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Lack of clarity in the definition of treatment-related mortality: pediatric acute leukemia and adult acute promyelocytic leukemia as examples (Perspectives)
O. Hrodek
Language Czech Country Czech Republic
Document type Overall
Digital library NLK
Issue
Volume
Source
NLK
ROAD: Directory of Open Access Scholarly Resources
from 2000
- MeSH
- Leukemia, Erythroblastic, Acute mortality therapy MeSH
- Precursor Cell Lymphoblastic Leukemia-Lymphoma mortality therapy MeSH
- Leukemia, Promyelocytic, Acute mortality therapy MeSH
- Child MeSH
- Adult MeSH
- Humans MeSH
- Cause of Death MeSH
- Randomized Controlled Trials as Topic MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Publication type
- Overall MeSH
Treatment-related mortality (TRM) is important in acute lymphoblastic leukemia and acute myeloid leukemia (AML); however, little is known about how TRM is defined across trials. Two major problems are related to what constitutes treatment versus disease-related cause of death and to TRM attribution (for example, death because of infection or hemorrhage). To address the former, we conducted a systematic review of randomized therapeutic pediatric acute leukemia and adult/pediatric acute promyelocytic leukemia trials and any study type focused on TRM in pediatric acute leukemia. We described definitions used for TRM. Sixty-six studies were included. Few therapeutic pediatric acute lymphoblastic leukemia studies (2/32, 6.3%) provided definitions for TRM, whereas more therapeutic pediatric AML studies (6/9, 66.7%) provided definitions. There was great heterogeneity in TRM classification. The authors of most studies relied on deaths during induction or in remission to delineate whether a death was TRM. However, 44.4% of therapeutic AML studies used death within a specific time frame to delineate TRM. We suggest that a consistent approach to defining and determining attribution for TRM in acute leukemia is an important future goal. Harmonization of definitions across the age spectrum would allow comparisons between pediatric and adult studies.
Citace: Marie-Chantal Ethier, Esther Blanco, Thomas Lehrnbecher, and Lillian Sung Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON; Division of Haematology/Oncology, Department of Paediatrics, The Hospital for Sick Children and Department of Paediatrics, University of Toronto, Toronto, ON, Canada; and Pediatric Hematology and Oncology, Johann-Wolfgang Goethe University Hospital, Frankfurt, Germany. Blood, 10 November 2011, Vol. 118, No. 19, pp. 5080-5083.
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- $a Citace: Marie-Chantal Ethier, Esther Blanco, Thomas Lehrnbecher, and Lillian Sung Program in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON; Division of Haematology/Oncology, Department of Paediatrics, The Hospital for Sick Children and Department of Paediatrics, University of Toronto, Toronto, ON, Canada; and Pediatric Hematology and Oncology, Johann-Wolfgang Goethe University Hospital, Frankfurt, Germany. Blood, 10 November 2011, Vol. 118, No. 19, pp. 5080-5083.
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- $a Treatment-related mortality (TRM) is important in acute lymphoblastic leukemia and acute myeloid leukemia (AML); however, little is known about how TRM is defined across trials. Two major problems are related to what constitutes treatment versus disease-related cause of death and to TRM attribution (for example, death because of infection or hemorrhage). To address the former, we conducted a systematic review of randomized therapeutic pediatric acute leukemia and adult/pediatric acute promyelocytic leukemia trials and any study type focused on TRM in pediatric acute leukemia. We described definitions used for TRM. Sixty-six studies were included. Few therapeutic pediatric acute lymphoblastic leukemia studies (2/32, 6.3%) provided definitions for TRM, whereas more therapeutic pediatric AML studies (6/9, 66.7%) provided definitions. There was great heterogeneity in TRM classification. The authors of most studies relied on deaths during induction or in remission to delineate whether a death was TRM. However, 44.4% of therapeutic AML studies used death within a specific time frame to delineate TRM. We suggest that a consistent approach to defining and determining attribution for TRM in acute leukemia is an important future goal. Harmonization of definitions across the age spectrum would allow comparisons between pediatric and adult studies.
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