Abstract

Objectives: Primary pulmonary lymphoepithelioma-like carcinoma (PPLELC) is an extremely rare subtype of non-small cell lung cancer (NSCLC). Currently, there are no established treatment protocols due to rarity of the cancer. Thus, this study aimed to explore the molecular and clinical characteristics of PPLELC. Study design and setting: Data from patients with PPLELC who were admitted to Zhejiang Cancer Hospital from August 2009 to September 2020 were retrospectively collected. Next-generation sequencing was performed to obtain a genomic profile and tumor mutation burden (TMB) value of patients with adequate tissue and divided them into two groups according to the expression level of PD-L1. The correlation of PD-L1 expression and the clinicopathological characteristics was evaluated by Pearson Chi-square test. Kaplan-Meier curves was applied to present the probability of survival between PD-L1 expression level and overall survival (OS). Moreover, the literature on the immunotherapy of advanced PPLELC published in PubMed between 2016 and 2020 were reviewed and the efficacy of immunotherapy were analyzed. Results: A total of 18 patients pathologically diagnosed as PPLELC were included. After a follow-up period of 8.8–138 months, 14 patients survived, three patients died and one patient lost, the median OS was 45.3 months Seven samples (tissue-available) tested by NGS and the median TMB was 2.5 mutations/Mb. 19 somatic mutated genes were recognized and TP53 (43%) and CYLD (43%) were the two most commonly mutated genes. Only seven patients who underwent NGS were tested for PD-L1. Three patients with high PD-L1 expression (PD-L1≥ 50%) and four patients with low PD-L1 expression (PD-L1 <50%) were included. No significant correlation was observed between PD-L1 expression and clinical characteristics (age, gender, smoking status, tumor stage, lymph node metastasis) (p > 0.05) and OS (p = 1). What’s more, 10 PPLELC patients involved in previous studies and one patient received nivolumab in the current study were collected retrospectively. 4/11 (36.4%) patients achieved PR, 6/11 (54.5%) patients achieved SD, and 1/11 (9.1%) patients achieved PD and the disease control rate (DCR) was 90.9%. Conclusions: The prognosis of PPLELC is better than that of other NSCLC, and immunotherapy may be a promising treatment to prolong the survival of advanced PPLELC patients. Whether the immunotherapy efficacy of PPLELC can be predicted by PD-L1 and TMB needs further clinical investigation. CYLD genetic alterations may participate in Epstein–Barr virus-mediated tumorigenesis in PPLELC, providing a novel therapeutic target.

Highlights

  • Lymphoepithelioma-like carcinoma (LELC) is a rare malignant tumor, which shares similar histology with undifferentiated nasopharyngeal carcinoma (NPC)

  • Palliative therapy, including concurrent chemoradiotherapy, was undertaken in four patients while one patient did not receive any treatment after diagnosis

  • The information of 11 immunotherapy patients (10 Primary pulmonary lymphoepithelioma-like carcinoma (PPLELC) patients involved in previous studies (Kim et al, 2016; Kumar et al, 2017; Narayanan et al, 2019; Qiu et al, 2019; Zhou et al, 2019; Tang et al, 2020; Xie et al, 2020) and one patient received nivolumab in the current study marked as “IP”) were collected retrospectively (Table 2). 4/11 (36.4%) patients achieved partial response (PR), 6/11 (54.5%) patients achieved stable disease (SD), and 1/11 (9.1%) patients achieved progressive disease (PD)

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Summary

Introduction

Lymphoepithelioma-like carcinoma (LELC) is a rare malignant tumor, which shares similar histology with undifferentiated nasopharyngeal carcinoma (NPC). It occurs in the submandibular gland, parotid gland, thymus, lung, stomach, uterus, bladder, and skin (Bégin et al, 1987). Primary pulmonary lymphoepithelioma-like carcinoma (PPLELC) is a rare lung tumor with specific clinicopathological characteristics (Liang et al, 2012), affecting younger patients (51–55-year-old), mostly non-smokers, and mainly Asian females and women from Southern China (Huang et al, 2007; Sun et al, 2014; Jiang et al, 2016). The efficacy of nivolumab in the treatment of advanced NSCLC is significantly related to tumor mutation burden (TMB), and it is more effective in patients with high TMB compared to chemotherapy (Carbone et al, 2017; Peters et al, 2017). The TMB of PPLELC is low, a large amount of gene copy number variations (CNVs), especially 11q13.3 amplification and 9p21.3 deletion, have been observed (Hong et al, 2019)

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