-
Something wrong with this record ?
Bortezomib-based therapy for newly diagnosed multiple myeloma patients ineligible for autologous stem cell transplantation: Czech Registry Data
V. Sandecká, L. Pour, I. Špička, J. Minařík, J. Radocha, T. Jelínek, A. Heindorfer, P. Pavlíček, M. Sýkora, A. Jungová, P. Kessler, M. Wróbel, D. Starostka, J. Ullrychová, L. Stejskal, M. Štork, J. Straub, T. Pika, L. Brožová, S. Ševčíková, V....
Language English Country Great Britain
Document type Journal Article
PubMed
34272773
DOI
10.1111/ejh.13683
Knihovny.cz E-resources
- MeSH
- Bortezomib therapeutic use MeSH
- Cyclophosphamide therapeutic use MeSH
- Dexamethasone therapeutic use MeSH
- Doxorubicin therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Melphalan therapeutic use MeSH
- Multiple Myeloma diagnosis drug therapy mortality pathology MeSH
- Prednisone therapeutic use MeSH
- Disease-Free Survival MeSH
- Antineoplastic Combined Chemotherapy Protocols therapeutic use MeSH
- Registries * MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Thalidomide therapeutic use MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Czech Republic MeSH
OBJECTIVES: This study compared the use of bortezomib in different combination regimens in newly diagnosed multiple myeloma (NDMM) patients who were transplant ineligible. PATIENTS AND METHODS: We analyzed data from the Registry of Monoclonal Gammopathies (RMG) of the Czech Myeloma Group (CMG) to provide real-world evidence of outcome for 794 newly diagnosed MM transplant ineligible patients. The most frequently used regimen was VCd (bortezomib-cyclophosphamide-dexamethasone) (47.5%) over VMP (bortezomib-melphalan-prednisone) (21.7%), BDd (bortezomib-doxorubicin-dexamethasone) (9.8%), and VTd (bortezomib-thalidomide-dexamethasone) (2.9%). RESULTS: The overall response rate (ORR) was 69.2% (478/691), including 12.6% (≥ CR); 34.7% very good partial responses (VGPR); and 21.9% partial responses (PR). Among triplet regimens, VMP was the most effective regimen compared to VCd, BDd, and VTd. Median PFS was 22.3 vs. 18.5 vs. 13.7 vs. 13.8 mo, (P = .275), respectively, and median OS was 49 vs. 41.7 vs. 37.9 vs. 32.2 mo (P = .004), respectively. The most common grade 3-4 toxicities were anemia in 17.4% and infections in 18% of patients. CONCLUSION: Our study confirmed that bortezomib-based treatment is effective and safe in NDMM transplant ineligible patients, especially VMP, which was identified as superior between bortezomib-based induction regimens not only in clinical trials, but also in real clinical practice.
Babak Myeloma Group Department of Pathophysiology Masaryk University Brno Czech Republic
Department of Clinical Hematology Hospital Ceske Budejovice Ceske Budejovice Czech Republic
Department of Clinical Hematology Hospital Havirov Czech Republic
Department of Clinical Hematology Hospital Liberec Czech Republic
Department of Clinical Hematology Hospital Novy Jicin Czech Republic
Department of Hemato Oncology University Hospital Olomouc Olomouc Czech Republic
Department of Hematology and Transfusion Medicine Hospital Pelhrimov Czech Republic
Department of Hematology Silesian Hospital in Opava Opava Czech Republic
Department of Internal Medicine Hematology and Oncology University Hospital Brno Czech Republic
Hematology and Oncology Department Charles University Hospital Pilsen Pilsen Czech Republic
Institute of Biostatistics and Analyses Masaryk University Brno Czech Republic
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22012133
- 003
- CZ-PrNML
- 005
- 20230714085129.0
- 007
- ta
- 008
- 220425s2021 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1111/ejh.13683 $2 doi
- 035 __
- $a (PubMed)34272773
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Sandecká, Viera $u Department of Internal Medicine, Hematology and Oncology, University Hospital, Brno, Czech Republic $1 https://orcid.org/0000000340748497
- 245 10
- $a Bortezomib-based therapy for newly diagnosed multiple myeloma patients ineligible for autologous stem cell transplantation: Czech Registry Data / $c V. Sandecká, L. Pour, I. Špička, J. Minařík, J. Radocha, T. Jelínek, A. Heindorfer, P. Pavlíček, M. Sýkora, A. Jungová, P. Kessler, M. Wróbel, D. Starostka, J. Ullrychová, L. Stejskal, M. Štork, J. Straub, T. Pika, L. Brožová, S. Ševčíková, V. Maisnar, R. Hájek
- 520 9_
- $a OBJECTIVES: This study compared the use of bortezomib in different combination regimens in newly diagnosed multiple myeloma (NDMM) patients who were transplant ineligible. PATIENTS AND METHODS: We analyzed data from the Registry of Monoclonal Gammopathies (RMG) of the Czech Myeloma Group (CMG) to provide real-world evidence of outcome for 794 newly diagnosed MM transplant ineligible patients. The most frequently used regimen was VCd (bortezomib-cyclophosphamide-dexamethasone) (47.5%) over VMP (bortezomib-melphalan-prednisone) (21.7%), BDd (bortezomib-doxorubicin-dexamethasone) (9.8%), and VTd (bortezomib-thalidomide-dexamethasone) (2.9%). RESULTS: The overall response rate (ORR) was 69.2% (478/691), including 12.6% (≥ CR); 34.7% very good partial responses (VGPR); and 21.9% partial responses (PR). Among triplet regimens, VMP was the most effective regimen compared to VCd, BDd, and VTd. Median PFS was 22.3 vs. 18.5 vs. 13.7 vs. 13.8 mo, (P = .275), respectively, and median OS was 49 vs. 41.7 vs. 37.9 vs. 32.2 mo (P = .004), respectively. The most common grade 3-4 toxicities were anemia in 17.4% and infections in 18% of patients. CONCLUSION: Our study confirmed that bortezomib-based treatment is effective and safe in NDMM transplant ineligible patients, especially VMP, which was identified as superior between bortezomib-based induction regimens not only in clinical trials, but also in real clinical practice.
