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头颈部癌症 10 年幸存者中辐射诱导的迟发性颅神经病变的发生率和结局。

Incidence and outcomes of radiation-induced late cranial neuropathy in 10-year survivors of head and neck cancer.

机构信息

Departments of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA.

Departments of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA.

出版信息

Oral Oncol. 2019 Aug;95:59-64. doi: 10.1016/j.oraloncology.2019.05.014. Epub 2019 Jun 8.

Abstract

OBJECTIVES

To characterize the late cranial neuropathy among 10-year survivors of head and neck cancer treatment.

MATERIALS AND METHODS

We retrospectively evaluated patients treated with curative-intent radiation for HNC between 1990 and 2005 at a single institution with systematic multidisciplinary follow-up ≥ 10 years. New findings of CNP were considered radiation-induced when examination, imaging and/or biopsy did not demonstrate a structural or malignant cause. Cox proportional hazards modeling was used for univariable analysis (UVA) and multivariable analysis (MVA) for time to CNP after completion of radiation.

RESULTS

We identified 112 patients with no evidence of disease and follow-up ≥ 10 years (median 12.2). Sixteen (14%) patients developed at least one CNP. The median time to CNP was 7.7 years (range 0.6-10.6 years). Most common was CN XII deficit in eight patients (7%), followed by CN X deficit in seven patients (6%). Others included CN V deficit in three, and CN XI deficit in two. Eight of the thirteen patients with a CN X and/or CN XII deficit required a permanent gastrostomy tube. On UVA, site of primary disease, post-radiation neck dissection, chemotherapy, and radiation dose were significantly associated with increased risk of CNP.

CONCLUSION

Iatrogenic CNP may develop years after head and neck cancer treatment and often leads to swallowing dysfunction. Long-term follow up is essential for these patients receiving head and neck radiation.

摘要

目的

描述头颈部癌症治疗后 10 年幸存者的晚期颅神经病变。

材料与方法

我们回顾性评估了 1990 年至 2005 年期间在一家机构接受根治性放疗的头颈部癌症患者,这些患者均接受了系统的多学科随访,随访时间≥10 年。当检查、影像学和/或活检未显示结构或恶性原因时,将新发现的颅神经病变视为放射性颅神经病变。使用 Cox 比例风险模型进行单变量分析(UVA)和多变量分析(MVA),以评估放疗完成后颅神经病变的时间。

结果

我们确定了 112 例无疾病证据且随访时间≥10 年(中位数为 12.2 年)的患者。16 例(14%)患者至少出现了一种颅神经病变。颅神经病变的中位时间为 7.7 年(范围为 0.6-10.6 年)。最常见的是 8 例(7%)患者的颅神经 XII 缺陷,其次是 7 例(6%)患者的颅神经 X 缺陷。其他包括 3 例颅神经 V 缺陷和 2 例颅神经 XI 缺陷。13 例颅神经 X 和/或颅神经 XII 缺陷患者中,有 8 例需要永久性胃造口管。在 UVA 中,原发疾病部位、放疗后颈部清扫术、化疗和放疗剂量与颅神经病变风险增加显著相关。

结论

头颈部癌症治疗后数年可能会出现医源性颅神经病变,常导致吞咽功能障碍。这些接受头颈部放疗的患者需要长期随访。

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