Key result
Patients with SCLC and neurologic paraneoplastic syndromes had improved median overall survival (24 months) compared to those with endocrinologic PNS (12 months) or controls (13 months).
Why the study?
Neurologic paraneoplastic syndromes in SCLC are thought to improve prognosis, hypothesized to relate to increased tumor-infiltrating lymphocytes and immune recognition.
Does the presence of neurologic paraneoplastic syndrome improve overall survival and correlate with increased tumor-infiltrating lymphocytes in patients with SCLC?
Cohort (n=145)
No
Does the presence of neurologic paraneoplastic syndrome improve overall survival and correlate with increased tumor-infiltrating lymphocytes in patients with SCLC?
Absolute Event Rate: 24% vs 13%
Neurologic paraneoplastic syndromes in SCLC are associated with improved overall survival and an inflamed tumor microenvironment characterized by increased T cell infiltrates and PD-1/PD-L1 interactions.
Neurologic PNS was associated with longer SCLC survival; leaves open whether immune activation drives benefit or reflects selection bias.
BACKGROUND: Approximately 10% of patients with SCLC develop a paraneoplastic syndrome (PNS). Neurologic PNS are thought to improve prognosis, which we hypothesized is related to increased tumor-infiltrating lymphocytes and immune recognition. METHODS: We queried 2,512,042 medical records from a single institution to identify patients who have SCLC with and without PNS and performed manual, retrospective chart review. We then performed multiplexed fluorescence immunohistochemistry and automated quantitative analysis (AQUA Technology) on tumors to assess CD3, CD4, and CD8 T cell infiltrates and programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) interactions. T cell infiltrates and PD-1/PD-L1 interaction scores were compared among patients with neurologic PNS, endocrinologic PNS, and a control group without PNS. Clinical outcomes were analyzed using the Kaplan-Meier method and Cox proportional hazards models. RESULTS: We evaluated 145 SCLC patients: 55 with PNS (25 neurologic and 30 endocrinologic) and 90 controls. Patients with neurologic PNS experienced improved overall survival compared to patients with endocrinologic PNS and controls (median overall survival of 24 months versus 12 months versus 13 months, respectively). Of the 145 patients, we identified tumor tissue from 34 patients that was adequate for AQUA analysis. Among 37 specimens from these 34 patients, patients with neurologic PNS had increased T cell infiltrates (p = 0.033) and PD-1/PD-L1 interaction (p = 0.014) compared to tumors from patients with endocrinologic PNS or controls. CONCLUSIONS: Tumor tissue from patients with SCLC with neurologic PNS showed increased tumor-infiltrating lymphocytes and PD-1/PD-L1 interaction consistent with an inflamed tumor microenvironment.
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Iams et al. (2019) conducted a cohort in Small Cell Lung Cancer (SCLC) (n=145). Neurologic paraneoplastic syndromes vs. Endocrinologic paraneoplastic syndromes and controls without PNS was evaluated on Median overall survival (months). Patients with SCLC and neurologic paraneoplastic syndromes had improved median overall survival (24 months) compared to those with endocrinologic PNS (12 months) or controls (13 months).
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