Treatment outcomes of sinonasal adenoid cystic carcinoma: a single-center experience
- Hye-Bin Jang 1, Dong Hoon Lee 1, Sang Chul Lim 1
- Hye-Bin Jang 1, Dong Hoon Lee 1, Sang Chul Lim 1
- 1Department of Otolaryngology-Head and Neck Surgery, Chonnam National University Medical School & Hwasun Hospital, Hwasun, Republic of Korea.
- 0Department of Otolaryngology-Head and Neck Surgery, Chonnam National University Medical School & Hwasun Hospital, Hwasun, Republic of Korea.
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View abstract on PubMed
Summary
This summary is machine-generated.Sinonasal adenoid cystic carcinoma (ACC) often presents at advanced stages and recurs frequently despite treatment. Tumor stage is the key factor influencing survival in these rare cancers.
Area Of Science
- Oncology
- Head and Neck Surgery
- Medical Malignancies
Background
- Sinonasal adenoid cystic carcinoma (ACC) is a rare malignancy with a propensity for perineural invasion and late recurrence.
- This study analyzes clinical characteristics and treatment outcomes of sinonasal ACC patients over 15 years.
Discussion
- Nasal obstruction is the most common symptom, with the maxillary sinus frequently involved.
- Advanced stage at diagnosis (Stage IV) and perineural invasion are notable findings.
- Multimodal treatment, primarily surgery followed by radiotherapy, is standard, though challenging in advanced cases.
Key Insights
- High recurrence rates (64.7%) are observed, with a mean time to recurrence of approximately 53 months.
- Tumor stage is identified as the sole significant prognostic factor for survival (p < 0.05).
- Early detection and aggressive treatment are crucial for improving outcomes in sinonasal ACC.
Outlook
- Further research into novel therapeutic strategies is warranted to combat the high recurrence rates.
- Improved diagnostic methods for earlier detection could significantly impact patient survival.
- Long-term surveillance is essential for patients with sinonasal ACC due to the risk of late recurrence.
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