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Mobilization and Hematopoietic Stem Cell Collection in Poor Mobilizing Patients with Lymphoma: Final Results of the German OPTIMOB Study.
Kriegsmann, Katharina; Bittrich, Max; Sauer, Sandra; Tietze-Stolley, Carola; Movassaghi, Kamran; Grube, Matthias; Vucinic, Vladan; Wehler, Daniela; Burchert, Andreas; Schmidt-Hieber, Martin; Rank, Andreas; Dürk, Heinz A; Metzner, Bernd; Kimmich, Christoph; Hentrich, Marcus; Kunz, Christian; Hartmann, Frank; Khandanpour, Cyrus; de Wit, Maike; Holtick, Udo; Kiehl, Michael; Stoltefuß, Andrea; Kiani, Alexander; Naumann, Ralph; Scholz, Christian W; Tischler, Hans-Joachim; Görner, Martin; Brand, Franziska; Ehmer, Martin; Kröger, Nicolaus.
Afiliação
  • Kriegsmann K; Department of Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
  • Bittrich M; Laborarztpraxis, Laborarztpraxis Rhein-Main MVZ GbR, Limbach Gruppe SE, Frankfurt, Germany.
  • Sauer S; Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany.
  • Tietze-Stolley C; Department of Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
  • Movassaghi K; Department of Hematology and Oncology, Stem Cell Facility, University Hospital Charité, Berlin, Germany.
  • Grube M; Department of Hematology and Oncology, Stem Cell Facility, University Hospital Charité, Berlin, Germany.
  • Vucinic V; Department of Hematology and Internistic Oncology, University Hospital Regensburg, Regensburg, Germany.
  • Wehler D; Klinik und Poliklinik für Hämatologie, Zelltherapie und Hämostaseologie, University Hospital Leipzig, Leipzig, Germany.
  • Burchert A; Klinik und Poliklinik für Innere Medizin III, University Hospital of Mainz, Mainz, Germany.
  • Schmidt-Hieber M; Klinik für Hämatologie, Onkologie und Immunologie, University Hospital of Gießen and Marburg (UKGM), Marburg, Germany.
  • Rank A; 2. Medizinische Klinik für Hämatologie, Onkologie, Pneumologie und Nephrologie, Carl-Thiem Hospital Cottbus gGmbH, Cottbus, Germany.
  • Dürk HA; 2. Medizinische Klinik - Hämatologie, Internistische Onkologie und Hämostaseologie, University Hospital of Augsburg, Augsburg, Germany.
  • Metzner B; Klinik für Hämatologie und Onkologie, St. Barbara Hospital Hamm-Heessen, Hamm, Germany.
  • Kimmich C; Universitätsklinik für Innere Medizin - Onkologie und Hämatologie, University Hospital Klinikum Oldenburg, Oldenburg, Germany.
  • Hentrich M; Universitätsklinik für Innere Medizin - Onkologie und Hämatologie, University Hospital Klinikum Oldenburg, Oldenburg, Germany.
  • Kunz C; Abteilung für Innere Medizin III -Hämatologie und Onkologie, Rotkreuzklinikum München, Munich, Germany.
  • Hartmann F; Innere Medizin I, Westpfalz-Klinikum Kaiserslautern, Kaiserslautern, Germany.
  • Khandanpour C; Klinik für Onkologie und Hämatologie, Hospital Lippe-Lemgo, Lemgo, Germany.
  • de Wit M; Medizinische Klinik A, University Hospital Münster, Münster, Germany.
  • Holtick U; Klinik für Hämatologie und Onkologie, University Hospital Schleswig-Holstein (Campus Lübeck) and University of Lübeck, Lübeck, Germany.
  • Kiehl M; Klinik für Innere Medizin - Hämatologie, Onkologie und Palliativmedizin, Vivantes Hospital Neukölln, Berlin, Germany.
  • Stoltefuß A; Department I of Internal Medicine, Medical Faculty and University Hospital of Cologne, University of Cologne, Cologne, Germany.
  • Kiani A; Medizinische Klinik I, Hospital Frankfurt (Oder), Frankfurt/Oder, Germany.
  • Naumann R; Klinik für Innere Medizin II, Evangelisches Krankenhaus Hamm, Hamm, Germany.
  • Scholz CW; Department of Hematology and Oncology, Klinikum Bayreuth, Bayreuth, Germany.
  • Tischler HJ; Comprehensive Cancer Center Erlangen-EMN (CCC ER-EMN), Erlangen, Germany.
  • Görner M; Klinik für Hämatologie, Medizinische Onkologie und Palliativmedizin, St. Marien-Krankenhaus Marien Gesellschaft Siegen gGmbH, Siegen, Germany.
  • Brand F; Klinik für Innere Medizin - Hämatologie und Onkologie, Vivantes Hospital Am Urban, Berlin, Germany.
  • Ehmer M; Universitätsklinik für Hämatologie, Onkologie, Hämostaseologie und Palliativmedizin, Johannes Wesling Hospital Minden, Mühlenkreiskliniken, Minden, Germany.
  • Kröger N; Klinik für Hämatologie, Onkologie, Palliativmedizin und Stammzelltherapie, Hospital Bielefeld-Mitte, Bielefeld, Germany.
Transfus Med Hemother ; 50(5): 403-416, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37899991
ABSTRACT

Introduction:

Successful mobilization and collection of peripheral hematopoietic stem cells (HSCs) are necessary for lymphoma patients eligible for myeloablative chemotherapy with subsequent autologous stem cell transplantation (ASCT). Albeit G-CSF alone or combined with chemotherapy is well-established methods for HSC mobilization, up to 40% of the patients fail to mobilize (poor mobilizer, PM). Plerixafor (PLX) is commonly used in PM patients resulting in increased migration of HSCs into peripheral blood and thus improves the collection outcome.

Methods:

The prospective, multicenter, open-label, non-interventional OPTIMOB study assessed mobilization and collection parameter of patients with lymphoma or multiple myeloma to get deep insights in the treatment of those patients in clinical routine focusing on PM patients. PM was defined as follows (1) no achievement of ≥20 CD34+ progenitor cells/µL before first apheresis, (2) PLX administration at any time point during the observational period, (3) reduction of the initially planned CD34+ progenitor cell yield as necessity due to failed mobilization or HSC collection, and (4) no performance of apheresis due to low CD34+ progenitor level. Primary objective of the study was to assess mobilization success by the proportion of PM patients achieving >2 × 106 CD34+ progenitor cells/kg body weight on the first day of apheresis. Here, the data of the lymphoma cohort are presented.

Results:

Out of 238 patients with lymphoma documented in the study, 32% were classified as PM. 87% of them received PLX. Demographic data revealed no obvious differences between PM and good mobilizing (GM) patients. All patients were treated highly individualized prior to mobilization. Majority of all PM patients were able to undergo apheresis (95%) and reached their individual requested CD34+ progenitor cell target (72%). 57% of the PM patients achieved >2.0 × 106 CD34+ progenitor cells/kg body weight on day 1 of apheresis and nearby 70% of them underwent ASCT. Median time to engraftment was similar in PM and GM patients of the lymphoma cohort.

Conclusions:

Majority of PM patients with lymphoma were successfully mobilized and underwent ASCT. Most of them received PLX during the study.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Transfus Med Hemother Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Transfus Med Hemother Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha