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Evaluation of the Khorana score for prediction of venous thromboembolism in patients with multiple myeloma.
Sanfilippo, Kristen M; Carson, Kenneth R; Wang, Tzu-Fei; Luo, Suhong; Edwin, Natasha; Kuderer, Nicole; Keller, Jesse M; Gage, Brian F.
Afiliação
  • Sanfilippo KM; Washington University School of Medicine in St. Louis St. Louis Missouri USA.
  • Carson KR; St. Louis Veterans Affairs Medical Center St. Louis Missouri USA.
  • Wang TF; Rush University Medical Center Chicago Illinois USA.
  • Luo S; University of Ottawa at The Ottawa Hospital and Ottawa Hospital Research Institute Ottawa Ontario Canada.
  • Edwin N; Washington University School of Medicine in St. Louis St. Louis Missouri USA.
  • Kuderer N; St. Louis Veterans Affairs Medical Center St. Louis Missouri USA.
  • Keller JM; ThedaCare Regional Cancer Center Appleton Wisconsin USA.
  • Gage BF; Advanced Cancer Research Group Kirkland Washington USA.
Res Pract Thromb Haemost ; 6(1): e12634, 2022 Jan.
Article em En | MEDLINE | ID: mdl-35028491
ABSTRACT

BACKGROUND:

Guidelines recommend thromboprophylaxis for patients with multiple myeloma (MM) at high risk for venous thromboembolism (VTE). However, the optimal risk prediction model for VTE in MM remains unclear. Khorana et al developed a VTE risk score (Khorana score) in ambulatory cancer patients receiving chemotherapy. We aimed to evaluate the predictive ability of the Khorana score in patients with MM.

METHODS:

We identified patients with MM within the Veterans Affairs health care system between 2006 and 2013. The Khorana score was calculated before treatment initiation. Using logistic regression, the relationship between risk group and VTE was assessed at 3 and 6 months. We tested model discrimination using the concordance statistic.

RESULTS:

In the cohort of 2870 patients with MM, there were 1328 at low risk (0 points), 1521 at intermediate risk (1-2 points), and 21 at high risk (≥3 points) for VTE by the Khorana score. The 6-month cumulative incidence of VTE was 5.1% (95% confidence interval [CI], 4.0%-6.4%) in low risk, 3.9% (95% CI, 3.0%-5.0%) in intermediate risk, 4.8% (95% CI, 0.3%-20.2%) in high risk. The Khorana score did not strongly discriminate between patients who did and did not develop VTEs at 3 or 6 months (concordance statistic, 0.58; 95% CI, 0.54-0.63; and 0.53, 95% CI, 0.50-0.57, respectively.

CONCLUSIONS:

In conclusion, in this cohort of 2870 patients with MM, the Khorana score did not predict VTE. Our study supports the need to use myeloma-specific risk models to predict VTE risk in patients with MM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Res Pract Thromb Haemost Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Res Pract Thromb Haemost Ano de publicação: 2022 Tipo de documento: Article