首页> 外文期刊>The Lancet >Radiotherapy plus chemotherapy with or without surgical resection for stage III non-small-cell lung cancer: a phase III randomised controlled trial.
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Radiotherapy plus chemotherapy with or without surgical resection for stage III non-small-cell lung cancer: a phase III randomised controlled trial.

机译:Ⅲ期非小细胞肺癌放疗加化疗,有无手术切除:Ⅲ期随机对照试验。

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BACKGROUND: Results from phase II studies in patients with stage IIIA non-small-cell lung cancer with ipsilateral mediastinal nodal metastases (N2) have shown the feasibility of resection after concurrent chemotherapy and radiotherapy with promising rates of survival. We therefore did this phase III trial to compare concurrent chemotherapy and radiotherapy followed by resection with standard concurrent chemotherapy and definitive radiotherapy without resection. METHODS: Patients with stage T1-3pN2M0 non-small-cell lung cancer were randomly assigned in a 1:1 ratio to concurrent induction chemotherapy (two cycles of cisplatin [50 mg/m(2) on days 1, 8, 29, and 36] and etoposide [50 mg/m(2) on days 1-5 and 29-33]) plus radiotherapy (45 Gy) in multiple academic and community hospitals. If no progression, patients in group 1 underwent resection and those in group 2 continued radiotherapy uninterrupted up to 61 Gy. Two additional cycles of cisplatin and etoposide were given in both groups. The primary endpoint was overall survival (OS). Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00002550. FINDINGS: 202 patients (median age 59 years, range 31-77) were assigned to group 1 and 194 (61 years, 32-78) to group 2. Median OS was 23.6 months (IQR 9.0-not reached) in group 1 versus 22.2 months (9.4-52.7) in group 2 (hazard ratio [HR] 0.87 [0.70-1.10]; p=0.24). Number of patients alive at 5 years was 37 (point estimate 27%) in group 1 and 24 (point estimate 20%) in group 2 (odds ratio 0.63 [0.36-1.10]; p=0.10). With N0 status at thoracotomy, the median OS was 34.4 months (IQR 15.7-not reached; 19 [point estimate 41%] patients alive at 5 years). Progression-free survival (PFS) was better in group 1 than in group 2, median 12.8 months (5.3-42.2) vs 10.5 months (4.8-20.6), HR 0.77 [0.62-0.96]; p=0.017); the number of patients without disease progression at 5 years was 32 (point estimate 22%) versus 13 (point estimate 11%), respectively. Neutropenia and oesophagitis were the main grade 3 or 4 toxicities associated with chemotherapy plus radiotherapy in group 1 (77 [38%] and 20 [10%], respectively) and group 2 (80 [41%] and 44 [23%], respectively). In group 1, 16 (8%) deaths were treatment related versus four (2%) in group 2. In an exploratory analysis, OS was improved for patients who underwent lobectomy, but not pneumonectomy, versus chemotherapy plus radiotherapy. INTERPRETATION: Chemotherapy plus radiotherapy with or without resection (preferably lobectomy) are options for patients with stage IIIA(N2) non-small-cell lung cancer. FUNDING: National Cancer Institute, Canadian Cancer Society, and National Cancer Institute of Canada.
机译:背景:IIIA期非小细胞肺癌同侧纵隔淋巴结转移(N2)患者的II期研究结果表明,同时进行化学疗法和放射疗法后,切除的可行性很高,生存率很高。因此,我们进行了此III期试验,比较了同时进行的化学疗法和放疗,然后将其与标准同期进行的化学疗法和明确的放疗(未切除)进行了比较。方法:将患有T1-3pN2M0期非小细胞肺癌的患者以1:1的比例随机分配至同步诱导化疗(在第1、8、29和22天进行两个周期的顺铂[50 mg / m(2))治疗[36]和依托泊苷[第1-5天和第29-33天的50 mg / m(2)]加上放疗(45 Gy)在多家学术和社区医院进行。如果没有进展,则第1组患者接受切除术,第2组患者继续放疗直至61 Gy。两组均进行了另外两个顺铂和依托泊苷循环治疗。主要终点是总体生存期(OS)。分析是按意向进行的。该研究已在ClinicalTrials.gov上注册,编号为NCT00002550。结果:第1组为202例患者(中位年龄59岁,范围31-77),第2组为194例(61岁,32-78岁)。与第1组相比,中位OS​​为23.6个月(未达到IQR 9.0)第2组22.2个月(9.4-52.7)(危险比[HR] 0.87 [0.70-1.10]; p = 0.24)。第1组5年存活的患者人数为37(点估计值27%),第2组为24(点估计值20%)(赔率比0.63 [0.36-1.10]; p = 0.10)。开胸手术时为N0状态,中位OS​​为34.4个月(未达到IQR 15.7; 19岁(估计41%)5岁时还活着)。第1组的无进展生存期(PFS)好于第2组,中位数分别为12.8个月(5.3-42.2)和10.5个月(4.8-20.6),HR 0.77 [0.62-0.96]; p = 0.017); 5年无疾病进展的患者人数分别为32(点估计值22%)和13(点估计值11%)。中性粒细胞减少和食管炎是第1组(分别为77 [38%]和20 [10%])和第2组(80 [41%]和44 [23%])中化学疗法和放疗相关的主要3或4级毒性,分别)。在第1组中,与治疗有关的死亡为16(8%),而在第2组中为4(2%)。在探索性分析中,与化学疗法加放疗相比,接受了肺叶切除而不是肺切除的患者的OS改善了。解释:IIIA(N2)期非小细胞肺癌患者可以选择化疗加放疗加或不加切除(最好是肺叶切除)。资金:国家癌症研究所,加拿大癌症协会和加拿大国家癌症研究所。

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