Ngoo Qi Zhe, Wan Hitam Wan Hazabbah, Tan Chai Lee, Krishna Bhavaraju Venkata Murali
Ophthalmology, Universiti Sains Malaysia School of Medical Sciences, Kota Bharu, MYS.
Oncology, Universiti Sains Malaysia School of Medical Sciences, Kota Bharu, MYS.
Cureus. 2022 Jan 9;14(1):e21042. doi: 10.7759/cureus.21042. eCollection 2022 Jan.
Introduction To evaluate if early tamoxifen toxicity can be detected by comparing pre-and post-treatment optic nerve head parameters and visual function using Heidelberg Retinal Tomograph III (HRT III) and Pattern Visual Evoked Potential (Pattern VEP). Method This is a prospective study involving 76 eyes of 38 breast cancer patients treated with tamoxifen in Hospital Universiti Sains Malaysia, Kelantan, Malaysia. These patients were examined by a single doctor and the investigations were done by a single technician. The visual acuity, optic nerve function, visual field, optic nerve head parameters on HRT III and Pattern VEP were assessed. The examination was performed before and three months after treatment initiation. Results There was no tamoxifen ocular toxicity found three months post-treatment with tamoxifen. There was no change in visual acuity and optic nerve function post-treatment initiation. There were no statistically significant changes found in optic nerve head parameters on HRT III and P 100 peak latency and amplitude on Pattern VEP. Conclusion Ocular toxicity is a recognized complication of tamoxifen treatment. Tamoxifen optic neuropathy is a potentially irreversible, visually disabling complication. Tamoxifen ocular toxicity was not found three months after tamoxifen treatment initiation among estrogen receptor (ER)-positive breast cancer patients. No early changes in optic nerve head parameters and P 100 peak latency and amplitude changes were found after three months of treatment. A longer duration of monitoring with HRT III and Pattern VEP may be needed to adequately observe for early, subclinical changes in optic nerve head parameters and visual function among tamoxifen users.
通过使用海德堡视网膜断层扫描仪III(HRT III)和图形视觉诱发电位(图形VEP)比较治疗前后的视神经乳头参数和视觉功能,以评估他莫昔芬早期毒性是否可被检测到。
这是一项前瞻性研究,纳入了马来西亚吉兰丹州马来西亚理科大学医院38例接受他莫昔芬治疗的乳腺癌患者的76只眼睛。这些患者由一名医生进行检查,检查由一名技术人员完成。评估了视力、视神经功能、视野、HRT III上的视神经乳头参数和图形VEP。在开始治疗前和治疗三个月后进行检查。
他莫昔芬治疗三个月后未发现他莫昔芬眼部毒性。开始治疗后视力和视神经功能没有变化。HRT III上的视神经乳头参数以及图形VEP上的P100峰潜伏期和波幅没有发现统计学上的显著变化。
眼部毒性是他莫昔芬治疗公认的并发症。他莫昔芬视神经病变是一种潜在的不可逆的、导致视力残疾的并发症。在雌激素受体(ER)阳性乳腺癌患者中,开始他莫昔芬治疗三个月后未发现眼部毒性。治疗三个月后,视神经乳头参数以及P100峰潜伏期和波幅未发现早期变化。可能需要使用HRT III和图形VEP进行更长时间的监测,以充分观察他莫昔芬使用者视神经乳头参数和视觉功能的早期亚临床变化。