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1000 Titel
  • Daratumumab, bortezomib, and dexamethasone in relapsed or refractory multiple myeloma: subgroup analysis of CASTOR based on cytogenetic risk
1000 Autor/in
  1. Weisel, Katja |
  2. Spencer, Andrew |
  3. Lentzsch, Suzanne |
  4. Avet-Loiseau, Hervé |
  5. Mark, Tomer M. |
  6. Spicka, Ivan |
  7. Masszi, Tamas |
  8. Lauri, Birgitta |
  9. Levin, Mark-David |
  10. Bosi, Alberto |
  11. Hungria, Vania |
  12. Cavo, Michele |
  13. Lee, Je-Jung |
  14. Nooka, Ajay |
  15. Quach, Hang |
  16. Munder, Markus |
  17. Lee, Cindy |
  18. Barreto, Wolney |
  19. Corradini, Paolo |
  20. Min, Chang-Ki |
  21. Chanan-Khan, Asher A. |
  22. Horvath, Noemi |
  23. Capra, Marcelo |
  24. Beksac, Meral |
  25. Ovilla, Roberto |
  26. Jo, Jae-Cheol |
  27. Shin, Ho-Jin |
  28. Sonneveld, Pieter |
  29. Casneuf, Tineke |
  30. DeAngelis, Nikki |
  31. Amin, Himal |
  32. Ukropec, Jon |
  33. Kobos, Rachel |
  34. Mateos, Maria-Victoria |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-08-20
1000 Erschienen in
1000 Quellenangabe
  • 13(1):115
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13045-020-00948-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439722/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Multiple myeloma (MM) patients with high cytogenetic risk have poor outcomes. In CASTOR, daratumumab plus bortezomib/dexamethasone (D-Vd) prolonged progression-free survival (PFS) versus bortezomib/dexamethasone (Vd) alone and exhibited tolerability in patients with relapsed or refractory MM (RRMM).!##!Methods!#!This subgroup analysis evaluated D-Vd versus Vd in CASTOR based on cytogenetic risk, determined using fluorescence in situ hybridization and/or karyotype testing performed locally. High-risk patients had t(4;14), t(14;16), and/or del17p abnormalities. Minimal residual disease (MRD; 10!##!Results!#!After a median follow-up of 40.0 months, D-Vd prolonged median PFS versus Vd in patients with standard (16.6 vs 6.6 months; HR, 0.26; 95% CI, 0.19-0.37; P < 0.0001) and high (12.6 vs 6.2 months; HR, 0.41; 95% CI, 0.21-0.83; P = 0.0106) cytogenetic risk. D-Vd achieved deep responses, including higher rates of MRD negativity and sustained MRD negativity versus Vd, regardless of cytogenetic risk. The safety profile was consistent with the overall population of CASTOR.!##!Conclusion!#!These updated data reinforce the effectiveness and tolerability of daratumumab-based regimens for RRMM, regardless of cytogenetic risk status.!##!Trial registration!#!ClinicalTrials.gov, NCT02136134 . Registered 12 May 2014.
1000 Sacherschließung
lokal Multiple myeloma
lokal Aged, 80 and over [MeSH]
lokal Multiple Myeloma/pathology [MeSH]
lokal Aged [MeSH]
lokal Bortezomib/administration
lokal Progression-Free Survival [MeSH]
lokal Myeloma therapy
lokal Multiple Myeloma/genetics [MeSH]
lokal Risk [MeSH]
lokal Male [MeSH]
lokal Antibodies, Monoclonal/administration
lokal Dexamethasone/administration
lokal Multiple Myeloma/drug therapy [MeSH]
lokal Female [MeSH]
lokal Follow-Up Studies [MeSH]
lokal Adult [MeSH]
lokal Kaplan-Meier Estimate [MeSH]
lokal Humans [MeSH]
lokal Middle Aged [MeSH]
lokal Abnormal Karyotype [MeSH]
lokal Antineoplastic Combined Chemotherapy Protocols/therapeutic use [MeSH]
lokal Recurrence [MeSH]
lokal Clinical trials
lokal Research
lokal Neoplasm, Residual [MeSH]
lokal In Situ Hybridization, Fluorescence [MeSH]
1000 Liste der Beteiligten
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