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局部晚期非小细胞肺癌患者预防性颅照射与观察:NRG 肿瘤学/RTOG 0214 期随机临床试验的长期更新。

Prophylactic Cranial Irradiation vs Observation in Patients With Locally Advanced Non-Small Cell Lung Cancer: A Long-term Update of the NRG Oncology/RTOG 0214 Phase 3 Randomized Clinical Trial.

机构信息

Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

NRG Oncology Statistics and Data Management Center, Philadelphia, Pennsylvania.

出版信息

JAMA Oncol. 2019 Jun 1;5(6):847-855. doi: 10.1001/jamaoncol.2018.7220.

Abstract

IMPORTANCE

Brain metastasis (BM) rates are high in locally advanced non-small cell lung cancer (LA-NSCLC), approaching rates seen in small cell lung cancer, where prophylactic cranial irradiation (PCI) is standard of care. Although PCI decreases the incidence of BM in LA-NSCLC, a survival advantage has not yet been shown.

OBJECTIVE

To determine if PCI improves survival in LA-NSCLC.

DESIGN, SETTING, AND PARTICIPANTS: Radiation Therapy Oncology Group (RTOG) 0214 was a randomized phase 3 clinical trial in stage III NSCLC stratified by stage (IIIA vs IIIB), histologic characteristics (nonsquamous vs squamous) and therapy (no surgery vs surgery). The study took place at 291 institutions in the United States, Canada, and internationally. Of 356 patients with stage III NSCLC entered onto this study, 16 were ineligible; therefore, 340 patients were randomized.

INTERVENTION FOR CLINICAL TRIALS

Observation vs PCI.

MAIN OUTCOMES AND MEASURES

The primary outcome was overall survival (OS). The secondary end points were disease-free survival (DFS) and incidence of BM.

RESULTS

Of the 340 total participants, mean (SD) age was 61 years; 213 of the participants were men and 127 were women. The median follow-up time was 2.1 years for all patients, and 9.2 years for living patients. The OS for PCI was not significantly better than observation (hazard ratio [HR], 0.82; 95% CI, 0.63-1.06; P = .12; 5- and 10-year rates, 24.7% and 17.6% vs 26.0% and 13.3%, respectively), while the DFS (HR, 0.76; 95% CI, 0.59-0.97; P = .03; 5- and 10-year rates, 19.0% and 12.6% vs 16.1% and 7.5% for PCI vs observation) and BM (HR, 0.43; 95% CI, 0.24-0.77; P = .003; 5- and 10-year rates, 16.7% vs 28.3% for PCI vs observation) were significantly different. Patients in the PCI arm were 57% less likely to develop BM than those in the observation arm. Younger patients (<60 years) and patients with nonsquamous disease developed more BM. On multivariable analysis, PCI was associated with decreased BM and improved DFS, but not improved OS. Multivariable analysis within the nonsurgical arm suggests that PCI effectively prolongs OS, DFS, and BM.

CONCLUSIONS AND RELEVANCE

In patients with stage III LA-NSCLC without progression of disease after therapy, PCI decreased the 5- and 10-year rate of BM and improved 5- and 10-year DFS, but did not improve OS. Although this study did not meet its primary end point, the long-term results reveal many important findings that will benefit future trials. Identifying the appropriate patient population and a safe intervention is critical.

TRIAL REGISTRATION

ClinicalTrials.gov identifier: NCT00048997.

摘要

重要性

局部晚期非小细胞肺癌(LA-NSCLC)的脑转移(BM)发生率很高,接近小细胞肺癌的发生率,小细胞肺癌中标准治疗方法是预防性颅脑照射(PCI)。虽然 PCI 降低了 LA-NSCLC 中 BM 的发生率,但尚未显示出生存优势。

目的

确定 PCI 是否能改善 LA-NSCLC 的生存。

设计、地点和参与者:放射治疗肿瘤学组(RTOG)0214 是一项在 III 期 NSCLC 中进行的随机 III 期临床试验,根据分期(IIIA 与 IIIB)、组织学特征(非鳞状与鳞状)和治疗(无手术与手术)进行分层。该研究在美国、加拿大和国际上的 291 个机构进行。在进入这项研究的 356 例 III 期 NSCLC 患者中,有 16 例不符合条件;因此,共有 340 例患者被随机分配。

临床试验干预措施

观察与 PCI。

主要结局和测量指标

主要结局是总生存(OS)。次要终点是无病生存(DFS)和 BM 的发生率。

结果

在 340 名总参与者中,平均(SD)年龄为 61 岁;213 名参与者为男性,127 名参与者为女性。所有患者的中位随访时间为 2.1 年,生存患者的中位随访时间为 9.2 年。PCI 的 OS 并不明显优于观察(风险比[HR],0.82;95%置信区间[CI],0.63-1.06;P=0.12;5 年和 10 年的生存率分别为 24.7%和 17.6%与 26.0%和 13.3%),而 DFS(HR,0.76;95%CI,0.59-0.97;P=0.03;5 年和 10 年的生存率分别为 19.0%和 12.6%与 16.1%和 7.5%,PCI 与观察)和 BM(HR,0.43;95%CI,0.24-0.77;P=0.003;5 年和 10 年的生存率分别为 16.7%与 28.3%,PCI 与观察)的差异有统计学意义。与观察组相比,PCI 组发生 BM 的可能性低 57%。年轻患者(<60 岁)和非鳞状疾病患者发生 BM 的可能性更高。多变量分析显示,PCI 与 BM 减少和 DFS 改善相关,但与 OS 改善无关。非手术组的多变量分析表明,PCI 可有效延长 OS、DFS 和 BM。

结论和相关性

在接受治疗后疾病无进展的 III 期 LA-NSCLC 患者中,PCI 降低了 5 年和 10 年的 BM 发生率,并改善了 5 年和 10 年的 DFS,但并未改善 OS。尽管这项研究未达到其主要终点,但长期结果揭示了许多将有益于未来试验的重要发现。确定合适的患者人群和安全的干预措施至关重要。

试验注册

ClinicalTrials.gov 标识符:NCT00048997。

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