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Single-dose Anti-CD20 Antibody With Bortezomib for Relapsed Refractory Autoimmune Hemolytic Anemia (RRAIHA01)

Primary Purpose

Autoimmune Hemolytic Anemia, Autoimmune Hemolytic Anemia and Autoimmune Thrombocytopenia

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
combination of a single dose anti-CD20 antibody and bortezomib
Sponsored by
Peking Union Medical College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Autoimmune Hemolytic Anemia focused on measuring warm autoimmune hemolytic anemia, relapsed, refractory, EVANS syndrome, anti-CD20 monoclonal antibody, bortezomib

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Peking Union Medical College HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

study group

Arm Description

The treatment regimen is a single dose anti-CD20 antibody injection (500mg iv drip,day0) combined with bortezomib injection (1.3mg/m2 subcutaneous injection,twice a week for two weeks,day1,4,8,11). The treatment course will be repeated three months later.

Outcomes

Primary Outcome Measures

response time
days hemoglobin increasing more than 20g/L
overall response
total of complete response and partial response
complete response
rate of achieving complete response
relapse rate
relapse rate of responders

Secondary Outcome Measures

relapse free survival
time duration of responders from first treatment to recurrence of decompensated hemolysis
overall survival
time from first treatment to death of any causes
side effects
side effects due to the combination of anti-CD20 antibody and bortezomib

Full Information

First Posted
August 31, 2019
Last Updated
October 12, 2021
Sponsor
Peking Union Medical College Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04083014
Brief Title
Single-dose Anti-CD20 Antibody With Bortezomib for Relapsed Refractory Autoimmune Hemolytic Anemia
Acronym
RRAIHA01
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 20, 2019 (Actual)
Primary Completion Date
August 20, 2022 (Anticipated)
Study Completion Date
August 20, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking Union Medical College Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autoimmune Hemolytic Anemia, Autoimmune Hemolytic Anemia and Autoimmune Thrombocytopenia
Keywords
warm autoimmune hemolytic anemia, relapsed, refractory, EVANS syndrome, anti-CD20 monoclonal antibody, bortezomib

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
43 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
study group
Arm Type
Experimental
Arm Description
The treatment regimen is a single dose anti-CD20 antibody injection (500mg iv drip,day0) combined with bortezomib injection (1.3mg/m2 subcutaneous injection,twice a week for two weeks,day1,4,8,11). The treatment course will be repeated three months later.
Intervention Type
Drug
Intervention Name(s)
combination of a single dose anti-CD20 antibody and bortezomib
Other Intervention Name(s)
Rituximab Injection, Bortezomib for Injection
Intervention Description
Relapsed and refractory warm AIHA patients receive treatment of combination of a single dose anti-CD20 antibody and bortezomib twice during three months interval.
Primary Outcome Measure Information:
Title
response time
Description
days hemoglobin increasing more than 20g/L
Time Frame
two years
Title
overall response
Description
total of complete response and partial response
Time Frame
two years
Title
complete response
Description
rate of achieving complete response
Time Frame
two years
Title
relapse rate
Description
relapse rate of responders
Time Frame
two years
Secondary Outcome Measure Information:
Title
relapse free survival
Description
time duration of responders from first treatment to recurrence of decompensated hemolysis
Time Frame
two years
Title
overall survival
Description
time from first treatment to death of any causes
Time Frame
two years
Title
side effects
Description
side effects due to the combination of anti-CD20 antibody and bortezomib
Time Frame
two years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of warm autoimmune hemolytic anemia or EVANS syndrome, primary or secondary. 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. Normal heart function, liver function (total bilirubin < 1.5×ULN, ALT, AST < 3.0 ×ULN), and renal function (serum creatinine < 1.0 ×ULN). No active infection. No malignant tumors (except carcinoma in situ). Patients understand the content of the study, participate the study and sign the informed consent voluntarily. Exclusion Criteria: Patients with malignant tumors (excluding carcinoma in situ); With uncontrollable infections or other serious diseases; Active hepatitis B, serume HBV-DNA > 104copies/ml; Women during pregnancy or lactation; Not strict contraception; Psychiatric patients and those with severe mental illness. Other conditions that researchers consider inappropriate to join the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Miao Chen
Phone
+86 13520112578
Email
chenm@pumch.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bing Han
Organizational Affiliation
Peking Union Medical College Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Peking Union Medical College Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Miao Chen
Phone
+86 13520112578
Email
chenm@pumch.cn
First Name & Middle Initial & Last Name & Degree
Bing Han
Phone
+86 69155028
Email
hanbingpumch@163.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Patients age,gender,diagnosis,treatment details, efficiency and survival.
IPD Sharing Time Frame
The data will become available 6 months after the publication of the study and for 2 years.
IPD Sharing Access Criteria
get permission from the researchers.
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Single-dose Anti-CD20 Antibody With Bortezomib for Relapsed Refractory Autoimmune Hemolytic Anemia

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