Reymen Bart, van Baardwijk Angela, Wanders Rinus, Borger Jacques, Dingemans Anne-Marie C, Bootsma Gerben, Pitz Cordula, Lunde Ragnar, Geraedts Wiel, Lambin Philippe, De Ruysscher Dirk
Department of Radiation Oncology (MAASTRO Clinic), The Netherlands.
Department of Radiation Oncology (MAASTRO Clinic), The Netherlands.
Radiother Oncol. 2014 Mar;110(3):482-7. doi: 10.1016/j.radonc.2013.12.005. Epub 2014 Jan 17.
Non-small cell lung cancer (NSCLC) stage T4N0-1 or single nodal station IIIA-N2 are two stage III sub-groups for which the outcome of non-surgical therapy is not well known. We investigated the results of individualised isotoxic accelerated radiotherapy (INDAR) and chemotherapy in this setting.
Analysis of NSCLC patients included in 2 prospective trials (NCT00573040 and NCT00572325) stage T4N0-1 or IIIA-N2 with 1 pathologic nodal station, treated with chemo-radiotherapy (CRT) using INDAR with concurrent or sequential platinum-based chemotherapy. Overall survival (OS) was updated and calculated from date of diagnosis (Kaplan-Meier). Toxicity was scored following CTCAEv3.0. To allow comparison with other articles the subgroups were also analysed separately for toxicity, progression free and overall survival.
83 patients (42 T4N0-1 and 41 IIIA-N2) were identified: the median radiotherapy dose was 65Gy. Thirty-seven percent of patients received sequential CRT and 63% received concurrent CRT. At a median follow-up of 48 months the median OS for T4N0-1 patients was 34 months with 55% 2-year survival and 25% 5-year survival. For stage IIIA-N2 at a median follow-up of 50 months the median OS was 26 months with 2- and 5-year survival rates of 53% and 24%, respectively.
Chemo-radiation using INDAR yields promising survival results in patients with single-station stage IIIA-N2 or T4N0-1 NSCLC.
非小细胞肺癌(NSCLC)的T4N0-1期或单个淋巴结转移的IIIA-N2期是两个III期亚组,其非手术治疗的结果尚不明确。我们研究了在这种情况下个体化等毒性加速放疗(INDAR)联合化疗的效果。
分析纳入两项前瞻性试验(NCT00573040和NCT00572325)的NSCLC患者,这些患者为T4N0-1期或IIIA-N2期且有1个病理淋巴结转移站,采用INDAR联合顺铂同步或序贯化疗进行放化疗(CRT)。从诊断日期开始更新并计算总生存期(OS)(Kaplan-Meier法)。按照CTCAEv3.0对毒性进行评分。为了与其他文章进行比较,还分别分析了亚组的毒性、无进展生存期和总生存期。
共纳入83例患者(42例T4N0-1期和41例IIIA-N2期):放疗中位剂量为65Gy。37%的患者接受序贯CRT,63%的患者接受同步CRT。中位随访48个月时,T4N0-1期患者的中位OS为34个月,2年生存率为55%,5年生存率为25%。IIIA-N2期患者中位随访50个月时,中位OS为26个月,2年和5年生存率分别为53%和24%。
使用INDAR进行放化疗在单站IIIA-N2期或T4N0-1期NSCLC患者中产生了有前景的生存结果。