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Targeted Therapies in Advanced Gastric Cancer
Timil H Patel1, Michael Cecchini2
1Department of Internal Medicine (Medical Oncology), Yale School of Medicine, 333 Cedar St, PO Box 208028, New Haven, CT, 06520, USA.
Opinion Statement:
Despite a decreasing incidence in the USA, gastric cancer is highly prevalent worldwide. Furthermore, gastric cancer remains highly lethal with median survival of less than 1 year for metastatic disease. The backbone of therapy against metastatic gastric cancer remains cytotoxic chemotherapy, but recent advances in the molecular understanding of gastric cancer have renewed hope within that targeted agents can be leveraged to improve survival and reduce toxicity. For example, in patients with human epidermal growth factor-2 (HER2)-positive gastric cancer, the addition of trastuzumab to frontline chemotherapy improves survival. In the second line, oncologists can now administer a vascular endothelial growth factor (VEGF) receptor inhibitor, ramucirumab, as a single agent or in combination with chemotherapy, and the immune checkpoint inhibitor pembrolizumab is approved in multiple settings dependent on the Programmed Death Ligand 1 (PD-L1) status. For patients with metastatic disease, our approach to standard of care in the first-line setting is a 5FU/platinum doublet with trastuzumab for HER2-positive tumors. In the second-line setting, most patients receive ramucirumab + paclitaxel, but those that are MSI high receive pembrolizumab. For squamous cell carcinoma of the esophagus with high PD-L1 status (combined positive score (CPS) ≥ 10), we recommend pembrolizumab in the second line. While for PD-L1 ≥ 1% gastroesophageal adenocarcinoma, we do not recommend pembrolizumab before the third-line setting, although this may change in the near future for CPS ≥ 10. The future landscape for targeted therapy in gastric cancer is promising. Numerous clinical trials evaluating the combination immune therapy with molecularly targeted agents are generating much excitement. Moreover, genomic data from The Cancer Center Genome (TCGA) and Asian Cancer Research Group (ACRG) classifications is being used to identify molecular subtypes to enable future clinical trials to include biomarker-enriched patient populations.
Insights
Gastric cancer treatment advances include targeted therapies like trastuzumab for HER2-positive cases and immune checkpoint inhibitors. Future research focuses on combining these for improved patient survival.
Area of Science:
- Medical Oncology
- Gastroenterology
- Cancer Research
Background:
- Gastric cancer remains a lethal malignancy worldwide, with limited survival for metastatic disease.
- Current standard treatment relies on cytotoxic chemotherapy, but targeted therapies offer new hope.
- Molecular understanding of gastric cancer is driving the development of novel treatment strategies.
Purpose of the Study:
- To review current and emerging therapeutic strategies for metastatic gastric cancer.
- To highlight the role of targeted agents and immune checkpoint inhibitors.
- To discuss the future landscape of personalized medicine in gastric cancer treatment.
Main Methods:
- Review of current clinical practice guidelines and recent clinical trial data.
- Analysis of targeted therapies including trastuzumab (for HER2-positive), ramucirumab (VEGF inhibitor), and pembrolizumab (immune checkpoint inhibitor).
- Discussion of molecular classifications (TCGA, ACRG) for identifying patient subgroups.
Main Results:
- First-line treatment for metastatic gastric cancer involves 5FU/platinum doublet chemotherapy, with trastuzumab for HER2-positive tumors.
- Second-line options include ramucirumab plus paclitaxel or pembrolizumab for MSI-high patients.
- Pembrolizumab use in esophageal squamous cell carcinoma and gastroesophageal adenocarcinoma is dependent on PD-L1 status and treatment line.
Conclusions:
- Targeted agents and immune checkpoint inhibitors are significantly improving outcomes in gastric cancer.
- Personalized medicine approaches, guided by molecular subtypes and biomarkers, are crucial for future treatment advancements.
- Ongoing clinical trials combining immunotherapy with targeted agents show promise for further enhancing survival and reducing toxicity.
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