PD-L1 evaluation in the gastrointestinal tract: from biological rationale to its clinical application

Luca Mastracci1,2, Federica Grillo1,2, Paola Parente3

  • 1IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Pathologica
|October 28, 2022
PubMed

Insights

Immune-checkpoint inhibitors show promise in gastrointestinal cancers, but only 20-40% of patients respond. PD-L1 expression is a key biomarker, currently used in upper gastrointestinal malignancies.

Area of Science:

  • Oncology
  • Immunology
  • Gastroenterology

Background:

  • Immune-checkpoint inhibitors targeting the PD-1/PD-L1 axis offer clinical benefits in solid tumors, including gastrointestinal malignancies.
  • However, response rates to these therapies remain limited, affecting only 20-40% of patients.
  • PD-L1 expression is a studied biomarker in gastrointestinal neoplasms, with established predictive value only in upper gastrointestinal cancers.

Purpose of the Study:

  • To review technical aspects and challenges of PD-L1 immunohistochemical assays.
  • To discuss the current clinical utility of PD-L1 as a biomarker.
  • To outline studies and trials evaluating PD-L1's prognostic and predictive value in gastrointestinal cancers.

Main Methods:

  • Literature review of studies and clinical trials.
  • Analysis of technical aspects of PD-L1 immunohistochemical assays.
  • Evaluation of PD-L1 expression patterns and biomarker utility.

Main Results:

  • PD-L1 expression is extensively studied in gastrointestinal neoplasms.
  • Predictive value of PD-L1 is currently established only for upper gastrointestinal adenocarcinomas and squamous cell carcinomas.
  • Technical challenges and clinical practice roles of PD-L1 assays are discussed.

Conclusions:

  • PD-L1 is a significant biomarker in gastrointestinal oncology, though its application is currently limited.
  • Further research is needed to optimize PD-L1 assays and expand their use across gastrointestinal cancer types.
  • Understanding PD-L1 expression is crucial for improving patient selection for immune-checkpoint inhibitor therapy.

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