Special Therapy and Psychosocial Needs Identified in a Multidisciplinary Cancer Predisposition Syndrome Clinic.


Journal

Journal of pediatric hematology/oncology
ISSN: 1536-3678
Titre abrégé: J Pediatr Hematol Oncol
Pays: United States
ID NLM: 9505928

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 22 7 2018
medline: 15 5 2019
entrez: 21 7 2018
Statut: ppublish

Résumé

Identification of patients with cancer predisposition syndromes (CPSs) can provide vital information to guide care of an existing cancer, survey for future malignancy, and counsel families. The same underlying mutation responsible for a CPS may also result in other phenotypic abnormalities amenable to therapeutic intervention. The purpose of this study was to examine patients followed in our multidisciplinary CPS clinic to determine the prevalence and scope of medical and psychosocial needs. Data from a baseline evaluation of a single-center patient registry was reviewed. Eligible patients included those with a known or suspected CPS. Over 3 years, 73 patients consented and had successful follow-up. Utilization rate of special therapies, defined as speech therapy, occupational therapy, and/or physical therapy, in the CPS population was 50.7%, significantly higher than a representative sample of children with special needs. Prevalence of 504/IEP (Individualized Education Program) utilization was 20.5%. Patients with CPSs have a high prevalence of medical and psychosocial needs beyond their risk for cancer, for which early screening for necessary interventions should be offered to maximize the patient's developmental potential. Future research is needed to further define the developmental and cognitive phenotypes of these syndromes, and to evaluate the effectiveness of subsequent interventions.

Identifiants

pubmed: 30028825
doi: 10.1097/MPH.0000000000001251
pmc: PMC6348029
mid: NIHMS976605
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

133-136

Subventions

Organisme : NCI NIH HHS
ID : P30 CA091842
Pays : United States

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Auteurs

Andrew P Groves (AP)

Division of General Pediatrics, Boston Children's Hospital, Boston, MA.

Katie Gettinger (K)

Departments of Pediatrics, Division of Pediatric Hematology and Oncology.

Todd E Druley (TE)

Departments of Pediatrics, Division of Pediatric Hematology and Oncology.

Beth A Kozel (BA)

Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO.

Marwan Shinawi (M)

Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO.

Caroline Mohrmann (C)

Departments of Pediatrics, Division of Pediatric Hematology and Oncology.

Jennifer Henry (J)

Departments of Pediatrics, Division of Pediatric Hematology and Oncology.

Celina Jacobi (C)

Departments of Pediatrics, Division of Pediatric Hematology and Oncology.

Kathryn Trinkaus (K)

Biostatistics.

Robert J Hayashi (RJ)

Departments of Pediatrics, Division of Pediatric Hematology and Oncology.

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Classifications MeSH