AI Article Synopsis

  • Eribulin is a synthetic drug used to treat locally advanced or metastatic breast cancer, showing potential effects on the tumor's immune environment and possibly indicating better survival predictions based on lymphocyte counts.
  • In a study involving 751 patients, those with higher absolute lymphocyte counts (≥1500/µl) experienced significantly prolonged overall survival when treated with eribulin, while those with counts below this threshold did not show a notable difference in survival outcomes compared to other treatments.
  • The analysis suggests baseline absolute lymphocyte count could serve as an independent predictor of overall survival in eribulin-treated patients, highlighting its clinical significance since it's non-invasive to assess.

Article Abstract

Background: Eribulin, a nontaxane synthetic inhibitor of microtubule dynamics, is widely used to manage locally advanced or metastatic breast cancer (MBC). Eribulin has demonstrated immunomodulatory activity on the tumour microenvironment. Baseline neutrophil-to-lymphocyte ratio (NLR), a marker of immune status, may predict progression-free survival in eribulin treatment. This post hoc analysis assessed predictors for overall survival (OS).

Methods: The phase 3 open-label study (EMBRACE) of eribulin versus treatment of physician's choice (TPC) in patients with MBC provided source data. Baseline absolute lymphocyte counts (ALCs) and NLR were evaluable in 751 and 713 patients, respectively.

Results: Eribulin prolonged OS versus TPC in patients with baseline ALC ≥ 1500/µl (hazard ratio [HR] 0.586; 95% confidence interval [CI] 0.437-0.784; P < 0.001). There was no significant difference by treatment for ALC < 1500/µl (HR 1.002; 95% CI 0.800-1.253; P = 0.989). Univariate and multivariate analyses were performed and identified baseline ALC as a potential predictor of OS in eribulin-treated patients. Interaction analysis of OS supported 1500/µl as a potentially differential cutoff value. NLR at a cutoff value of 3 was associated with prolonged OS (eribulin group). However, similar results were also observed in the TPC group, without apparent interaction effect, suggesting that NLR may be a general prognostic marker rather than a specific predictor of OS for eribulin.

Discussion: This hypothesis-generating study speculates that baseline ALC may be an independent predictor for longer OS in eribulin-treated MBC patients and could be clinically impactful because it can be evaluated without the need for additional invasive procedures.

Trial Registration: www.ClinicalTrials.gov code: NCT00388726.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297864PMC
http://dx.doi.org/10.1007/s12282-020-01067-2DOI Listing

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