Department of Oncology and Palliative Medicine, Nordland Hospital, Bodø, Norway.
Radiat Oncol. 2012 Jan 11;7:3. doi: 10.1186/1748-717X-7-3.
Treatment of non-small cell lung cancer (NSCLC) is challenging in many ways. One of the problems is disappointing local control rates in larger volume disease. Moreover, the likelihood of both nodal and distant spread increases with primary tumour (T-) stage. Many patients are elderly and have considerable comorbidity. Therefore, aggressive combined modality treatment might be contraindicated or poorly tolerated. In many cases with larger tumour volume, sufficiently high radiation doses can not be administered because the tolerance of surrounding normal tissues must be respected. Under such circumstances, simultaneous administration of radiosensitizing agents, which increase tumour cell kill, might improve the therapeutic ratio. If such agents have a favourable toxicity profile, even elderly patients might tolerate concomitant treatment. Based on sound preclinical evidence, several relatively small studies have examined radiotherapy (RT) with cetuximab in stage III NSCLC. Three different strategies were pursued: 1) RT plus cetuximab (2 studies), 2) induction chemotherapy followed by RT plus cetuximab (2 studies) and 3) concomitant RT and chemotherapy plus cetuximab (2 studies). Radiation doses were limited to 60-70 Gy. As a result of study design, in particular lack of randomised comparison between cetuximab and no cetuximab, the efficacy results are difficult to interpret. However, strategy 1) and 3) appear more promising than induction chemotherapy followed by RT and cetuximab. Toxicity and adverse events were more common when concomitant chemotherapy was given. Nevertheless, combined treatment appears feasible. The role of consolidation cetuximab after RT is uncertain. A large randomised phase III study of combined RT, chemotherapy and cetuximab has been initiated.
治疗非小细胞肺癌(NSCLC)在很多方面都具有挑战性。其中一个问题是,在更大体积的疾病中局部控制率令人失望。此外,随着原发肿瘤(T-)分期的增加,淋巴结和远处转移的可能性也会增加。许多患者年龄较大且合并症较多。因此,强烈的联合治疗可能是禁忌的或难以耐受的。在许多情况下,由于必须考虑周围正常组织的耐受性,因此不能给予足够高的肿瘤剂量。在这种情况下,同时给予增敏剂(可增加肿瘤细胞杀伤)可能会改善治疗效果比。如果这些药物具有良好的毒性特征,即使是老年患者也可能耐受同时治疗。基于可靠的临床前证据,一些相对较小的研究已经检查了 III 期 NSCLC 的放射治疗(RT)联合西妥昔单抗。有三种不同的策略:1)RT 联合西妥昔单抗(两项研究),2)诱导化疗后 RT 联合西妥昔单抗(两项研究)和 3)同期 RT 和化疗联合西妥昔单抗(两项研究)。辐射剂量限制在 60-70 Gy。由于研究设计,特别是缺乏西妥昔单抗与无西妥昔单抗之间的随机比较,因此疗效结果难以解释。然而,策略 1)和 3)似乎比诱导化疗后 RT 和西妥昔单抗更有希望。同时给予化疗时,毒性和不良事件更为常见。尽管如此,联合治疗似乎是可行的。RT 后巩固西妥昔单抗的作用尚不确定。一项关于联合 RT、化疗和西妥昔单抗的大型随机 III 期研究已经启动。