-
Je něco špatně v tomto záznamu ?
Real-world data on efficacy and safety of obinutuzumab plus chlorambucil, rituximab plus chlorambucil, and rituximab plus bendamustine in the frontline treatment of chronic lymphocytic leukemia: The GO-CLLEAR Study by the Czech CLL Study Group
A. Panovská, L. Němcová, L. Nekvindová, M. Špaček, M. Šimkovič, T. Papajík, M. Brejcha, D. Lysák, J. Zuchnická, J. Novák, D. Starostka, H. Poul, F. Vrbacký, P. Vodárek, R. Urbanová, K. Plevová, Š. Pospíšilová, S. Mašlejová, Y. Brychtová, E....
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, pozorovací studie
Grantová podpora
NA
Czech CLL Study Group
Czech Leukemia Study Group
ML41010
F. Hoffmann-La Roche
MH CZ-RVO 65269705
Ministerstvo Zdravotnictví Ceské Republiky
LQ1601
Ministry of Education, Youth and Sport, CR project NPUII CEITEC 2020
Q28/LF1
Charles University Prague
Q40/08
Charles University Prague
PubMed
32400885
DOI
10.1002/hon.2744
Knihovny.cz E-zdroje
- MeSH
- bendamustin hydrochlorid aplikace a dávkování MeSH
- chlorambucil aplikace a dávkování MeSH
- chronická lymfatická leukemie farmakoterapie patologie MeSH
- humanizované monoklonální protilátky aplikace a dávkování MeSH
- indukce remise MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití MeSH
- následné studie MeSH
- prognóza MeSH
- protokoly protinádorové kombinované chemoterapie terapeutické užití MeSH
- retrospektivní studie MeSH
- rituximab aplikace a dávkování MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
Until recently, a combination of anti-CD20 antibody plus less intensive chemotherapy was a standard of care in elderly population with previously untreated chronic lymphocytic leukemia (CLL). The aim of this observational study was to retrospectively assess efficacy and safety of obinutuzumab + chlorambucil (G-Clb), rituximab + chlorambucil (R-Clb), and bendamustine + rituximab (BR) given as the frontline therapy within routine practice. The final analyzed dataset included 398 consecutive CLL patients from 10 hematology centers cooperating within the Czech CLL Study Group: 63 treated with G-Clb, 78 with R-Clb, and 257 with BR. There were no significant differences in prognostic and predictive markers among the groups. On the contrary, median age at the start of therapy and cumulative illness rating scale (CIRS) score was significantly higher in R-Clb group. Obinutuzumab plus chlorambucil regimen was preferably offered to elderly patients (compared to BR) with less severe comorbidities and lower CIRS score (compared to R-Clb). A time period when a treatment was indicated had also a strong impact on the choice of the regimen. The overall response rate reached 76% (30% complete remissions, CRs) in G-Clb, 75% (22% CRs) in R-Clb, and 85% (47% CRs) in BR group. Median event-free survival was 49.0 months for G-Clb, 20.3 months for R-Clb, and 37.0 months for BR group. Neutropenia grade ≥ 3 developed in 43% of G-Clb, 31% of R-Clb and in 49% of BR patients, grade ≥ 3 infections were recorded in 17% of G-Clb, 6.4% of R-Clb, and 17% of BR patients. In conclusion, real-world therapeutic activity of G-Clb appears to be at least comparable to prospective clinical trial data. R-Clb yields relatively good results in very old and severely comorbid patients.
Department of Hematology and Oncology University Hospital Plzeň Czech Republic
Department of Hematology Havirov Hospital and Polyclinic Havířov Czech Republic
Department of Hematology Hospital Pelhřimov Pelhřimov Czech Republic
Department of Hematology University Hospital Ostrava Czech Republic
Department of Hematooncology University Hospital Olomouc Czech Republic
Institute of Biostatistics and Analyses Ltd Brno Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20027771
- 003
- CZ-PrNML
- 005
- 20250114091500.0
- 007
- ta
- 008
- 210105s2020 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1002/hon.2744 $2 doi
- 035 __
- $a (PubMed)32400885
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Panovská, Anna $u Department of Internal Medicine-Hematology and Oncology, University Hospital and Masaryk University, Brno, Czech Republic.
