TY - JOUR
T1 - Richter transformation of chronic lymphocytic leukemia in the era of novel agents
AU - Wang, Yucai
AU - Ding, Wei
N1 - Funding Information:
Dr Wang has no conflicts of interest to disclose. Dr Ding has received research funding from Merck and DTRM, and has participated in advisory boards for Merck and Alexion.
Publisher Copyright:
© 2020, Millennium Medical Publishing, Inc.. All rights reserved.
PY - 2020
Y1 - 2020
N2 - The increased use of several effective novel targeted therapy agents has revolutionized therapy for patients with chronic lymphocytic leukemia (CLL). Disease progression in patients with CLL continues to occur, however. In particular, 3% to 25% of patients treated with a novel agent develop Richter transformation (RT); that is, histologic transformation of CLL to an aggressive lymphoma, most commonly diffuse large B-cell lymphoma (DLBCL). RT that develops in the novel agent era is frequently associated with adverse molecular alterations, such as TP53 disrup-tion and complex karyotype. As a result, patients with RT in the era of novel agents typically have poor responses to the traditional chemotherapy used to treat de novo DLBCL. These patients also tend to have poor survival outcomes, with a median overall survival of less than 1 year. In this article, we review the contemporary literature of RT, particularly in the context of novel agents used for CLL, and discuss the management approach of RT in the novel agent era.
AB - The increased use of several effective novel targeted therapy agents has revolutionized therapy for patients with chronic lymphocytic leukemia (CLL). Disease progression in patients with CLL continues to occur, however. In particular, 3% to 25% of patients treated with a novel agent develop Richter transformation (RT); that is, histologic transformation of CLL to an aggressive lymphoma, most commonly diffuse large B-cell lymphoma (DLBCL). RT that develops in the novel agent era is frequently associated with adverse molecular alterations, such as TP53 disrup-tion and complex karyotype. As a result, patients with RT in the era of novel agents typically have poor responses to the traditional chemotherapy used to treat de novo DLBCL. These patients also tend to have poor survival outcomes, with a median overall survival of less than 1 year. In this article, we review the contemporary literature of RT, particularly in the context of novel agents used for CLL, and discuss the management approach of RT in the novel agent era.
KW - Chronic lymphocytic leukemia
KW - Ibrutinib
KW - Immune checkpoint inhibitor
KW - Richter transformation
KW - Venetoclax
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M3 - Article
C2 - 32649656
AN - SCOPUS:85086043588
SN - 1543-0790
VL - 18
SP - 348
EP - 357
JO - Clinical Advances in Hematology and Oncology
JF - Clinical Advances in Hematology and Oncology
IS - 6
ER -