Histiocytosis, Langerhans-Cell
Conditions
Keywords
LANGERHANS, HISTIOCYTOSIS
Brief summary
The purpose of this study is to learn about the response of Langerhans cell histiocytosis (LCH) to Enbrel in patients who have failed to respond to standard therapies. We are also looking specifically at what side effects Enbrel has on patients. We expect to enroll 20 patients on this study and anticipate the subjects active participation to last up to one year.
Detailed description
After subjects have completed the pretreatment evaluations, they will receive an injection of Enbrel - the study drug -(given under the skin) twice weekly. If the subjects disease stabilizes or regresses, they may continue to receive treatment for up to 1 year. Subjects with disease involvement of risk organs (this means patients have disease in their liver, lung, spleen, or bone marrow): will be admitted to the hospital for observation during the first week of administration of Enbrel. If after the first two doses there appears to be no problems, subjects may be followed as an outpatient with twice weekly evaluation visits (similar to those performed before treatment began) until abnormal blood tests have become normal. Then the frequency of clinic visits will decrease and be similar to those described below for subjects without disease involvement of risk organs. Subjects without disease involvement of risk organs will be treated as an outpatient. While receiving the treatment, subjects may not receive any other chemotherapy agents. Doctors will be monitoring subjects closely for side effects. Most side effects usually disappear after the treatment is stopped. In the meantime, however, the doctor may prescribe medication to keep these side effects under control.
Interventions
DRUGEtanercept
Sponsors
The Methodist Hospital Research Institute
Baylor College of Medicine
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
1 Days to 65 Years
Healthy volunteers
No
Inclusion criteria
INCLUSION: * Age: Patients of any age greater than 1 year and up to 65 years of age. An internal medicine board-certified physician will also evaluate adult patients. * Histologic diagnosis: Patients must have a histologically confirmed LCH that is refractory to standard therapy. * Recovery from prior therapy: Patients must have recovered from the toxic effects of all prior therapy but may have abnormal hematologic, hepatic, or other lab values secondary to the disease. * Life expectancy: Patients must have a life expectancy of at least 8 weeks. * Performance status: Patients must have a Lansky performance status greater than 40 or Karnofsky status greater than 40. * Informed consent: All patients or their legal guardians (if the patient is \< 18 years of age) must sign a document of informed consent indicating their awareness of the investigational nature and the risks of this study. When appropriate the patient will be included in all discussions in order to obtain verbal consent. * Hematologic status: Patients of any hematologic status may be enrolled since resistant LCH may require considerable transfusion support. * Durable Power of Attorney (DPA): A DPA must be offered to all patients 18 years of age or older. EXCLUSION: * Women of childbearing potential who are pregnant or lactating are excluded. * Patients with active infections must be treated prior to entry. * Significant other diseases that the investigator feels will complicate review/evaluation of the study data (example: uncontrolled diabetes, multiple sclerosis).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Response of Langerhans cell histiocytosis | — |
Countries
United States
Outcome results
None listed