- 245 10
- $a Real-world data on efficacy and safety of obinutuzumab plus chlorambucil, rituximab plus chlorambucil, and rituximab plus bendamustine in the frontline treatment of chronic lymphocytic leukemia: The GO-CLLEAR Study by the Czech CLL Study Group / $c A. Panovská, L. Němcová, L. Nekvindová, M. Špaček, M. Šimkovič, T. Papajík, M. Brejcha, D. Lysák, J. Zuchnická, J. Novák, D. Starostka, H. Poul, F. Vrbacký, P. Vodárek, R. Urbanová, K. Plevová, Š. Pospíšilová, S. Mašlejová, Y. Brychtová, E. Koriťáková, L. Smolej, M. Doubek,
- 520 9_
- $a Until recently, a combination of anti-CD20 antibody plus less intensive chemotherapy was a standard of care in elderly population with previously untreated chronic lymphocytic leukemia (CLL). The aim of this observational study was to retrospectively assess efficacy and safety of obinutuzumab + chlorambucil (G-Clb), rituximab + chlorambucil (R-Clb), and bendamustine + rituximab (BR) given as the frontline therapy within routine practice. The final analyzed dataset included 398 consecutive CLL patients from 10 hematology centers cooperating within the Czech CLL Study Group: 63 treated with G-Clb, 78 with R-Clb, and 257 with BR. There were no significant differences in prognostic and predictive markers among the groups. On the contrary, median age at the start of therapy and cumulative illness rating scale (CIRS) score was significantly higher in R-Clb group. Obinutuzumab plus chlorambucil regimen was preferably offered to elderly patients (compared to BR) with less severe comorbidities and lower CIRS score (compared to R-Clb). A time period when a treatment was indicated had also a strong impact on the choice of the regimen. The overall response rate reached 76% (30% complete remissions, CRs) in G-Clb, 75% (22% CRs) in R-Clb, and 85% (47% CRs) in BR group. Median event-free survival was 49.0 months for G-Clb, 20.3 months for R-Clb, and 37.0 months for BR group. Neutropenia grade ≥ 3 developed in 43% of G-Clb, 31% of R-Clb and in 49% of BR patients, grade ≥ 3 infections were recorded in 17% of G-Clb, 6.4% of R-Clb, and 17% of BR patients. In conclusion, real-world therapeutic activity of G-Clb appears to be at least comparable to prospective clinical trial data. R-Clb yields relatively good results in very old and severely comorbid patients.
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a senioři nad 80 let $7 D000369
- 650 _2
- $a humanizované monoklonální protilátky $x aplikace a dávkování $7 D061067
- 650 _2
- $a protokoly protinádorové kombinované chemoterapie $x terapeutické užití $7 D000971
- 650 _2
- $a bendamustin hydrochlorid $x aplikace a dávkování $7 D000069461
- 650 _2
- $a chlorambucil $x aplikace a dávkování $7 D002699
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a následné studie $7 D005500
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a chronická lymfatická leukemie $x farmakoterapie $x patologie $7 D015451
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a prognóza $7 D011379
- 650 _2
- $a indukce remise $7 D012074
- 650 _2
- $a retrospektivní studie $7 D012189
- 650 _2
- $a rituximab $x aplikace a dávkování $7 D000069283
- 650 _2
- $a míra přežití $7 D015996
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a pozorovací studie $7 D064888
- 700 1_
- $a Němcová, Lucie $u Department of Internal Medicine-Hematology and Oncology, University Hospital and Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Nekvindová, Lucie $u Institute of Biostatistics and Analyses, Ltd., Brno, Czech Republic.
