Serum metabolomic signatures predict clinical outcomes in advanced non-small cell lung cancer treated with pembrolizumab plus platinum-based chemotherapy - Summary - MDSpire

Serum metabolomic signatures predict clinical outcomes in advanced non-small cell lung cancer treated with pembrolizumab plus platinum-based chemotherapy

  • By

  • Peter May

  • Christof Winter

  • Inga Hubrecht

  • Adrian Patenge

  • Selina Strathmeyer

  • Roland Geyer

  • Steffen Heelemann

  • Jan Stratmann

  • Seyer Safi

  • Henriette Klein

  • Folker Schneller

  • Florian Bassermann

  • Aaron Becker von Rose

  • May 18, 2026

  • 0 min

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Objective:

To determine the correlation between serum metabolite profiles and specific clinical outcomes, such as overall survival and progression-free survival, in advanced NSCLC patients treated with pembrolizumab plus chemotherapy.

Key Findings:
  • Lower serum levels of branched-chain amino acids (BCAAs) valine and isoleucine were linked to disease progression within 60 days.
  • Long-term survivors exhibited higher levels of lipids, including total phospholipids and sphingomyelin.
  • Patients who died during follow-up had elevated inflammatory markers like glycoprotein acetyls.
  • An RF model achieved high accuracy (AUC = 0.93) in predicting survival status, with key contributors being sphingomyelin, apolipoprotein A2, and glycoprotein acetyls B.
Interpretation:

Serum metabolomic profiles can serve as non-invasive biomarkers for predicting clinical outcomes in advanced NSCLC patients undergoing pembrolizumab and chemotherapy.

Limitations:
  • The study's sample size was relatively small with only 36 patients, which may limit the statistical power and generalizability of the findings.
  • Findings may not be generalizable to all NSCLC patient populations due to specific inclusion criteria, particularly the exclusion of patients with certain genetic mutations.
Conclusion:

Serum metabolomic profiling reveals significant associations with clinical outcomes in advanced NSCLC, highlighting the potential of specific metabolites as biomarkers for treatment response.

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