The current management and biomarkers of immunotherapy in advanced gastric cancer

Xiaojing Chang1, Xiaohui Ge, Yufeng Zhang

  • 1Department of Radiotherapy, the Second Hospital of Hebei Medical University, Shijiazhuang, China.

Medicine
|May 27, 2022
PubMed
Abstract

Insights

Immune checkpoint inhibitors (ICIs) show promise for advanced gastric cancer (GC). Biomarkers like PD-L1 and TMB may predict treatment response to these immunotherapies.

Area of Science:

  • Oncology
  • Immunotherapy
  • Gastrointestinal Cancer Research

Background:

  • Gastric carcinoma (GC) is a leading cause of cancer mortality globally.
  • Late-stage diagnosis and limited treatment options contribute to poor prognosis in GC.
  • Immune checkpoint inhibitors (ICIs) represent a significant advancement in GC treatment.

Purpose of the Study:

  • To summarize current treatments for advanced gastric cancer.
  • To review the latest advances in immune checkpoint inhibitor therapy for advanced GC.

Main Methods:

  • Comprehensive literature search of databases including WANFANG MED ONLINE, CNKI, NCBI PubMed, and clinicaltrials.gov.
  • Inclusion of studies from 2000 to 2021 focusing on advanced gastric or gastro-oesophageal junction cancer, ICIs, PD-1, PD-L1, CTLA-4, and immunotherapy.

Main Results:

  • Nivolumab and pembrolizumab are recommended for third-line or subsequent therapy in advanced GC.
  • Nivolumab plus chemotherapy is a recommended first-line treatment in China for advanced GC.
  • Potential biomarkers for ICI response include PD-L1, MSI-H, Epstein-Barr virus (EBV), and tumor mutational burden (TMB).

Conclusions:

  • ICIs demonstrate encouraging efficacy and a manageable safety profile in gastric cancer treatment.
  • Biomarkers such as PD-L1, MSI-H, EBV, and TMB status can help evaluate ICI efficacy in GC.

Related Concept Videos

Tumor Immunotherapy01:27

Tumor Immunotherapy

Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
677
Cancer Vaccines01:30

Cancer Vaccines

Cancer treatment vaccines are a rapidly evolving field that offers a promising approach to immunotherapy. Unlike traditional vaccines that prevent diseases, cancer treatment vaccines are designed to treat existing cancers by stimulating the immune system to recognize and attack cancer cells.
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...
526
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
7.8K
Inflammatory Bowel Disease IV: Pharmacological Management01:29

Inflammatory Bowel Disease IV: Pharmacological Management

Upon diagnosis, managing Inflammatory Bowel Disease (IBD) involves addressing several crucial aspects. The primary goals include resting the bowel, correcting malnutrition, and providing symptomatic relief. Resting the bowel may consist of medications to reduce inflammation and promote healing. Correcting malnutrition is essential, often requiring dietary adjustments and nutritional supplements. Symptomatic relief aims to ease pain, diarrhea, and other discomforts in IBD.
Pharmacologic...
206