Identifying the optimum first-line therapy in BRAF-mutant metastatic melanoma

被引:6
作者
Ziogas, Dimitrios C. [1 ]
Konstantinou, Frosso [1 ]
Bouros, Spyros [1 ]
Gogas, Helen [1 ]
机构
[1] Univ Athens, Sch Med, Laiko Gen Hosp, Dept Med 1, Athens, Greece
关键词
First-line; metastatic melanoma; BRAF; MEK inhibitors; targeted therapy; immunotherapy; DABRAFENIB PLUS TRAMETINIB; T-CELL RECOGNITION; OPEN-LABEL; PD-L1; EXPRESSION; ADJUVANT DABRAFENIB; COMBINED NIVOLUMAB; ANTITUMOR-ACTIVITY; POOLED ANALYSIS; MEK INHIBITION; DOUBLE-BLIND;
D O I
10.1080/14737140.2020.1711737
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The emergence of molecularly targeted agents and immune checkpoint inhibitors has positively revolutionized the management and prognosis of BRAF-mutant metastatic melanoma. However, the availability of both therapeutic options, with their pros and cons, rationally triggered clinical considerations for the optimum frontline and subsequent treatment decisions. Areas covered: Here, we debate all approved therapies in patients with BRAF-mutant metastatic melanoma evaluating their efficacy and safety based on their pivotal trials. With prospective randomized data pending, retrospective comparisons of BRAF/MEK versus immune checkpoint inhibitors are reviewed to recognize any advantage between these two alternatives and to optimize their implementation. Preclinical and early clinical results of combining concurrently or sequentially targeted therapy and immunotherapy are also discussed. Expert opinion: BRAF/MEK inhibitors produce rapid and deep responses and should be included in first-line approaches, particularly in cases with aggressive and bulky disease, while single or double checkpoint inhibition lead to more durable responses and could be involved either in frontline treatment of BRAF-mutant melanoma with less unfavorable characteristics or in maintenance after initial targeted induction or in future immune/targeted regimens for high-risk groups. Data from ongoing trials directly comparing or combining these strategies are expected to update their role in a more individualized basis.
引用
收藏
页码:53 / 62
页数:10
相关论文
共 67 条
  • [21] Immune-Based Antitumor Effects of BRAF Inhibitors Rely on Signaling by CD40L and IFNγ
    Ho, Ping-Chih
    Meeth, Katrina M.
    Tsui, Yao-Chen
    Srivastava, Bhaskar
    Bosenberg, Marcus W.
    Kaech, Susan M.
    [J]. CANCER RESEARCH, 2014, 74 (12) : 3205 - 3217
  • [22] Improved Survival with Ipilimumab in Patients with Metastatic Melanoma
    Hodi, F. Stephen
    O'Day, Steven J.
    McDermott, David F.
    Weber, Robert W.
    Sosman, Jeffrey A.
    Haanen, John B.
    Gonzalez, Rene
    Robert, Caroline
    Schadendorf, Dirk
    Hassel, Jessica C.
    Akerley, Wallace
    van den Eertwegh, Alfons J. M.
    Lutzky, Jose
    Lorigan, Paul
    Vaubel, Julia M.
    Linette, Gerald P.
    Hogg, David
    Ottensmeier, Christian H.
    Lebbe, Celeste
    Peschel, Christian
    Quirt, Ian
    Clark, Joseph I.
    Wolchok, Jedd D.
    Weber, Jeffrey S.
    Tian, Jason
    Yellin, Michael J.
    Nichol, Geoffrey M.
    Hoos, Axel
    Urba, Walter J.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (08) : 711 - 723
  • [23] Nivolumab plus ipilimumab or nivolumab alone versus ipilimumab alone in advanced melanoma (CheckMate 067): 4-year outcomes of a multicentre, randomised, phase 3 trial
    Hodi, Frank Stephen
    Chiarion-Sileni, Vanna
    Gonzalez, Rene
    Grob, Jean-Jacques
    Rutkowski, Piotr
    Cowey, Charles Lance
    Lao, Christopher D.
    Schadendorf, Dirk
    Wagstaff, John
    Dummer, Reinhard
    Ferrucci, Pier Francesco
    Smylie, Michael
    Hill, Andrew
    Hogg, David
    Marquez-Rodas, Ivan
    Jiang, Joel
    Rizzo, Jasmine
    Larkin, James
    Wolchok, Jedd D.
