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首页> 外文期刊>Journal of Thoracic Disease >Adjuvant immunotherapy in resected early non-small cell lung cancer—battle lost, hopefully not the war!
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Adjuvant immunotherapy in resected early non-small cell lung cancer—battle lost, hopefully not the war!

机译:切除早期非小细胞肺癌的辅助免疫疗法-战败,希望不是战争!

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Lung cancer is major cancer killer in both sexes (1). In spite of improvements in diagnostic and therapeutic efforts in recent decades, still only a vast minority of patients with non-small cell lung cancer (NSCLC) undergo surgery. In these patients, additional chemotherapy (CHT) is considered a standard of care worldwide (2). Unfortunately, in spite of the lowest possible T and/or N burden of the disease, many people experience relapse, leading to a 5-year survival rates which range from more than 70% for stage IA to less than 25% in stage IIIA NSCLC (3). It is, therefore, not surprising that many efforts have been attempted to improve these figures. Building on recent success of drug therapy in advanced disease, usually labeled as targeted agents, some studies investigated adjuvant use of drugs such as erlotinib or gefitinib, but failed to demonstrate superiority over existing standards of care (4,5). Besides studies which showed the failure of tyrosine kinase inhibitors (TKIs), there were studies investigating the use of the DNA repair marker ERCC1 in adjuvant setting of NSCLC. While initial results were optimistic (6), more recent results were disappointing, leading to suggestion to abandon this research pathway (7-10).
机译:肺癌是男女的主要癌症杀手(1)。尽管近几十年来在诊断和治疗方面有所改进,但仍然只有极少数的非小细胞肺癌(NSCLC)患者接受手术治疗。在这些患者中,附加化疗(CHT)被认为是全球范围的护理标准(2)。不幸的是,尽管该疾病的T和/或N负担尽可能低,但许多人仍会复发,导致5年生存率从IA期的70%以上到IIIA期NSCLC的不到25%不等。 (3)。因此,为改善这些数字而进行了许多努力也就不足为奇了。在药物治疗通常被标记为靶向药物的晚期疾病的近期成功的基础上,一些研究调查了辅助药物如厄洛替尼或吉非替尼的使用,但未能证明其优于现有的治疗标准(4,5)。除了显示酪氨酸激酶抑制剂(TKIs)失败的研究外,还有研究调查DNA修复标记ERCC1在NSCLC辅助治疗中的用途。尽管最初的结果是乐观的(6),但最近的结果却令人失望,这提示放弃该研究途径的建议(7-10)。

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