Long-term health-related outcomes in survivors of childhood cancer treated with HSCT versus conventional therapy: a report from the Bone Marrow Transplant Survivor Study (BMTSS) and Childhood Cancer Survivor Study (CCSS)

Author:

Armenian Saro H.1,Sun Can-Lan1,Kawashima Toana2,Arora Mukta3,Leisenring Wendy2,Sklar Charles A.4,Baker K. Scott5,Francisco Liton1,Teh Jennifer Berano1,Mills George1,Wong F. Lennie1,Rosenthal Joseph6,Diller Lisa R.7,Hudson Melissa M.8,Oeffinger Kevin C.4,Forman Stephen J.9,Robison Leslie L.8,Bhatia Smita1

Affiliation:

1. Population Sciences, City of Hope, Duarte, CA;

2. Clinical Statistics and Cancer Prevention, Fred Hutchinson Cancer Research Center, Seattle, WA;

3. Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN;

4. Memorial Sloan-Kettering Cancer Center, New York, NY;

5. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;

6. Hematology/Oncology, Children's Hospital of Central California, Madera; CA;

7. Dana-Farber Cancer Institute, Boston, MA;

8. Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, TN; and

9. Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA

Abstract

Abstract HSCT is being increasingly offered as a curative option for children with hematologic malignancies. Although survival has improved, the long-term morbidity ascribed to the HSCT procedure is not known. We compared the risk of chronic health conditions and adverse health among children with cancer treated with HSCT with survivors treated conventionally, as well as with sibling controls. HSCT survivors were drawn from BMTSS (N = 145), whereas conventionally treated survivors (N = 7207) and siblings (N = 4020) were drawn from CCSS. Self-reported chronic conditions were graded with CTCAEv3.0. Fifty-nine percent of HSCT survivors reported ≥ 2 conditions, and 25.5% reported severe/life-threatening conditions. HSCT survivors were more likely than sibling controls to have severe/life-threatening (relative risk [RR] = 8.1, P < .01) and 2 or more (RR = 5.7, P < .01) conditions, as well as functional impairment (RR = 7.7, P < .01) and activity limitation (RR = 6.3, P < .01). More importantly, compared with CCSS survivors, BMTSS survivors demonstrated significantly elevated risks (severe/life-threatening conditions: RR = 3.9, P < .01; multiple conditions: RR = 2.6, P < .01; functional impairment: RR = 3.5, P < .01; activity limitation: RR = 5.8, P < .01). Unrelated donor HSCT recipients were at greatest risk. Childhood HSCT survivors carry a significantly greater burden of morbidity not only compared with noncancer populations but also compared with conventionally treated cancer patients, providing evidence for close monitoring of this high-risk population.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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