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Childhood cancer survivors face markedly worse overall survival after diagnosis with breast cancer, melanoma, or colorectal cancer.
Lynch, Kevin T; Kane, William J; Fleming, Mark A; Desai, Raj P; Showalter, Shayna L; Slingluff, Craig L; Levin, Daniel E; Hedrick, Traci L.
Afiliação
  • Lynch KT; Department of Surgery, University of Virginia, Charlottesville, Virginia, USA.
  • Kane WJ; Department of Surgery, University of Virginia, Charlottesville, Virginia, USA.
  • Fleming MA; Department of Surgery, University of Virginia, Charlottesville, Virginia, USA.
  • Desai RP; Department of Public Health Sciences, University of Virginia Cancer Center, Charlottesville, Virginia, USA.
  • Showalter SL; Department of Surgery, University of Virginia, Charlottesville, Virginia, USA.
  • Slingluff CL; Department of Surgery, University of Virginia, Charlottesville, Virginia, USA.
  • Levin DE; Department of Surgery, University of Virginia, Charlottesville, Virginia, USA.
  • Hedrick TL; Department of Surgery, University of Virginia, Charlottesville, Virginia, USA.
J Surg Oncol ; 124(1): 16-24, 2021 Jul.
Article em En | MEDLINE | ID: mdl-33788957
ABSTRACT

BACKGROUND:

Childhood cancer survivors (CCS) are at elevated risk of secondary malignancies (SM). Enhanced screening for SM is recommended, but compliance is poor. We hypothesized that CCS with adult-onset SM (colorectal cancer [CRC], melanoma, or breast cancer [BC]) would present with more advanced disease and have decreased overall survival (OS).

METHODS:

The Surveillance, Epidemiology, and End Results Program was queried for patients diagnosed with cancer at age less than or equal to 18 also diagnosed with adult-onset CRC, melanoma, or BC. A cohort without a history of prior malignancy was likewise identified. Tumor features and clinical outcomes were compared.

RESULTS:

CCS with a SM (n = 224) were compared with patients without a childhood cancer history (n = 1,392,670). CCS were diagnosed younger (BC = 37.6 vs. 61.3, p < 0.01, CRC = 35.0 vs. 67.1, p < 0.01, melanoma = 29.6 vs. 61.3 years old, p < 0.01). CCS with BC were more likely to have Stage III or IV disease (25.2% vs. 16.5%, p = 0.01). Hormone-receptor expression also differed; CCS were less likely to develop Luminal A-type tumors (48.6% vs. 66.9%, p = 0.01). After age-adjustment, CCS had worse OS (Hazard ratio CRC = 2.449, p < 0.01, melanoma = 6.503, p < 0.01, BC = 3.383, p < 0.01).

CONCLUSION:

CCS were younger when diagnosed with a SM. After age-adjustment, OS was diminished. Heightened surveillance may be necessary for CCS diagnosed with SM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Neoplasias Colorretais / Programa de SEER / Sobreviventes de Câncer / Melanoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male Idioma: En Revista: J Surg Oncol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Neoplasias Colorretais / Programa de SEER / Sobreviventes de Câncer / Melanoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male Idioma: En Revista: J Surg Oncol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos