Immunotherapy has revolutionised cancer treatment over the past decade. Long-term durable responses can be achieved in some cancer patient populations that were previously facing terminal disease. In this chapter, we summarise current phase 3 clinical trial evidence for the use of immunotherapy in gastrointestinal cancers (oesophageal squamous cell carcinoma, oesophago-gastric adenocarcinoma, pancreatic cancer, biliary cancer, hepatocellular carcinoma, colorectal cancer, and squamous cell cancer of the anus). We discuss meaningful biomarkers used in clinical trials to select patients most likely to benefit from immunotherapy, such as mismatch-repair deficiency (MMRd)/microsatellite instability (MSI) and programmed-death-ligand-1 (PD-L1) immunohistochemistry (IHC) expression. Clinical questions are arising regarding the role of immunotherapy in the adjuvant/perioperative setting, optimal timing of surgery in patients who respond to immunotherapy, and toxicities specific to patients with gastrointestinal malignancies. We outline the current landscape and future horizon of immunotherapy in gastrointestinal cancers, such as strategies to increase effectiveness of checkpoint blockade through combinations with other checkpoint inhibitors, cytotoxic chemotherapy, targeted agents, radiotherapy, CAR-T therapy, and cancer vaccines.
Keyphrases
- squamous cell
- clinical trial
- papillary thyroid
- squamous cell carcinoma
- locally advanced
- lymph node metastasis
- dna damage
- early stage
- end stage renal disease
- systematic review
- childhood cancer
- chronic kidney disease
- poor prognosis
- prognostic factors
- radiation therapy
- ejection fraction
- oxidative stress
- bone marrow
- coronary artery disease
- acute kidney injury
- coronary artery bypass
- single cell
- young adults
- atrial fibrillation
- phase ii
- current status
- percutaneous coronary intervention
- cell therapy
- acute coronary syndrome