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...
Autores principales: | , , , , , , , , |
---|---|
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 |