Wang Shulian, Liao Zhongxing, Wei Xiong, Liu H Helen, Tucker Susan L, Hu Chaosu, Ajani Jaffer A, Phan Alexandria, Swisher Stephen G, Mohan Radhe, Cox James D, Komaki Ritsuko
Department of Radiation Oncology, Cancer Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
J Thorac Oncol. 2008 Mar;3(3):277-82. doi: 10.1097/JTO.0b013e3181653ca6.
There is limited information on risk factors for treatment-related pneumonitis in esophageal cancer patients.
To determine factors associated with treatment-related pneumonitis in esophageal cancer patients treated with definitive chemoradiotherapy.
We retrospectively reviewed clinical data from esophageal cancer patients treated with definitive chemoradiotherapy from 2000 to 2003. Demographic, clinical, and treatment-related data were collected for all patients. The time to occurrence of grade > or =2 pneumonitis was calculated from the end of radiotherapy. Univariate analyses were performed to determine the existence of any association between patient demographic, clinical, or treatment characteristics and pneumonitis.
In total, 96 patients were included in the study with a median follow-up of 8 months (range, <1-48 months). Among them, 23 patients also received an average of two cycles of systemic chemotherapy before the initiation of concurrent chemoradiation. The incidence of grade > or =2 pneumonitis was 22% at 1 year. Systemic chemotherapy before concurrent chemoradiation was significantly associated with an increased risk of grade > or =2 pneumonitis (p = 0.003), with the 1-year incidence of grade > or =2 pneumonitis for patients with and without systemic chemotherapy being 49 and 14%, respectively. No other clinical or dosimetric factors investigated were associated with the risk of grade > or =2 pneumonitis.
Systemic chemotherapy before concurrent chemoradiation was significantly associated with an increased risk of grade > or =2 pneumonitis, suggesting that induction chemotherapy may have sensitized the lung tissue to radiation damage in esophageal cancer patients.
关于食管癌患者治疗相关肺炎的危险因素,目前信息有限。
确定接受根治性放化疗的食管癌患者中与治疗相关肺炎相关的因素。
我们回顾性分析了2000年至2003年接受根治性放化疗的食管癌患者的临床资料。收集了所有患者的人口统计学、临床和治疗相关数据。从放疗结束开始计算≥2级肺炎发生的时间。进行单因素分析以确定患者人口统计学、临床或治疗特征与肺炎之间是否存在关联。
本研究共纳入96例患者,中位随访时间为8个月(范围:<1至48个月)。其中,23例患者在同步放化疗开始前还平均接受了两个周期的全身化疗。1年时≥2级肺炎的发生率为22%。同步放化疗前的全身化疗与≥2级肺炎风险增加显著相关(p = 0.003),接受和未接受全身化疗的患者1年时≥2级肺炎的发生率分别为49%和14%。所研究的其他临床或剂量学因素均与≥2级肺炎风险无关。
同步放化疗前的全身化疗与≥2级肺炎风险增加显著相关,提示诱导化疗可能使食管癌患者的肺组织对辐射损伤更敏感。