Monocytes-to-lymphocytes ratio increases the prognostic value of circulating tumor cells in non-small cell lung cancer: a prospective study

  • 0Department of Clinical Medicine, Henan Medical College, Zhengzhou, China.

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Summary

This summary is machine-generated.

Combining circulating tumor cells (CTCs) with the monocytes-to-lymphocytes ratio (MLR) significantly improves prognostic value in non-small cell lung cancer (NSCLC). This combined approach aids in patient stratification and monitoring immunotherapy response.

Area Of Science

  • Oncology
  • Biomarkers
  • Cancer Research

Background

  • Circulating tumor cells (CTCs) hold prognostic significance in non-small cell lung cancer (NSCLC).
  • Current CTC detection sensitivity limits clinical utility.
  • This study investigates combining inflammation-based scores with CTCs to enhance prognostic capabilities in NSCLC.

Purpose Of The Study

  • To explore the feasibility of integrating peripheral blood cell (PBC)-derived inflammation scores with CTC analysis.
  • To improve the prognostic value of CTCs in NSCLC patients.
  • To assess the potential for better patient stratification and personalized treatment strategies.

Main Methods

  • Sixty NSCLC patients were enrolled.
  • CTC counts and six inflammation-based scores, including monocytes-to-lymphocytes ratio (MLR), were analyzed.
  • Association with progression-free survival (PFS) and overall survival (OS) was evaluated, alongside changes in CTC counts post-immunotherapy.

Main Results

  • Elevated CTCs (>7) and MLR (>0.2) were independently associated with shorter OS and PFS in NSCLC.
  • Patients with both high CTCs and MLR faced significantly increased risks of death and disease progression.
  • Decreased CTC counts post-immunotherapy correlated with disease control.

Conclusions

  • CTCs and MLR are independent prognostic factors in NSCLC.
  • Combining CTCs with MLR substantially enhances prognostic accuracy, aiding in patient stratification.
  • Dynamic CTC monitoring effectively predicts immunotherapy response in NSCLC.