Favorable response to PD-1 receptor inhibitor pembrolizumab as a third-line therapy in ROS1-rearranged advanced lung cancer: A case report and review of the literature

被引:0
作者
Chaudhry, Akriti [1 ]
Schuppe, Kyle [2 ]
Burke, Skyler [2 ]
Lobova, Veronika [2 ]
Seigel, Quincy [3 ]
Kirby, Carsten [4 ]
Chitlik, Sara [5 ]
Andrei, Mirela [1 ]
Kaya, Erin [1 ,2 ,6 ,7 ]
机构
[1] Summit Canc Ctr Amer Oncol Partners, 6001 N Mayfair St, Spokane, WA 99208 USA
[2] Washington State Univ, Elson S Floyd Coll Med, 412 Spokane Falls Blvd, Spokane, WA 99202 USA
[3] Univ Texas Med Branch Galveston, 301 Univ Blvd, Galveston, TX 77555 USA
[4] Spokane Teaching Hlth Clin Internal Med, 624 Front Ave, Spokane, WA 99202 USA
[5] Rush Med Coll, 600 S Paulina St, Chicago, IL 60612 USA
[6] Oregon Hlth Sci Univ Radiat Oncol, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA
[7] 809 Main Ave Unit 308, Spokane, WA 99201 USA
来源
CURRENT PROBLEMS IN CANCER: CASE REPORTS | 2022年 / 8卷
关键词
Lung adenocarcinoma; ROS1; mutation; Pembrolizumab; Targeted cancer therapy; Case report;
D O I
10.1016/j.cpccr.2022.100190
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ROS chromosomal rearrangements, which compromise around 1-2% of non-small cell carcinomas, have become an established therapeutic target. While targeted therapy for this mutation usually includes tyrosine kinase inhibitors such as crizotinib or alectinib, we present a unique case of a patient with stage 4 adenocarcinoma of the lung with ROS1 mutation who failed multiple targeted therapies, but was successfully treated on the immunotherapy pembrolizumab, a PD-1 receptor inhibitor, which is usually used for advanced non-small cell lung cancer without targetable mutations. From a review of the literature, this is an uncommon treatment course and patient response. Further studies are needed of this clinical situation in order to better understand and optimize future treatments for patients with advanced stage lung adenocarcinoma with ROS1 rearrangements and to develop better predictive testing to assess which patients are likely to respond to immune checkpoint inhibitors such as pembrolizumab.
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页数:5
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