Trends in Melanoma Phase 3 Clinical Trials since 2010: Is there Hope for Advanced Melanoma Therapies beyond Approved Treatment Mechanisms?

被引:9
作者
Kakish, Hanna H. [1 ]
Ahmed, Fasih Ali [1 ]
Elshami, Mohamedraed [1 ]
Loftus, Alexander W. [1 ]
Hoehn, Richard S. [1 ]
Ammori, John B. [1 ]
Ocuin, Lee M. [1 ]
Winter, Jordan M. [1 ]
Bordeaux, Jeremy S. [2 ]
Mangla, Ankit [3 ]
Rothermel, Luke D. [1 ]
机构
[1] Univ Hosp Cleveland Med Ctr, Dept Surg, Div Surg Oncol, Cleveland Hts, OH 44106 USA
[2] Univ Hospitals Cleveland Med Ctr, Dept Dermatol, Cleveland Hts, OH 44106 USA
[3] Univ Hosp Seidman Canc Ctr, Div Hematol & Oncol, Cleveland Hts, OH 44106 USA
关键词
cutaneous melanoma; clinical trials; immunotherapy; targeted therapy; chemotherapy; metabolic therapy; emerging therapy; STAGE-III MELANOMA; BETA-BLOCKERS; DOUBLE-BLIND; GM-CSF; IPILIMUMAB; PLACEBO; NIVOLUMAB; SURVIVAL; PEMBROLIZUMAB; BRAF;
D O I
10.3390/cancers14215184
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Several drugs and treatment modalities are under investigation to improve current melanoma therapy options. This review profiles the trends in clinical trial investment in late-stage melanoma, and anticipates what changes are expected in melanoma treatment, with a focus on exploratory drug mechanisms. Methods: We reviewed nine international clinical trial databases for registered, interventional, and phase 3 cutaneous melanoma clinical trials since 2010. Results: 73 trials studied drug therapies in late-stage (stage III and IV) melanoma. Exploratory mechanisms were investigated in 32% (23/73) of the late-stage melanoma drug therapy trials. Most exploratory drug trials include immunotherapy drug mechanisms (15/23 trials). Two exploratory mechanisms showed promise: the anti-LAG3 antibody, relatlimab, and the hapten modified vaccine, MVax. Many (52%) trials of exploratory mechanisms are ongoing including the use of adoptive cell transfer immunotherapies, dendritic cell vaccine therapy, and histone deacetylase (HDAC) inhibitors, among others. Conclusions: Since most clinical trials focus on previously approved drug mechanisms, it is likely that paradigm-changing treatments will involve these therapies being used in new treatment contexts or combinations. Only 2 exploratory drug mechanisms studied since 2010 have achieved promising results in the phase 3 setting, though many other trials are ongoing at this time.
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页数:16
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共 62 条
  • [41] Single Institution Experience of Ipilimumab 3 mg/kg with Sargramostim (GM-CSF) in Metastatic Melanoma
    Luke, Jason J.
    Donahue, Hilary
    Nishino, Mizuki
    Giobbie-Hurder, Anita
    Davis, Meredith
    Bailey, Nancy
    Ott, Patrick A.
    Hodi, F. Stephen
    [J]. CANCER IMMUNOLOGY RESEARCH, 2015, 3 (09) : 986 - 991
  • [42] Macia S., PHASE 2 SINGLE ARM C
  • [43] National Library of Medicine (U.S.), PHAS 3 RAND PLAC CON
  • [44] National Library of Medicine (U.S.), ALL VACC MOD EXPR HL
  • [45] National Library of Medicine (U.S.), PHAS 3 RAND DOUBL BL
  • [46] National Library of Medicine (U.S.), MEL MULT RAND DOUBL
  • [47] Ning J.T., MULTICENTER RANDOMIZ
  • [48] First-in-human study of the PARP/tankyrase inhibitor E7449 in patients with advanced solid tumours and evaluation of a novel drug-response predictor
    Plummer, Ruth
    Dua, Divyanshu
    Cresti, Nicola
    Drew, Yvette
    Stephens, Peter
    Foegh, Marie
    Knudsen, Steen
    Sachdev, Pallavi
    Mistry, Bipin M.
    Dixit, Vaishali
    McGonigle, Sharon
    Hall, Nancy
    Matijevic, Mark
    McGrath, Shannon
    Sarker, Debashis
    [J]. BRITISH JOURNAL OF CANCER, 2020, 123 (04) : 525 - 533
  • [49] SELECTIVE TOXICITY OF BUTHIONINE SULFOXIMINE (BSO) TO MELANOMA-CELLS IN-VITRO AND IN-VIVO
    REVESZ, L
    EDGREN, MR
    WAINSON, AA
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1994, 29 (02): : 403 - 406
  • [50] Nivolumab in Previously Untreated Melanoma without BRAF Mutation
    Robert, Caroline
    Long, Georgina V.
    Brady, Benjamin
    Dutriaux, Caroline
    Maio, Michele
    Mortier, Laurent
    Hassel, Jessica C.
    Rutkowski, Piotr
    McNeil, Catriona
    Kalinka-Warzocha, Ewa
    Savage, Kerry J.
    Hernberg, Micaela M.
    Lebbe, Celeste
    Charles, Julie
    Mihalcioiu, Catalin
    Chiarion-Sileni, Vanna
    Mauch, Cornelia
    Cognetti, Francesco
    Arance, Ana
    Schmidt, Henrik
    Schadendorf, Dirk
    Gogas, Helen
    Lundgren-Eriksson, Lotta
    Horak, Christine
    Sharkey, Brian
    Waxman, Ian M.
    Atkinson, Victoria
    Ascierto, Paolo A.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (04) : 320 - 330