Danazol for Genetic Bone Marrow and Lung Disorders
This trial has been completed.
|Phase||phase 1/phase 2|
|Sponsor||National Heart, Lung, and Blood Institute (NHLBI)|
|Start date||July 2011|
|End date||November 2016|
|Trial size||27 participants|
|Trial identifier||NCT01441037, 11-H-0209, 110209|
- Some people have bone marrow and lung disorders that are caused by genetic problems. These problems often involve damage to the ends of the chromosomes that pass down genes. One of these disorders is aplastic anemia. This is a disorder in which the bone marrow does not make enough blood cells. Currently, doctors use a male hormone-based drug called Danazol to improve bone marrow function and treat aplastic anemia. More information is needed on whether Danazol can help repair the damaged chromosomes that cause aplastic anemia and similar disorders that cause low blood cell counts or lung problems.
- To study the safety and effectiveness of Danazol for bone marrow and lung disorders caused by damaged genes.
- Individuals at least 2 years of age who have low blood cell counts or lung fibrosis caused by damaged genes.
- Participants will be screened with a physical exam and medical history. Then they will have blood and urine tests, imaging studies, and a lung function test. They will also take a 6-minute walking test and have a bone marrow biopsy.
- Participants will receive Danazol to take twice a day for the duration of the study.
- Participants will have regular study visits at 6, 12, and 24 months, with blood tests, imaging studies, a lung function test, and a 6-minute walking test. A bone marrow sample will be collected at the 12-month visit.
- Participants will remain on the study for up to 2 years. Researchers will follow up with them for 2 years after the end of the study.
|Endpoint classification||safety/efficacy study|
|Intervention model||single group assignment|
Toxicity profile in the 24 months following danazol therapy. The biologic endpoint is reduction in telomere attrition rate yearly.
time frame: 2 years
a) hematologic response
time frame: 2 years
time frame: 2 years
c) clonal evolution
time frame: 2 years
d) myelodysplasia or acute leukemia
time frame: 2 years
f) progression of PETs and CT scans
time frame: months and yearly thereafter
g) 6-minute walk test
time frame: 6 months and yearly thereafter
Male or female participants at least 2 years old.
- INCLUSION CRITERIA: 1. Short age-adjusted telomere length in the first percentile and/or a mutation in telomerase genes 2. One or more of the following cytopenia(s). - Anemia 1. Symptomatic anemia with a hemoglobin < 9.5 g/dL or red cell transfusion requirements > 2 units/month for at least 2 months 2. Reticulocyte count < 60,000 /microL - Thrombocytopenia 1. Platelet count < 30,000 /microL or < 50,000 /microL associated with bleeding 2. Decreased megakaryocytic precursors in the bone marrow - Neutropenia 1. Absolute neutrophil count < 1,000 /microL OR 3. Idiopathic pulmonary fibrosis diagnosed by either a lung biopsy of high resolution computed tomography scan of the chest according to guidelines from the American Thoracic Society and European Respiratory Society 4. Age greater than or equal to 2 years 5. Weight > 12 kg EXCLUSION CRITERIA: 1. Moribund status or concurrent hepatic, renal, cardiac, neurologic, pulmonary, infectious, or metabolic disease of such severity that it would preclude the patient s ability to tolerate protocol therapy, or that death within 30 days is likely 2. Potential subjects with cancer who are on active chemotherapeutic treatment 3. Current pregnancy, or unwillingness to avoid pregnancy if of childbearing potential 4. Not able to understand the investigational nature of the study or give informed consent or does not have a legally authorized representative or surrogate that can provide informed consent.
|Official title||Male Hormones for Telomere Related Diseases|
|Principal investigator||Danielle M Townsley, M.D.|
|Description||Severe aplastic anemia (SAA) is a life-threatening bone marrow failure disorder characterized by pancytopenia and a hypocellular bone marrow. Telomeres were reported to be short in up to one-third of patients with SAA.Initially this occurrence was presumed to be secondary to hematopoietic stress. However, the discovery of loss-of-function mutations in genes of the telomerase complex (TERC, TERT) established a genetic etiology for telomere attrition in some patients with marrow failure who did not have the stigmata associated to an inherited bone marrow failure syndrome. These findings implicated telomerase dysfunction in failed hematopoiesis. In family members of probands with SAA, telomerase mutations have been observed which were associated to varying degrees of cytopenias, idiopathic pulmonary fibrosis (IPF) and/or cirrhosis. Telomere length has been associated with human cancer. Telomere attrition has been implicated in a variety of solid organ malignancies including esophageal and colon adenocarcinoma. In a longitudinal population based study, shorter telomere length associated to a higher cancer mortality risk overtime. It is plausible that a shorter telomere length is not just a biomarker associated to development of cancer, but involved in its pathogenesis. Ample experimental data supports an important role of critically short telomere length in genomic instability. Furthermore, our laboratory data (unpublished) shows that similar chromosome instability occurs in bone marrow cells of mutant patients, confirming the experimental data. Thus, a common molecular mechanism appears to underlie risk for cancer and a range of clinical entities. In vitro studies suggest that telomere length could, in theory, be modulated with sex hormones.15 Exposure of normal peripheral blood lymphocytes and human bone marrow derived CD34+ cells to androgens increased telomerase activity in vitro and androgens increased low baseline telomerase activity in individuals carrying a loss-of-function TERT mutation to normal levels. In retrospect, the beneficial effects of sex hormones on telomerase activity may be the mechanism by which SAA patients treated over 40 years ago with male hormones showed hematologic improvement in some cases. In recent years we have seen patients referred to our clinic with varying degree of cytopenia(s) who had significant family history for cytopenia(s), IPF and/or cirrhosis. We have identified very short telomeres in these patients and in some mutations in TERC and TERT. We hypothesize that male hormone therapy might modulate telomere attrition in vivo and ameliorate progression or reverse the clinical consequences of accelerated telomere attrition. Therefore, we propose male hormone therapy in patients with cytopenia(s) and/or IPF who show evidence of telomere dysfunction by a short age adjusted telomere length associated to telomerase gene mutations. The primary biologic endpoint will be delay of telomere attrition over time compared to known rates of telomere erosion in normal individuals and in those who carry mutation in the telomerase genes. The main clinical endpoint will be tolerability of oral danazol over two years. Secondary endpoints will be improvement in blood counts and/or pulmonary function. The small sample size, lack of control groups, and variable clinical course among those with marrow failure and IPF, will not allow for definitive assessment of clinical benefit. Nevertheless, we believe this protocol will provide insight into the possible effects of androgen therapy on telomere attrition in humans and of possible clinical benefit in telomere related disorders, and serve as hypothesis generating for further larger controlled studies.|
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