Department of Thoracic Surgery Department of Experimental Research.
Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou.
Ann Oncol. 2015 Mar;26(3):504-9. doi: 10.1093/annonc/mdu567. Epub 2014 Dec 15.
This study compared prophylactic cranial irradiation (PCI) with observation in patients with resected stage IIIA-N2 non-small-cell lung cancer (NSCLC) and high risk of cerebral metastases after adjuvant chemotherapy.
In this open-label, randomized, phase III trial, patients with fully resected postoperative pathologically confirmed stage IIIA-N2 NSCLC and high cerebral metastases risk without recurrence after postoperative adjuvant chemotherapy were randomly assigned to receive PCI (30 Gy in 10 fractions) or observation. The primary end point was disease-free survival (DFS). The secondary end points included the incidence of brain metastases, overall survival (OS), toxicity and quality of life.
This trial was terminated early after the random assignment of 156 patients (81 to PCI group and 75 to control group). The PCI group had significantly lengthened DFS compared with the control group, with a median DFS of 28.5 months versus 21.2 months [hazard ratio (HR), 0.67; 95% confidence interval (CI) 0.46-0.98; P = 0.037]. PCI was associated with a decrease in risk of brain metastases (the actuarial 5-year brain metastases rate, 20.3% versus 49.9%; HR, 0.28; 95% CI 0.14-0.57; P < 0.001). The median OS was 31.2 months in the PCI group and 27.4 months in the control group (HR, 0.81; 95% CI 0.56-1.16; P = 0.310). While main toxicities were headache, nausea/vomiting and fatigue in the PCI group, they were generally mild.
In patients with fully resected postoperative pathologically confirmed stage IIIA-N2 NSCLC and high risk of cerebral metastases after adjuvant chemotherapy, PCI prolongs DFS and decreases the incidence of brain metastases.
本研究比较了根治性手术后 IIIA-N2 期非小细胞肺癌(NSCLC)患者辅助化疗后颅内转移高风险患者预防性颅照射(PCI)与观察结果。
在这项开放标签、随机、III 期临床试验中,完全切除术后病理证实的 IIIA-N2 期 NSCLC 患者和辅助化疗后无复发的高颅内转移风险患者被随机分配接受 PCI(30 Gy,10 个分数)或观察。主要终点是无病生存(DFS)。次要终点包括脑转移发生率、总生存(OS)、毒性和生活质量。
在 156 例患者(PCI 组 81 例,对照组 75 例)随机分组后,该试验提前终止。PCI 组的 DFS 明显长于对照组,中位 DFS 为 28.5 个月对 21.2 个月[风险比(HR),0.67;95%置信区间(CI)0.46-0.98;P=0.037]。PCI 可降低脑转移风险(5 年脑转移率的实际值为 20.3%对 49.9%;HR,0.28;95%CI 0.14-0.57;P<0.001)。PCI 组中位 OS 为 31.2 个月,对照组为 27.4 个月(HR,0.81;95%CI 0.56-1.16;P=0.310)。虽然 PCI 组的主要毒性反应为头痛、恶心/呕吐和疲劳,但一般为轻度。
对于完全切除术后病理证实的 IIIA-N2 期 NSCLC 患者和辅助化疗后颅内转移高风险患者,PCI 可延长 DFS 并降低脑转移发生率。