TY - JOUR
T1 - Adjuvant rituximab causes prolonged hypogammaglobulinaemia following autologous stem cell transplant for non-Hodgkin's lymphoma
AU - Shortt, Jake
AU - Spencer, Andrew
PY - 2006
Y1 - 2006
N2 - Rituximab is an anti-CD20 monoclonal antibody that has efficacy in B-cell non-Hodgkin s lymphoma (NHL). Adjuvant immunotherapy with rituximab may reduce relapse rates for high-risk B-cell NHL following high-dose chemotherapy with autologous stem cell transplantation (SCT). However, the potential adverse effects of rituximab on immune reconstitution following SCT are not fully characterized. We performed a retrospective analysis of immunoglobulin (Ig) levels and peripheral blood neutrophil counts in 11 patients who received adjuvant rituximab following autologous SCT for B-cell NHL. Results were compared to a contemporaneous group of 24 patients who received an identical conditioning regimen and autologous SCT for lymphoma, but no adjuvant rituximab. Adjuvant rituximab was associated with a significantly increased incidence of hypogammaglobulinaemia between 12 and 24 months post-SCT, but not neutropenia. Despite suppression of Igs, there were no late or atypical infective complications attributable to rituximab.
AB - Rituximab is an anti-CD20 monoclonal antibody that has efficacy in B-cell non-Hodgkin s lymphoma (NHL). Adjuvant immunotherapy with rituximab may reduce relapse rates for high-risk B-cell NHL following high-dose chemotherapy with autologous stem cell transplantation (SCT). However, the potential adverse effects of rituximab on immune reconstitution following SCT are not fully characterized. We performed a retrospective analysis of immunoglobulin (Ig) levels and peripheral blood neutrophil counts in 11 patients who received adjuvant rituximab following autologous SCT for B-cell NHL. Results were compared to a contemporaneous group of 24 patients who received an identical conditioning regimen and autologous SCT for lymphoma, but no adjuvant rituximab. Adjuvant rituximab was associated with a significantly increased incidence of hypogammaglobulinaemia between 12 and 24 months post-SCT, but not neutropenia. Despite suppression of Igs, there were no late or atypical infective complications attributable to rituximab.
UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-33748431654&partnerID=40&md5=bda1b47ae462eb92bc3b9082074573b4
U2 - 10.1038/sj.bmt.1705463
DO - 10.1038/sj.bmt.1705463
M3 - Article
SN - 0268-3369
VL - 38
SP - 433
EP - 436
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 6
ER -