- 700 1_
- $a Špaček, Martin $u 1st Department of Medicine-Department of Hematology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
- 700 1_
- $a Šimkovič, Martin $u 4th Department of Internal Medicine-Hematology, University Hospital and Charles University Faculty of Medicine, Hradec Králové, Czech Republic.
- 700 1_
- $a Papajík, Tomáš $u Department of Hematooncology, University Hospital, Olomouc, Czech Republic.
- 700 1_
- $a Brejcha, Martin $u Oncology Center, Nový Jičín, Czech Republic. $7 xx0105595
- 700 1_
- $a Lysák, Daniel $u Department of Hematology and Oncology, University Hospital, Plzeň, Czech Republic.
- 700 1_
- $a Zuchnická, Jana $u Department of Hematology, University Hospital, Ostrava, Czech Republic.
- 700 1_
- $a Novák, Jan $u Department of Internal Medicine and Hematology, University Hospital Kralovske Vinohrady and Third Faculty of Medicine, Charles University, Prague, Czech Republic.
- 700 1_
- $a Starostka, David $u Department of Hematology, Havirov Hospital and Polyclinic, Havířov, Czech Republic.
- 700 1_
- $a Poul, Hynek $u Department of Hematology, Hospital Pelhřimov, Pelhřimov, Czech Republic.
- 700 1_
- $a Vrbacký, Filip $u 4th Department of Internal Medicine-Hematology, University Hospital and Charles University Faculty of Medicine, Hradec Králové, Czech Republic.
- 700 1_
- $a Vodárek, Pavel $u 4th Department of Internal Medicine-Hematology, University Hospital and Charles University Faculty of Medicine, Hradec Králové, Czech Republic. $7 xx0262638
- 700 1_
- $a Urbanová, Renata $u Department of Hematooncology, University Hospital, Olomouc, Czech Republic.
- 700 1_
- $a Plevová, Karla $u Department of Internal Medicine-Hematology and Oncology, University Hospital and Masaryk University, Brno, Czech Republic. Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Pospíšilová, Šárka $u Department of Internal Medicine-Hematology and Oncology, University Hospital and Masaryk University, Brno, Czech Republic. Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Mašlejová, Stanislava $u Department of Internal Medicine-Hematology and Oncology, University Hospital and Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Brychtová, Yvona $u Department of Internal Medicine-Hematology and Oncology, University Hospital and Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Koriťáková, Eva $u Institute of Biostatistics and Analyses, Ltd., Brno, Czech Republic.
- 700 1_
- $a Smolej, Lukáš $u 4th Department of Internal Medicine-Hematology, University Hospital and Charles University Faculty of Medicine, Hradec Králové, Czech Republic.
- 700 1_
- $a Doubek, Michael $u Department of Internal Medicine-Hematology and Oncology, University Hospital and Masaryk University, Brno, Czech Republic. Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
- 773 0_
- $w MED00002019 $t Hematological oncology $x 1099-1069 $g Roč. 38, č. 4 (2020), s. 509-516
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/32400885 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20210105 $b ABA008
- 991 __
- $a 20250114091457 $b ABA008
- 999 __
- $a ok $b bmc $g 1608106 $s 1118951
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 38 $c 4 $d 509-516 $e 20200601 $i 1099-1069 $m Hematological oncology $n Hematol Oncol $x MED00002019
- GRA __
- $a NA $p Czech CLL Study Group
- GRA __
- $p Czech Leukemia Study Group
- GRA __
- $a ML41010 $p F. Hoffmann-La Roche
- GRA __
- $a MH CZ-RVO 65269705 $p Ministerstvo Zdravotnictví Ceské Republiky
- GRA __
- $a LQ1601 $p Ministry of Education, Youth and Sport, CR project NPUII CEITEC 2020
- GRA __
- $a Q28/LF1 $p Charles University Prague
- GRA __
- $a Q40/08 $p Charles University Prague
- LZP __
- $a Pubmed-20210105