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Lactate Dehydrogenase (LDH) Response to First-Line Treatment Predicts Survival in Metastatic Breast Cancer: First Clues for A Cost-Effective and Dynamic Biomarker. | LitMetric

AI Article Synopsis

  • * A study of 392 women with MBC found that those with high LDH levels after 12 weeks of initial treatment had significantly worse progression-free survival (PFS) and overall survival (OS) compared to those with normal levels.
  • * The research suggests that monitoring LDH levels could be a useful way to predict treatment outcomes in MBC, indicating a need for further studies to see how LDH changes could inform treatment decisions.

Article Abstract

Elevated plasmatic lactate dehydrogenase (LDH) levels are associated with worse prognosis in various malignancies, including metastatic breast cancer (MBC). Nevertheless, no data are available on the prognostic role of LDH as a dynamic biomarker during first-line treatment in unselected MBC. We reviewed data of 392 women with MBC to evaluate the association between LDH variation after 12 weeks of first-line treatment and survival. The prognostic impact was tested by multivariate Cox regression analysis. Results: Plasmatic LDH was confirmed as an independent prognostic factor in MBC. Patients who maintained elevated LDH levels after 12 weeks of first-line treatment experienced worse progression-free survival (PFS, HR 2.88, 95% CI: 1.40-5.89, = 0.0038) and overall survival (OS, HR 2.61, 95% CI 1.16-5.86, = 0.02) compared to patients with stable normal LDH levels, even after adjustment for other prognostic factors. Notably, LDH low-to-high variation emerged as an unfavorable prognostic factor for PFS (HR 3.96, 95% CI 2.00-7.82, = 0.0001). Plasmatic LDH and its variation during first-line treatment predict PFS and OS in MBC, providing independent prognostic information. It would be worthwhile to prospectively evaluate the association between LDH variation and therapeutic benefit in MBC, and explore how it may affect treatment strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770929PMC
http://dx.doi.org/10.3390/cancers11091243DOI Listing

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