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Single-dose Anti-CD20 Antibody With Bortezomib for Relapsed Refractory Autoimmune Hemolytic Anemia

An Open, One-arm, Prospective Study of a Single Dose Anti-CD20 Monoclonal Antibody Combined With Bortezomib for Treatment of Relapsed Refractory Autoimmune Hemolytic Anemia

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04083014
Acronym
RRAIHA01
Enrollment
33
Registered
2019-09-10
Start date
2019-08-20
Completion date
2024-03-20
Last updated
2024-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autoimmune Hemolytic Anemia, Autoimmune Hemolytic Anemia and Autoimmune Thrombocytopenia

Keywords

warm autoimmune hemolytic anemia, relapsed, refractory, EVANS syndrome, anti-CD20 monoclonal antibody, bortezomib

Brief summary

Patients of relapsed and refractory warm autoimmune hemolytic anemia or EVANS syndrome aged 18 to 80 will be included in this study. The treatment regimen is a single dose anti-CD20 antibody (500mg) combined with bortezomib (1.3mg/m2 twice a week for two weeks). The treatment course would be repeated three months later.

Detailed description

Glucocorticoids are the first-line treatment of warm AIHA. The overall response is 70-90%, but 10% to 20% patients are refractory to GCs and more than 50% patients will relapse after GCs tapering or cessation. Anti-CD20 monoclonal antibody is the preferred second-line treatment for relapsed refractory wAIHA. Anti-CD20 antibody 375 mg/m2, once a week, four times, is the standard treatment regimen. Low dose anti-CD20 antibody, 100mg once a week, four times, also showed similar response rate. However, the use of four times of intravenous infusion is trouble. So the investigators intend to explore the efficiency of the singe dose of 500mg anti-CD20 antibody. Anti-CD20 antibody takes median 6-8 weeks to response and only about 50% patients achieving long-term response. Plasma cells produce antibodies and long-lived plasma cells in bone marrow and spleen continuously work. Bortezomib is a proteasome inhibitor and targets plasma cells. Bortezomib has become a first-line treatment for clonal plasma cell diseases (such as multiple myeloma, systemic amyloidosis, POEMS syndrome, etc.). Bortezomib can also induce reactive plasma cell apoptosis and has a variety of immunomodulatory effects. The investigators try to combine bortezomib with anti-CD20 antibody, which may play a synergistic role and improve the efficacy. Patients of relapsed and refractory warm autoimmune hemolytic anemia or EVANS syndrome will receive a single dose anti-CD20 antibody (500mg) and bortezomib (1.3mg/m2 twice a week for two weeks) twice for three months interval.

Interventions

DRUGcombination of a single dose anti-CD20 antibody and bortezomib

Relapsed and refractory warm AIHA patients receive treatment of combination of a single dose anti-CD20 antibody and bortezomib twice during three months interval.

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of warm autoimmune hemolytic anemia or EVANS syndrome, primary or secondary. 2. Patients refractory to glucocorticoids (HGB increase less than 20g/L after three weeks full dose glucocorticoids treatment). Or patients relapse after at least one course of glucocorticoids therapy (HGB \< 110g/L in female and HGB \< 120g/L in male). Or glucocorticoids dependence (prednisone maintenance dose \> 10mg a day). Or glucocorticoids intolerance. 3. Normal heart function, liver function (total bilirubin \< 1.5×ULN, ALT, AST \< 3.0 ×ULN), and renal function (serum creatinine \< 1.0 ×ULN). 4. No active infection. 5. No malignant tumors (except carcinoma in situ). 6. Patients understand the content of the study, participate the study and sign the informed consent voluntarily.

Exclusion criteria

1. Patients with malignant tumors (excluding carcinoma in situ); 2. With uncontrollable infections or other serious diseases; 3. Active hepatitis B, serume HBV-DNA \> 104copies/ml; 4. Women during pregnancy or lactation; 5. Not strict contraception; 6. Psychiatric patients and those with severe mental illness. 7. Other conditions that researchers consider inappropriate to join the study.

Design outcomes

Primary

MeasureTime frameDescription
response timetwo yearsdays hemoglobin increasing more than 20g/L
overall responsetwo yearstotal of complete response and partial response
complete responsetwo yearsrate of achieving complete response
relapse ratetwo yearsrelapse rate of responders

Secondary

MeasureTime frameDescription
overall survivaltwo yearstime from first treatment to death of any causes
side effectstwo yearsside effects due to the combination of anti-CD20 antibody and bortezomib
relapse free survivaltwo yearstime duration of responders from first treatment to recurrence of decompensated hemolysis

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026