    [J]. LANCET ONCOLOGY, 2018, 19 (11) : 1480 - 1492
  • [24] Improved antitumor activity of immunotherapy with BRAF and MEK inhibitors in BRAFV600E melanoma
    Hu-Lieskovan, Siwen
    Mok, Stephen
    Moreno, Blanca Homet
    Tsoi, Jennifer
    Robert, Lidia
    Goedert, Lucas
    Pinheiro, Elaine M.
    Koya, Richard C.
    Graeber, Thomas G.
    Comin-Anduix, Begona
    Ribas, Antoni
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2015, 7 (279)
  • [25] Genomic and Transcriptomic Features of Response to Anti-PD-1 Therapy in Metastatic Melanoma
    Hugo, Willy
    Zaretsky, Jesse M.
    Sun, Lu
    Song, Chunying
    Moreno, Blanca Homet
    Hu-Lieskovan, Siwen
    Berent-Maoz, Beata
    Pang, Jia
    Chmielowski, Bartosz
    Cherry, Grace
    Seja, Elizabeth
    Lomeli, Shirley
    Kong, Xiangju
    Kelley, Mark C.
    Sosman, Jeffrey A.
    Johnson, Douglas B.
    Ribas, Antoni
    Lo, Roger S.
    [J]. CELL, 2016, 165 (01) : 35 - 44
  • [26] Discontinuation of anti-PD-1 antibody therapy in the absence of disease progression or treatment limiting toxicity: clinical outcomes in advanced melanoma
    Jansen, Y. J. L.
    Rozeman, E. A.
    Mason, R.
    Goldinger, S. M.
    Foppen, M. H. Geukes
    Hoejberg, L.
    Schmidt, H.
    van Thienen, J., V
    Haanen, J. B. A. G.
    Tiainen, L.
    Svane, I. M.
    Makela, S.
    Seremet, T.
    Arance, A.
    Dummer, R.
    Bastholt, L.
    Nyakas, M.
    Straume, O.
    Menzies, A. M.
    Long, G., V
    Atkinson, V
    Blank, C. U.
    Neyns, B.
    [J]. ANNALS OF ONCOLOGY, 2019, 30 (07) : 1154 - 1161
  • [27] The Activation of MAPK in Melanoma Cells Resistant to BRAF Inhibition Promotes PD-L1 Expression That Is Reversible by MEK and PI3K Inhibition
    Jiang, Xiaofeng
    Zhou, Jun
    Giobbie-Hurder, Anita
    Wargo, Jennifer
    Hodi, F. Stephen
    [J]. CLINICAL CANCER RESEARCH, 2013, 19 (03) : 598 - 609
  • [28] Sequencing Treatment in BRAFV600 Mutant Melanoma: Anti-PD-1 Before and After BRAF Inhibition
    Johnson, Douglas B.
    Pectasides, Eirini
    Feld, Emily
    Ye, Fei
    Zhao, Shilin
    Johnpulle, Romany
    Merritt, Ryan
    McDermott, David F.
    Puzanov, Igor
    Lawrence, Donald
    Sosman, Jeffrey A.
    Buchbinder, Elizabeth
    Sullivan, Ryan J.
    [J]. JOURNAL OF IMMUNOTHERAPY, 2017, 40 (01) : 31 - 35
  • [29] PD-L1 Expression and Immune Escape in Melanoma Resistance to MAPK Inhibitors
    Kakavand, Hojabr
    Rawson, Robert V.
    Pupo, Gulietta M.
    Yang, Jean Y. H.
    Menzies, Alexander M.
    Carlino, Matteo S.
    Kefford, Richard F.
    Howle, Julie R.
    Saw, Robyn P. M.
    Thompson, John F.
    Wilmott, James S.
    Long, Georgina V.
    Scolyer, Richard A.
    Rizos, Helen
    [J]. CLINICAL CANCER RESEARCH, 2017, 23 (20) : 6054 - 6061
  • [30] PD-L1 Expression and Tumor-Infiltrating Lymphocytes Define Different Subsets of MAPK Inhibitor-Treated Melanoma Patients
    Kakavand, Hojabr
    Wilmott, James S.
    Menzies, Alexander M.
    Vilain, Ricardo
    Haydu, Lauren E.
    Yearley, Jennifer H.
    Thompson, John F.
    Kefford, Richard F.
    Hersey, Peter
    Long, Georgina V.
    Scolyer, Richard A.
    [J]. CLINICAL CANCER RESEARCH, 2015, 21 (14) : 3140 - 3148