Anti-PD-1 antibodies, a novel treatment option for advanced chemoresistant pulmonary lymphoepithelioma carcinoma

• DOI: 10.3389/fimmu.2022.1001414
• Publication Date: 2022-12-06T04:47:02Z
• Authors: Na Zhou; Hui Tang; Shuangni Yu; Yi Lin; Yingyi Wang; Yuzhou Wang
• Keywords: Lung Neoplasms; efficacy; Immunology; RC581-607; Middle Aged; Lymphoepithelioma-like carcinoma; B7-H1 Antigen; Antibodies; 3. Good health; lung cancer; 03 medical and health sciences; 0302 clinical medicine; Carcinoma, Non-Small-Cell Lung; Tumor Microenvironment; Humans; Prospective Studies; Immunotherapy; rare subtype; immunotherpay; Immunologic diseases. Allergy; Immune Checkpoint Inhibitors; Retrospective Studies

BackgroundPulmonary lymphoepithelioma-like carcinoma (LELC) exhibits a unique immune microenvironment, including high PD-L1 expression and abundant infiltrating-immune cells. However, the availability of PD-1/PD-L1 inhibitors in patients with LELC is still not determined.MethodsA total of 36 cases of pulmonary LELC treated with PD-1/PD-L1 inhibitors were reviewed, including 10 cases from our institute and 26 cases included from the literature. The Kaplan-Meier method and log-rank test were utilized to analyze the survival outcomes of LELC patients receiving immunotherapy, and the factors related to immunotherapy response were further examined.ResultsOf the 10 patients from our institute, the median age was 53.5 years, adrenal glands and distant lymph nodes were the most common metastatic sites, and 4 of 8 (50%) patients had a PD-L1 TPS ≥50%. The median progression-free survival and overall survival in patients from our institute and from the literature were 11.6 and 27.3 months, 17.2 months and not reached, respectively. In all 36 patients, the objective response rate was as high as 57.6%. Patients with higher PD-L1 expression were more likely to have a tumor response, but the association of PD-L1 expression with survival time remains to be determined.ConclusionsPD-1/PD-L1 inhibitors in patients with pulmonary LELC demonstrated a promising efficacy in retrospective cohorts, and deserve further validation in prospective studies administrating in front-line setting.