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针对寡进展性致癌基因成瘾型非小细胞肺癌的立体定向体部放疗

SBRT for oligoprogressive oncogene addicted NSCLC.

作者信息

Basler L, Kroeze S G C, Guckenberger M

机构信息

Department of Radiation Oncology, University Hospital Zurich, Rämistrasse 100, CH 8091 Zurich, Switzerland.

Department of Radiation Oncology, University Hospital Zurich, Rämistrasse 100, CH 8091 Zurich, Switzerland.

出版信息

Lung Cancer. 2017 Apr;106:50-57. doi: 10.1016/j.lungcan.2017.02.007. Epub 2017 Feb 6.

DOI:10.1016/j.lungcan.2017.02.007
PMID:28285694
Abstract

Lung cancer is one of the leading causes of cancer death in men and women and treatment outcome continues to lag behind other common cancer types. A subset of lung adenocarcinoma patients exhibit a somatic mutation in EGFR or an ALK rearrangement. In these patients, targeted TKI therapy results in higher response rates, improved PFS and reduced side effects compared with platinum-based chemotherapy. Despite initial activity of the TKIs, ultimately all patients present with disease progression after about a year on TKI therapy due to resistance development. About 15-47% of patients present with limited oligoprogressive disease (OPD): such patients show only a limited number of metastases with progression in radiological imaging. Radical local treatment to all oligoprogressive lesions is thought to eradicate the de-differentiated clones and restore overall sensitivity of the metastatic disease. Retrospective studies suggest that aggressive local treatment using stereotactic body radiotherapy (SBRT), surgery or others can be used to eradicate TKI-resistant subpopulations enabling prolonged TKI treatment "beyond progression", which may lead to increased PFS and overall survival. This review focuses on the biological background of resistance development, systemic and local treatment options with a focus on SBRT, as well as challenges in defining the state of OPD and current clinical studies in oligoprogressive oncogene addicted NSCLC.

摘要

肺癌是男性和女性癌症死亡的主要原因之一,其治疗效果仍落后于其他常见癌症类型。一部分肺腺癌患者表现出表皮生长因子受体(EGFR)的体细胞突变或间变性淋巴瘤激酶(ALK)重排。在这些患者中,与铂类化疗相比,靶向酪氨酸激酶抑制剂(TKI)治疗可带来更高的缓解率、更长的无进展生存期(PFS)并减少副作用。尽管TKI最初有活性,但由于耐药性的产生,所有患者在接受TKI治疗约一年后最终都会出现疾病进展。约15%-47%的患者出现局限性寡进展性疾病(OPD):此类患者在影像学检查进展时仅显示有限数量的转移灶。对所有寡进展性病灶进行根治性局部治疗被认为可以根除去分化克隆并恢复转移性疾病的整体敏感性。回顾性研究表明,使用立体定向体部放疗(SBRT)、手术或其他方法进行积极的局部治疗可用于根除TKI耐药亚群,从而实现“疾病进展后”延长TKI治疗,这可能会延长PFS和总生存期。本综述重点关注耐药性产生的生物学背景、以SBRT为重点的全身和局部治疗选择,以及定义OPD状态的挑战和寡进展性致癌基因成瘾非小细胞肺癌(NSCLC)的当前临床研究。

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