SANDECKÁ, Viera, Luděk POUR, Ivan SPICKA, Jiri MINARIK, Jakub RADOCHA, Tomas JELINEK, Adriana HEINDORFER, Petr PAVLICEK, Michal SYKORA, Alexandra JUNGOVA, Petr KESSLER, Marek WROBEL, David STAROSTKA, Jana ULLRYCHOVA, Lukas STEJSKAL, Martin ŠTORK, Jan STRAUB, Tomas PIKA, Lucie KUBÍNOVÁ, Sabina ŠEVČÍKOVÁ, Vladimir MAISNAR and Roman HAJEK. Bortezomib-based therapy for newly diagnosed multiple myeloma patients ineligible for autologous stem cell transplantation: Czech Registry Data. European Journal of Haematology. Hoboken: Wiley-Blackwell, 2021, vol. 107, No 4, p. 466-474. ISSN 0902-4441. Available from: https://dx.doi.org/10.1111/ejh.13683.
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Basic information
Original name Bortezomib-based therapy for newly diagnosed multiple myeloma patients ineligible for autologous stem cell transplantation: Czech Registry Data
Authors SANDECKÁ, Viera (703 Slovakia), Luděk POUR (203 Czech Republic), Ivan SPICKA (203 Czech Republic), Jiri MINARIK (203 Czech Republic), Jakub RADOCHA (203 Czech Republic), Tomas JELINEK (203 Czech Republic), Adriana HEINDORFER (203 Czech Republic), Petr PAVLICEK (203 Czech Republic), Michal SYKORA (203 Czech Republic), Alexandra JUNGOVA (203 Czech Republic), Petr KESSLER (203 Czech Republic), Marek WROBEL (203 Czech Republic), David STAROSTKA (203 Czech Republic), Jana ULLRYCHOVA (203 Czech Republic), Lukas STEJSKAL (203 Czech Republic), Martin ŠTORK (203 Czech Republic, guarantor), Jan STRAUB (203 Czech Republic), Tomas PIKA (203 Czech Republic), Lucie KUBÍNOVÁ (203 Czech Republic, belonging to the institution), Sabina ŠEVČÍKOVÁ (203 Czech Republic, belonging to the institution), Vladimir MAISNAR (203 Czech Republic) and Roman HAJEK (203 Czech Republic).
Edition European Journal of Haematology, Hoboken, Wiley-Blackwell, 2021, 0902-4441.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30205 Hematology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.674
RIV identification code RIV/00216224:14110/21:00123612
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1111/ejh.13683
UT WoS 000678205200001
Keywords in English bortezomib; multiple myeloma; patient; treatment
Tags 14110518, 14119612, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 10/1/2022 13:46.
Abstract
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.
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