Active clinical trials for laryngeal cancer with immune checkpoint inhibitors (ICIs) that are no longer recruiting [26]
Trial identifier | Number of cancer patients | Intervention/Treatment regimen | Setting | Primary outcome(s) | Secondary outcome(s) |
---|---|---|---|---|---|
NCT04943445 | 43 laryngeals | Pembrolizumab-based therapy | Neoadjuvant (organ preservation) | Two-year laryngectomy-free survival | Two-year larynx dysfunction-free survival (alive without local recurrence or laryngoesophageal dysfunction) |
NCT04030455 | 27 laryngeals | Cisplatin, docetaxel, pembrolizumab | Neoadjuvant | Disease control rate, pathological complete response rate | Incidence of adverse events, laryngeal preservation rate, relapse-free survival, overall survival, patient-reported quality of life |
NCT04590963 | 370 head and neck (laryngeal unspecified) | Monalizumab, cetuximab | Recurrent/Metastatic | Overall survival in HPV-unrelated analysis set | Overall survival in full analysis set, progression-free survival, duration of response |
NCT02586207 | 59 head and neck (laryngeal unspecified) | Pembrolizumab + chemoradiotherapy (CRT) | Neoadjuvant | Safety & tolerability | Efficacy, response rate |
NCT03082534 | 78 head and neck (laryngeal unspecified) | Pembrolizumab + cetuximab | Recurrent/Metastatic | Clinical efficacy | Progression-free survival, overall survival, duration of response |
NCT04576091 | 7 head and neck (laryngeal unspecified) | Pembrolizumab + radiation + BAY 1895344 (elimusertib) | Recurrent | Safety & tolerability | Incidence of adverse events, locoregional control, progression-free survival, overall response rate, 1-year overall survival, quality of life |
NCT03370276 | 95 head and neck (laryngeal unspecified) | Cetuximab + nivolumab | Recurrent/Metastatic | Phase I: maximum tolerated dose, Phase II: overall survival | Overall response rate, progression-free survival, treatment-related adverse events |
NCT03468218 | 36 head and neck (laryngeal unspecified) | Pembrolizumab + cabozantinib | Recurrent/Metastatic | Overall response rate | Progression-free survival |
MA: Investigation, Writing—original draft. PS: Conceptualization, Writing—original draft. GA, IA, NK, and EK: Writing—review & editing. NSM: Writing—review & editing, Supervision. All authors read and approved the submitted version.
The authors declare that they have no conflicts of interest.
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