Javascript must be enabled to continue!
Alemtuzumab and Rituximab in the treatment of refractory autoimmune Cytopenias.
View through CrossRef
Abstract
Abstract 4458
Introduction
The combination of rituximab and alemtuzumab have been used to treat CLL. This combination is feasible without excessive toxicity. Both antibodies have been used as monotherapy for the treatment of autoimmune diseases, including autoimmune hemolytic anemia (AHA) and Immune thrombocytopenic purpura (ITP).
Objective
Evaluate the efficacy and safety of the combination of low dose alemtuzumab and rituximab in patients with AHA and ITP.
Material and methods
patients diagnosed with AHA (clinical and biochemical data of hemolysis) or ITP (less than < 50 K/μl) who failed or relapsed after first line therapy (steroids) were included. Basal lymphocyte count and immunoglobulin levels were assessed. Patients received alemtuzumab 10 mg SC on days 1,2 and 3 followed by rituximab 100 mg IV on days 4,11,18 and 25. Complete response (CR) was defined as normal hemoglobin in the absence of hemolysis and platelet count >150K/μl; and partial response (PR): increase of 2 g/dl of hemoglobin and platelets 50-149K/μl The effect of the antibodies combination was evaluated by lymphocyte B, T and NK count 8 and 24 weeks after their administration. Prophylactic bactrim, acyclovir and itraconazole were given for the first 2 months.
Results
We included 13 patients, and eleven were evaluable, 5 patients in the AHA group and 6 in the ITP group, demographic data is shown on table 1. For AHA the 5 patients achieved CR with a median follow up of 37 weeks; only 1 patient relapsed after the 49th week of follow up. For the ITP group 2 patients achieved CR, 2 patients PR and 2 were classified as non responders. Alemtuzumab and rituximab combination quickly depleted B lymphocites falling to zero or near zero at the 8th week determination, with a sustained decrease at 24th week, in which levels did not return to pre-treatment levels.
Conclusions
These initial results indicate that low dose alemtuzumab and rituximab combination is safe and demonstrate promising activity for AHA and ITP refractory patients including durable complete responses and as a steroid spring therapy.
Disclosures:
Off Label Use: alemtuzumab for refractory autoimmune cytopenias rituximab for refractory autoimmune cytopenias.
Title: Alemtuzumab and Rituximab in the treatment of refractory autoimmune Cytopenias.
Description:
Abstract
Abstract 4458
Introduction
The combination of rituximab and alemtuzumab have been used to treat CLL.
This combination is feasible without excessive toxicity.
Both antibodies have been used as monotherapy for the treatment of autoimmune diseases, including autoimmune hemolytic anemia (AHA) and Immune thrombocytopenic purpura (ITP).
Objective
Evaluate the efficacy and safety of the combination of low dose alemtuzumab and rituximab in patients with AHA and ITP.
Material and methods
patients diagnosed with AHA (clinical and biochemical data of hemolysis) or ITP (less than < 50 K/μl) who failed or relapsed after first line therapy (steroids) were included.
Basal lymphocyte count and immunoglobulin levels were assessed.
Patients received alemtuzumab 10 mg SC on days 1,2 and 3 followed by rituximab 100 mg IV on days 4,11,18 and 25.
Complete response (CR) was defined as normal hemoglobin in the absence of hemolysis and platelet count >150K/μl; and partial response (PR): increase of 2 g/dl of hemoglobin and platelets 50-149K/μl The effect of the antibodies combination was evaluated by lymphocyte B, T and NK count 8 and 24 weeks after their administration.
Prophylactic bactrim, acyclovir and itraconazole were given for the first 2 months.
Results
We included 13 patients, and eleven were evaluable, 5 patients in the AHA group and 6 in the ITP group, demographic data is shown on table 1.
For AHA the 5 patients achieved CR with a median follow up of 37 weeks; only 1 patient relapsed after the 49th week of follow up.
For the ITP group 2 patients achieved CR, 2 patients PR and 2 were classified as non responders.
Alemtuzumab and rituximab combination quickly depleted B lymphocites falling to zero or near zero at the 8th week determination, with a sustained decrease at 24th week, in which levels did not return to pre-treatment levels.
Conclusions
These initial results indicate that low dose alemtuzumab and rituximab combination is safe and demonstrate promising activity for AHA and ITP refractory patients including durable complete responses and as a steroid spring therapy.
Disclosures:
Off Label Use: alemtuzumab for refractory autoimmune cytopenias rituximab for refractory autoimmune cytopenias.
Related Results
Alemtuzumab as First Line Treatment in Children with Familial Lymphohistiocytosis
Alemtuzumab as First Line Treatment in Children with Familial Lymphohistiocytosis
Background
Hemophagocytic lymphohistiocytosis (HLH) is an inflammatory condition caused by uncontrolled proliferation of activated lymphocytes and macrophages secret...
Could rituximab be a silver lining in refractory bone marrow fibrosis caused by lupus?
Could rituximab be a silver lining in refractory bone marrow fibrosis caused by lupus?
Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that can present with a variety of clinical manifestations, ranging from mild skin involvement to multisystemic ...
Treatment of Refractory Autoimmune Hemolytic Anemia in B-CLL with Alemtuzumab (Humanized CD52 MAb).
Treatment of Refractory Autoimmune Hemolytic Anemia in B-CLL with Alemtuzumab (Humanized CD52 MAb).
Abstract
Alemtuzumab is a humanized monoclonal antibody that targets the CD52 antigen. CD52 is abundantly expressed on leukemic B-CLL cells (approximately 4 x 105 bi...
Autoimmune Cytopenia in Chronic Lymphocytic Leukemia: Effect on Outcome and Survival, a Population Based Analysis in British Columbia, Canada
Autoimmune Cytopenia in Chronic Lymphocytic Leukemia: Effect on Outcome and Survival, a Population Based Analysis in British Columbia, Canada
Abstract
Background: Among Chronic Lymphocytic Leukemia (CLL) patients (pts), 4-10% are diagnosed with autoimmune cytopenias (AC) at some point during the course of ...
Antitumor Activity of An RNA-Based Agonist of TLR7 and 8 In Preclinical Models of Hematological Malignancies
Antitumor Activity of An RNA-Based Agonist of TLR7 and 8 In Preclinical Models of Hematological Malignancies
Abstract
Abstract 421
Treatment of hematological malignancies, non-Hodgkins lymphoma in particular, has evolved greatly in the past decade with the ad...
Commensalism or symbiosis: The potential use of rituximab in steroid-refractory Evans syndrome in a patient with ulcerative colitis
Commensalism or symbiosis: The potential use of rituximab in steroid-refractory Evans syndrome in a patient with ulcerative colitis
Evans syndrome (ES) is defined as simultaneous or sequential association of direct Coombs-positive autoimmune hemolytic anemia (AIHA) with superimposed immune-mediated thrombocytop...
Alemtuzumab Induction in Septuagenarians Undergoing Deceased Donor Kidney Transplantation
Alemtuzumab Induction in Septuagenarians Undergoing Deceased Donor Kidney Transplantation
ABSTRACT
Introduction
The anti‐CD52 monoclonal antibody alemtuzumab is used as an induction agent in kidney transplantati...
Rituximab Induces Long Lasting Clinical and Serological Remission in Refractory Antiphospholipid Syndrome (APS) and Related Disorders.
Rituximab Induces Long Lasting Clinical and Serological Remission in Refractory Antiphospholipid Syndrome (APS) and Related Disorders.
Abstract
INTRODUCTION. Rituximab, a chimeric monoclonal antibody against CD20 expressed on B cells, has been approved for the treatment of B cell neoplasms. Recently...

