4.5 Article

High proportion of tumor necrosis predicts poor survival in surgically resected high-grade neuroendocrine carcinoma of the lung

Journal

LUNG CANCER
Volume 157, Issue -, Pages 1-8

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.lungcan.2021.05.018

Keywords

Tumor necrosis; High-grade neuroendocrine carcinoma; Small cell lung cancer; Large cell neuroendocrine carcinoma; Prognosis

Funding

  1. National Cancer Center Research Fund [20-TR-9]

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This study investigated the prognostic value of tumor necrosis in surgically resected high-grade neuroendocrine carcinomas of the lung, finding that a necrosis proportion of over 10% was significantly associated with higher rates of recurrence and lung cancer-specific deaths. Additionally, genomic alterations did not differ significantly based on the level of necrosis in both small cell lung cancer and large cell neuroendocrine carcinoma.
Objectives: Tumor necrosis is a negative prognostic factor in various cancers. High-grade neuroendocrine carci-nomas (HGNEC) of the lung, such as small cell lung cancer (SCLC) and large cell neuroendocrine carcinoma (LCNEC), commonly have histopathological features of tumor necrosis. However, the prognostic value of tumor necrosis remains unknown. Materials and methods: A total of 81 patients with HGNEC (SCLC, n = 42; LCNEC, n = 39) who underwent complete resection were enrolled. The proportion of necrosis in the tumor tissues was quantified using digital image analysis. We analyzed the relationship between the proportion of necrosis, clinicopathological factors, and prognosis. Moreover, we examined the correlation between genomic alterations and proportion of necrosis. Results: The median proportion of necrosis was 10.6 % (range, 0-62.8 %). The proportion of necrosis was not significantly different between SCLC (median, 5.1 %; range, 0-62.8 %) and LCNEC (median: 14.2 %; range, 0-59.3 %) (p = 0.14). The cumulative incidence of recurrence (CIR) and lung cancer-specific cumulative incidence of death (LC-CID) were significantly higher in patients with 10 % or higher necrosis (necrosis > 10 %) than in those with less than 10 % (necrosis < 10 %) (hazard ratio [HR], 2.94; 95 % confidence interval [CI], 1.30-6.64, and HR, 2.87; 95 % CI, 1.13-7.29, respectively). In the bivariate analysis, necrosis > 10 % was independently associated with higher CIR and tended to be associated with higher LC-CID. The frequency of genomic alterations in the PI3K/AKT/mTOR pathway, MYC family, MAPK/ERK pathway, and major RTK signaling pathways were not different between the necrosis > 10 % and necrosis < 10 % groups for both SCLC and LCNEC. Conclusion: High proportion of tumor necrosis (> 10 %) had a negative prognostic value in surgically resected HGNEC.

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