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Clinical applicability of proposed algorithm for identifying individuals at risk for hereditary hematologic malignancies.
Clifford, Maggie; Bannon, Sarah; Bednar, Erica M; Czerwinski, Jennifer; Davis, Jessica; Dunnington, Leslie; Shahrukh Hashmi, S; DiNardo, Courtney D.
Afiliação
  • Clifford M; Baylor Charles A. Sammons Cancer Center, Baylor University Medical Center, Dallas, TX, USA.
  • Bannon S; The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX, USA.
  • Bednar EM; Department of Clinical Cancer Genetics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
  • Czerwinski J; Department of Clinical Cancer Genetics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
  • Davis J; Department of Obstetrics and Gynecology, McGovern Medical School at the University of Texas at Houston, Houston, TX, USA.
  • Dunnington L; Greenwood Genetic Center, Greenville, SC, USA.
  • Shahrukh Hashmi S; Department of Pediatrics, McGovern Medical School at the University of Texas at Houston, Houston, TX, USA.
  • DiNardo CD; Pediatric Research Center, Department of Pediatrics, McGovern Medical School at the University of Texas at Houston, Houston, TX, USA.
Leuk Lymphoma ; 60(12): 3020-3027, 2019 12.
Article em En | MEDLINE | ID: mdl-31274040
ABSTRACT
Multiple genes have been identified to cause hereditary predispositions to hematologic malignancies, and characterized by an increased risk to develop myelodysplastic syndromes (MDS), acute myeloid leukemia (AML), and/or aplastic anemia (AA). Referral algorithms for patients who may be at higher risk have been proposed, with limited data regarding applicability. Our study aimed to evaluate referral criteria on a population of MDS/AML/AA patients. Demographic information and medical history were obtained from 608 patients referred over a 9-month period. Median age at diagnosis was 67 years (56-73), 387 (64%) were male, and the majority of individuals (54.9%) had AML. Overall, 406 individuals (66.8%) had insufficient documentation to determine whether certain criteria were met. Two hundred and two (33.2%) individuals met at least one criteria for genetic counseling referral; however, only nine (4.5%) were referred. Increased documentation of personal and family history is necessary to better assess and validate the applicability of these criteria.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Hematológicas / Predisposição Genética para Doença / Estudos de Associação Genética Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Hematológicas / Predisposição Genética para Doença / Estudos de Associação Genética Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article