Nivolumab to pembrolizumab switch induced a durable melanoma response A case report

被引:15
作者
Lepir, Tanja [1 ]
Zaghouani, Mehdi [2 ]
Roche, Stephane P. [2 ,3 ]
Li, Ying-Ying [1 ]
Suarez, Miguel [1 ]
Irias, Maria Jose [1 ]
Savaraj, Niramol [1 ]
机构
[1] Bruce W Carter VA Med Ctr, Dept Vet Affairs, 1201 NW 16th St, Miami, FL 33125 USA
[2] Florida Atlantic Univ, Dept Chem & Biochem, Boca Raton, FL 33431 USA
[3] Florida Atlantic Univ, Ctr Mol Biol & Biotechnol, Boca Raton, FL 33431 USA
关键词
melanoma; molecular interaction; PD-1; epitopes; PD-1/PD-L1; blockers; DEATH; 1; BRAF; SURVIVAL; DABRAFENIB; COMPLEX; PD-1; IMMUNOTHERAPY; MULTICENTER; VEMURAFENIB; ANTIBODIES;
D O I
10.1097/MD.0000000000013804
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: While checkpoint inhibitors have revolutionized the treatment of melanoma, it is not known whether switching from one monoclonal antibody drug to another one would be justified in the case of a treatment failure. Herein, we report a case illustrating a durable response to pembrolizumab after a failure with nivolumab. Patient concerns: A 76-year-old white male noticed an enlarging papular lesion on his neck. Diagnosis: Malignant melanoma. Interventions: The patient underwent surgery in December 2013 and was found to have a B-Rapidly Accelerated Fibrosarcoma (BRAF) V600E mutated melanoma. Treatment with BRAF and MAPK/Erk kinase (MEK) inhibitors along with radiation was initiated. After 1 year, the disease progressed, and the treatment was switched to the cytotoxic T-lymphocyte antigen 4 (CTLA-4) blocking antibody, ipilimumab. As the tumor did not respond, the treatment was changed to programmed cell death receptor-1 (PD-1) blockers: nivolumab followed by pembrolizumab. Since the initial diagnosis, the tumor response was monitored by computed tomography (CT) scans. Immunohistochemistry (IHC) was also used for the assessment of programmed death ligand 1 PD-L1) expression in the neck, lung, and spleen lesions. Outcomes: The patient had an initial mixed response to nivolumab, but the disease ultimately progressed as evidenced by new metastases to the spleen, thus the treatment was switched to pembrolizumab. After 46 cycles of treatment, all sites of metastases disappeared, including a substantial shrinkage of the splenic metastasis. To gain understanding about the pharmacological differences between nivolumab and pembrolizumab, the PD-1-ligands interactions and conformational dynamics responsible for the PD-1/PD-L1 checkpoint blockade were investigated. The higher affinity of pembrolizumab might likely arise from a unique and large patch of interactions engaging the C'D loop of PD-1, thus forcing an important motion across the PD-1 immunoreceptor. Lessons: In this case report, we described the tolerance and response of a melanoma patient to a sequence of various agents, including ipilimumab, nivolumab, and pembrolizumab. To the best of our knowledge, this is the first clinical report highlighting differences between PD-1 blockers, as shown by the unexpected and durable response of the tumor to pembrolizumab, after a treatment failure with nivolumab.
引用
收藏
页数:7
相关论文
共 28 条
[1]  
[Anonymous], 2016, LEX ONL VEM LEX DRUG
[2]   The role of BRAF V600 mutation in melanoma [J].
Ascierto, Paolo A. ;
Kirkwood, John M. ;
Grob, Jean-Jacques ;
Simeone, Ester ;
Grimaldi, Antonio M. ;
Maio, Michele ;
Palmieri, Giuseppe ;
Testori, Alessandro ;
Marincola, Francesco M. ;
Mozzillo, Nicola .
JOURNAL OF TRANSLATIONAL MEDICINE, 2012, 10
[3]   Response of metastatic mucosal melanoma to immunotherapy: It can get worse before it gets better [J].
Atrash, Shebli ;
Makhoul, Issam ;
Mizell, Jason S. ;
Hutchins, Laura ;
Mahmoud, Fade .
JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2017, 23 (03) :215-219
[4]   Vemurafenib-induced toxic epidermal necrolysis: possible cross-reactivity with other sulfonamide compounds [J].
Bellon, T. ;
Lerma, V. ;
Gonzalez-Valle, O. ;
Gonzalez Herrada, C. ;
de Abajo, F. J. .
BRITISH JOURNAL OF DERMATOLOGY, 2016, 174 (03) :621-624
[5]   Molecular and Biochemical Aspects of the PD-1 Checkpoint Pathway [J].
Boussiotis, Vassiliki A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 375 (18) :1767-1778
[6]   Structure and Interactions of the Human Programmed Cell Death 1 Receptor [J].
Cheng, Xiaoxiao ;
Veverka, Vaclav ;
Radhakrishnan, Anand ;
Waters, Lorna C. ;
Muskett, Frederick W. ;
Morgan, Sara H. ;
Huo, Jiandong ;
Yu, Chao ;
Evans, Edward J. ;
Leslie, Alasdair J. ;
Griffiths, Meryn ;
Stubberfield, Colin ;
Griffin, Robert ;
Henry, Alistair J. ;
Jansson, Andreas ;
Ladbury, John E. ;
Ikemizu, Shinji ;
Carr, Mark D. ;
Davis, Simon J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (17) :11771-11785
[7]   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
[8]   Improved Survival with MEK Inhibition in BRAF-Mutated Melanoma [J].
Flaherty, Keith T. ;
Robert, Caroline ;
Hersey, Peter ;
Nathan, Paul ;
Garbe, Claus ;
Milhem, Mohammed ;
Demidov, Lev V. ;
Hassel, Jessica C. ;
Rutkowski, Piotr ;
Mohr, Peter ;
Dummer, Reinhard ;
Trefzer, Uwe ;
Larkin, James M. G. ;
Utikal, Jochen ;
Dreno, Brigitte ;
Nyakas, Marta ;
Middleton, Mark R. ;
Becker, Juergen C. ;
Casey, Michelle ;
Sherman, Laurie J. ;
Wu, Frank S. ;
Ouellet, Daniele ;
Martin, Anne-Marie ;
Patel, Kiran ;
Schadendorf, Dirk .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (02) :107-114
[9]  
For Zelboraf (vemurafenib) Prescribing Information: Genentech Inc. 1 DNA Way Co-promoted by: Genentech USA Inc. and Daiichi Sankyo Inc, 2014, ZELB VEM PRESCR INF
[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