Sirolimus Combined With ATRA for the Treatment of Auto-Immune Anemia

NCT04324411 | Unknown Phase 2 DMC

• 1 other identifier: sirolimus-3
• Study Type: interventional
• Target: 50
• Locations: 1 country
• Sites: 1

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.

Conditions

Autoimmune Anemia

Outcome Measures

Primary Outcomes (2)

• overall response rate

  overall response rate

  1 year

• rate of side effects

  rates and types of all side effects

  1 year

Secondary Outcomes (5)

• change of HGB concentration

  through study completion, an average of 1 year

• frequency of HGB transfusion

  through study completion, an average of 1 year

• time to response

  through study completion, an average of 1 year

• response duration

  through study completion, an average of 1 year

• life quality score (SF 36)

  through study completion, an average of 1 year

Study Arms (1)

treatment group

EXPERIMENTAL

combined sirolimus(serum concentration to be 4-10ng/ml) and ATRA (20mg bid) for at least 6 months

Drug: sirolimus and ATRA

Interventions

sirolimus and ATRA DRUG

sirolimus (serum concentration 4-10ng/ml) and ATRA 20mg bid

treatment group

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• diagnosed as autoimmune anemia (autoimmune hemolytic anemia, pure red aplastic anemia, events syndrome) without organ complications;
• 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) ;
• normal cardiac function, liver function (total bilirubin ≤ 1.5 × ULN, ALT/AST ≤ 3.0 × ULN) and renal function (serum creatinine ≤ 1 × ULN);
• no secondary disease;
• unable to accept hematopoietic stem cell transplantation;
• ECoG score ≤ 2;
• able to sign the informed consent form.

You may not qualify if:

• failure to make a definite diagnosis;
• AIA secondary to known diseases such as systemic lupus erythematosus, rheumatoid arthritis, tumor or other inflammatory diseases;
• severe hepatorenal insufficiency (creatinine, transaminase more than 3 times of the upper limit of normal value);
• uncontrollable systemic infection or other serious diseases;
• pregnant or lactating women;
• patients with mental disease who are unable to sign the informed consent;
• taking other AIA drugs or stopping the drugs for less than 3 months;
• allergic to the study drug;
• participation in other clinical studies;
• patients in any other circumstances considered unsuitable by the investigator.

Sponsors & Collaborators

• Peking Union Medical College Hospital: lead

Study Sites (1)

Peking union medical college hospital

Beijing, China

Location

MeSH Terms

Interventions

Sirolimus; Tretinoin

Intervention Hierarchy (Ancestors)

Macrolides; Lactones; Organic Chemicals; Vitamin A; Retinoids; Carotenoids; Polyenes; Alkenes; Hydrocarbons, Acyclic; Hydrocarbons; Cyclohexenes; Cyclohexanes; Cycloparaffins; Hydrocarbons, Alicyclic; Hydrocarbons, Cyclic; Terpenes; Diterpenes; Pigments, Biological; Biological Factors

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: March 23, 2020
• First Posted: March 27, 2020
• Study Start: April 1, 2020
• Primary Completion: April 1, 2022
• Study Completion: December 1, 2022
• Last Updated: March 27, 2020

Record last verified: 2020-03

Data Sharing

• IPD Sharing: Will share
• Shared Documents: STUDY PROTOCOL, SAP, ICF, CSR
• Time Frame: always
• Access Criteria: email request

Locations

CN (1)