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The relationship between PARP inhibitors with the relapse and leukemisation of lymphomas: a case report

BACKGROUND: Nowadays the poly-ADP ribose polymerase inhibitors (iPARPs) are the mainly treatment for the ovarian cancer and other solid tumours. However, given its recent use, long-term toxicity is still under study. The occurrence of acute leukaemias and myelodysplastic syndromes (MDS) secondarily...

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Autores principales: Navalón-Jiménez, Marta, Olivares-Hernández, Alejandro, Figuero-Pérez, Luis, Miramontes-González, José Pablo, Montero-Mateos, Enrique, Cruz-Hernández, Juan Jesús, Fonseca-Sánchez, Emilio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130682/
https://www.ncbi.nlm.nih.gov/pubmed/37122963
http://dx.doi.org/10.21037/acr-22-91
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author Navalón-Jiménez, Marta
Olivares-Hernández, Alejandro
Figuero-Pérez, Luis
Miramontes-González, José Pablo
Montero-Mateos, Enrique
Cruz-Hernández, Juan Jesús
Fonseca-Sánchez, Emilio
author_facet Navalón-Jiménez, Marta
Olivares-Hernández, Alejandro
Figuero-Pérez, Luis
Miramontes-González, José Pablo
Montero-Mateos, Enrique
Cruz-Hernández, Juan Jesús
Fonseca-Sánchez, Emilio
author_sort Navalón-Jiménez, Marta
collection PubMed
description BACKGROUND: Nowadays the poly-ADP ribose polymerase inhibitors (iPARPs) are the mainly treatment for the ovarian cancer and other solid tumours. However, given its recent use, long-term toxicity is still under study. The occurrence of acute leukaemias and myelodysplastic syndromes (MDS) secondarily to iPARPs is known (0.5–1%). CASE DESCRIPTION: We present the case of a 78-year-old patient with a serous carcinoma of ovary in maintenance treatment with Niraparib after response to platinum. Along with the ovarian carcinoma the patient developed a diffuse large cell B lymphoma (DLBCL) five years ago, treated with R-CHOP (Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisolone) with complete response. The patient was evaluated in the emergency due to constitutional syndrome, objectifying a bicytopenia (platelets 28,000/mcL, haemoglobin 9.6 g/dL). In the study of bicytopenia, a bone marrow infiltration by high-grade B lymphoma was diagnosed. CONCLUSIONS: The action of iPARPs on the selection of acquired mutations in clonal haematopoiesis maybe have been able to accelerate the process of relapse and leukemisation of the previous lymphoma. The association of treatment with iPARPs and the development of lymphomas is key for increasing knowledge of the safety profiles these drugs.
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spelling pubmed-101306822023-04-27 The relationship between PARP inhibitors with the relapse and leukemisation of lymphomas: a case report Navalón-Jiménez, Marta Olivares-Hernández, Alejandro Figuero-Pérez, Luis Miramontes-González, José Pablo Montero-Mateos, Enrique Cruz-Hernández, Juan Jesús Fonseca-Sánchez, Emilio AME Case Rep Case Report BACKGROUND: Nowadays the poly-ADP ribose polymerase inhibitors (iPARPs) are the mainly treatment for the ovarian cancer and other solid tumours. However, given its recent use, long-term toxicity is still under study. The occurrence of acute leukaemias and myelodysplastic syndromes (MDS) secondarily to iPARPs is known (0.5–1%). CASE DESCRIPTION: We present the case of a 78-year-old patient with a serous carcinoma of ovary in maintenance treatment with Niraparib after response to platinum. Along with the ovarian carcinoma the patient developed a diffuse large cell B lymphoma (DLBCL) five years ago, treated with R-CHOP (Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisolone) with complete response. The patient was evaluated in the emergency due to constitutional syndrome, objectifying a bicytopenia (platelets 28,000/mcL, haemoglobin 9.6 g/dL). In the study of bicytopenia, a bone marrow infiltration by high-grade B lymphoma was diagnosed. CONCLUSIONS: The action of iPARPs on the selection of acquired mutations in clonal haematopoiesis maybe have been able to accelerate the process of relapse and leukemisation of the previous lymphoma. The association of treatment with iPARPs and the development of lymphomas is key for increasing knowledge of the safety profiles these drugs. AME Publishing Company 2023-02-17 /pmc/articles/PMC10130682/ /pubmed/37122963 http://dx.doi.org/10.21037/acr-22-91 Text en 2023 AME Case Reports. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Navalón-Jiménez, Marta
Olivares-Hernández, Alejandro
Figuero-Pérez, Luis
Miramontes-González, José Pablo
Montero-Mateos, Enrique
Cruz-Hernández, Juan Jesús
Fonseca-Sánchez, Emilio
The relationship between PARP inhibitors with the relapse and leukemisation of lymphomas: a case report
title The relationship between PARP inhibitors with the relapse and leukemisation of lymphomas: a case report
title_full The relationship between PARP inhibitors with the relapse and leukemisation of lymphomas: a case report
title_fullStr The relationship between PARP inhibitors with the relapse and leukemisation of lymphomas: a case report
title_full_unstemmed The relationship between PARP inhibitors with the relapse and leukemisation of lymphomas: a case report
title_short The relationship between PARP inhibitors with the relapse and leukemisation of lymphomas: a case report
title_sort relationship between parp inhibitors with the relapse and leukemisation of lymphomas: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130682/
https://www.ncbi.nlm.nih.gov/pubmed/37122963
http://dx.doi.org/10.21037/acr-22-91
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