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III 期肺腺癌患者根治性同步放化疗后脑转移:癌胚抗原作为一种潜在的预测因素。

Brain metastases after definitive concurrent chemoradiotherapy in patients with stage III lung adenocarcinoma: carcinoembryonic antigen as a potential predictive factor.

机构信息

Division of Internal Medicine and Thoracic Oncology, National Cancer Center Hospital, Chuo-ku, Tokyo, Japan.

出版信息

Cancer Sci. 2012 Apr;103(4):756-9. doi: 10.1111/j.1349-7006.2012.02217.x. Epub 2012 Feb 20.

Abstract

The predictive factors for the development of brain metastases in patients with stage III non-small-cell lung cancer receiving concurrent chemoradiotherapy remain unclear. Several studies have suggested adenocarcinoma as a predictive factor of brain relapses. In the current analysis, we tried to identify the factors associated with brain metastases in stage III lung adenocarcinoma. The demographic and clinical characteristics, site and date of recurrence, and date of death were reviewed in patients with unresectable stage III lung adenocarcinoma who underwent concurrent platinum-based chemoradiotherapy. In total, 116 patients were identified with a median (range) age of 57 (35-74) years. Of these, 86 (74%) were men, all patients had platinum-based chemotherapy, and 100 (86%) received a total dose of 60 Gy in 30 fractions as definitive thoracic radiotherapy. Of the 95 patients with disease progression or recurrence, 19 (16%) developed brain metastases as the sole site of initial recurrence. A total of 43 (37%) patients developed brain metastases at some time during follow-up. Time to brain metastases was significantly associated with the pretreatment carcinoembryonic antigen (CEA) value, with a hazard ratio (95% confidence interval) of 2.64 (1.39-5.02, P = 0.003). Patients who developed brain metastases as the first recurrent site had marginally better survival (log-rank test, P = 0.066) than those with metastases other than brain. In conclusion, stage III lung adenocarcinoma patients with an elevated CEA value before treatment had a higher risk of developing brain metastases after chemoradiotherapy. Further effort is mandatory to control brain metastases in this patient population by a therapeutic strategy based on the tumor histology and pretreatment CEA value.

摘要

接受同步放化疗的 III 期非小细胞肺癌患者发生脑转移的预测因素尚不清楚。一些研究表明腺癌是脑复发的预测因素。在目前的分析中,我们试图确定与 III 期肺腺癌脑转移相关的因素。对接受含铂同步放化疗的不可切除 III 期肺腺癌患者的人口统计学和临床特征、复发部位和时间以及死亡日期进行了回顾性分析。共确定了 116 例中位(范围)年龄为 57(35-74)岁的患者。其中,86 例(74%)为男性,所有患者均接受了含铂化疗,100 例(86%)接受了总剂量为 60 Gy 的 30 次分割作为确定性胸部放疗。在 95 例疾病进展或复发的患者中,19 例(16%)作为初始复发的唯一部位发生脑转移。共有 43 例(37%)患者在随访期间的某个时间发生脑转移。脑转移的时间与治疗前癌胚抗原(CEA)值显著相关,风险比(95%置信区间)为 2.64(1.39-5.02,P=0.003)。作为首发复发病灶发生脑转移的患者的生存时间略长(对数秩检验,P=0.066),而不是脑外转移。总之,治疗前 CEA 值升高的 III 期肺腺癌患者在接受放化疗后发生脑转移的风险更高。需要进一步努力,通过基于肿瘤组织学和治疗前 CEA 值的治疗策略来控制这部分患者的脑转移。

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