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Second allogeneic stem cell transplantation for relapse after allografting in multiple myeloma using CD 34+ selected donor cells without immunosuppression

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References

  1. Sobh M, Michallet M, Gahrton G, Iacobelli S, van Biezen A, Schonland S, et al. Allogeneic hematopoietic cell transplantation for multiple myeloma in Europe: trends and outcomes over 25 years. A study by the EBMT Chronic Malignancies Working Party. Leukemia. 2016;30:2047–54. https://doi.org/10.1038/leu.2016.101

    Article  CAS  PubMed  Google Scholar 

  2. Gahrton G, Iacobelli S, Bjorkstrand B, Hegenbart U, Gruber A, Greinix H, et al. Autologous/reduced-intensity allogeneic stem cell transplantation vs autologous transplantation in multiple myeloma: long-term results of the EBMT-NMAM2000 study. Blood. 2013;121:5055–63. https://doi.org/10.1182/blood-2012-11-469452

    Article  CAS  PubMed  Google Scholar 

  3. Rasche L, Rollig C, Stuhler G, Danhof S, Mielke S, Grigoleit GU, et al. Allogeneic hematopoietic cell transplantation in multiple myeloma: focus on longitudinal assessment of donor chimerism, extramedullary disease, and high-risk cytogenetic features. Biol Blood Marrow Transplant. 2016;22:1988–96. https://doi.org/10.1016/j.bbmt.2016.08.024

    Article  PubMed  Google Scholar 

  4. Hatsuse M, Taniguchi-Yoshihara K, Yagyu S, Fuchida S, Okano A, Murakami S, et al. Successful treatment with pseudo-autologous bloodstem cell transplantation for an adolescent-onset multiple myeloma whorelapsed after allogenic bone marrow transplantation. Rinsho Ketsueki. 2015;56:428–431. https://doi.org/10.11406/rinketsu.56.428

    Article  PubMed  Google Scholar 

  5. Palfreyman E, Song K, Nantel S. Pseudo-autologous hematopoietic SCT as treatment for a patient with multiple myeloma who relapsed following an allogeneic hematopoietic SCT. Bone Marrow Transplant. 2013;48:1138 https://doi.org/10.1038/bmt.2013.12

    Article  CAS  PubMed  Google Scholar 

  6. Rajkumar SV, Richardson P, San Miguel JF. Guidelines for determination of the number of prior lines of therapy in multiple myeloma. Blood. 2015;126:921–2. https://doi.org/10.1182/blood-2015-05-647636

    Article  CAS  PubMed  Google Scholar 

  7. Klyuchnikov E, El-Cheikh J, Sputtek A, Lioznov M, Calmels B, Furst S, et al. CD34(+)-selected stem cell boost without further conditioning for poor graft function after allogeneic stem cell transplantation in patients with hematological malignancies. Biol Blood Marrow Transplant. 2014;20:382–6. https://doi.org/10.1016/j.bbmt.2013.11.034

    Article  CAS  PubMed  Google Scholar 

  8. Smith E, Devlin SM, Kosuri S, Orlando E, Landau H, Lesokhin AM, et al. CD34-selected allogeneic hematopoietic stem cell transplantation for patients with relapsed, high-risk multiple myeloma. Biol Blood Marrow Transplant. 2016;22:258–67. https://doi.org/10.1016/j.bbmt.2015.08.025

    Article  PubMed  Google Scholar 

  9. Kroger N, Badbaran A, Zabelina T, Ayuk F, Wolschke C, Alchalby H, et al. Impact of high-risk cytogenetics and achievement of molecular remission on long-term freedom from disease after autologous-allogeneic tandem transplantation in patients with multiple myeloma. Biol Blood Marrow Transplant. 2013;19:398–404. https://doi.org/10.1016/j.bbmt.2012.10.008

    Article  CAS  PubMed  Google Scholar 

  10. Lokhorst HM, Wu K, Verdonck LF, Laterveer LL, van de Donk NW, van Oers MH, et al. The occurrence of graft-versus-host disease is the major predictive factor for response to donor lymphocyte infusions in multiple myeloma. Blood. 2004;103:4362–4. https://doi.org/10.1182/blood-2003-11-3862

    Article  CAS  PubMed  Google Scholar 

  11. Kroger N, Kruger W, Renges H, Zabelina T, Stute N, Jung R, et al. Donor lymphocyte infusion enhances remission status in patients with persistent disease after allografting for multiple myeloma. Br J Haematol. 2001;112:421–3.

    Article  CAS  PubMed  Google Scholar 

  12. Kroger N, Zabelina T, Klyuchnikov E, Kropff M, Pfluger KH, Burchert A, et al. Toxicity-reduced, myeloablative allograft followed by lenalidomide maintenance as salvage therapy for refractory/relapsed myeloma patients. Bone Marrow Transplant. 2013;48:403–7. https://doi.org/10.1038/bmt.2012.142

    Article  CAS  PubMed  Google Scholar 

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Authors and Affiliations

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Contributions

NK designed the study and wrote the paper. PN analysed data, interpreted results, and wrote the paper. MG prepared CD34 selection. EK, UvP, MG, MC, FA, and CW analysed data, interpreted results, and approved the final version of the paper.

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Correspondence to Nicolaus Kröger.

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Novak, P., Klyuchnikov, E., von Pein, UM. et al. Second allogeneic stem cell transplantation for relapse after allografting in multiple myeloma using CD 34+ selected donor cells without immunosuppression. Bone Marrow Transplant 55, 1817–1820 (2020). https://doi.org/10.1038/s41409-020-0912-7

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