-
Something wrong with this record ?
Allogeneic hematopoietic stem cell transplantation for adult patients with t(4;11)(q21;q23) KMT2A/AFF1 B-cell precursor acute lymphoblastic leukemia in first complete remission: impact of pretransplant measurable residual disease (MRD) status. An analysis from the Acute Leukemia Working Party of the EBMT
J. Esteve, S. Giebel, M. Labopin, T. Czerw, D. Wu, L. Volin, G. Socié, I. Yakoub-Agha, J. Maertens, JJ. Cornelissen, A. Pigneux, A. Shimoni, R. Schwerdtfeger, H. Labussière-Wallet, N. Russell, A. Schattenberg, P. Chevallier, V. Koza, R. Foà, C....
Language English Country Great Britain
Document type Journal Article, Multicenter Study
NLK
ProQuest Central
from 2000-01-01 to 1 year ago
Open Access Digital Library
from 1997-01-01
Nursing & Allied Health Database (ProQuest)
from 2000-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 2000-01-01 to 1 year ago
Public Health Database (ProQuest)
from 2000-01-01 to 1 year ago
- MeSH
- DNA-Binding Proteins genetics metabolism MeSH
- Adult MeSH
- Histone-Lysine N-Methyltransferase genetics metabolism MeSH
- Transplantation, Homologous MeSH
- Remission Induction MeSH
- Humans MeSH
- Chromosomes, Human, Pair 11 genetics MeSH
- Chromosomes, Human, Pair 4 genetics MeSH
- Survival Rate MeSH
- Follow-Up Studies MeSH
- Precursor B-Cell Lymphoblastic Leukemia-Lymphoma genetics pathology therapy MeSH
- Transplantation Conditioning MeSH
- Prognosis MeSH
- Myeloid-Lymphoid Leukemia Protein genetics metabolism MeSH
- Retrospective Studies MeSH
- Neoplasm, Residual genetics pathology therapy MeSH
- Transcriptional Elongation Factors genetics metabolism MeSH
- Translocation, Genetic MeSH
- Hematopoietic Stem Cell Transplantation methods MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
Adult B-cell precursor acute lymphoblastic leukemia (BCP-ALL) with t(4;11)(q21;q23);KMT2A/AFF1 is a poor-prognosis entity. This registry-based study was aimed to analyze outcome of patients with t(4;11) BCP-ALL treated with allogeneic hematopoietic stem cell transplantation (alloHSCT) in first complete remission (CR1) between 2000 and 2017, focusing on the impact of measurable residual disease (MRD) at the time of transplant. Among 151 patients (median age, 38) allotransplanted from either HLA-matched siblings or unrelated donors, leukemia-free survival (LFS) and overall survival (OS) at 2 years were 51% and 60%, whereas relapse incidence (RI) and non-relapse mortality (NRM) were 30% and 20%, respectively. These results were comparable to a cohort of contemporary patients with diploid normal karyotype (NK) BCP-ALL with equivalent inclusion criteria (n = 567). Among patients with evaluable MRD pre-alloHSCT, a negative status was the strongest beneficial factor influencing LFS (hazard ratio [HR] = 0.2, p < 0.001), OS (HR = 0.14, p < 0.001), RI (HR = 0.23, p = 0.001), and NRM (HR = 0.16, p = 0.002), with a similar outcome to MRD-negative NK BCP-ALL patients. In contrast, among patients with detectable pretransplant MRD, outcome in t(4;11) BCP-ALL was inferior to NK BCP-ALL (LFS: 27% vs. 50%, p = 0.02). These results support indication of alloHSCT in CR1 for t(4;11) BCP-ALL patients, provided a negative MRD status is achieved. Conversely, pre-alloHSCT additional therapy is warranted in MRD-positive patients.
