Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd-4th, 2021, Italy)

被引:2
|
作者
Ascierto, Paolo A. [1 ]
Agarwala, Sanjiv S. [2 ,3 ]
Blank, Christian [4 ]
Caraco, Corrado [5 ]
Carvajal, Richard D. [6 ]
Ernstoff, Marc S. [7 ]
Ferrone, Soldano [8 ]
Fox, Bernard A. [9 ]
Gajewski, Thomas F. [10 ,11 ]
Garbe, Claus [12 ]
Grob, Jean-Jacques [13 ]
Hamid, Omid [14 ]
Krogsgaard, Michelle [15 ]
Lo, Roger S. [16 ]
Lund, Amanda W. [17 ]
Madonna, Gabriele [18 ]
Michielin, Olivier [19 ,20 ]
Neyns, Bart [21 ]
Osman, Iman [22 ]
Peters, Solange [23 ]
Poulikakos, Poulikos, I [24 ]
Quezada, Sergio A. [25 ]
Reinfeld, Bradley [26 ]
Zitvogel, Laurence [27 ]
Puzanov, Igor [28 ]
Thurin, Magdalena [29 ]
机构
[1] Ist Nazl Tumor IRCCS Fdn G Pascale, Dept Melanoma Canc Immunotherapy & Innovat Therap, Naples, Italy
[2] Temple Univ, Hematol & Oncol, Bethlehem, PA USA
[3] Canc Expert Now, Bethlehem, PA USA
[4] Netherlands Canc Inst, Amsterdam, Netherlands
[5] Ist Nazl Tumori Fdn Pascale IRCCS, Div Surg Melanoma & Skin Canc, Naples, Italy
[6] Columbia Univ, Dept Med, Div Hematol & Oncol, Irving Med Ctr, New York, NY USA
[7] NCI, Dev Therapeut Program, Div Canc Therapy & Diag, NIHMD, Bethesda, MD 20892 USA
[8] Harvard Med Sch, Massachusetts Gen Hosp, Dept Surg, Boston, MA 02115 USA
[9] Providence Canc Inst, Earle A Chiles Res Inst, Robert W Franz Canc Res Ctr, Portland, OR USA
[10] Univ Chicago, Dept Pathol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[11] Univ Chicago, Dept Med, Sect Hematol Oncol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[12] Univ Dept Dermatol, Ctr Dermatooncol, Tubingen, Germany
[13] Aix Marseille, Dermatol Dept, Hop La Timone, Marseille, France
[14] Angeles Clin & Res Inst, Med Oncol, Los Angeles, CA USA
[15] New York Univ Langone, New York Grossman Sch Med, New York, NY USA
[16] Univ Calif Los Angeles, David Geffen Sch Med, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[17] NYU, Dept Pathol, Grossman Sch Med, Ronald O Perelman Dept Dermatol, 550 1St Ave, New York, NY 10016 USA
[18] Ist Nazl Tumori IRCCS Fdn G Pascale, Dept Melanoma Canc Immunotherapy & Innovat Therap, Naples, Italy
[19] Lausanne Univ Hosp CHUV, Precis Oncol Ctr, Lausanne, Switzerland
[20] Lausanne Univ Hosp CHUV, Oncol Dept, Melanoma Clin, Lausanne, Switzerland
[21] Univ Ziekenhuis Brussel, Med Oncol, Brussels, Belgium
[22] NYU, Langone Med Ctr, New York, NY USA
[23] UNIL, Med Oncol Dept European Thorac Oncol Platform Sto, Specialized Thorac Tumor Consultat, Oncol Dept UNIL CHUV Thorac Tumor Ctr, Lausanne, Switzerland
[24] Icahn Sch Med Mt Sinai, Tisch Canc Inst, Dept Oncol Sci, Dept Dermatol, New York, NY 10029 USA
[25] Univ Coll London Canc Inst, Res Dept Hematol, Canc Immunol Unit, London, England
[26] Vanderbilt Univ, Dept Med, Vanderbilt Univ Med Ctr VUMC, Div Hematol Oncol,Grad Program Canc Biol, Nashville, TN USA
[27] Univ Paris Saclay, European Acad Tumor Immunol, Gustave Roussy, INSERM,Tumour Immunol & Immunotherapy Canc, Villejuif Grand Paris, France
[28] Roswell Park Comprehens Canc Ctr, Dept Med, Buffalo, NY USA
[29] NCI, Canc Diag Program, Div Canc Treatment & Diag, NIHMD, Rockville, MD USA
关键词
Melanoma; Immunotherapy; Anti-PD-1; Anti-CTLA-4; Target therapy; Biomarkers; BRAF inhibitor; MEK inhibitor; Adjuvant; Neoadjuvant; Combination strategies; DABRAFENIB PLUS TRAMETINIB; DOUBLE-BLIND; IMMUNE CHECKPOINT; ANTI-PD-1; THERAPY; POOLED ANALYSIS; FREE SURVIVAL; VISTA; IPILIMUMAB; EXPRESSION; IMMUNOTHERAPY;
D O I
10.1186/s12967-022-03592-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Advances in immune checkpoint and combination therapy have led to improvement in overall survival for patients with advanced melanoma. Improved understanding of the tumor, tumor microenvironment and tumor immune-evasion mechanisms has resulted in new approaches to targeting and harnessing the host immune response. Combination modalities with other immunotherapy agents, chemotherapy, radiotherapy, electrochemotherapy are also being explored to overcome resistance and to potentiate the immune response. In addition, novel approaches such as adoptive cell therapy, oncogenic viruses, vaccines and different strategies of drug administration including sequential, or combination treatment are being tested. Despite the progress in diagnosis of melanocytic lesions, correct classification of patients, selection of appropriate adjuvant and systemic theraapies, and prediction of response to therapy remain real challenges in melanoma. Improved understanding of the tumor microenvironment, tumor immunity and response to therapy has prompted extensive translational and clinical research in melanoma. There is a growing evidence that genomic and immune features of pre-treatment tumor biopsies may correlate with response in patients with melanoma and other cancers, but they have yet to be fully characterized and implemented clinically. Development of novel biomarker platforms may help to improve diagnostics and predictive accuracy for selection of patients for specific treatment. Overall, the future research efforts in melanoma therapeutics and translational research should focus on several aspects including: (a) developing robust biomarkers to predict efficacy of therapeutic modalities to guide clinical decision-making and optimize treatment regimens, (b) identifying mechanisms of therapeutic resistance to immune checkpoint inhibitors that are potentially actionable, (c) identifying biomarkers to predict therapy-induced adverse events, and (d) studying mechanism of actions of therapeutic agents and developing algorithms to optimize combination treatments. During the Melanoma Bridge meeting (December 2nd-4th, 2021, Naples, Italy) discussions focused on the currently approved systemic and local therapies for advanced melanoma and discussed novel biomarker strategies and advances in precision medicine as well as the impact of COVID-19 pandemic on management of melanoma patients.
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页数:21
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