A narrative review of the evolving role of immunotherapy in the management of esophageal and gastric cancer

Background and ObjectiveDespite recent advances in the multidisciplinary management of esophagogastric cancer, overall prognosis remains poor. There is a need for improved treatment options, along with predictive biomarkers that improve therapeutic decision-making. MethodsWe conducted an extensive r...

Full description

Saved in:
Bibliographic Details
Published inJournal of gastrointestinal oncology Vol. 13; no. 4; pp. 2007 - 2019
Main Authors Madan, Ankit, Uronis, Hope E., Strickler, John H.
Format Journal Article
LanguageEnglish
Published AME Publishing Company 01.08.2022
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background and ObjectiveDespite recent advances in the multidisciplinary management of esophagogastric cancer, overall prognosis remains poor. There is a need for improved treatment options, along with predictive biomarkers that improve therapeutic decision-making. MethodsWe conducted an extensive review of immunotherapy articles in the PubMed database between December 2013 and October 2021. Articles in English were included. We included phase 1, 2, and 3 clinical trials for immunotherapy review, and prospective, retrospective, and meta-analyses for biomarker review. Key Content and FindingsInitial studies of immunotherapy were performed in patients with relapsed refractory metastatic disease and demonstrated a modest survival benefit. Subsequent studies have evaluated the use of these agents in combination with first line chemotherapy for metastatic disease. Finally, recent data indicates that immunotherapy in the adjuvant setting after concurrent chemoradiation and surgery improves disease free survival. Both microsatellite instability high (MSI-H) status and Epstein-Barr virus (EBV) positivity predict response to immunotherapy, but many patients without these biomarkers still benefit. The predictive impact of programmed cell death-ligand 1 (PD-L1) expression and tumor mutational burden (TMB) have been variable, and the optimal cutoff point for these biomarkers remains poorly defined. ConclusionsWhile immunotherapy agents have demonstrated clinical benefit and are now incorporated into the current standard of care, novel immunotherapy approaches such as dual immunotherapy combinations, chimeric antigen receptor (CAR) T cells, and tumor vaccines need to be further investigated. As the era of precision medicine beckons, refined biomarkers to predict benefit are needed.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
Contributions: (I) Conception and design: A Madan, JH Strickler; (II) Administrative support: A Madan, JH Strickler; (III) Provision of study materials: A Madan, JH Strickler; (IV) Collection and assembly of data: A Madan, JH Strickler; (V) Data analysis and interpretation: All authors; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.
ISSN:2078-6891
2219-679X
DOI:10.21037/jgo-22-55