2006•Zhongguo xin yao zazhiRequires access

Advances of rituximab in the treatment of malignant lymphoma

Cai Qing-qing

Open publisher page 0 citations

Abstract

The chimeric anti-CD20 monoclonal antibody rituximab is the first humanized monoclonal antibody approved for patients with malignant lymphoma with CD20 expression. Rituximab has been approved to treat indolent non-Hodgkin's lymphoma and aggressive non-Hodgkin's lymphoma as first-line medication. Other indications of this agent used to manage Hodgkin's lymphoma and other B-cell malignancies were in the clinical trial stage. The adjunctive therapy of rituximab with cytotoxic agents or cyto-kines has been impressed in many clinical studies. The maintenance treatment of indolent non-Hodgkin's lymphoma with rituximab also yielded promising results. Rituximab has become the part of standard therapy for B cell non-Hodgkin's lymphoma.

About this research paper

What this paper is about

The chimeric anti-CD20 monoclonal antibody rituximab is the first humanized monoclonal antibody approved for patients with malignant lymphoma with CD20 expression. Rituximab has been approved to treat indolent non-Hodgkin's lymphoma and aggressive non-Hodgkin's lymphoma as first-line medication. Other indications of this agent used to manage Hodgkin's lymphoma and other B-cell malignancies were in the clinical trial stage. The adjunctive therapy of rituximab with cytotoxic agents or cyto-kines has been impressed in many clinical studies. The maintenance treatment of indolent non-Hodgkin's lymphoma with rituximab also yielded promising results. Rituximab has become the part of standard therapy for B cell non-Hodgkin's lymphoma.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The chimeric anti-CD20 monoclonal antibody rituximab is the first humanized monoclonal antibody approved for patients with malignant lymphoma with CD20 expression. Rituximab has been approved to treat indolent non-Hodgkin's lymphoma and aggressive non-Hodgkin's lymphoma as first-line medication. Other indications of this agent used to manage Hodgkin's lymphoma and other B-cell malignancies were in the clinical trial stage. The adjunctive therapy of rituximab with cytotoxic agents or cyto-kines has been impressed in many clinical studies. The maintenance treatment of indolent non-Hodgkin's lymphoma with rituximab also yielded promising results. Rituximab has become the part of standard therapy for B cell non-Hodgkin's lymphoma.

Key concepts: Rituximab, Medicine, Lymphoma, CD20, Monoclonal antibody, Oncology, Monoclonal antibody therapy, Monoclonal

Related papers

Back to paper searchBrowse research topicsOriginal source
Advances of rituximab in the treatment of malignant lymphoma — Research Paper | ScholarLens