Charles University Hospital Pilsen Czech Republic
CHU Bordeaux Hôpital Haut Lévêque Pessac France
Department d'Hematologie CHU Nantes Nantes France
Department of Hematology and Oncology Augsburg University Hospital Augsburg Germany
Department of Hematology Hospital Saint Antoine Paris France
Department of Hematology Nijmegen Medical Centre Radboud University Nijmegen The Netherlands
Department of Hematology The 1st Hospital Affiliated to Soochow University Suzhou China
Department of Translational and Precision Medicine Sapienza University Rome Italy
Division of Hematology Hospital St Louis and University Paris Paris France
EBMT Paris Study Office Department of Hematology and Cell Therapy Hôpital Saint Antoine Paris France
Erasmus MC Daniel den Hoed Cancer Centre Rotterdam The Netherlands
Hematology Department Hospital Clínic of Barcelona IDIBAPS University of Barcelona Barcelona Spain
Hematology Division Chaim Sheba Medical Center Tel Hashomer Israel
Hôpital Claude Huriez Lille France
Hôpital Edouard Herriot Lyon France
Nottingham University Hospitals and University of Nottingham Nottingham UK
University Hospital Center Zagreb School of Medicine University of Zagreb Zagreb Croatia
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21025245
- 003
- CZ-PrNML
- 005
- 20240528151424.0
- 007
- ta
- 008
- 211013s2021 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1038/s41375-021-01135-2 $2 doi
- 035 __
- $a (PubMed)33542481
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Esteve, Jordi $u Hematology Department, Hospital Clínic of Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain. jesteve@clinic.cat
- 245 10
- $a Allogeneic hematopoietic stem cell transplantation for adult patients with t(4;11)(q21;q23) KMT2A/AFF1 B-cell precursor acute lymphoblastic leukemia in first complete remission: impact of pretransplant measurable residual disease (MRD) status. An analysis from the Acute Leukemia Working Party of the EBMT / $c J. Esteve, S. Giebel, M. Labopin, T. Czerw, D. Wu, L. Volin, G. Socié, I. Yakoub-Agha, J. Maertens, JJ. Cornelissen, A. Pigneux, A. Shimoni, R. Schwerdtfeger, H. Labussière-Wallet, N. Russell, A. Schattenberg, P. Chevallier, V. Koza, R. Foà, C. Schmid, Z. Peric, M. Mohty, A. Nagler
- 520 9_
- $a Adult B-cell precursor acute lymphoblastic leukemia (BCP-ALL) with t(4;11)(q21;q23);KMT2A/AFF1 is a poor-prognosis entity. This registry-based study was aimed to analyze outcome of patients with t(4;11) BCP-ALL treated with allogeneic hematopoietic stem cell transplantation (alloHSCT) in first complete remission (CR1) between 2000 and 2017, focusing on the impact of measurable residual disease (MRD) at the time of transplant. Among 151 patients (median age, 38) allotransplanted from either HLA-matched siblings or unrelated donors, leukemia-free survival (LFS) and overall survival (OS) at 2 years were 51% and 60%, whereas relapse incidence (RI) and non-relapse mortality (NRM) were 30% and 20%, respectively. These results were comparable to a cohort of contemporary patients with diploid normal karyotype (NK) BCP-ALL with equivalent inclusion criteria (n = 567). Among patients with evaluable MRD pre-alloHSCT, a negative status was the strongest beneficial factor influencing LFS (hazard ratio [HR] = 0.2, p < 0.001), OS (HR = 0.14, p < 0.001), RI (HR = 0.23, p = 0.001), and NRM (HR = 0.16, p = 0.002), with a similar outcome to MRD-negative NK BCP-ALL patients. In contrast, among patients with detectable pretransplant MRD, outcome in t(4;11) BCP-ALL was inferior to NK BCP-ALL (LFS: 27% vs. 50%, p = 0.02). These results support indication of alloHSCT in CR1 for t(4;11) BCP-ALL patients, provided a negative MRD status is achieved. Conversely, pre-alloHSCT additional therapy is warranted in MRD-positive patients.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a lidské chromozomy, pár 11 $x genetika $7 D002880
- 650 _2
- $a lidské chromozomy, pár 4 $x genetika $7 D002894
- 650 _2
- $a DNA vazebné proteiny $x genetika $x metabolismus $7 D004268
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a následné studie $7 D005500
- 650 _2
