Idarubicin versus Doxorubicin in Acute Myeloid Leukemia: A Parallel Randomized Trial with Pharmacoeconomic Analysis

Background: Acute Myeloid Leukemia (AML) is the most common form of acute leukemia among adults. Treatment of acute leukemia has been divided into induction chemotherapy and post-remission therapy. The goal of induction chemotherapy, that consists of anthracycline and cytarabine, is to achieve morph...

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Main Authors: Amany El Zeiny, Raafat Abdel-Fattah, Maggie Abbassie, Samar Farid
Format: Article
Language:English
Published: Tabriz University of Medical Sciences 2024-01-01
Series:Pharmaceutical Sciences
Subjects:
Online Access:https://ps.tbzmed.ac.ir/PDF/ps-30-135.pdf
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author Amany El Zeiny
Raafat Abdel-Fattah
Maggie Abbassie
Samar Farid
author_facet Amany El Zeiny
Raafat Abdel-Fattah
Maggie Abbassie
Samar Farid
author_sort Amany El Zeiny
collection DOAJ
description Background: Acute Myeloid Leukemia (AML) is the most common form of acute leukemia among adults. Treatment of acute leukemia has been divided into induction chemotherapy and post-remission therapy. The goal of induction chemotherapy, that consists of anthracycline and cytarabine, is to achieve morphologic complete remission (CR), but the main problem is that it has a high economic burden. Idarubicin is the anthracycline of choice used in AML, while doxorubicin, is mainly used in other types of cancer. The aims of this study were evaluating the use of doxorubicin versus idarubicin in the induction phase for the treatment of AML and analysis the impact of the adoption of this anthracycline in Egypt’s public health system. Methods: A randomized controlled trial was undertaken in 244 patients with AML. A decision tree was developed based on the clinical outcome of the study, safety and efficacy, aiming to get the expected cost of doxorubicin compared with idarubicin in AML management. Results: In the doxorubicin group, 52.5% had a CR, versus 49.2 % in the idarubicin group (P=0.6). The most common toxicities among the 2 groups were febrile neutropenia, diarrhea and vomiting. Oral mucositis (OM) was higher in the doxorubicin group (70.8% vs 37%, P=0.0001), while invasive fungal infections were greater in the idarubicin group (75% vs 88.7%, P=0.004). Doxorubicin arm had a lower cost than idarubicin arm in treatment success group (39,492 LE vs 44,323 LE). Conclusion: Doxorubicin provides a treatment option with comparable efficacy, toxicity profile and survival rates at a lower cost compared to the traditional treatment, idarubicin.
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spelling doaj.art-cca99ef724764a5eb36c5cf1057f9a0b2024-02-07T06:58:43ZengTabriz University of Medical SciencesPharmaceutical Sciences2383-28862024-01-0130113514210.34172/PS.2023.28ps-39960Idarubicin versus Doxorubicin in Acute Myeloid Leukemia: A Parallel Randomized Trial with Pharmacoeconomic AnalysisAmany El Zeiny0Raafat Abdel-Fattah1Maggie Abbassie2Samar Farid3Clinical Pharmacy Department, National Cancer Institute, Cairo University, Cairo, Egypt.Clinical Pharmacy Department, National Cancer Institute, Cairo University, Cairo, Egypt.Clinical Pharmacy Department, National Cancer Institute, Cairo University, Cairo, Egypt.Clinical Pharmacy Department, National Cancer Institute, Cairo University, Cairo, Egypt.Background: Acute Myeloid Leukemia (AML) is the most common form of acute leukemia among adults. Treatment of acute leukemia has been divided into induction chemotherapy and post-remission therapy. The goal of induction chemotherapy, that consists of anthracycline and cytarabine, is to achieve morphologic complete remission (CR), but the main problem is that it has a high economic burden. Idarubicin is the anthracycline of choice used in AML, while doxorubicin, is mainly used in other types of cancer. The aims of this study were evaluating the use of doxorubicin versus idarubicin in the induction phase for the treatment of AML and analysis the impact of the adoption of this anthracycline in Egypt’s public health system. Methods: A randomized controlled trial was undertaken in 244 patients with AML. A decision tree was developed based on the clinical outcome of the study, safety and efficacy, aiming to get the expected cost of doxorubicin compared with idarubicin in AML management. Results: In the doxorubicin group, 52.5% had a CR, versus 49.2 % in the idarubicin group (P=0.6). The most common toxicities among the 2 groups were febrile neutropenia, diarrhea and vomiting. Oral mucositis (OM) was higher in the doxorubicin group (70.8% vs 37%, P=0.0001), while invasive fungal infections were greater in the idarubicin group (75% vs 88.7%, P=0.004). Doxorubicin arm had a lower cost than idarubicin arm in treatment success group (39,492 LE vs 44,323 LE). Conclusion: Doxorubicin provides a treatment option with comparable efficacy, toxicity profile and survival rates at a lower cost compared to the traditional treatment, idarubicin.https://ps.tbzmed.ac.ir/PDF/ps-30-135.pdfacute myeloid leukemiadoxorubicinidarubicinpharmacoeconomic
spellingShingle Amany El Zeiny
Raafat Abdel-Fattah
Maggie Abbassie
Samar Farid
Idarubicin versus Doxorubicin in Acute Myeloid Leukemia: A Parallel Randomized Trial with Pharmacoeconomic Analysis
Pharmaceutical Sciences
acute myeloid leukemia
doxorubicin
idarubicin
pharmacoeconomic
title Idarubicin versus Doxorubicin in Acute Myeloid Leukemia: A Parallel Randomized Trial with Pharmacoeconomic Analysis
title_full Idarubicin versus Doxorubicin in Acute Myeloid Leukemia: A Parallel Randomized Trial with Pharmacoeconomic Analysis
title_fullStr Idarubicin versus Doxorubicin in Acute Myeloid Leukemia: A Parallel Randomized Trial with Pharmacoeconomic Analysis
title_full_unstemmed Idarubicin versus Doxorubicin in Acute Myeloid Leukemia: A Parallel Randomized Trial with Pharmacoeconomic Analysis
title_short Idarubicin versus Doxorubicin in Acute Myeloid Leukemia: A Parallel Randomized Trial with Pharmacoeconomic Analysis
title_sort idarubicin versus doxorubicin in acute myeloid leukemia a parallel randomized trial with pharmacoeconomic analysis
topic acute myeloid leukemia
doxorubicin
idarubicin
pharmacoeconomic
url https://ps.tbzmed.ac.ir/PDF/ps-30-135.pdf
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