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Tislelizumab for the treatment of advanced esophageal squamous cell carcinoma
Kazuhiro Shiraishi1, Shun Yamamoto1, Ken Kato1
1Department of Head and Neck, Esophageal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Abstract:
Advanced esophageal squamous cell carcinoma (ESCC) patients had poor prognosis and few effective drugs based on the randomized controlled trials (RCTs). In such a circumstance, recent RCTs have shown the clinical efficacy of immune checkpoint inhibitors (ICIs) as first- or second-line treatment for advanced ESCC patients. Tislelizumab is one of the anti-Programmed-Death-1 (PD-1) antibodies; at first, tislelizumab monotherapy showed clinical efficacy as a second-line treatment for advanced ESCC patients based on the results of the RATIONALE-302 trial. Since then, tislelizumab plus doublet chemotherapy has shown superiority in overall survival compared to doublet chemotherapy for untreated advanced ESCC patients in the RATIONALE-306 trial. In this review, we share the overview of the development of tislelizumab and discuss the future perspectives on ICIs for advanced ESCC patients. In our opinion, tislelizumab plus doublet chemotherapy is one of the first-line standard treatments for advanced ESCC patients regardless of Programmed cell Death ligand 1 expression. Some other ICI-containing treatments showed clinical efficacy for untreated ESCC patients; we need further investigation to select these treatments appropriately.
Insights
Tislelizumab, an immune checkpoint inhibitor, shows efficacy in advanced esophageal squamous cell carcinoma (ESCC). Tislelizumab plus chemotherapy is a recommended first-line treatment for ESCC patients, regardless of PD-L1 status.
Area of Science:
- Oncology
- Immunotherapy
- Gastrointestinal Oncology
Background:
- Advanced esophageal squamous cell carcinoma (ESCC) presents a poor prognosis with limited therapeutic options.
- Immune checkpoint inhibitors (ICIs) have emerged as a promising treatment modality for advanced ESCC.
- Tislelizumab, an anti-Programmed-Death-1 (PD-1) antibody, has demonstrated clinical activity in this patient population.
Purpose of the Study:
- To review the development and clinical efficacy of tislelizumab in advanced ESCC.
- To discuss the role of ICIs, including tislelizumab, in the treatment landscape of advanced ESCC.
- To provide perspectives on future directions for ICI-based therapies in advanced ESCC.
Main Methods:
- Review of randomized controlled trials (RCTs) evaluating tislelizumab in advanced ESCC.
- Analysis of data from RATIONALE-302 and RATIONALE-306 trials.
- Discussion of clinical outcomes and treatment strategies involving tislelizumab and other ICIs.
Main Results:
- Tislelizumab monotherapy demonstrated efficacy as a second-line treatment for advanced ESCC (RATIONALE-302).
- Tislelizumab plus doublet chemotherapy showed superior overall survival compared to chemotherapy alone in untreated advanced ESCC (RATIONALE-306).
- Tislelizumab plus doublet chemotherapy is considered a first-line standard treatment for advanced ESCC, irrespective of PD-L1 expression.
Conclusions:
- Tislelizumab-based therapies represent a significant advancement in treating advanced ESCC.
- Tislelizumab plus doublet chemotherapy is a recommended first-line treatment option for advanced ESCC.
- Further research is needed to optimize the selection and sequencing of various ICI-containing treatments for advanced ESCC.
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