Chronic conditions, late mortality, and health status after childhood AML: a Childhood Cancer Survivor Study report

Author:

Turcotte Lucie M.1ORCID,Whitton Jillian A.2,Leisenring Wendy M.2ORCID,Howell Rebecca M.3,Neglia Joseph P.1ORCID,Phelan Rachel45,Oeffinger Kevin C.6,Ness Kirsten K.7ORCID,Woods William G.8,Kolb E. Anders9,Robison Leslie L.7ORCID,Armstrong Gregory T.7,Chow Eric J.2ORCID

Affiliation:

1. 1Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN

2. 2Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA

3. 3Department of Radiation Physics, University of Texas MD Anderson Cancer Center, Houston, TX

4. 4Center for International Blood and Marrow Transplantation, Milwaukee, WI

5. 5Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI

6. 6Department of Medicine, Duke University School of Medicine, Durham, NC

7. 7Department of Epidemiology and Cancer Control, St. Jude Children’s Research Hospital, Memphis, TN

8. 8Aflac Cancer Center, Children’s Healthcare of Atlanta/Emory University, Atlanta, GA

9. 9Nemours Center for Cancer and Blood Disorders, Nemours Children’s Health System, Wilmington, DE

Abstract

Abstract Five-year survival following childhood acute myeloid leukemia (AML) has increased following improvements in treatment and supportive care. Long-term health outcomes are unknown. To address this, cumulative incidence of late mortality and grades 3 to 5 chronic health condition (CHC) were estimated among 5-year AML survivors diagnosed between 1970 and 1999. Survivors were compared by treatment group (hematopoietic cell transplantation [HCT], chemotherapy with cranial radiation [chemo + CRT], chemotherapy only [chemo-only]), and diagnosis decade. Self-reported health status was compared across treatments, diagnosis decade, and with siblings. Among 856 survivors (median diagnosis age, 7.1 years; median age at last follow-up, 29.4 years), 20-year late mortality cumulative incidence was highest after HCT (13.9%; 95% confidence interval [CI], 10.0%-17.8%; chemo + CRT, 7.6%; 95% CI, 2.2%-13.1%; chemo-only, 5.1%; 95% CI, 2.8%-7.4%). Cumulative incidence of mortality for HCT survivors diagnosed in the 1990s (8.5%; 95% CI, 4.1%-12.8%) was lower vs those diagnosed in the 1970s (38.9%; 95% CI, 16.4%-61.4%). Most survivors did not experience any grade 3 to 5 CHC after 20 years (HCT, 45.8%; chemo + CRT, 23.7%; chemo-only, 27.0%). Furthermore, a temporal reduction in CHC cumulative incidence was seen after HCT (1970s, 76.1%; 1990s, 38.3%; P = .02), mirroring reduced use of total body irradiation. Self-reported health status was good to excellent for 88.2% of survivors; however, this was lower than that for siblings (94.8%; P < .0001). Although HCT is associated with greater long-term morbidity and mortality than chemotherapy-based treatment, gaps have narrowed, and all treatment groups report favorable health status.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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