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Prostate cancer-specific mortality burden by risk group among men with localized disease: Implications for research and clinical trial priorities.
Dee, Edward Christopher; Nezolosky, Michelle D; Chipidza, Fallon E; Arega, Melaku A; Butler, Santino S; Sha, Sybil T; Mahal, Brandon A; Nguyen, Paul L; Yang, David D; Muralidhar, Vinayak.
Afiliação
  • Dee EC; Dana-Farber Cancer Institute/Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Nezolosky MD; Harvard Medical School, Boston, Massachusetts.
  • Chipidza FE; Dana-Farber Cancer Institute/Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Arega MA; Dana-Farber Cancer Institute/Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Butler SS; Harvard Medical School, Boston, Massachusetts.
  • Sha ST; Dana-Farber Cancer Institute/Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Mahal BA; Harvard Medical School, Boston, Massachusetts.
  • Nguyen PL; Dana-Farber Cancer Institute/Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Yang DD; Geisel School of Medicine at Dartmouth, Hanover, New Hampshire.
  • Muralidhar V; Department of Radiation Oncology, University of Miami Miller School of Medicine, Miami, Florida.
Prostate ; 80(13): 1128-1133, 2020 09.
Article em En | MEDLINE | ID: mdl-32659024
ABSTRACT

OBJECTIVE:

To estimate contemporary population-based patterns of the relative burden of prostate cancer-specific mortality (PCSM) attributable to each N0M0 prostate cancer risk-group, that may guide prioritization in research, trial design, and clinical practice.

METHODS:

We categorized 2004-2015 Surveillance, Epidemiology, and End Results database patients by risk group (low, favorable intermediate, unfavorable intermediate, high, and very highrisk). Using the Fine-Gray method, we calculated the relative burden of 10-year PCSM attributable to each risk group.

RESULTS:

Among N = 337 162 men (6.8-year median follow-up; median age 65 years), the relative proportion of low-, favorable intermediate-, unfavorable intermediate-, high-, and very high-risk diagnoses were 29.9% (N = 100 969), 31.1% (N = 104 696), 17.9% (N = 60 360), 18.1% (N = 61 023), and 3.0% (N = 10 114). Within 10 years of diagnosis, among patients who died of prostate cancer (N = 15 064), 5.0% (N = 746) had low-risk, 13.7% (N = 2060) had favorable intermediate-risk, 16.1% (N = 2429) had unfavorable intermediate-risk, 47.8% (N = 7196) had high-risk, and 17.5% (N = 2633) had very high-risk disease at diagnosis. Patients aged 65 and older accounted for 51.9% of all diagnoses and 72.3% of 10-year PCSM. Although black patients accounted for 15.0% of low-risk diagnoses, they accounted for 20.6% of 10-year PCSM. White patients accounted for 80.3% of low-risk diagnoses and 75.7% of 10-year PCSM.

CONCLUSION:

Although high-risk and very high-risk disease account for one-fifth of diagnoses, they account for two-thirds of 10-year PCSM. Older patients and black patients with low-risk disease accounted for a disproportionately large proportion of deaths. These findings support targeting research toward high-risk disease and ensuring adequate representation of older and black men in clinical trials.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata Tipo de estudo: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Prostate Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata Tipo de estudo: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Prostate Ano de publicação: 2020 Tipo de documento: Article