Azathioprine/hydroxyurea preconditioning prior to nonmyeloablative matched sibling donor hematopoietic stem cell transplantation in adults with sickle cell disease: A prospective observational cohort study

被引:0
|
作者
Dovern, Elisabeth [1 ]
Aydin, Mesire [1 ]
Hazenberg, Mette D. [1 ]
Tang, Man Wai [1 ]
Suijk, Elisabeth M. [1 ]
Hoogendoorn, Gerianne M. [1 ]
Van Tuijn, Charlotte F. J. [1 ]
Kerkhoffs, Jean-Louis [2 ]
Rutten, Caroline E. [1 ]
Zeerleder, Sacha S. [3 ]
de la Fuente, Josu [4 ,5 ]
Biemond, Bart J. [1 ]
Nur, Erfan [1 ,6 ]
机构
[1] Amsterdam UMC Locat Univ Amsterdam, Dept Hematol, De Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
[2] HagaZiekenhuis, Dept Hematol, The Hague, Netherlands
[3] Luzerner Kantonsspital Lucerne, Dept Hematol, Div Internal Med, Luzern, Switzerland
[4] Imperial Healthcare NHS Trust, St Marys Hosp, Dept Paediat, London, England
[5] Imperial Coll London, Dept Immunol & Inflammat, London, England
[6] Sanquin Res, Dept Blood Cell Res, Amsterdam, Netherlands
关键词
YOUNGER; ANEMIA;
D O I
10.1002/ajh.27360
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nonmyeloablative, matched sibling donor hematopoietic stem cell transplantation with alemtuzumab/total body irradiation (TBI) conditioning is a curative therapy with low toxicity for adults with sickle cell disease (SCD). However, relatively low donor chimerism levels and graft rejection remain important challenges. We hypothesized that adding azathioprine/hydroxyurea preconditioning will improve donor chimerism levels and reduce graft failure rate. In this prospective cohort study, we enrolled consecutive adult patients with SCD undergoing matched sibling donor transplantation at the Amsterdam UMC. Patients received azathioprine 150 mg/day and hydroxyurea 25 mg/kg/day for 3 months prior to alemtuzumab 1 mg/kg and 300 cGy TBI conditioning. Twenty patients with SCD (median age 26 years [range 19-49], 13 females) were transplanted. Median follow-up was 46.0 months (IQR 21.8-57.9). One-year overall survival and event-free survival (graft failure or death) were both 95% (95% confidence interval 86-100). Mean donor myeloid and T-cell chimerism 1-year post-transplant were 95.2% (SD +/- 10.6) and 67.3% (+/- 15.3), respectively. One patient (5%) experienced graft failure without autologous regeneration, resulting in infections and death. All other patients had a corrected SCD phenotype and were able to discontinue sirolimus. Three patients were successfully treated with alemtuzumab (1 mg/kg) after the transplant because of declining donor chimerism and cytopenias to revert impending graft rejection. Toxicity was mostly related to sirolimus and alemtuzumab. One patient developed steroid-responsive grade II intestinal acute graft-versus-host disease. Collectively, preconditioning with azathioprine/hydroxyurea prior to nonmyeloablative matched sibling donor transplantation resulted in excellent event-free survival and robust donor T-cell chimerism, enabling the successful withdrawal of sirolimus. : NCT05249452. Azathioprine/hydroxyurea preconditioning prior to nonmyeloablative matched sibling donor hematopoietic stem cell transplantation in adults with sickle cell disease: a prospective observational cohort study. image
引用
收藏
页码:1523 / 1531
页数:9
相关论文
共 50 条
  • [41] Comparable Outcome of CD3+-/CD19+Depleted Haploidentical with Matched Sibling Donor Hematopoietic Stem Cell Transplantation for Advanced Stage Sickle Cell Disease: Result of a Pilot Study
    Corbacioglu, Selim
    Foell, Juergen
    Wolff, Daniel
    Holler, Ernst
    Pfirstinger, Beatrix
    Rehe, Klaus Thorsten
    Hoffmann, Petra
    Edinger, Matthias
    Troeger, Anja
    Srutkova, Svatava
    BLOOD, 2017, 130
  • [42] The role of HLA matching in unrelated donor hematopoietic stem cell transplantation for sickle cell disease in Europe
    Gluckman, Eliane
    de la Fuente, Josu
    Cappelli, Barbara
    Scigliuolo, Graziana M.
    Volt, Fernanda
    Tozatto-Maio, Karina
    Rocha, Vanderson
    Tommaso, Mina
    O'Boyle, Farah
    Smiers, Frans
    Da Cunha-Riehm, Claudia Bettoni
    Calore, Elisabetta
    Bonanomi, Sonia
    Graphakos, Stelios
    Paisiou, Anna
    Albert, Michael H.
    Ruggeri, Annalisa
    Zecca, Marco
    Lankester, Arjan C.
    Corbacioglu, Selim
    BONE MARROW TRANSPLANTATION, 2020, 55 (10) : 1946 - 1954
  • [43] The Role of HLA Matching In Unrelated Donor Hematopoietic Stem Cell Transplantation for Sickle Cell Disease in Europe
    Gluckman, Eliane
    De la Fuente, Josu
    Cappelli, Barbara
    Scigliuolo, Graziana M.
    Volt, Fernanda
    Maio, Karina Tozatto
    Rocha, Vanderson
    Mina, Tommaso
    O'Boyle, Farah
    Smiers, Frans
    Da Cunha-Riehm, Claudia Bettoni
    Calore, Elisabetta
    Bonanomi, Sonia
    Graphakos, Stelios
    Paisiou, Anna
    Albert, Michael H.
    Ruggeri, Annalisa
    Zecca, Marco
    Lankester, Arjan C.
    Corbacioglu, Selim
    BONE MARROW TRANSPLANTATION, 2020, 55 (SUPPL 1) : 97 - 98
  • [44] The role of HLA matching in unrelated donor hematopoietic stem cell transplantation for sickle cell disease in Europe
    Eliane Gluckman
    Josu de la Fuente
    Barbara Cappelli
    Graziana M. Scigliuolo
    Fernanda Volt
    Karina Tozatto-Maio
    Vanderson Rocha
    Mina Tommaso
    Farah O’Boyle
    Frans Smiers
    Claudia Bettoni Da Cunha-Riehm
    Elisabetta Calore
    Sonia Bonanomi
    Stelios Graphakos
    Anna Paisiou
    Michael H. Albert
    Annalisa Ruggeri
    Marco Zecca
    Arjan C. Lankester
    Selim Corbacioglu
    Bone Marrow Transplantation, 2020, 55 : 1946 - 1954
  • [45] Stable long term engraftment and amelioration of clinical phenotype following hematopoietic stem cell transplantation from a matched sibling donor for sickle cell disease using a reduced intensity conditioning regimen
    Krishnamurti, L
    Wu, C
    Baker, S
    Yeager, AM
    Wagner, JE
    BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2005, 11 (02) : 28 - 28
  • [46] HLA-matched related donor hematopoietic stem cell transplantation is a suitable treatment in adolescents and adults with sickle cell disease: Comparison of myeloablative and non-myeloablative approaches
    Dhedin, Nathalie
    Chevillon, Florian
    Castelle, Martin
    Lavoipiere, Virginie
    Vasseur, Loic
    Dalle, Jean-Hugues
    Joseph, Laure
    Beckerich, Florence
    Buchbinder, Nimrod
    Coman, Tereza
    Garban, Frederic
    Ferster, Alina
    Nguyen, Stephanie
    Boissel, Nicolas
    Arlet, Jean-Benoit
    Pondarre, Corinne
    AMERICAN JOURNAL OF HEMATOLOGY, 2022, 97 (09) : E359 - E362
  • [47] Physical Performance Following Hematopoietic Stem Cell Transplantation: A Prospective Observational Study
    Rindflesch, Aaron B.
    Hake, Melissa P.
    Spiten, Megan A.
    Trueblood, Jinise K.
    Reiplinger, Allison F.
    Dykstra, Rebecca L.
    Hollman, John H.
    REHABILITATION ONCOLOGY, 2020, 38 (03) : 122 - 126
  • [48] Hemophagocytic syndrome after hematopoietic stem cell transplantation: a prospective observational study
    Abderrahman Abdelkefi
    Wassim Ben Jamil
    Lamia Torjman
    Saloua Ladeb
    Habib Ksouri
    Amel Lakhal
    Assia Ben Hassen
    Abdeladhim Ben Abdeladhim
    Tarek Ben Othman
    International Journal of Hematology, 2009, 89 : 368 - 373
  • [49] Hemophagocytic syndrome after hematopoietic stem cell transplantation: a prospective observational study
    Abdelkefi, Abderrahman
    Ben Jamil, Wassim
    Torjman, Lamia
    Ladeb, Saloua
    Ksouri, Habib
    Lakhal, Amel
    Ben Hassen, Assia
    Ben Abdeladhim, Abdeladhim
    Ben Othman, Tarek
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2009, 89 (03) : 368 - 373
  • [50] Curative Allogeneic Stem Cell Transplantation Is Safe and Feasible in Adult Patients with Sickle Cell Disease Despite Lack of Matched Sibling Donor and Presence of Sickle Cell Related Co-Morbidities
    Assal, Amer
    George, Diane
    Bhatia, Monica
    Gordillo, Christian
    Howard, Nicole
    Reshef, Ran
    Mapara, Markus Y.
    BLOOD, 2018, 132