AI Article Synopsis

  • Recent studies indicate that the lymphocyte-to-monocyte ratio (LMR) at diagnosis can predict survival in tumor patients, including those with multiple myeloma (MM).
  • In a study of 285 MM patients undergoing treatment with novel drugs, an LMR ≤ 4.2 was associated with significantly poorer overall survival (OS) and progression-free survival (PFS) compared to those with LMR > 4.2.
  • LMR < 4.2 was identified as an independent prognostic factor for worse OS and PFS, highlighting its potential as a simple index for assessing systemic immunity and predicting clinical outcomes in MM patients.

Article Abstract

The survival of individuals with tumors may be predicted by the peripheral blood lymphocyte-to-monocyte ratio (LMR) upon diagnosis in recent studies. For patients with multiple myeloma (MM) in the era of novel agents, the prognostic significance of LMR remains unclear. In this study, the prognostic impact of LMR is evaluated by 285 patients with MM who are treated with proteasome inhibitor and/or immunomodulatory drug. LMR is a proven predictor of survival using the receiver operating characteristic curve, with 4.2 as the cutoff point. Patients with LMR ≤ 4.2 at diagnosis had poorer overall survival (OS) and progression-free survival (PFS) than those with LMR > 4.2. In addition, multivariate analysis showed that LMR less than 4.2 is an independent predictor for the OS (hazard ratio [HR]: 1.703; 95% confidence interval [CI]: 1.020-2.842; = 0.042) and PFS (HR: 1.831; 95% CI: 1.098-3.053; = 0.021). According to the test, the LMR at diagnosis, which functions as a simple index reflecting host systemic immunity, can predict clinical outcomes in patients with MM who are treated with new agents.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287166PMC
http://dx.doi.org/10.1155/2018/9434637DOI Listing

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