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1000 Titel
  • Long-term results and GvHD after prophylactic and preemptive donor lymphocyte infusion after allogeneic stem cell transplantation for acute leukemia
1000 Autor/in
  1. Schmid, Christoph |
  2. LABOPIN, Myriam |
  3. Schaap, Nicolaas |
  4. Veelken, Hendrik |
  5. Brecht, Arne |
  6. Stadler, Michael |
  7. Finke, Juergen |
  8. Baron, Frederic |
  9. Collin, Matthew |
  10. Bug, Gesine |
  11. Ljungman, Per |
  12. Blaise, Didier |
  13. Tischer, Johanna |
  14. Bloor, Adrian |
  15. Kulagin, Alexander |
  16. Giebel, Sebastian |
  17. Gorin, Norbert-Claude |
  18. Esteve Reyner, Jordi |
  19. CICERI, Fabio |
  20. Savani, Bipin |
  21. Nagler, Arnon |
  22. Mohty, Mohamad |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-11-08
1000 Erschienen in
1000 Quellenangabe
  • 57(2):215-223
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1038/s41409-021-01515-3 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821014/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • We report on 318 patients with acute leukemia, receiving donor lymphocyte infusion (DLI) in complete hematologic remission (CHR) after allogeneic stem cell transplantation (alloSCT). DLI were applied preemptively (preDLI) for minimal residual disease (MRD, n = 23) or mixed chimerism (MC, n = 169), or as prophylaxis in high-risk patients with complete chimerism and molecular remission (proDLI, n = 126). Median interval from alloSCT to DLI1 was 176 days, median follow-up was 7.0 years. Five-year cumulative relapse incidence (CRI), non-relapse mortality (NRM), leukemia-free and overall survival (LFS/OS) of the entire cohort were 29.1%, 12.7%, 58.2%, and 64.3%. Cumulative incidences of acute graft-versus-host disease (aGvHD) grade II-IV°/chronic GvHD were 11.9%/31%. Nineteen patients (6%) died from DLI-induced GvHD. Age ≥60 years (p = 0.046), advanced stage at transplantation (p = 0.003), shorter interval from transplantation (p = 0.018), and prior aGvHD ≥II° (p = 0.036) were risk factors for DLI-induced GvHD. GvHD did not influence CRI, but was associated with NRM and lower LFS/OS. Efficacy of preDLI was demonstrated by decreasing MRD/increasing blood counts in 71%, and increasing chimerism in 70%. Five-year OS after preDLI for MRD/MC was 51%/68% among responders, and 37% among non-responders. The study describes response and outcome of DLI in CHR and helps to identify candidates without increased risk of severe GvHD.
1000 Sacherschließung
lokal Lymphocyte Transfusion/adverse effects [MeSH]
lokal Cancer
lokal Humans [MeSH]
lokal Lymphocytes [MeSH]
lokal Retrospective Studies [MeSH]
lokal Middle Aged [MeSH]
lokal Leukemia, Myeloid, Acute/complications [MeSH]
lokal Recurrence [MeSH]
lokal Acute Disease [MeSH]
lokal Article
lokal Immunotherapy
lokal Transplantation Conditioning/adverse effects [MeSH]
lokal Graft vs Host Disease/etiology [MeSH]
lokal Cancer immunotherapy
lokal Hematopoietic Stem Cell Transplantation/methods [MeSH]
lokal Neoplasm, Residual [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0001-7070-487X|https://orcid.org/0000-0003-4514-4748|https://frl.publisso.de/adhoc/uri/U2NoYWFwLCBOaWNvbGFhcw==|https://orcid.org/0000-0002-9108-3125|https://frl.publisso.de/adhoc/uri/QnJlY2h0LCBBcm5l|https://frl.publisso.de/adhoc/uri/U3RhZGxlciwgTWljaGFlbA==|https://frl.publisso.de/adhoc/uri/Rmlua2UsIEp1ZXJnZW4=|https://orcid.org/0000-0002-2944-3812|https://orcid.org/0000-0001-6585-9586|https://frl.publisso.de/adhoc/uri/QnVnLCBHZXNpbmU=|https://orcid.org/0000-0002-8281-3245|https://orcid.org/0000-0002-5684-9447|https://frl.publisso.de/adhoc/uri/VGlzY2hlciwgSm9oYW5uYQ==|https://orcid.org/0000-0003-4550-220X|https://orcid.org/0000-0002-9589-4136|https://orcid.org/0000-0002-4827-4401|https://frl.publisso.de/adhoc/uri/R29yaW4sIE5vcmJlcnQtQ2xhdWRl|https://orcid.org/0000-0002-8056-648X|https://orcid.org/0000-0003-0873-0123|https://orcid.org/0000-0002-3304-9965|https://frl.publisso.de/adhoc/uri/TmFnbGVyLCBBcm5vbg==|https://orcid.org/0000-0002-7264-808X
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