医学
慢性淋巴细胞白血病
侵袭性淋巴瘤
淋巴瘤
弥漫性大B细胞淋巴瘤
肿瘤科
淋巴结活检
内科学
临床试验
伊布替西坦
滤泡性淋巴瘤
淋巴结
美罗华
白血病
放射免疫疗法
免疫学
抗体
单克隆抗体
作者
Robert Briski,Justin Taylor
出处
期刊:Cancers
[MDPI AG]
日期:2023-03-20
卷期号:15 (6): 1857-1857
被引量:3
标识
DOI:10.3390/cancers15061857
摘要
Richter Transformation (RT) refers to the development of an aggressive lymphoma in the setting of chronic lymphocytic leukemia (CLL). While many variants of RT are recognized, diffuse large B-cell lymphoma (RT-DLBCL) is the most common (80%), followed by Hodgkin's lymphoma (RT-HL, 19%). Diagnosis is based upon histologic evaluation of clinically suspicious lymph nodes. Positron emission tomography (PET) may be used to select the node of interest for biopsy. Although clonality testing is not a prerequisite of RT diagnosis, it has significant implications for survival. Clonally related DLBCL carries the worst prognosis with a median overall survival (OS) of less than one year in the era of combination chemotherapies with or without anti-CD20 antibodies. Prognosis has improved with the use of stem cell transplant and newer agents such as targeted therapy and newer forms of immunotherapy. Consideration of a clinical trial is encouraged. This review describes our current understanding of RT and focuses on treatment of RT-DLBCL, including clinical trials in progress and new therapies in development. We also report an illustrative example of a patient with clonally related DLBCL who survived two years after diagnosis without the use of combination chemotherapy.
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