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Not all IGHV3-21 chronic lymphocytic leukemias are equal: prognostic considerations

Authors :
Eva Minga
Karin E. Smedby
Lesley-Ann Sutton
Nicholas Chiorazzi
Myriam Boudjogra
Kostas Stamatopoulos
Karla Plevová
Lone Bredo Pedersen
Zadie Davis
Lydia Scarfò
Andreas Agathangelidis
Monica Facco
Achilles Anagnostopoulos
Maria Chatzouli
Chrysoula Belessi
Athina Tsanousa
Panagiotis Baliakas
Kirsten van Lom
Lefteris Angelis
Yorick Sandberg
Gunnar Juliusson
Diane F. Jelinek
Fie Juhl Vojdeman
Anne Gardiner
Panagiotis Panagiotidis
Anton W. Langerak
Florence Nguyen-Khac
Hana Skuhrová Francová
Frederic Davi
Denis Moreno
Silvio Veronese
Richard Rosenquist
Marie-Paule Lefranc
Nikos Darzentas
Šárka Pospíšilová
Véronique Giudicelli
Xiao-Jie Yan
Charles C. Chu
Christian H. Geisler
Larry Mansouri
David Oscier
Mark Catherwood
Marco Montillo
Anastasia Hadzidimitriou
Livio Trentin
Paolo Ghia
Tait D. Shanafelt
Tatiana Tzenou
Baliakas, P
Agathangelidis, A
Hadzidimitriou, A
Sutton, La
Minga, E
Tsanousa, A
Scarfò, L
Davis, Z
Yan, Xj
Shanafelt, T
Plevova, K
Sandberg, Y
Vojdeman, Fj
Boudjogra, M
Tzenou, T
Chatzouli, M
Chu, Cc
Veronese, S
Gardiner, A
Mansouri, L
Smedby, Ke
Pedersen, Lb
Moreno, D
Van Lom, K
Giudicelli, V
Francova, H
Nguyen Khac, F
Panagiotidis, P
Juliusson, G
Angelis, L
Anagnostopoulos, A
Lefranc, Mp
Facco, M
Trentin, L
Catherwood, M
Montillo, M
Geisler, Ch
Langerak, Aw
Pospisilova, S
Chiorazzi, N
Oscier, D
Jelinek, Df
Darzentas, N
Belessi, C
Davi, F
Ghia, PAOLO PROSPERO
Rosenquist, R
Stamatopoulos K. Ghia P., is Co senior author
Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden
Università Vita-Salute San Raffaele, Milan, Italy
Division of Molecular Oncology and Department of Onco-Hematology, Istituto di Ricovero e Cura a Carattere Scientifico, San Raffaele Scientific Institute, Milan, Italy
Institute of Applied Biosciences, Centre for Research and Technology-Hellas, Thessaloniki, Greece
Department of Informatics, Aristotle University of Thessaloniki, Thessaloniki, Greece
Department of Haematology, Royal Bournemouth Hospital, Bournemouth, United Kingdom
The Feinstein Institute for Medical Research
Mayo Clinic [Rochester]
Central European Institute of Technology [Brno] (CEITEC MU)
Brno University of Technology [Brno] (BUT)
Erasmus University Medical Center [Rotterdam] (Erasmus MC)
Department of Hematology, Rigshospitalet, Copenhagen, Denmark
Service d'Hématologie Biologique [CHU Pitié-Salpêtrière]
CHU Pitié-Salpêtrière [AP-HP]
Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
First Department of Propaedeutic Medicine, University of Athens, Athens, Greece
Hematology Department, Nikea General Hospital, Piraeus, Greece
Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico
Department of Medicine, Solna, Clinical Epidemiology Unit, Karolinska Institutet, Stockholm, Sweden
Institut de génétique humaine (IGH)
Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Lund University and Hospital Department of Hematology, Lund Stem Cell Center, Lund, Sweden
Hematology Department and Hematopoietic Cell Transplantation Unit, Georgios Papanicolaou Hospital, Thessaloniki, Greece
Universita degli Studi di Padova
Department of Hemato-Oncology, Belfast City Hospital, Belfast, United Kingdom
Immunology
Hematology
Source :
Blood, Blood, American Society of Hematology, 2015, 125 (5), pp.856-859. ⟨10.1182/blood-2014-09-600874⟩, Blood, 125(5), 856-859. American Society of Hematology
Publication Year :
2015
Publisher :
American Society of Hematology, 2015.

Abstract

An unresolved issue in chronic lymphocytic leukemia (CLL) is whether IGHV3-21 gene usage, in general, or the expression of stereotyped B-cell receptor immunoglobulin defining subset # 2 (IGHV3-21/IGLV3-21), in particular, determines outcome for IGHV3-21-utilizing cases. We reappraised this issue in 8593 CLL patients of whom 437 (5%) used the IGHV3-21 gene with 254/437 (58%) classified as subset # 2. Within subset # 2, immunoglobulin heavy variable (IGHV)-mutated cases predominated, whereas non-subset # 2/IGHV3-21 was enriched for IGHV-unmutated cases (P =.002). Subset # 2 exhibited significantly shorter time-to-first-treatment (TTFT) compared with non-subset # 2/IGHV3-21 (22 vs 60 months, P =.001). No such difference was observed between non-subset # 2/IGHV3-21 vs the remaining CLL with similar IGHV mutational status. In conclusion, IGHV3-21 CLL should not be axiomatically considered a homogeneous entity with adverse prognosis, given that only subset # 2 emerges as uniformly aggressive, contrasting non-subset # 2/IGVH3-21 patients whose prognosis depends on IGHV mutational status as the remaining CLL.

Details

ISSN :
15280020 and 00064971
Volume :
125
Database :
OpenAIRE
Journal :
Blood
Accession number :
edsair.doi.dedup.....3af82c0b22edf5f8a9a1063132ac6a41