Comparison of Mitoxantrone-Melphalan and BEAM Conditioning Regimens in Patients with Lymphoma.


Journal

Hematology/oncology and stem cell therapy
ISSN: 2589-0646
Titre abrégé: Hematol Oncol Stem Cell Ther
Pays: Saudi Arabia
ID NLM: 101468532

Informations de publication

Date de publication:
23 Dec 2022
Historique:
received: 16 12 2020
accepted: 27 03 2021
pubmed: 3 5 2021
medline: 3 1 2023
entrez: 2 5 2021
Statut: epublish

Résumé

Lymphoma is seen as a highly treatable and curable malignancy with aggressive treatment methods. Efficacy is often limited by toxicity and many patients need alternative treatment strategies as they cannot tolerate existing high cytotoxic approaches. Our aim is to compare BEAM [carmustine (BCNU), etoposide, cytarabine (ARA-C, cytosine arabinoside), and melphalan] and mitoxantrone-melphalan (Mx-Mel) regimens utilized in our patients with a diagnosis of lymphoma who underwent autologous stem cell transplantation (ASCT), and to demonstrate that the Mx-Mel regimen has similar but less toxic results than the BEAM regimen we have been using frequently as standard conditioning regimen. A total of 101 patients with lymphoma who underwent ASCT were included in our study. The BEAM regimen included BCNU, etoposide, ARA-C, and melphalan. The Mx-Mel regimen included mitoxantrone and melphalan. Of 101 patients included in the study, 60 (59.4%) received BEAM and 41 (40.6%) received Mx-Mel (40.6%) conditioning regimen. The median time to neutrophil engraftment was 10 (range: 9-20) days and 12 (range: 9-12) days in the BEAM and Mx-Mel arms, respectively; it was statistically significantly shorter in the BEAM arm (p = .001). This study demonstrates that the Mx-Mel regimen has similar efficacy and toxicity compared with the BEAM regimen. Although time to neutrophil engraftment was shorter in the BEAM arm, it did not result as significant transplant-related complications between the two regimens. The Mx-Mel regimen is seen as a good alternative with low toxicity and high efficacy.

Sections du résumé

OBJECTIVE/BACKGROUND OBJECTIVE
Lymphoma is seen as a highly treatable and curable malignancy with aggressive treatment methods. Efficacy is often limited by toxicity and many patients need alternative treatment strategies as they cannot tolerate existing high cytotoxic approaches. Our aim is to compare BEAM [carmustine (BCNU), etoposide, cytarabine (ARA-C, cytosine arabinoside), and melphalan] and mitoxantrone-melphalan (Mx-Mel) regimens utilized in our patients with a diagnosis of lymphoma who underwent autologous stem cell transplantation (ASCT), and to demonstrate that the Mx-Mel regimen has similar but less toxic results than the BEAM regimen we have been using frequently as standard conditioning regimen.
METHODS METHODS
A total of 101 patients with lymphoma who underwent ASCT were included in our study. The BEAM regimen included BCNU, etoposide, ARA-C, and melphalan. The Mx-Mel regimen included mitoxantrone and melphalan.
RESULTS RESULTS
Of 101 patients included in the study, 60 (59.4%) received BEAM and 41 (40.6%) received Mx-Mel (40.6%) conditioning regimen. The median time to neutrophil engraftment was 10 (range: 9-20) days and 12 (range: 9-12) days in the BEAM and Mx-Mel arms, respectively; it was statistically significantly shorter in the BEAM arm (p = .001).
CONCLUSION CONCLUSIONS
This study demonstrates that the Mx-Mel regimen has similar efficacy and toxicity compared with the BEAM regimen. Although time to neutrophil engraftment was shorter in the BEAM arm, it did not result as significant transplant-related complications between the two regimens. The Mx-Mel regimen is seen as a good alternative with low toxicity and high efficacy.

Identifiants

pubmed: 33933474
pii: j.hemonc.2021.03.005
doi: 10.1016/j.hemonc.2021.03.005
doi:

Substances chimiques

Carmustine U68WG3173Y
Melphalan Q41OR9510P
Etoposide 6PLQ3CP4P3
Mitoxantrone BZ114NVM5P
Cytarabine 04079A1RDZ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

201-207

Auteurs

Ahmet Kursad Gunes (AK)

Ankara City Hospital, Department of Hematology, Ankara, Turkey.

Istemi Serin (I)

University of Health Sciences, Istanbul Training and Research Hospital, Department of Hematology, Istanbul, Turkey.

Ilknur Demir (I)

Gaziantep Abdulkadir Yuksel State Hospital, Gaziantep, Turkey.

Serpil Sarifakiogullari (S)

Giresun University, Faculty of Medicine, Department of Hematology, Giresun, Turkey.

Salih Sertac Durusoy (SS)

Van Training and Research Hospital, Department of Hematology, Van, Turkey.

Dervis Murad Akkurt (DM)

Gaziantep University, Faculty of Medicine, Department of Hematology, Gaziantep, Turkey.

Idris Ince (I)

Dr. Ersin Aslan Training and Research Hospital, Department of Hematology, Gaziantep, Turkey.

Gulkan Ozkan (G)

Istanbul Hamidiye Sisli Etfal Training and Research Hospital, Department of Hematology, Istanbul, Turkey.

Tahir Alper Cinli (TA)

University of Health Sciences, Istanbul Training and Research Hospital, Department of Hematology, Istanbul, Turkey.

Mustafa Pehlivan (M)

Gaziantep University, Faculty of Medicine, Department of Hematology, Gaziantep, Turkey.

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Classifications MeSH