Emergence of ocular toxicities associated with novel anticancer therapeutics: What the oncologist needs to know

被引:9
作者
Ali, Azka [1 ,2 ]
Shah, Ankit A. [4 ]
Jeang, Lauren J. [4 ]
Fallgatter, Kyle S. [4 ]
George, Thomas J. [1 ,2 ]
DeRemer, David L. [2 ,3 ]
机构
[1] Univ Florida, Dept Med, Div Hematol & Oncol, Gainesville, FL 32610 USA
[2] Univ Florida, Hlth Canc Ctr, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Pharm, Dept Pharmacotherapy & Translat Res, Gainesville, FL 32610 USA
[4] Univ Florida, Coll Med, Dept Ophthalmol, Gainesville, FL 32610 USA
关键词
ADVERSE EVENTS; SOLID TUMORS; TARGETED AGENTS; MEK INHIBITORS; OPEN-LABEL; PHASE-I; IMATINIB; DRUG; CRIZOTINIB; ERLOTINIB;
D O I
10.1016/j.ctrv.2022.102376
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As cancer treatment evolves in the era of precision oncology, molecularly targeted agents (MTAs) have become frontline therapy for many cancers. MTAs are biologically targeted and thought to have less off-target toxicity; however, the eye is particularly susceptible to off-target toxicities given its unique microenvironment. In this review, we present commonly used FDA-approved MTAs, any associated ocular toxicities and review the mechanisms, frequency, severity, and management. Increased awareness and communication between clinicians caring for cancer patients is needed for individualized risk assessment, earlier diagnosis, and mitigation of ocular toxicities.
引用
收藏
页数:10
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