Cargando…

Unusually swift response of relapsed Burkitt leukemia to R‐DHAP

Burkitt leukemia (BL) represents a highly aggressive lymphoma characterized by proliferation rates of around 100%, and a frequent spread into the central nervous system. If standard frontline chemotherapy fails, the prognosis is usually dismal, and reports on successful effective salvage therapy str...

Descripción completa

Detalles Bibliográficos
Autores principales: Harrer, Dennis Christoph, Denk, Alexander, Keil, Felix, Menhart, Karin, Mayer, Stephanie, Wolff, Daniel, Edinger, Matthias, Herr, Wolfgang, Grube, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422005/
https://www.ncbi.nlm.nih.gov/pubmed/36051076
http://dx.doi.org/10.1002/jha2.501
_version_ 1784777722486063104
author Harrer, Dennis Christoph
Denk, Alexander
Keil, Felix
Menhart, Karin
Mayer, Stephanie
Wolff, Daniel
Edinger, Matthias
Herr, Wolfgang
Grube, Matthias
author_facet Harrer, Dennis Christoph
Denk, Alexander
Keil, Felix
Menhart, Karin
Mayer, Stephanie
Wolff, Daniel
Edinger, Matthias
Herr, Wolfgang
Grube, Matthias
author_sort Harrer, Dennis Christoph
collection PubMed
description Burkitt leukemia (BL) represents a highly aggressive lymphoma characterized by proliferation rates of around 100%, and a frequent spread into the central nervous system. If standard frontline chemotherapy fails, the prognosis is usually dismal, and reports on successful effective salvage therapy strategies for patients with relapsed/refractory BL are scant. Here, we report on a 40‐year‐old female patient who suffered an early relapse of BL three months after the completion of frontline chemoimmunotherapy. Strikingly, after only one cycle of R‐DHAP chemotherapy, the patient showed CR of BL enabling swift transition to a consolidating allogeneic stem cell transplantation. A 40‐year‐old previously healthy woman presented to the hospital with fatigue and incessant epistaxis, and a diagnosis of BL was made upon histological examination of a bone marrow biopsy. Treatment was initiated according to the GMALL 2002 B‐NHL/ALL protocol, which could induce complete molecular remission. Nevertheless, three months after chemotherapy, the patient exhibited BL relapse in the bone marrow, and on Fluorodeoxyglucose (FDG)–PET‐imaging. The relapse therapy was started with R‐DHAP, and after only one cycle, the patient once again entered complete remission (CR) paving the way for allogeneic stem cell transplantation. Unfortunately, the patient again relapsed five months after transplantation prompting salvage therapy with R‐DHAC and the execution of the second stem cell transplantation. However, one month after the second transplantation the patient presented with chemorefractory meningeosis leukemia resulting in the initiation of palliative care treatment. In summary, we report on rapid CR of relapsed BL after a single cycle of rituximab‐DHAP. Given a paucity of clinical trials on the treatment of patients with r/r BL, we intend to highlight the potential efficacy of rituximab‐DHAP as salvage therapy in those patients.
format Online
Article
Text
id pubmed-9422005
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-94220052022-08-31 Unusually swift response of relapsed Burkitt leukemia to R‐DHAP Harrer, Dennis Christoph Denk, Alexander Keil, Felix Menhart, Karin Mayer, Stephanie Wolff, Daniel Edinger, Matthias Herr, Wolfgang Grube, Matthias EJHaem Case Reports Burkitt leukemia (BL) represents a highly aggressive lymphoma characterized by proliferation rates of around 100%, and a frequent spread into the central nervous system. If standard frontline chemotherapy fails, the prognosis is usually dismal, and reports on successful effective salvage therapy strategies for patients with relapsed/refractory BL are scant. Here, we report on a 40‐year‐old female patient who suffered an early relapse of BL three months after the completion of frontline chemoimmunotherapy. Strikingly, after only one cycle of R‐DHAP chemotherapy, the patient showed CR of BL enabling swift transition to a consolidating allogeneic stem cell transplantation. A 40‐year‐old previously healthy woman presented to the hospital with fatigue and incessant epistaxis, and a diagnosis of BL was made upon histological examination of a bone marrow biopsy. Treatment was initiated according to the GMALL 2002 B‐NHL/ALL protocol, which could induce complete molecular remission. Nevertheless, three months after chemotherapy, the patient exhibited BL relapse in the bone marrow, and on Fluorodeoxyglucose (FDG)–PET‐imaging. The relapse therapy was started with R‐DHAP, and after only one cycle, the patient once again entered complete remission (CR) paving the way for allogeneic stem cell transplantation. Unfortunately, the patient again relapsed five months after transplantation prompting salvage therapy with R‐DHAC and the execution of the second stem cell transplantation. However, one month after the second transplantation the patient presented with chemorefractory meningeosis leukemia resulting in the initiation of palliative care treatment. In summary, we report on rapid CR of relapsed BL after a single cycle of rituximab‐DHAP. Given a paucity of clinical trials on the treatment of patients with r/r BL, we intend to highlight the potential efficacy of rituximab‐DHAP as salvage therapy in those patients. John Wiley and Sons Inc. 2022-06-13 /pmc/articles/PMC9422005/ /pubmed/36051076 http://dx.doi.org/10.1002/jha2.501 Text en © 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Harrer, Dennis Christoph
Denk, Alexander
Keil, Felix
Menhart, Karin
Mayer, Stephanie
Wolff, Daniel
Edinger, Matthias
Herr, Wolfgang
Grube, Matthias
Unusually swift response of relapsed Burkitt leukemia to R‐DHAP
title Unusually swift response of relapsed Burkitt leukemia to R‐DHAP
title_full Unusually swift response of relapsed Burkitt leukemia to R‐DHAP
title_fullStr Unusually swift response of relapsed Burkitt leukemia to R‐DHAP
title_full_unstemmed Unusually swift response of relapsed Burkitt leukemia to R‐DHAP
title_short Unusually swift response of relapsed Burkitt leukemia to R‐DHAP
title_sort unusually swift response of relapsed burkitt leukemia to r‐dhap
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422005/
https://www.ncbi.nlm.nih.gov/pubmed/36051076
http://dx.doi.org/10.1002/jha2.501
work_keys_str_mv AT harrerdennischristoph unusuallyswiftresponseofrelapsedburkittleukemiatordhap
AT denkalexander unusuallyswiftresponseofrelapsedburkittleukemiatordhap
AT keilfelix unusuallyswiftresponseofrelapsedburkittleukemiatordhap
AT menhartkarin unusuallyswiftresponseofrelapsedburkittleukemiatordhap
AT mayerstephanie unusuallyswiftresponseofrelapsedburkittleukemiatordhap
AT wolffdaniel unusuallyswiftresponseofrelapsedburkittleukemiatordhap
AT edingermatthias unusuallyswiftresponseofrelapsedburkittleukemiatordhap
AT herrwolfgang unusuallyswiftresponseofrelapsedburkittleukemiatordhap
AT grubematthias unusuallyswiftresponseofrelapsedburkittleukemiatordhap