TY - JOUR
T1 - Causes of early death and treatment-related death in newly diagnosed pediatric acute myeloid leukemia
T2 - Recent experiences of the Dutch Childhood Oncology Group
AU - Klein, Kim
AU - van Litsenburg, Raphaële R L
AU - de Haas, Valérie
AU - Dors, Natasja
AU - van den Heuvel-Eibrink, Marry M
AU - Knops, Rutger R G
AU - Tissing, Wim J E
AU - Versluys, Birgitta A
AU - Zwaan, C Michel
AU - Kaspers, Gertjan J L
N1 - © 2019 The Authors. Pediatric Blood & Cancer published by Wiley Periodicals, Inc.
PY - 2020/4
Y1 - 2020/4
N2 - BACKGROUND: With the current more effective treatment regimens for pediatric acute myeloid leukemia (AML), research on early death (ED), treatment-related mortality (TRM), and toxicity becomes increasingly important. The aim of this study was to give an overview of the frequency, clinical features, and risk factors associated with ED and TRM in first complete remission (CR1) during the last three consecutive treatment protocols of the Dutch Childhood Oncology Group (DCOG) between 1998 and 2014.METHODS: Incidence and risk factors associated with ED and TRM in CR1 were retrospectively studied in 245 patients treated according to the Dutch ANLL-97/AML-12 (n = 118), AML-15 (n = 60), or DB AML-01 (n = 67) protocols.RESULTS: The incidence of ED was, respectively, 5.1%, 6.7%, and 3.0% excluding deaths before treatment (P = NS), and 7.4%, 11.1%, and 4.4% including deaths before the onset of treatment. Severe underweight at initial diagnosis was significantly associated with more frequent ED. When relapse was included as a competing risk, cumulative incidence of death in CR1 were 5.9%, 5.0%, and 4.6% for ANLL97, AML15, and DB01, respectively (P = NS). The most important cause of TRM included infectious and SCT-related complications.CONCLUSION: We report relatively stable rates of ED and TRM in CR1 in the latest completed DCOG protocols for newly diagnosed AML patients. The most important causes of TRM were SCT- or infection-related, warranting further evaluation and awareness.
AB - BACKGROUND: With the current more effective treatment regimens for pediatric acute myeloid leukemia (AML), research on early death (ED), treatment-related mortality (TRM), and toxicity becomes increasingly important. The aim of this study was to give an overview of the frequency, clinical features, and risk factors associated with ED and TRM in first complete remission (CR1) during the last three consecutive treatment protocols of the Dutch Childhood Oncology Group (DCOG) between 1998 and 2014.METHODS: Incidence and risk factors associated with ED and TRM in CR1 were retrospectively studied in 245 patients treated according to the Dutch ANLL-97/AML-12 (n = 118), AML-15 (n = 60), or DB AML-01 (n = 67) protocols.RESULTS: The incidence of ED was, respectively, 5.1%, 6.7%, and 3.0% excluding deaths before treatment (P = NS), and 7.4%, 11.1%, and 4.4% including deaths before the onset of treatment. Severe underweight at initial diagnosis was significantly associated with more frequent ED. When relapse was included as a competing risk, cumulative incidence of death in CR1 were 5.9%, 5.0%, and 4.6% for ANLL97, AML15, and DB01, respectively (P = NS). The most important cause of TRM included infectious and SCT-related complications.CONCLUSION: We report relatively stable rates of ED and TRM in CR1 in the latest completed DCOG protocols for newly diagnosed AML patients. The most important causes of TRM were SCT- or infection-related, warranting further evaluation and awareness.
KW - Adolescent
KW - Antineoplastic Combined Chemotherapy Protocols/adverse effects
KW - Child
KW - Child, Preschool
KW - Female
KW - Hematopoietic Stem Cell Transplantation/adverse effects
KW - Humans
KW - Incidence
KW - Infant
KW - Infant, Newborn
KW - Leukemia, Myeloid, Acute/mortality
KW - Male
KW - Retrospective Studies
KW - Young Adult
UR - http://www.scopus.com/inward/record.url?scp=85076900599&partnerID=8YFLogxK
U2 - 10.1002/pbc.28099
DO - 10.1002/pbc.28099
M3 - Article
C2 - 31872548
SN - 1545-5009
VL - 67
SP - e28099
JO - Pediatric blood & cancer
JF - Pediatric blood & cancer
IS - 4
M1 - e28099
ER -