Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Cancer Treat Rev. 2014 Feb;40(1):197-203. doi: 10.1016/j.ctrv.2013.05.005. Epub 2013 Jul 10.
The treatment of advanced disease (stage IIIb and IV) of non-small cell lung cancer (NSCLC) is based on systemic treatment with platinum-based chemotherapy or biological compounds depending on the disease molecular profile. In the last few years, intensive investigational efforts in anticancer therapy have led to the registration of new active chemotherapeutic agents, combination regimens, and biological drugs, expanding choices for customizing individual treatment. However, the introduction of new drugs in the clinical setting has led to several new toxicities, creating some difficulties in daily management. Among these, ocular toxicity is generally overlooked as more common toxicities such as myelosuppression, stomatitis, diarrhea, vomiting, "hand-foot syndrome", and neurological alterations attract greater attention. Ophthalmic complications from cytotoxic chemotherapeutics are rare, transient, and of mild/moderate intensity but irreversible acute disorders are possible. The best way to prevent potential irreversible visual complications is an awareness of the potential for ocular toxicity because dose reductions or early drug cessation can prevent serious ocular complications in the majority of cases. However, given the novelty of many therapeutic agents and the complexity of ocular pathology, oncologists may be unfamiliar with these adverse effects of anticancer therapy. Although toxicities from chemotherapy are generally intense but short lasting, toxicities related to targeted drugs are often milder but longer lasting and can persist throughout treatment. Here we review the principal clinical presentations of ocular toxicity arising from chemotherapy [1-3], target therapies [4], and newly developed drugs and provide some recommendations for monitoring and management of ocular toxicity.
晚期非小细胞肺癌(NSCLC)的治疗(IIIb 期和 IV 期)基于基于铂类化疗或生物化合物的全身治疗,具体取决于疾病的分子特征。在过去的几年中,癌症治疗的深入研究努力导致了新的活性化疗药物、联合方案和生物药物的注册,扩大了为定制个体化治疗而选择的范围。然而,新药物在临床环境中的引入导致了一些新的毒性,在日常管理中造成了一些困难。其中,眼部毒性通常被忽视,因为更常见的毒性如骨髓抑制、口腔炎、腹泻、呕吐、“手足综合征”和神经改变引起了更多的关注。细胞毒性化疗药物引起的眼部并发症罕见、短暂且为轻度/中度,但也可能发生不可逆的急性疾病。预防潜在不可逆视觉并发症的最佳方法是意识到眼部毒性的可能性,因为在大多数情况下,减少剂量或早期停药可以预防严重的眼部并发症。然而,由于许多治疗药物的新颖性和眼部病理学的复杂性,肿瘤学家可能不熟悉这些抗癌治疗的不良反应。虽然化疗引起的毒性通常强烈但持续时间短,但靶向药物引起的毒性通常较轻但持续时间较长,并且可能在整个治疗过程中持续存在。在这里,我们回顾了化疗[1-3]、靶向治疗[4]和新开发药物引起的眼部毒性的主要临床表现,并提供了一些关于眼部毒性监测和管理的建议。