Autoimmune Anemia
Conditions
Brief summary
Autoimmune anemia (AIA), including autoimmune hemolytic anemia (AIHA), EVENs' syndrome (ES), acquired pure red aplastic anemia (PRCA), is a kind of anemia disease mediated by autoimmunity, which can be primary or secondary to other diseases including autoimmune disease, malignant tumor, infection, etc. Glucocorticoid is the first-line treatment. However, the recurrence rate is very high and some patients may not response to steroids, the latter defined as refractory autoimmune anemia (RAIA). Second-line therapies include cyclosporine A (CSA), cyclophosphamide, 6-mercaptopurine, CD20 monoclonal antibody, anti human lymphocyte immunoglobulin (ATG), and even splenectomy. Cyclosporine A is easy to accept while some patients may have side effects such as renal function damage, gingival hyperplasia, hypertension and so on. Other second-line drugs also have many problems, such as low effective rate, slow onset, expensive price, and large side effects, and some patients do not response to these treatments. The refractory/relapsed AIA patients have increased cardiovascular events, increased opportunities for infections, decreased quality of life, and even death. At present, there is still no effective treatment for these patients. Our previous retrospective study showed that sirolimus was effective in cyclosporine refractory PRCA with an effective rate of 70% and slight side effects. In addition, we used sirolimus in refractory AIHA and ES, with an effective rate of 60-70%. However, there are still some non-responsive patients. Recently, it has been reported that all trans retinoic acid (ATRA) combined with danazol was effective in the treatment of refractory immune thrombocytopenic purpura (ITP). Therefore, we plans to combine sirolimus and ATRA in the treatment of refractory AIA to improve the efficacy. Since both sirolimus and ATRA are cheap and have slight side effects, this combination may reduce the economic burden of patients and reduce the side effects related to treatment.
Interventions
DRUGsirolimus and ATRA
sirolimus (serum concentration 4-10ng/ml) and ATRA 20mg bid
DRUGsirolimus
Since ATRA is not available in China for a variety of reasons, it was only used for less than 6 months. Then, sirolimus (serum concentration 4-10ng/ml) monotherapy was used.
Sponsors
Peking Union Medical College Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
1. diagnosed as autoimmune anemia (autoimmune hemolytic anemia, pure red aplastic anemia, events syndrome) without organ complications; 2. ineffective, relapsed or intolerant patients who have been treated with at least one kind of sufficient current conventional drug (steroids, CsA, CD20 monoclonal antibody, tacrolimus and others) ; 3. normal cardiac function, liver function (ALT/AST ≤ 3.0 × ULN) and renal function (serum creatinine ≤ 1 × ULN); 4. no secondary disease; 5. unable to accept hematopoietic stem cell transplantation; 6. ECoG score ≤ 2; 7. able to sign the informed consent form.
Exclusion criteria
1. failure to make a definite diagnosis; 2. AIA secondary to known diseases such as systemic lupus erythematosus, rheumatoid arthritis, tumor or other inflammatory diseases; 3. severe hepatorenal insufficiency (creatinine, transaminase more than 3 times of the upper limit of normal value); 4. uncontrollable systemic infection or other serious diseases; 5. pregnant or lactating women; 6. patients with mental disease who are unable to sign the informed consent; 7. taking other AIA drugs or stopping the drugs for less than 3 months; 8. allergic to the study drug; 9. participation in other clinical studies; 10. patients in any other circumstances considered unsuitable by the investigator.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| overall response rate | 1 year | overall response rate |
| rate of side effects | 1 year | rates and types of all side effects |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| change of HGB concentration | through study completion, an average of 1 year | change of HGB concentration |
| frequency of HGB transfusion | through study completion, an average of 1 year | frequency of HGB transfusion |
| time to response | through study completion, an average of 1 year | time to response |
| response duration | through study completion, an average of 1 year | CR/PR duration |
| change of bilirubin concentration | through study completion, an average of 1 year | change of bilirubin concentration |
Countries
China
Outcome results
None listed