Clonal haematopoiesis as a risk factor for therapy-related
myeloid neoplasms in patients with chronic lymphocytic
leukaemia treated with chemo-(immuno)therapy

J 2022

Clonal haematopoiesis as a risk factor for therapy-related myeloid neoplasms in patients with chronic lymphocytic leukaemia treated with chemo-(immuno)therapy

VOSO, Maria-Teresa, Tatjana PANDZIC, Giulia FALCONI, Marija DENCIC-FEKETE, De Bellis ELEONORA et. al.

Basic information

Original name

Clonal haematopoiesis as a risk factor for therapy-related myeloid neoplasms in patients with chronic lymphocytic leukaemia treated with chemo-(immuno)therapy

Authors

VOSO, Maria-Teresa, Tatjana PANDZIC, Giulia FALCONI, Marija DENCIC-FEKETE, De Bellis ELEONORA, Lydia SCARFO, Viktor LJUNGSTROM, Michail ISKAS, Del Poeta GIOVANNI, Pamela RANGHETTI, Stamatia LAIDOU, Antonio CRISTIANO, Karla PLEVOVÁ (203 Czech Republic, belonging to the institution), Silvia IMBERGAMO, Marie ENGVALL, Antonella ZUCCHETTO, Chiara SALVETTI, Francesca R MAURO, Niki STAVROYIANNI, Lucia CAVELIER, Paolo GHIA, Kostas STAMATOPOULOS, Emiliano FABIANI (guarantor) and Panagiotis BALIAKAS

Edition

British journal of haematology, England, Wiley-Blackwell, 2022, 0007-1048

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30205 Hematology

Country of publisher

United States of America

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

URL

Impact factor

Impact factor: 6.500

RIV identification code

RIV/00216224:14110/22:00126416

Organization unit

Faculty of Medicine

DOI

http://dx.doi.org/10.1111/bjh.18129

UT WoS

000767753800001

Keywords in English

CHIP and FCR; CLL; t-MN

Abstract

V originále

Clonal haematopoiesis of indeterminate potential (CHIP) may predispose for the development of therapy-related myeloid neoplasms (t-MN). Using target next-generation sequencing (t-NGS) panels and digital droplet polymerase chain reactions (ddPCR), we studied the myeloid gene mutation profiles of patients with chronic lymphocytic leukaemia (CLL) who developed a t-MN after treatment with chemo-(immuno)therapy. Using NGS, we detected a total of 30 pathogenic/likely pathogenic (P/LP) variants in 10 of 13 patients with a t-MN (77%, median number of variants for patient: 2, range 0-6). The prevalence of CHIP was then backtracked in paired samples taken at CLL diagnosis in eight of these patients. Six of them carried at least one CHIP-variant at the time of t-MN (median: 2, range: 1-5), and the same variants were present in the CLL sample in five cases. CHIP variants were present in 34 of 285 patients from a population-based CLL cohort, which translates into a significantly higher prevalence of CHIP in patients with a CLL who developed a t-MN, compared to the population-based cohort (5/8, 62.5% vs. 34/285, 12%, p = 0.0001). Our data show that CHIP may be considered as a novel parameter affecting treatment algorithms in patients with CLL, and highlight the potential of using chemo-free therapies in CHIP-positive cases.

Citovat

VOSO, Maria-Teresa, Tatjana PANDZIC, Giulia FALCONI, Marija DENCIC-FEKETE, De Bellis ELEONORA, Lydia SCARFO, Viktor LJUNGSTROM, Michail ISKAS, Del Poeta GIOVANNI, Pamela RANGHETTI, Stamatia LAIDOU, Antonio CRISTIANO, Karla PLEVOVÁ, Silvia IMBERGAMO, Marie ENGVALL, Antonella ZUCCHETTO, Chiara SALVETTI, Francesca R MAURO, Niki STAVROYIANNI, Lucia CAVELIER, Paolo GHIA, Kostas STAMATOPOULOS, Emiliano FABIANI and Panagiotis BALIAKAS. Clonal haematopoiesis as a risk factor for therapy-related myeloid neoplasms in patients with chronic lymphocytic leukaemia treated with chemo-(immuno)therapy. British journal of haematology. England: Wiley-Blackwell, 2022, vol. 198, No 1, p. 103-113. ISSN 0007-1048. Available from: https://dx.doi.org/10.1111/bjh.18129.

