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Pretreatment Blood Parameters Predict Efficacy from Immunotherapy Agents in Early Phase Clinical Trials

Oncologist, ISSN: 1549-490X, Vol: 25, Issue: 11, Page: e1732-e1742
2020
  • 20
    Citations
  • 0
    Usage
  • 51
    Captures
  • 1
    Mentions
  • 10
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    20
  • Captures
    51
  • Mentions
    1
    • News Mentions
      1
      • 1
  • Social Media
    10
    • Shares, Likes & Comments
      10
      • Facebook
        10

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Article Description

Background: Peripheral blood parameters are correlated to immune-checkpoint inhibitor efficacy in solid tumors, such as melanoma and non-small cell lung cancer. Few data are currently available on the prognostic role of these immune-inflammatory biomarkers for other solid tumors and immunotherapy combinations. Material and Methods: From August 2014 to May 2019, 153 patients with metastatic solid tumors were enrolled in phase I clinical trials testing immunotherapy both as single agents and as combinations. Primary endpoint was to evaluate the impact of baseline blood parameters on progression-free survival (PFS) and overall survival (OS). Results: The most common tumor types were gastrointestinal, breast, and gynecological cancers (22.9%, 22.2%, and 15.0%, respectively). Higher lactate dehydrogenase (LDH) and derived neutrophil-to-lymphocyte ratio (dNLR) were independently associated with reduced PFS (hazard ratio [HR], 1.97; 95% confidence interval [CI], 1.30–2.99; p =.001, and HR, 2.29; 95% CI, 1.39–3.77; p =.001, respectively) and reduced OS (HR, 2.04; 95% CI, 1.26–3.28; p =.004, and HR, 2.06; 95% CI, 1.12–3.79; p =.02, respectively). In the subgroup analysis, (single agent vs. combination), patients at “good” (dNLR <3 and LDH < upper limit of normal [ULN]) and “intermediate and poor” (dNLR >3 and/or LDH > ULN) risk had higher and lower PFS, respectively (p for interaction =.002). Conversely, patients receiving monotherapy presented statistically significant difference in OS according to the risk group, whereas this effect was not observed for those treated with combinations (p for interaction =.004). Conclusion: Elevated LDH and dNLR are associated with poorer survival outcomes in patients treated with immunotherapy in phase I clinical trials, regardless of tumor type. These parameters represent an easy tool that might be considered as stratification factors in immunotherapy-based clinical trials. Implications for Practice: In this retrospective cohort study of 153 patients with metastatic solid tumors treated with immunotherapy in the context of phase I clinical trials, elevated baseline lactate dehydrogenase and derived neutrophil-to-lymphocyte ratio were associated with reduced survival regardless of tumor subtype. If prospectively validated, these parameters might represent low-cost and easy biomarkers that could help patient selection for early phase immunotherapy trials and be applied as a stratification factor in randomized studies testing immunotherapy agents.

Bibliographic Details

Criscitiello, Carmen; Marra, Antonio; Morganti, Stefania; Zagami, Paola; Viale, Giulia; Esposito, Angela; Curigliano, Giuseppe

Oxford University Press (OUP)

Medicine; Biochemistry, Genetics and Molecular Biology

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