Late-Occurring Neurologic Sequelae in Adult Survivors of Childhood Acute Lymphoblastic Leukemia: A Report From the Childhood Cancer Survivor Study

Author:

Goldsby Robert E.1,Liu Qi1,Nathan Paul C.1,Bowers Daniel C.1,Yeaton-Massey Amanda1,Raber Shannon H.1,Hill Daniel1,Armstrong Gregory T.1,Yasui Yutaka1,Zeltzer Lonnie1,Robison Leslie L.1,Packer Roger J.1

Affiliation:

1. From the Pediatric Hematology/Oncology, University of California at San Francisco Children's Hospital, San Francisco; Pediatric Hematology/Oncology, University of California at Los Angeles David Geffen School of Medicine, Los Angeles, CA; Public Health Sciences, University of Alberta, Edmonton, AB; Pediatric Hematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada; Pediatric Hematology/Oncology, University of Texas Southwestern Medical Center, Dallas, TX; Epidemiology and Cancer Control, St....

Abstract

Purpose Children with acute lymphoblastic leukemia (ALL) are often cured, but the therapies they receive may be neurotoxic. Little is known about the incidence and severity of late-occurring neurologic sequelae in ALL survivors. Data were analyzed to determine the incidence of adverse long-term neurologic outcomes and treatment-related risk factors. Patients and Methods We analyzed adverse neurologic outcomes that occurred after diagnosis in 4,151 adult survivors of childhood ALL who participated in the Childhood Cancer Survivor Study (CCSS), a retrospective cohort of 5-year survivors of childhood cancer diagnosed between 1970 and 1986. A randomly selected cohort of the survivors' siblings served as a comparison group. Self-reported auditory-vestibular-visual sensory deficits, focal neurologic dysfunction, seizures, and serious headaches were assessed. Results The median age at outcome assessment was 20.2 years for survivors. The median follow-up time to death or last survey since ALL diagnosis was 14.1 years. Of the survivors, 64.5% received cranial radiation and 94% received intrathecal chemotherapy. Compared with the sibling cohort, survivors were at elevated risk for late-onset auditory-vestibular-visual sensory deficits (rate ratio [RR], 1.8; 95% CI, 1.5 to 2.2), coordination problems (RR, 4.1; 95% CI, 3.1 to 5.3), motor problems (RR, 5.0; 95% CI, 3.8 to 6.7), seizures (RR, 4.6; 95% CI, 3.4 to 6.2), and headaches (RR, 1.6; 95% CI, 1.4 to 1.7). In multivariable analysis, relapse was the most influential factor that increased risk of late neurologic complications. Conclusion Children treated with regimens that include cranial radiation for ALL and those who suffer a relapse are at increased risk for late-onset neurologic sequelae.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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