Emerging toxicities in the treatment of non-small cell lung cancer: Ocular disorders

被引:33
作者
Agustoni, Francesco [1 ]
Platania, Marco [1 ]
Vitali, Milena [1 ]
Zilembo, Nicoletta [1 ]
Haspinger, Eva [1 ]
Sinno, Valentina [1 ]
Gallucci, Rosaria [1 ]
de Braud, Filippo [1 ]
Garassino, Marina Chiara [1 ]
机构
[1] Ist Nazl Tumori, Fdn IRCCS, Dept Med Oncol, I-20133 Milan, Italy
关键词
Non-small-cell lung cancer; Chemotherapy; Target therapies; Ocular toxicity; Ophthalmology; INHIBITOR AZD6244 ARRY-142886; TYROSINE KINASE INHIBITOR; PHASE-I; OPEN-LABEL; OPHTHALMOLOGIC TOXICITY; MACULAR EDEMA; GEFITINIB; CISPLATIN; ERLOTINIB; CHEMOTHERAPY;
D O I
10.1016/j.ctrv.2013.05.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:197 / 203
页数:7
相关论文
共 76 条
[31]   Randomized Phase II Study of Gefitinib Compared With Placebo in Chemotherapy-Naive Patients With Advanced Non-Small-Cell Lung Cancer and Poor Performance Status [J].
Goss, Glenwood ;
Ferry, David ;
Wierzbicki, Rafal ;
Laurie, Scott A. ;
Thompson, Joyce ;
Biesma, Bonne ;
Hirsch, Fred R. ;
Varella-Garcia, Marileila ;
Duffield, Emma ;
Ataman, Ozlem U. ;
Zarenda, Marc ;
Armour, Alison A. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (13) :2253-2260
[32]   A Phase II, Open-Label, Randomized Study to Assess the Efficacy and Safety of AZD6244 (ARRY-142886) Versus Pemetrexed in Patients with Non-small Cell Lung Cancer Who Have Failed One or Two Prior Chemotherapeutic Regimens [J].
Hainsworth, John D. ;
Cebotaru, Cristina L. ;
Kanarev, Vladimir ;
Ciuleanu, Tudor E. ;
Damyanov, Danail ;
Stella, Phillip ;
Ganchev, Hristo ;
Pover, Gillian ;
Morris, Clive ;
Tzekova, Valentina .
JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (10) :1630-1636
[33]   First-SIGNAL: First-Line Single-Agent Iressa Versus Gemcitabine and Cisplatin Trial in Never-Smokers With Adenocarcinoma of the Lung [J].
Han, Ji-Youn ;
Park, Keunchil ;
Kim, Sang-We ;
Lee, Dae Ho ;
Kim, Hyae Young ;
Kim, Heung Tae ;
Ahn, Myung Ju ;
Yun, Tak ;
Ahn, Jin Seok ;
Suh, Cheolwon ;
Lee, Jung-Shin ;
Yoon, Sung Jin ;
Han, Jong Hee ;
Lee, Jae Won ;
Jo, Sook Jung ;
Lee, Jin Soo .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (10) :1122-1128
[34]   Ocular complications of cancer therapy: a primer for the ophthalmologist treating cancer patients [J].
Hazin, Ribhi ;
Abuzetun, Jamil Y. ;
Daoud, Yassine J. ;
Abu-Khalaf, Maysa M. .
CURRENT OPINION IN OPHTHALMOLOGY, 2009, 20 (04) :308-317
[35]   OCULAR COMPLICATIONS OF SYSTEMIC CANCER-CHEMOTHERAPY [J].
IMPERIA, PS ;
LAZARUS, HM ;
LASS, JH .
SURVEY OF OPHTHALMOLOGY, 1989, 34 (03) :209-230
[36]  
Isomura M, 2004, J CLIN ONCOL, V22, p200S
[37]   Selumetinib plus docetaxel for KRAS-mutant advanced non-small-cell lung cancer: a randomised, multicentre, placebo-controlled, phase 2 study [J].
Jaenne, Pasi A. ;
Shaw, Alice T. ;
Pereira, Jose Rodrigues ;
Jeannin, Gaelle ;
Vansteenkiste, Johan ;
Barrios, Carlos ;
Franke, Fabio Andre ;
Grinsted, Lynda ;
Zazulina, Victoria ;
Smith, Paul ;
Smith, Ian ;
Crino, Lucio .
LANCET ONCOLOGY, 2013, 14 (01) :38-47
[38]   Paclitaxel maculopathy [J].
Joshi, Mandar M. ;
Garretson, Bruce R. .
ARCHIVES OF OPHTHALMOLOGY, 2007, 125 (05) :709-710
[39]   Persistent severe visual and electroretinographic abnormalities after intravenous cisplatin therapy [J].
Katz, BJ ;
Ward, JH ;
Digre, KB ;
Creel, DJ ;
Mamalis, N .
JOURNAL OF NEURO-OPHTHALMOLOGY, 2003, 23 (02) :132-135
[40]  
Kim DW, 2011, EUR MULT CANC C SEP