Dept. of Pulmonary Diseases, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center+, PO Box 5800, 6202 AZ Maastricht, The Netherlands.
Dept. of Radiation Oncology (MAASTRO Clinic), GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center+, Doctor Tanslaan 12, 6229 ET Maastricht, The Netherlands.
Cancer Treat Rev. 2015 Jul;41(7):634-45. doi: 10.1016/j.ctrv.2015.05.005. Epub 2015 May 13.
Recently, non-small cell lung cancer (NSCLC) has been partly subclassified into molecularly-defined oncogene "addicted" tumors for which targeted agents are available. Tyrosine kinase inhibitors (TKI) are currently approved for patients with an activating epidermal growth factor receptor (EGFR) mutation or anaplastic lymphoma kinase (ALK) rearrangement. In these patients, brain metastases are often the first site of progression while on TKI treatment. The TKI may however still be active on extra-cranial sites and clinicians are thus faced with the question if the TKI may be continued during cranial radiotherapy. Advantages of combining TKI with cranial radiotherapy would be a possible synergistic effect on the brain metastases and the prevention of a systemic disease flare-up. A disadvantage is the possibly increased risk of (neuro)toxicity. The present systematic review addresses the toxicity of combining TKI with cranial radiotherapy in NSCLC patients.
最近,非小细胞肺癌(NSCLC)部分细分为分子定义的致癌基因“成瘾”肿瘤,这些肿瘤有可用的靶向药物。酪氨酸激酶抑制剂(TKI)目前批准用于具有激活表皮生长因子受体(EGFR)突变或间变性淋巴瘤激酶(ALK)重排的患者。在这些患者中,脑转移通常是 TKI 治疗时疾病进展的第一个部位。然而,TKI 在颅外部位可能仍然活跃,因此临床医生面临着一个问题,即在颅部放疗期间是否可以继续使用 TKI。将 TKI 与颅部放疗联合使用的优点是可能对脑转移有协同作用,并可预防全身疾病的爆发。缺点是(神经)毒性增加的风险。本系统评价旨在探讨 NSCLC 患者 TKI 联合颅部放疗的毒性。