last contact |
Up to 6 months from study entry
|
|
Pharmacokinetic (PK) Parameters
Periodo de tiempo: Pre-dose Cycle 2 Day 1; 1-hour post-dose Cycle 2 Day 1; 2-hour post dose Cycle 2, Day 1; 4-hour post-dose Cycle 2, Day 1; 6-8-hour post-dose, Cycle 2 Day 1; 24-hour post dose, Cycle 2, Day 2
|
A descriptive analysis of PK parameters will be performed to define systemic exposure, drug clearance, and other pharmacokinetic parameters. The PK parameters will be summarized with simple summary statistics, including means, medians, ranges, and standard deviations (if numbers and distribution permit). |
Pre-dose Cycle 2 Day 1; 1-hour post-dose Cycle 2 Day 1; 2-hour post dose Cycle 2, Day 1; 4-hour post-dose Cycle 2, Day 1; 6-8-hour post-dose, Cycle 2 Day 1; 24-hour post dose, Cycle 2, Day 2
|
Otras medidas de resultado
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Changes in Tumor Genomic Profile
Periodo de tiempo: Up to 3 years
|
A descriptive analysis will be performed and will be summarized with simple summary statistics. All of these analyses will be descriptive in nature. |
Up to 3 years
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Investigador principal: Alice Lee, Children's Oncology Group
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Inicio del estudio
Finalización primaria (Actual)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades urogenitales
- Enfermedades del Sistema Nervioso
- Neoplasias urogenitales
- Neoplasias por sitio
- Neoplasias
- Enfermedades urogenitales masculinas
- Enfermedades Renales
- Enfermedades urológicas
- Enfermedades urogenitales femeninas
- Enfermedades urogenitales femeninas y complicaciones del embarazo
- Enfermedades Genéticas Congénitas
- Enfermedades del sistema inmunológico
- Enfermedades de las vías respiratorias
- Neoplasias por tipo histológico
- Enfermedades pulmonares
- Neoplasias Glandulares y Epiteliales
- Enfermedades linfáticas
- Trastornos linfoproliferativos
- Trastornos inmunoproliferativos
- Neoplasias Urológicas
- Neoplasias Neuroepiteliales
- Tumores neuroectodérmicos
- Neoplasias De Células Germinales Y Embrionarias
- Neoplasias De Tejido Nervioso
- Linfoma
- Neoplasias del Sistema Nervioso
- Enfermedades Pulmonares Intersticiales
- Neoplasias Renales
- Síndromes Neoplásicos Hereditarios
- Tumores Neuroectodérmicos Primitivos
- Neoplasias Complejas y Mixtas
- Histiocitosis
- Enfermedades y anomalías congénitas, hereditarias y neonatales
- Enfermedades hemic y linfáticas
- Glioma
- Neuroblastoma
- Linfoma No Hodgkin
- Tumores Neuroectodérmicos Primitivos Periféricos
- Neoplasias del Sistema Nervioso Central
- Ependimoma
- Meduloblastoma
- Tumor de Wilms
- Tumor rabdoide
- Hepatoblastoma
- Histiocitosis de células de Langerhans
- Ependimoma familiar
- Organización y administración
- Administración de Servicios de Salud
- Técnicas de investigación
- Técnicas de laboratorio clínico
- Técnicas y procedimientos de diagnóstico
- Diagnóstico
- Procedimientos quirúrgicos, operativo
- Técnicas citológicas
- Citodiagnóstico
- Fenómeno físico
- Equipos y suministros
- Técnicas de diagnóstico, quirúrgico
- Técnicas de química, analítica
- Análisis de espectro
- Fenómenos electromagnéticos
- Fenómeno magnético
- Administración hospitalaria
- Administración de instalaciones de salud
- Radiación electromagnética
- Radiación
- Radiación, ionizante
- Biopsia
- Manejo de muestras
- Espectroscopía de resonancia magnética
- Departamento de medicina nuclear, hospital
- erdafitinib
- Rayos X
- Fantasmas, imágenes
Otros números de identificación del estudio
Otros números de identificación del estudio
- NCI-2017-01159
- U10CA180886 (Subvención/contrato del NIH de EE. UU.)
- UM1CA081457 (Subvención/contrato del NIH de EE. UU.)
- NCI-2017-01159 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
- APEC1621B (Otro identificador: CTEP)
- APEC1621B (Otro identificador: Children's Oncology Group)
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .