Kaitlyn E Aragon, Nathan R Lindquist, Meera Patel, Erich M Sturgis, Ray Y Wang, Neil D Gross, Marc-Elie Nader, Neal S Akhave, Paul W Gidley
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引用次数: 0
Abstract
Objective: To present immune checkpoint inhibitor immunotherapy (IO) outcomes for temporal bone-involving squamous cell carcinoma and guide neurotologic decision-making.
Study design: Multi-institutional retrospective cohort.
Setting: Two tertiary-care referral centers.
Patients: Twenty-three patients (42 to 86 years old) with biopsy-proven temporal bone-involving squamous cell carcinoma (SCC).
Interventions: Neoadjuvant IO, imaging to assess response, and surgical interventions.
Main outcome measures: Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 outcomes, pathologic response, surgery de-escalation, and overall survival.
Results: For final RECIST 1.1 response, 6 (26.1%, 95% CI: 10%-48%) patients completely responded (CR), 4 (17.4%, 95% CI: 5%-39%) patients partially responded (PR), 3 (13.0%, 95% CI: 3%-34%) patients had stable disease (SD), and disease progressed (PD) in 10 (43.5%, 95% CI 23%-66%) patients. For primary temporal bone tumors, 36.4% (95% CI: 11%-69%) achieved pathologic CR, radiologic CR, or radiologic PR; cutaneous SCC tumors had a 66.7% (95% CI: 35%-90%) response rate. Two (8.7%) patients with resectable disease were de-escalated to nonsurgical management, and 2 (8.7%) patients were de-escalated from lateral temporal bone resection (LTBR) to mastoidectomy. Overall 3-year survival for patients with CR, PR, or SD was 100% versus 78% for PD patients (P=0.029, HR 13.2, 95% CI: 1.3-134).
Conclusions: Neoadjuvant IO is an option for early-stage and advanced temporal bone SCC, with roughly 50% of patients exhibiting response and avoidance of radical surgery and/or adjuvant radiation in selected cases; ongoing phase 3 trials of neoadjuvant IO will add prospective evidence.
期刊介绍:
Otology & Neurotology publishes original articles relating to both clinical and basic science aspects of otology, neurotology, and cranial base surgery. As the foremost journal in its field, it has become the favored place for publishing the best of new science relating to the human ear and its diseases. The broadly international character of its contributing authors, editorial board, and readership provides the Journal its decidedly global perspective.