Intermittent dosing with vemurafenib in BRAF V600E-mutant melanoma: review of a case series

被引:32
作者
Dooley, Andrew J. [2 ]
Gupta, Avinash [1 ]
Bhattacharyya, Madhumita [3 ]
Middleton, Mark R. [1 ]
机构
[1] Churchill Hosp, Dept Oncol, NIHR Biomed Res Ctr, Oxford Canc & Haematol Ctr, Oxford OX3 7LE, England
[2] Univ Oxford, John Radcliffe Hosp, Oxford OX3 9DU, England
[3] Royal Berkshire Hosp, Dept Oncol, Reading RG1 5AN, Berks, England
关键词
melanoma; vemurafenib; intermittent; toxicity; resistance; MUTATED METASTATIC MELANOMA; RENAL-CELL CARCINOMA; OPEN-LABEL; PHASE-II; CANCER; MULTICENTER; INHIBITOR; TRIAL; CAPECITABINE; SUNITINIB;
D O I
10.1177/1758834014548187
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The selective BRAF inhibitors, vemurafenib and dabrafenib, yield high response rates and improved overall survival in patients with BRAF V600E-mutant metastatic melanoma. Acquired drug resistance and drug toxicity are key challenges when using these drugs. We investigated whether vemurafenib toxicity could successfully be managed with intermittent dosing, and if its therapeutic efficacy could be maintained on intermittent dosing. Six patients with BRAF V600E-mutated metastatic melanoma were treated with an intermittent dosing regimen of vemurafenib. In three patients, toxicities were successfully managed with an intermittent dosing regimen. In the other three patients, intolerable toxicities continued on intermittent dosing. Our experience shows that intermittent dosing can successfully manage vemurafenib toxicities where continuous dosing at a reduced dose does not. Intermittent treatment improves drug tolerability and can achieve or maintain melanoma shrinkage. We recommend that in clinical practice, intermittent dosing should be considered as an alternative to dose reduction/termination in the management of vemurafenib toxicity.
引用
收藏
页码:262 / 266
页数:5
相关论文
共 17 条
[1]   Intermittent versus continuous oxaliplatin and fluoropyrimidine combination chemotherapy for first-line treatment of advanced colorectal cancer: results of the randomised phase 3 MRC COIN trial [J].
Adams, Richard A. ;
Meade, Angela M. ;
Seymour, Matthew T. ;
Wilson, Richard H. ;
Madi, Ayman ;
Fisher, David ;
Kenny, Sarah L. ;
Kay, Edward ;
Hodgkinson, Elizabeth ;
Pope, Malcolm ;
Rogers, Penny ;
Wasan, Harpreet ;
Falk, Stephen ;
Gollins, Simon ;
Hickish, Tamas ;
Bessell, Eric M. ;
Propper, David ;
Kennedy, M. John ;
Kaplan, Richard ;
Maughan, Timothy S. .
LANCET ONCOLOGY, 2011, 12 (07) :642-653
[2]  
Blum JL, 2001, CANCER, V92, P1759, DOI 10.1002/1097-0142(20011001)92:7<1759::AID-CNCR1691>3.0.CO
[3]  
2-A
[4]   Improved Survival with Vemurafenib in Melanoma with BRAF V600E Mutation [J].
Chapman, Paul B. ;
Hauschild, Axel ;
Robert, Caroline ;
Haanen, John B. ;
Ascierto, Paolo ;
Larkin, James ;
Dummer, Reinhard ;
Garbe, Claus ;
Testori, Alessandro ;
Maio, Michele ;
Hogg, David ;
Lorigan, Paul ;
Lebbe, Celeste ;
Jouary, Thomas ;
Schadendorf, Dirk ;
Ribas, Antoni ;
O'Day, Steven J. ;
Sosman, Jeffrey A. ;
Kirkwood, John M. ;
Eggermont, Alexander M. M. ;
Dreno, Brigitte ;
Nolop, Keith ;
Li, Jiang ;
Nelson, Betty ;
Hou, Jeannie ;
Lee, Richard J. ;
Flaherty, Keith T. ;
McArthur, Grant A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (26) :2507-2516
[5]   Modelling vemurafenib resistance in melanoma reveals a strategy to forestall drug resistance [J].