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a senioři nad 80 let $7 D000369
- 650 _2
- $a protokoly protinádorové kombinované chemoterapie $x terapeutické užití $7 D000971
- 650 _2
- $a bortezomib $x terapeutické užití $7 D000069286
- 650 _2
- $a cyklofosfamid $x terapeutické užití $7 D003520
- 650 _2
- $a dexamethason $x terapeutické užití $7 D003907
- 650 _2
- $a přežití bez známek nemoci $7 D018572
- 650 _2
- $a doxorubicin $x terapeutické užití $7 D004317
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a melfalan $x terapeutické užití $7 D008558
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a mnohočetný myelom $x diagnóza $x farmakoterapie $x mortalita $x patologie $7 D009101
- 650 _2
- $a prednison $x terapeutické užití $7 D011241
- 650 12
- $a registrace $7 D012042
- 650 _2
- $a thalidomid $x terapeutické užití $7 D013792
- 650 _2
- $a výsledek terapie $7 D016896
- 651 _2
- $a Česká republika $7 D018153
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Pour, Luděk $u Department of Internal Medicine, Hematology and Oncology, University Hospital, Brno, Czech Republic
- 700 1_
- $a Špička, Ivan $u 1st Department of Medicine, Department of Hematology, Charles University and General Hospital, Prague, Czech Republic
- 700 1_
- $a Minařík, Jiří $u Department of Hemato-Oncology, University Hospital Olomouc, Olomouc, Czech Republic $1 https://orcid.org/000000030513326X
- 700 1_
- $a Radocha, Jakub $u 4th Department of Internal Medicine, Hematology, University Hospital and Charles University in Hradec Kralove, Hradec Kralove, Czech Republic
- 700 1_
- $a Jelínek, Tomáš $u Department of Hematooncology, University Hospital Ostrava, University of Ostrava, Ostrava, Czech Republic
- 700 1_
- $a Heindorfer, Adriana $u Department of Clinical Hematology, Hospital Liberec, Czech Republic
- 700 1_
- $a Pavlíček, Petr $u Department of Internal Medicine and Hematology, Charles University and Faculty Hospital Kralovske Vinohrady, Prague, Czech Republic
- 700 1_
- $a Sýkora, Michal $u Department of Clinical Hematology, Hospital Ceske Budejovice, Ceske Budejovice, Czech Republic
- 700 1_
- $a Jungová, Alexandra $u Hematology and Oncology Department, Charles University Hospital Pilsen, Pilsen, Czech Republic
- 700 1_
- $a Kessler, Petr $u Department of Hematology and Transfusion Medicine, Hospital Pelhrimov, Czech Republic
- 700 1_
- $a Wróbel, Marek $u Department of Clinical Hematology, Hospital Novy Jicin, Czech Republic $7 xx0303976
- 700 1_
- $a Starostka, David $u Department of Clinical Hematology, Hospital Havirov, Czech Republic
- 700 1_
- $a Ullrychová, Jana $u Department of Clinical Hematology, Regional Health Corporation, Masaryk Hospital, Usti nad Labem, Czech Republic
- 700 1_
- $a Stejskal, Lukáš $u Department of Hematology, Silesian Hospital in Opava, Opava, Czech Republic
- 700 1_
- $a Štork, Martin $u Department of Internal Medicine, Hematology and Oncology, University Hospital, Brno, Czech Republic $1 https://orcid.org/0000000270728537
- 700 1_
- $a Straub, Jan $u 1st Department of Medicine, Department of Hematology, Charles University and General Hospital, Prague, Czech Republic
- 700 1_
- $a Pika, Tomáš $u Department of Hemato-Oncology, University Hospital Olomouc, Olomouc, Czech Republic
- 700 1_
- $a Brožová, Lucie $u Institute of Biostatistics and Analyses, Masaryk University, Brno, Czech Republic
- 700 1_
- $a Ševčíková, Sabina $u Babak Myeloma Group, Department of Pathophysiology, Masaryk University, Brno, Czech Republic $1 https://orcid.org/0000000271946771
- 700 1_
- $a Maisnar, Vladimír $u 4th Department of Internal Medicine, Hematology, University Hospital and Charles University in Hradec Kralove, Hradec Kralove, Czech Republic
- 700 1_
- $a Hájek, Roman $u Department of Hematooncology, University Hospital Ostrava, University of Ostrava, Ostrava, Czech Republic $1 https://orcid.org/0000000169556267 $7 nlk20000083645
- 773 0_
- $w MED00001620 $t European journal of haematology $x 1600-0609 $g Roč. 107, č. 4 (2021), s. 466-474
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34272773 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220425 $b ABA008
- 991 __
- $a 20230714085129 $b ABA008
- 999 __
- $a ok $b bmc $g 1789637 $s 1163334
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 107 $c 4 $d 466-474 $e 20210728 $i 1600-0609 $m European journal of haematology $n Eur J Haematol $x MED00001620
- LZP __
- $a Pubmed-20220425