@article{2211023,
   author = {Voso, MariaandTeresa and Pandzic, Tatjana and Falconi, Giulia and DencicandFekete, Marija and Eleonora, De Bellis and Scarfo, Lydia and Ljungstrom, Viktor and Iskas, Michail and Giovanni, Del Poeta and Ranghetti, Pamela and Laidou, Stamatia and Cristiano, Antonio and Plevová, Karla and Imbergamo, Silvia and Engvall, Marie and Zucchetto, Antonella and Salvetti, Chiara and Mauro, Francesca R and Stavroyianni, Niki and Cavelier, Lucia and Ghia, Paolo and Stamatopoulos, Kostas and Fabiani, Emiliano and Baliakas, Panagiotis},
   article_location = {England},
   article_number = {1},
   doi = {http://dx.doi.org/10.1111/bjh.18129},
   keywords = {CHIP and FCR; CLL; t-MN},
   language = {eng},
   issn = {0007-1048},
   journal = {British journal of haematology},
   title = {Clonal haematopoiesis as a risk factor for therapy-related myeloid neoplasms in patients with chronic lymphocytic leukaemia treated with chemo-(immuno)therapy},
   url = {https://onlinelibrary.wiley.com/doi/10.1111/bjh.18129},
   volume = {198},
   year = {2022}
}

TY  - JOUR
ID  - 2211023
AU  - Voso, Maria-Teresa - Pandzic, Tatjana - Falconi, Giulia - Dencic-Fekete, Marija - Eleonora, De Bellis - Scarfo, Lydia - Ljungstrom, Viktor - Iskas, Michail - Giovanni, Del Poeta - Ranghetti, Pamela - Laidou, Stamatia - Cristiano, Antonio - Plevová, Karla - Imbergamo, Silvia - Engvall, Marie - Zucchetto, Antonella - Salvetti, Chiara - Mauro, Francesca R - Stavroyianni, Niki - Cavelier, Lucia - Ghia, Paolo - Stamatopoulos, Kostas - Fabiani, Emiliano - Baliakas, Panagiotis
PY  - 2022
TI  - Clonal haematopoiesis as a risk factor for therapy-related myeloid neoplasms in patients with chronic lymphocytic leukaemia treated with chemo-(immuno)therapy
JF  - British journal of haematology
VL  - 198
IS  - 1
SP  - 103-113
EP  - 103-113
PB  - Wiley-Blackwell
SN  - 00071048
KW  - CHIP and FCR
KW  - CLL
KW  - t-MN
UR  - https://onlinelibrary.wiley.com/doi/10.1111/bjh.18129
N2  - Clonal haematopoiesis of indeterminate potential (CHIP) may predispose for the development of therapy-related myeloid neoplasms (t-MN). Using target next-generation sequencing (t-NGS) panels and digital droplet polymerase chain reactions (ddPCR), we studied the myeloid gene mutation profiles of patients with chronic lymphocytic leukaemia (CLL) who developed a t-MN after treatment with chemo-(immuno)therapy. Using NGS, we detected a total of 30 pathogenic/likely pathogenic (P/LP) variants in 10 of 13 patients with a t-MN (77%, median number of variants for patient: 2, range 0-6). The prevalence of CHIP was then backtracked in paired samples taken at CLL diagnosis in eight of these patients. Six of them carried at least one CHIP-variant at the time of t-MN (median: 2, range: 1-5), and the same variants were present in the CLL sample in five cases. CHIP variants were present in 34 of 285 patients from a population-based CLL cohort, which translates into a significantly higher prevalence of CHIP in patients with a CLL who developed a t-MN, compared to the population-based cohort (5/8, 62.5% vs. 34/285, 12%, p = 0.0001). Our data show that CHIP may be considered as a novel parameter affecting treatment algorithms in patients with CLL, and highlight the potential of using chemo-free therapies in CHIP-positive cases.
ER  -

VOSO, Maria-Teresa, Tatjana PANDZIC, Giulia FALCONI, Marija DENCIC-FEKETE, De Bellis ELEONORA, Lydia SCARFO, Viktor LJUNGSTROM, Michail ISKAS, Del Poeta GIOVANNI, Pamela RANGHETTI, Stamatia LAIDOU, Antonio CRISTIANO, Karla PLEVOVÁ, Silvia IMBERGAMO, Marie ENGVALL, Antonella ZUCCHETTO, Chiara SALVETTI, Francesca R MAURO, Niki STAVROYIANNI, Lucia CAVELIER, Paolo GHIA, Kostas STAMATOPOULOS, Emiliano FABIANI and Panagiotis BALIAKAS. Clonal haematopoiesis as a risk factor for therapy-related myeloid neoplasms in patients with chronic lymphocytic leukaemia treated with chemo-(immuno)therapy. \textit{British journal of haematology}. England: Wiley-Blackwell, 2022, vol.~198, No~1, p.~103-113. ISSN~0007-1048. Available from: https://dx.doi.org/10.1111/bjh.18129.

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