Back to Search Start Over

Chronic Lymphocytic Leukemia (CLL) with Borderline Immunoglobulin Heavy Chain Mutational Status, a Rare Subgroup of CLL with Variable Disease Course.

Authors :
Angotzi F
Cellini A
Ruocco V
Cavarretta CA
Zatta I
Serafin A
Pravato S
Pagnin E
Bonaldi L
Frezzato F
Facco M
Piazza F
Trentin L
Visentin A
Source :
Cancers [Cancers (Basel)] 2024 Mar 08; Vol. 16 (6). Date of Electronic Publication: 2024 Mar 08.
Publication Year :
2024

Abstract

Chronic lymphocytic leukemia (CLL) exhibits substantial variability in disease course. The mutational status of the B-cell receptor immunoglobulin heavy variable (IGHV) chain is a critical prognostic factor, categorizing patients into mutated (M-IGHV) and unmutated (U-IGHV) groups. Recently, a third subgroup with borderline mutational status (BL-IGHV) has been identified, comprising approximately 5% of CLL cases. This study retrospectively analyzes the outcomes of 30 BL-IGHV mutated patients among a cohort of 653 CLL patients, focusing on time to first treatment (TTFT) and overall survival (OS). BL-IGHV patients had a short TTFT similar to U-IGHV patients (median 30.2 vs. 34 months; p = 0.9). Conversely, the OS of BL-IGHV patients resembled M-IGHV patients (median NR vs. 258 months; p = 1). Despite a similar incidence in unfavorable prognostic factors, the TTFT was shorter compared to other published cohorts. However, striking similarities with other experiences suggest that BL-IGHV mutated patients share common biological characteristics, biased IGHV gene usage and BCR subset frequency. These findings also underscore the need for multicentric efforts aggregating data on BL-IGHV CLL in order to elucidate its disease course and optimize therapeutic approaches for this rare subgroup. Until then, predicting outcomes and optimal management of BL-IGHV CLL will remain challenging.

Details

Language :
English
ISSN :
2072-6694
Volume :
16
Issue :
6
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
38539430
Full Text :
https://doi.org/10.3390/cancers16061095