- $a transplantace hematopoetických kmenových buněk $x metody $7 D018380
- 650 _2
- $a histonlysin-N-methyltransferasa $x genetika $x metabolismus $7 D011495
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a protoonkogenní protein MLL $x genetika $x metabolismus $7 D051788
- 650 _2
- $a reziduální nádor $x genetika $x patologie $x terapie $7 D018365
- 650 _2
- $a pre-B-buněčná leukemie $x genetika $x patologie $x terapie $7 D015452
- 650 _2
- $a prognóza $7 D011379
- 650 _2
- $a indukce remise $7 D012074
- 650 _2
- $a retrospektivní studie $7 D012189
- 650 _2
- $a míra přežití $7 D015996
- 650 _2
- $a transkripční elongační faktory $x genetika $x metabolismus $7 D035602
- 650 _2
- $a translokace genetická $7 D014178
- 650 _2
- $a příprava pacienta k transplantaci $7 D019172
- 650 _2
- $a homologní transplantace $7 D014184
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a multicentrická studie $7 D016448
- 700 1_
- $a Giebel, Sebastian $u Department of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie Institute-Oncology Center, Gliwice Branch, Gliwice, Poland. sgiebel@io.gliwice.pl
- 700 1_
- $a Labopin, Myriam $u EBMT Paris Study Office, Department of Hematology and Cell Therapy, Hôpital Saint-Antoine, Paris, France
- 700 1_
- $a Czerw, Tomasz $u Department of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie Institute-Oncology Center, Gliwice Branch, Gliwice, Poland
- 700 1_
- $a Wu, Depei $u Department of Hematology, The First Hospital Affiliated to Soochow University, Suzhou, China
- 700 1_
- $a Volin, Liisa $u Stem Cell Transplantation Unit, Comprehensive Cancer Center, Helsinki University Hospital, Helsinki, Finland
- 700 1_
- $a Socié, Gerard $u Division of Hematology, Hospital St Louis and University Paris, Paris, France
- 700 1_
- $a Yakoub-Agha, Ibrahim $u Hôpital Claude Huriez, Lille, France
- 700 1_
- $a Maertens, Johan $u University Hospital Gasthuisberg, Leuven, Belgium
- 700 1_
- $a Cornelissen, Jan J $u Erasmus MC-Daniel den Hoed Cancer Centre, Rotterdam, The Netherlands
- 700 1_
- $a Pigneux, Arnaud $u CHU Bordeaux, Hôpital Haut-Lévêque, Pessac, France
- 700 1_
- $a Shimoni, Avichai $u Hematology Division, Chaim Sheba Medical Center, Tel-Hashomer, Israel
- 700 1_
- $a Schwerdtfeger, Rainer $u Center for Hematopoietic Cell Transplantation, Deutsche Klinik für Diagnostik Helios Klinik, Wiesbaden, Germany
- 700 1_
- $a Labussière-Wallet, Hélène $u Hôpital Edouard Herriot, Lyon, France
- 700 1_
- $a Russell, Nigel $u Nottingham University Hospitals and University of Nottingham, Nottingham, UK
- 700 1_
- $a Schattenberg, Anton $u Department of Hematology, Nijmegen Medical Centre, Radboud University, Nijmegen, The Netherlands
- 700 1_
- $a Chevallier, Patrice $u Department d'Hematologie, CHU Nantes, Nantes, France
- 700 1_
- $a Koza, Vladimir $u Charles University Hospital, Pilsen, Czech Republic
- 700 1_
- $a Foa, Robin $u Department of Translational and Precision Medicine, "Sapienza" University, Rome, Italy $7 xx0317383
- 700 1_
- $a Schmid, Christoph $u Department of Hematology and Oncology, Augsburg University Hospital, Augsburg, Germany
- 700 1_
- $a Peric, Zinaida $u University Hospital Center Zagreb, School of Medicine, University of Zagreb, Zagreb, Croatia
- 700 1_
- $a Mohty, Mohamad $u EBMT Paris Study Office, Department of Hematology and Cell Therapy, Hôpital Saint-Antoine, Paris, France $u Department of Hematology, Hospital Saint Antoine, Paris, France $7 xx0317729
- 700 1_
- $a Nagler, Arnon $u EBMT Paris Study Office, Department of Hematology and Cell Therapy, Hôpital Saint-Antoine, Paris, France $u Hematology Division, Chaim Sheba Medical Center, Tel-Hashomer, Israel
- 773 0_
- $w MED00003138 $t Leukemia $x 1476-5551 $g Roč. 35, č. 8 (2021), s. 2232-2242
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33542481 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20211013 $b ABA008
- 991 __
- $a 20240528151421 $b ABA008
- 999 __
- $a ok $b bmc $g 1714344 $s 1145752
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 35 $c 8 $d 2232-2242 $e 20210204 $i 1476-5551 $m Leukemia $n Leukemia $x MED00003138
- LZP __
- $a Pubmed-20211013