Das Thakur, Meghna ;
Salangsang, Fernando ;
Landman, Allison S. ;
Sellers, William R. ;
Pryer, Nancy K. ;
Levesque, Mitchell P. ;
Dummer, Reinhard ;
McMahon, Martin ;
Stuart, Darrin D. .
NATURE, 2013, 494 (7436) :251-255
[6]   Mutations of the BRAF gene in human cancer [J].
Davies, H ;
Bignell, GR ;
Cox, C ;
Stephens, P ;
Edkins, S ;
Clegg, S ;
Teague, J ;
Woffendin, H ;
Garnett, MJ ;
Bottomley, W ;
Davis, N ;
Dicks, N ;
Ewing, R ;
Floyd, Y ;
Gray, K ;
Hall, S ;
Hawes, R ;
Hughes, J ;
Kosmidou, V ;
Menzies, A ;
Mould, C ;
Parker, A ;
Stevens, C ;
Watt, S ;
Hooper, S ;
Wilson, R ;
Jayatilake, H ;
Gusterson, BA ;
Cooper, C ;
Shipley, J ;
Hargrave, D ;
Pritchard-Jones, K ;
Maitland, N ;
Chenevix-Trench, G ;
Riggins, GJ ;
Bigner, DD ;
Palmieri, G ;
Cossu, A ;
Flanagan, A ;
Nicholson, A ;
Ho, JWC ;
Leung, SY ;
Yuen, ST ;
Weber, BL ;
Siegler, HF ;
Darrow, TL ;
Paterson, H ;
Marais, R ;
Marshall, CJ ;
Wooster, R .
NATURE, 2002, 417 (6892) :949-954
[7]   Safety, pharmacokinetic, and antitumor activity of SU11248, a novel oral multitarget tyrosine kinase inhibitor, in patients with cancer [J].
Faivre, S ;
Delbaldo, C ;
Vera, K ;
Robert, C ;
Lozahic, S ;
Lassau, N ;
Bello, C ;
Deprimo, S ;
Brega, A ;
Massimini, G ;
Armand, JP ;
Scigalla, P ;
Raymond, E .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (01) :25-35
[8]   The MAPK pathway in melanoma [J].
Fecher, Leslie A. ;
Arnaravadi, Ravi K. ;
Flaherty, Keith T. .
CURRENT OPINION IN ONCOLOGY, 2008, 20 (02) :183-189
[9]   Inhibition of Mutated, Activated BRAF in Metastatic Melanoma [J].
Flaherty, Keith T. ;
Puzanov, Igor ;
Kim, Kevin B. ;
Ribas, Antoni ;
McArthur, Grant A. ;
Sosman, Jeffrey A. ;
O'Dwyer, Peter J. ;
Lee, Richard J. ;
Grippo, Joseph F. ;
Nolop, Keith ;
Chapman, Paul B. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (09) :809-819
[10]   Dabrafenib in BRAF-mutated metastatic melanoma: a multicentre, open-label, phase 3 randomised controlled trial [J].
Hauschild, Axel ;
Grob, Jean-Jacques ;
Demidov, Lev V. ;
Jouary, Thomas ;
Gutzmer, Ralf ;
Millward, Michael ;
Rutkowski, Piotr ;
Blank, Christian U. ;
Miller, Wilson H., Jr. ;
Kaempgen, Eckhart ;
Martin-Algarra, Salvador ;
Karaszewska, Boguslawa ;
Mauch, Cornelia ;
Chiarion-Sileni, Vanna ;
Martin, Anne-Marie ;
Swann, Suzanne ;
Haney, Patricia ;
Mirakhur, Beloo ;
Guckert, Mary E. ;
Goodman, Vicki ;
Chapman, Paul B. .
LANCET, 2012, 380 (9839) :358-365