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H. Kaur



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    P1.07 - Poster Session/ Small Cell Lung Cancer (ID 221)

    • Event: WCLC 2015
    • Type: Poster
    • Track: Small Cell Lung Cancer
    • Presentations: 1
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      P1.07-015 - The Prognostic Value of the Neutrophil Lymphocyte Ratio in Patients with Small Cell Lung Cancer (ID 964)

      09:30 - 17:00  |  Author(s): H. Kaur

      • Abstract
      • Slides

      Background:
      A high neutrophil to lymphocyte ratio (NLR) is reported to be a poor prognostic indicator in several malignancies and is associated with inferior survival. There is limited data exploring the prognostic role of NLR in small cell lung cancer (SCLC). The aim of the study was to evaluate the prognostic role of the NLR at the time of diagnosis in patients with SCLC.

      Methods:
      We retrospectively analyzed data from July 2010 to June 2013 of patients diagnosed with SCLC at a single tertiary care center. NLR ≥4 at the time of diagnosis was correlated with other prognostic variables to estimate its effect on the overall survival (OS).

      Results:
      There were a total of 80 eligible patients, including 33 males and 47 females. At the time of diagnosis, NLR ≥4 was seen in 36 (45%) patients. Overall, median absolute neutrophil count was 6.15 K/uL and absolute lymphocyte count was 1.6 K/uL. Both groups were comparable for age, gender, body mass index and ECOG functional score. We found 31/36 (86.11%) patients with NLR ≥4 who had extensive stage disease. In contrast, only 24/44 (54.55%) patients with NLR <4 had extensive stage disease (P= 0.0024). All 25/25 (100%) patients with limited stage disease received chemoradiation, while 44/55 (80%) of patients with extensive stage disease received chemotherapy. The median overall survival was 8.7 versus 11.2 months for patients with NLR ≥4 versus NLR <4 (log-rank P=0.014) (Figure 1). Multivariate Cox regression detected a strong interaction (P=0.0024) between NLR and the combined status of chemotherapy and stage. In the limited stage group, NLR ≥4 patients had slightly worse OS (HR=2.13, 95% CI: 0.66-6.86; P=0.20), whereas in the extensive stage group which received chemotherapy, NLR ≥4 patients had slightly better OS (HR=0.80, 95% CI: 0.42-1.53; P=0.50). In the extensive-stage group which did not receive chemotherapy, NLR ≥4 patients had significantly worse OS (HR=12.7, 95% CI: 2.94-55.2; P=0.0007).

      Conclusion:
      Similar to the other studies in solid tumors, we found a prognostic value of NLR in all patients with SCLC. However, NLR was prognostically significant only among patients with extensive-stage disease who did not receive chemotherapy. Among patients of both stage groups who received chemotherapy, NLR had little prognostic value. NLR ≥4 appears to be more prevalent in patients with extensive stage disease probably reflecting an impaired immune system. Further research exploring the role of immune system and associated immune surrogate markers in SCLC is needed. Figure 1



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