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Feasibility of CXCR4-Directed Radioligand Therapy in Advanced Diffuse Large B-Cell Lymphoma.
Lapa, Constantin; Hänscheid, Heribert; Kircher, Malte; Schirbel, Andreas; Wunderlich, Gerd; Werner, Rudolf A; Samnick, Samuel; Kotzerke, Jörg; Einsele, Hermann; Buck, Andreas K; Wester, Hans-Jürgen; Grigoleit, Götz Ulrich.
Afiliação
  • Lapa C; Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany lapa_c@ukw.de.
  • Hänscheid H; Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
  • Kircher M; Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
  • Schirbel A; Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
  • Wunderlich G; Department of Nuclear Medicine, University Hospital Dresden, Dresden, Germany.
  • Werner RA; Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
  • Samnick S; Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
  • Kotzerke J; Department of Nuclear Medicine, University Hospital Dresden, Dresden, Germany.
  • Einsele H; Division of Hematology and Medical Oncology, Department of Internal Medicine II, Universitätsklinikum Würzburg, Würzburg, Germany; and.
  • Buck AK; Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
  • Wester HJ; Pharmaceutical Radiochemistry, Technische Universität München, Munich, Germany.
  • Grigoleit GU; Division of Hematology and Medical Oncology, Department of Internal Medicine II, Universitätsklinikum Würzburg, Würzburg, Germany; and.
J Nucl Med ; 60(1): 60-64, 2019 01.
Article em En | MEDLINE | ID: mdl-29777009
ABSTRACT
We have recently reported on our experience with C-X-C-motif chemokine receptor 4 (CXCR4)-directed radioligand therapy (RLT) in multiple myeloma and acute leukemia.

Methods:

Six patients with heavily pretreated relapsed diffuse large B-cell lymphoma (3 men, 3 women; aged, 54 ± 8 y) underwent CXCR4-directed RLT in combination with conditioning chemotherapy and allogeneic stem cell transplantation. In 2 patients, radioimmunotherapy targeting CD20 or CD66 was added to enhance antilymphoma activity. Endpoints were incidence and severity of adverse events, progression-free survival, and overall survival.

Results:

RLT and additional radioimmunotherapy were well tolerated, without any acute adverse events or changes in vital signs. Successful engraftment was recorded after a median of 11 d (range, 9-13 d). Of the 4 patients who were available for follow-up (one patient died of CNS aspergillosis 29 d after RLT and another of sepsis in aplasia 34 d after RLT), CXCR4-directed RLT resulted in a partial response in two (both treated with additional radioimmunotherapy) and a mixed response in the remaining two. The response duration was rather short-lived, with a median progression-free survival of 62 d (range, 29-110 d) and a median overall survival of 76 d (range, 29-334 d).

Conclusion:

CXCR4-directed RLT (in combination with additional radioimmunotherapy) is feasible as a conditioning regimen before allogeneic stem cell transplantation in diffuse large B-cell lymphoma.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma Difuso de Grandes Células B / Receptores CXCR4 Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma Difuso de Grandes Células B / Receptores CXCR4 Idioma: En Ano de publicação: 2019 Tipo de documento: Article