The Relationship between Tumor-infiltrating Lymphocytes (TILs) and Nasopharyngeal Carcinoma (NPC): A Systematic

Awal Prasetyo1,2, Jethro Budiman3, Udadi Sadhana1,2

  • 1Department of Biomedical Science, Faculty of Medicine, Diponegoro University, Semarang, Indonesia.

Abstract

Insights

Tumor-infiltrating lymphocytes (TILs) are linked to better outcomes in nasopharyngeal carcinoma (NPC). High TILs indicate a stronger anti-tumor response, improving survival and cancer-immune microenvironment. Further research into TILs and gene expression is crucial.

Area of Science:

  • Oncology
  • Immunology
  • Head and Neck Cancer Research

Background:

  • Nasopharyngeal carcinoma (NPC) is an aggressive head and neck cancer.
  • Tumor-infiltrating lymphocytes (TILs) show potential as prognostic markers and therapeutic targets in cancer.
  • The relationship between TILs and NPC prognosis requires systematic investigation.

Purpose of the Study:

  • To systematically review and analyze existing literature on the role of TILs in nasopharyngeal carcinoma.
  • To explore the prognostic significance and therapeutic implications of TILs in NPC.

Main Methods:

  • A systematic literature search was conducted for articles published between January 2000 and January 2020.
  • Three independent reviewers screened articles based on inclusion/exclusion criteria.
  • Risk of bias was assessed, and consensus was reached among reviewers. 12 articles were included from 1233 identified.

Main Results:

  • The majority of included studies (9/12) were cohort studies focusing on the prognostic significance of TILs in NPC.
  • Two studies explored the use of expanded TILs for NPC treatment.
  • One study investigated TILs based on gene expression.

Conclusions:

  • TILs are significant prognostic factors in NPC and play a role in immunotherapy development.
  • Higher TIL levels correlate with improved patient outcomes and survival rates.
  • TILs are associated with effective anti-tumor immunity, delayed tumor progression, and enhanced cancer-immune microenvironment.

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