2020-01-09
既往多项研究显示,对于携带EGFR或ALK突变的NSCLC患者,PD-1/PD-L1抑制剂的有效率只有3%~7%【1】,远不如靶向治疗,而如果将靶向治疗与PD-1/PD-L1抑制剂联合,免疫相关性肺炎的发生率高(TATTON和CAURAL研究均因此提前终止)【2,3】。因此,目前证据不支持PD-1/PD-L1抑制剂联合靶向治疗。
参考文献
[1] Gainor JF, et al. EGFR Mutations and ALK Rearrangements Are Associated with Low Response Rates to PD-1. Pathway Blockade in Non-Small Cell Lung Cancer. Clin Cancer Res. 2016;22:4585-4593.
[2] NIH. AZD9291 in Combination With Ascending Doses of Novel Therapeutics (TATTON); [accessed 2018 May 21]; Available from: https://clinicaltrials.gov/ct2/show/NCT02143466.
[3] NIH. Study of AZD9291 Plus MEDI4736 Versus AZD9291 Monotherapy in NSCLC After Previous EGFR TKI Therapy in T790M Mutation Positive Tumours (CAURAL); [accessed 2018 May 21]; Available from: https://clinicaltrials.gov/ct2/show/NCT02454933.
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