Brentuximab Vedotin A nursing perspective on best practices and management of associated adverse events

被引:10
作者
Clifford, Kathleen [1 ]
Copeland, Amanda [2 ]
Knutzen, Gregory [3 ]
Samuelson, Ellen [4 ]
Grove, Laurie [5 ]
Schiavo, Karen [6 ]
机构
[1] St Lukes Mt States Tumor Inst, Boise, ID 83712 USA
[2] Mem Sloan Kettering Canc Ctr, Clin Trials Nursing, 1275 York Ave, New York, NY 10021 USA
[3] City Hope Colton, Colton, CA USA
[4] Seattle Genet, Bothell, WA USA
[5] Seattle Genet, Safety Evaluat & Risk Management, Bothell, WA USA
[6] Seattle Canc Care Alliance, Washington, DC USA
关键词
brentuximab vedotin; adverse events; peripheral neuropathy; management; INDUCED PERIPHERAL NEUROPATHY; ANTIBODY-DRUG CONJUGATE; HODGKIN LYMPHOMA; CELL TRANSPLANTATION; UNITED-STATES; RISK; THERAPY; AGENTS; DESENSITIZATION; PANCREATITIS;
D O I
10.1188/18.CJON.E103-E114
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Brentuximab vedotin (BV) is an antibody-drug conjugate that targets CD30-expressing cells. OBJECTIVES:This article assesses the occurrence and management of the most frequent and clinically relevant BV-associated adverse events (AEs), with a focus on Hodgkin lymphoma and systemic anaplastic large cell lymphoma trials, and shares practical tips that may help decrease occurrence and severity. METHODS: Peer-reviewed literature was surveyed to collect safety data from sponsored clinical trials of BV and to compile associated management guidelines. FINDINGS: Peripheral neuropathy was the most common BV-associated AE across clinical trials. Other clinically relevant AEs included neutropenia, infection, and infusion-related reactions. Awareness of and preparedness for these common BV-associated AEs and other less common but significant AEs will help nurse clinicians and patients maximize the clinical benefit for patients receiving BV.
引用
收藏
页码:E103 / E114
页数:12
相关论文
共 55 条
[1]   Growth factors in idiopathic pulmonary fibrosis: relative roles [J].
Allen, JT ;
Spiteri, MA .
RESPIRATORY RESEARCH, 2001, 3 (01)
[2]  
[Anonymous], 2018, NCCN Clinical Practice Guidelines in Oncology, DOI DOI 10.1016/B978-0-323-35762-3.00092-5
[3]  
[Anonymous], 2010, Common terminology criteria for adverse events, v4.03
[4]   Hodgkin lymphoma: 2016 update on diagnosis, risk-stratification, and management [J].
Ansell, Stephen M. .
AMERICAN JOURNAL OF HEMATOLOGY, 2016, 91 (04) :434-442
[5]   Brentuximab vedotin desensitization in a patient with refractory Hodgkin's lymphoma [J].
Arora, Anubha ;
Bhatt, Vijaya Raj ;
Liewer, Susanne ;
Armitage, James O. ;
Bociek, R. Gregory .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2015, 95 (04) :361-364
[6]  
Boussios S, 2012, ANN GASTROENTEROL, V25, P106
[7]   Incidence of infusion reactions to anti-neoplastic agents in early phase clinical trials: The MD Anderson Cancer Center experience [J].
Bupathi, Manojkumar ;
Hajjar, Joud ;
Bean, Stacie ;
Fu, Siqing ;
Hong, David ;
Karp, Daniel ;
Stephen, Bettzy ;
Hess, Kenneth ;
Meric-Bernstam, Funda ;
Naing, Aung .
INVESTIGATIONAL NEW DRUGS, 2017, 35 (01) :59-67
[8]  
Center for Drug Evaluation and Research, 2011, ADC BRENT VED
[9]   Five-year survival and durability results of brentuximab vedotin in patients with relapsed or refractory Hodgkin lymphoma [J].
Chen, Robert ;
Gopal, Ajay K. ;
Smith, Scott E. ;
Ansell, Stephen M. ;
Rosenblatt, Joseph D. ;
Savage, Kerry J. ;
Connors, Joseph M. ;
Engert, Andreas ;
Larsen, Emily K. ;
Huebner, Dirk ;
Fong, Abraham ;
Younes, Anas .
BLOOD, 2016, 128 (12) :1562-1566
[10]   Multiple Successful Desensitizations to Brentuximab Vedotin: A Case Report and Literature Review [J].
DeVita, Michael D. ;
Evens, Andrew M. ;
Rosen, Steven T. ;
Greenberger, Paul A. ;
Petrich, Adam M. .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2014, 12 (04) :465-471