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Richter transformation in chronic lymphocytic leukemia (CLL)-a pooled analysis of German CLL Study Group (GCLLSG) front line treatment trials.

Authors :
Al-Sawaf O
Robrecht S
Bahlo J
Fink AM
Cramer P
V Tresckow J
Lange E
Kiehl M
Dreyling M
Ritgen M
Dürig J
Tausch E
Schneider C
Stilgenbauer S
Wendtner CM
Fischer K
Goede 5th
Hallek M
Eichhorst B
Source :
Leukemia [Leukemia] 2021 Jan; Vol. 35 (1), pp. 169-176. Date of Electronic Publication: 2020 Mar 17.
Publication Year :
2021

Abstract

Richter transformation (RT) is defined as development of aggressive lymphoma in patients (pts) with CLL. The incidence rates of RT among pts with CLL range from 2 to 10%. The aim of this analysis is to report the frequency, characteristics and outcomes of pts with RT enrolled in trials of the GCLLSG. A total of 2975 pts with advanced CLL were reviewed for incidence of RT. Clinical, laboratory, and genetic data were pooled. Time-to-event data, starting from time of CLL diagnosis, of first-line therapy or of RT diagnosis, were analyzed by Kaplan-Meier methodology. One hundred and three pts developed RT (3%): 95 pts diffuse large B-cell lymphoma (92%) and eight pts Hodgkin lymphoma (8%). Median observation time was 53 months (interquartile range 38.1-69.5). Median OS from initial CLL diagnosis for pts without RT was 167 months vs 71 months for pts with RT (HR 2.64, CI 2.09-3.33). Median OS after diagnosis of RT was 9 months. Forty-seven pts (46%) received CHOP-like regimens for RT treatment. Three pts subsequently underwent allogeneic and two pts autologous stem cell transplantation. Our findings show that within a large cohort of GCLLSG trial participants, 3% of the pts developed RT after receiving first-line chemo- or chemoimmunotherapy. This dataset confirms the ongoing poor prognosis and high mortality associated with RT.

Details

Language :
English
ISSN :
1476-5551
Volume :
35
Issue :
1
Database :
MEDLINE
Journal :
Leukemia
Publication Type :
Academic Journal
Accession number :
32203141
Full Text :
https://doi.org/10.1038/s41375-020-0797-x