The Incidence of Brain Metastases in Stage IV ROS1-Rearranged Non-Small Cell Lung Cancer and Rate of Central Nervous System Progression on Crizotinib.
The Incidence of Brain Metastases in Stage IV ROS1-Rearranged Non-Small Cell Lung Cancer and Rate of Central Nervous System Progression on Crizotinib.
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DOI:
10.1016/j.jtho.2018.07.001
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发表时间:
2018-11
期刊:
影响因子:
--
通讯作者:
Doebele RC
中科院分区:
文献类型:
--
作者:
Patil T;Smith DE;Bunn PA;Aisner DL;Le AT;Hancock M;Purcell WT;Bowles DW;Camidge DR;Doebele RC
Central nervous system (CNS) metastases in lung cancer are a frequent cause of morbidity and mortality. There are conflicting data on the incidence of CNS metastases in stage IV ROS1+ non-small cell lung cancer (NSCLC) and rate of CNS progression on crizotinib. A retrospective review of 579 patients with stage IV NSCLC between June 2008 to December 2017 was performed. Brain metastases and oncogene status (ROS1, ALK, EGFR, KRAS, BRAF, and other) were recorded. We measured progression free survival (PFS) and time to CNS progression (P-CNS) in ROS1+ and ALK+ patients on crizotinib. We identified 33 ROS1+ and 115 ALK+ patients with stage IV NSCLC. The incidence of brain metastases for treatment-naïve, stage IV ROS1+ and ALK+ NSCLC was 36% (12/33) and 34% (39/115) respectively. There were no statistically significant differences in incidence of brain metastases across ROS1, ALK, EGFR, KRAS, BRAF or other mutations. Complete survival data was available for 19 ROS1+ and 83 ALK+ patients. Median PFS for ROS1+ and ALK+ patients was 11 and 8 months (p = 0.304). The CNS was the first and sole site of progression in 47% (9/19) of ROS1+ and 33% ALK+ (28/83) patients with no differences between these groups (p = 0.610). Brain metastases are common in treatment-naïve stage IV ROS1+ NSCLC, though the incidence does not differ from other oncogene cohorts. The CNS is a common first site of progression in ROS1+ patients on crizotinib. This study reinforces the importance of developing CNS-penetrant TKIs for patients with ROS1+ NSCLC.
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DOI:
10.1158/1078-0432.ccr-12-0550
发表时间:
2012-09-01
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
--
作者:
Davies KD;Le AT;Theodoro MF;Skokan MC;Aisner DL;Berge EM;Terracciano LM;Cappuzzo F;Incarbone M;Roncalli M;Alloisio M;Santoro A;Camidge DR;Varella-Garcia M;Doebele RC
通讯作者:
Doebele RC
DOI:
10.1016/j.lungcan.2015.01.020
发表时间:
2015-04
期刊:
Lung cancer (Amsterdam, Netherlands)
影响因子:
--
作者:
Rangachari D;Yamaguchi N;VanderLaan PA;Folch E;Mahadevan A;Floyd SR;Uhlmann EJ;Wong ET;Dahlberg SE;Huberman MS;Costa DB
通讯作者:
Costa DB
影响因子:
6.2
作者:
Doebele RC;Lu X;Sumey C;Maxson DA;Weickhardt AJ;Oton AB;Bunn PA Jr;Barón AE;Franklin WA;Aisner DL;Varella-Garcia M;Camidge DR
通讯作者:
Camidge DR
影响因子:
20.4
作者:
Li, Ziming;Shen, Lan;Lu, Shun
通讯作者:
Lu, Shun
影响因子:
45.3
作者:
Kim, Dong-Wan;Tiseo, Marcello;Camidge, D. Ross
通讯作者:
Camidge, D. Ross