Neurosensory deficits and functional outcomes in childhood cancer survivors: A report from the Childhood Cancer Survivor Study (CCSS).

C Chiara Papini (St. Jude Children's Research Hospital, Memphis, TN) P Pinki Kumari Prasad (Louisiana State University Health Sciences Center New Orleans, Children’s Hospital of New Orleans, New Orleans, LA) M Mengqi Xing (St. Jude Children's Research Hospital, Memphis, TN) S Sedigheh Mirzaei (1St. Jude Children's Research Hospital, Memphis, United States) E Emily S. Tonorezos (Weill Cornell Medicine, New York, NY) D David R. Freyer C Christopher Bertero Weldon (Boston Children's Hospital, Boston, MA) A Austin L. Brown (Baylor College of Medicine, Houston, TX) E Eric Jessen Chow (Fred Hutch Cancer Center, Seattle, WA) R Rebecca M. Howell A Annalynn Williams (13Wilmot Cancer Institute, University of Rochester, Rochester, United States) K Kirsten K. Ness D Deokumar Srivastava V Vikki G. Nolan (St. Jude Children's Research Hospital, Memphis, TN) G Gregory T. Armstrong K Kevin R. Krull R Robert J. Hayashi (Washington University School of Medicine, St. Louis, MO) T Tara M. Brinkman

Abstract

10046 Background: Survivors of childhood cancer are at risk for neurosensory deficits secondary to their disease and treatment. Previous research has characterized system-specific (e.g., visual) impairments; however, the prevalence of multisystem neurosensory deficits and their functional impact remain unknown. Methods: Adult 5-year survivors (n=20037, median age 36 [range 18-69] years, 53.4% male) and sibling controls (n=4121) reported neurosensory deficits related to vision, hearing, vestibular, and neuropathy. Comorbidities were graded using modified CTCAE v5 and defined as having at least one grade 1 neurosensory deficit in one, two, and three/four systems. Survivors reported neurocognitive function (CCSS Neurocognitive questionnaire; impairment: <10 th %ile of sibling distribution), emotional distress (BSI-18; impairment: T score ≥63), quality of life (SF-36; impairment: T score <40), and functional independence. Multivariable models estimated the prevalence of neurosensory comorbidities, adjusted for age, sex, and race. Multivariable models further adjusted for other chronic conditions and neurotoxic therapies examined associations between comorbidities and functional outcomes in survivors. Results: Survivors had higher prevalence of neurosensory deficits in one (31% vs. 24%; prevalence ratio [PR] 1.4, 95% confidence interval [CI] 1.3-1.5), two (14% vs. 8%; 2.2, 1.9-2.5) and three/four systems (9% vs. 3%; 3.3, 2.9-4.1) than siblings. Neurosensory comorbidities were associated with greater risk of neurocognitive impairment (task efficiency and memory), emotional distress (anxiety) and poor quality of life (physical and social function) in a dose-dependent manner in survivors (Table). Similar effects were observed for indicators of functional independence: assistance with personal care/routine needs (one system: relative risk [RR] 2.7, 95% CI 2.2-3.3; two systems: 4.1, 3.3-5.0; three/four systems: 6.5, 5.4-7.9), interference with job/school (2.5, 2.2-3.0; 3.8, 3.2-4.5; 6.1, 5.2-7.1), no driver’s license (1.5, 1.3-1.8; 2.4, 2.1-2.8; 3.8, 3.2-4.4), and non-independent living (1.3, 1.2-1.4; 1.8, 1.6-2.0; 2.1, 1.9-2.4). Conclusions: Adult survivors of childhood cancer have high rates of comorbid neurosensory deficits that have a dose-dependent impact on functional outcomes. Survivors with multisystem deficits should be prioritized for interventions to support functional independence. Relative risk (95% CI) of impaired outcomes in survivors with neurosensory comorbidities. Neurosensory comorbidities(# organ systems) Memory TaskEfficiency Anxiety Physical Function Social Function 0 (ref.) - - - - - 1 1.6 (1.4-1.8) 1.8 (1.6-2.0) 2.6 (2.2-3.1) 2.2 (1.9-2.6) 1.9 (1.7-2.1) 2 2.2 (2.0-2.5) 2.4 (2.2-2.7) 3.4 (2.8-4.1) 3.1 (2.7-3.5) 2.5 (2.2-2.8) 3/4 3.1 (2.7-3.4) 3.3 (3.0-3.7) 5.2 (4.4-6.3) 4.4 (3.8-5.0) 3.2 (2.9-3.7)

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 10046-10046
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

C

Chiara Papini

St. Jude Children's Research Hospital, Memphis, TN

P

Pinki Kumari Prasad

Louisiana State University Health Sciences Center New Orleans, Children’s Hospital of New Orleans, New Orleans, LA

M

Mengqi Xing

St. Jude Children's Research Hospital, Memphis, TN

S

Sedigheh Mirzaei

1St. Jude Children's Research Hospital, Memphis, United States

E

Emily S. Tonorezos

Weill Cornell Medicine, New York, NY

D

David R. Freyer

C

Christopher Bertero Weldon

Boston Children's Hospital, Boston, MA

A

Austin L. Brown

Baylor College of Medicine, Houston, TX

E

Eric Jessen Chow

Fred Hutch Cancer Center, Seattle, WA

R

Rebecca M. Howell

A

Annalynn Williams

13Wilmot Cancer Institute, University of Rochester, Rochester, United States

K

Kirsten K. Ness

D

Deokumar Srivastava

V

Vikki G. Nolan

St. Jude Children's Research Hospital, Memphis, TN

G

Gregory T. Armstrong

K

Kevin R. Krull

R

Robert J. Hayashi

Washington University School of Medicine, St. Louis, MO

T

Tara M. Brinkman