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The impact of baseline brain metastases on clinical benefits and progression patterns after first-line crizotinib in anaplastic lymphoma kinase-rearranged non-small cell lung cancer

机译:基线脑转移对急性淋巴瘤激酶重排非小细胞肺癌术后一线蠕变后临床益处和进展模式的影响

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ABSTRACT:Baseline brain metastasis (BBM) commonly occurs in anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer. Crizotinib prolongs the survival of patients with ALK rearrangement but lacks significant effect on brain metastasis. It remains unclear whether BBM and local therapy affect therapeutic outcomes and progression patterns during crizotinib treatment.Patients with ALK-positive (immunotherapy) non-small cell lung cancer were screened from West China Hospital between May 2013 and January 2019. A total of 155 patients were enrolled in this research, with entirely recorded statistics to analyze retrospectively.Baseline brain metastasis occurred in 64 patients (55.7%). Thirty-seven patients received local therapy, while 24 patients did not. We observed higher overall response rate in patients receiving local therapy (70.2% vs. 41.7%, P?=?.026), but no statistical difference was found in median progression free survival (mPFS) (12.0?months vs 13.0?months, P?=?.633). A significantly shorter mPFS was found in patients not receiving local treatment compared with the 16.5?months mPFS of patients without BBM (P?=?.029). Intracranial progressions were recorded in 35 patients with BBM (71%) and 16 patients who don't have (30%). As for extracranial progression, there is a higher occurrence rate (75.5%) in patients who had baseline extracranial metastases versus 49.0% in BBM patients. A significantly higher occurrence rate of multiple progression was noted in patients with BBM (14/49 vs. 6/53).Baseline intracranial metastasis changes the location and number of progressions after the first-line crizotinib and results in poor prognosis. There is no evidence that local treatment for brain metastasis had a protective effect on intracranial progression.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:摘要:基线脑转移(BBM)通常发生在促进淋巴瘤激酶(ALK) - 再装非小细胞肺癌中。 Crizotinib延长了ALK重排患者的存活率,但对脑转移缺乏显着影响。仍然尚不清楚BBM和局部治疗是否会影响蠕虫治疗期间的治疗结果和进展模式。在2013年5月至2019年5月期间,从西部医院筛选了具有ALK阳性(免疫疗法)非小细胞肺癌的患者。共有155名患者在本研究中注册,具有完全记录的统计数据来分析回顾性。34名患者(55.7%)发生的基础脑转移。三十七名患者接受局部治疗,而24名患者没有。我们观察到患者接受局部治疗的患者的较高总体反应率(70.2%,p?= 026),但在中位进展免费生存(MPF)没有发现统计学差异(12.0?个月与13.0?月, p?= 633)。与15.5岁的患者没有接受局部治疗的患者发现明显较短的MPFS,没有BBM的患者MPF(P?= 029)。颅内进展于35例BBM(71%)和16名没有(30%)的患者中记录。对于颅外进展,在BBM患者中具有基线颅颅转移的患者患者存在较高的患者(75.5%)。 BBM患者(14/49对6/53)中,注意到多次进展的显着较高率没有证据表明脑转移的局部治疗对颅内进展有一种保护作用。 2021提交人。由Wolters Kluwer Health,Inc。出版

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