Evolving impact of long-term survival results on metastatic melanoma treatment

被引:70
作者
Michielin, Olivier [1 ,2 ]
Atkins, Michael B. [3 ,4 ]
Koon, Henry B. [5 ]
Dummer, Reinhard [6 ]
Ascierto, Paolo Antonio [7 ]
机构
[1] Precis Oncol Ctr, Oncol Dept, Lausanne, Switzerland
[2] Lausanne Univ Hosp, Oncol Dept, Lausanne, Switzerland
[3] Georgetown Univ, Med Ctr, Georgetown Lombardi Comprehens Canc Ctr, Med Oncol, Washington, DC 20007 USA
[4] Georgetown Univ, Med Ctr, Oncol Acad Dept, Washington, DC 20007 USA
[5] Bristol Myers Squibb, Clin Res, Princeton, NJ USA
[6] Univ Spital, Dermatol, Zurich, Switzerland
[7] Ist Nazl Tumori IRCCS Fdn Pascale, Melanoma Canc Immunotherapy & Innovat Therapy Uni, Naples, Italy
关键词
immunomodulation; immunotherapy; CTLA-4; antigen; review; programmed cell death 1 receptor; QUALITY-OF-LIFE; TUMOR-INFILTRATING LYMPHOCYTES; MUTANT ADVANCED MELANOMA; RANDOMIZED PHASE-III; STAGE-III; RECOMBINANT INTERLEUKIN-2; COMBINED NIVOLUMAB; LANDMARK ANALYSIS; TARGETED THERAPY; DOUBLE-BLIND;
D O I
10.1136/jitc-2020-000948
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Melanoma treatment has been revolutionized over the past decade. Long-term results with immuno-oncology (I-O) agents and targeted therapies are providing evidence of durable survival for a substantial number of patients. These results have prompted consideration of how best to define long-term benefit and cure. Now more than ever, oncologists should be aware of the long-term outcomes demonstrated with these newer agents and their relevance to treatment decision-making. As the first tumor type for which I-O agents were approved, melanoma has served as a model for other diseases. Accordingly, discussions regarding the value and impact of long-term survival data in patients with melanoma may be relevant in the future to other tumor types. Current findings indicate that, depending on the treatment, over 50% of patients with melanoma may gain durable survival benefit. The best survival outcomes are generally observed in patients with favorable prognostic factors, particularly normal baseline lactate dehydrogenase and/or a low volume of disease. Survival curves from melanoma clinical studies show a plateau at 3 to 4 years, suggesting that patients who are alive at the 3-year landmark (especially in cases in which treatment had been stopped) will likely experience prolonged cancer remission. Quality-of-life and mixture-cure modeling data, as well as metrics such as treatment-free survival, are helping to define the value of this long-term survival. In this review, we describe the current treatment landscape for melanoma and discuss the long-term survival data with immunotherapies and targeted therapies, discussing how to best evaluate the value of long-term survival. We propose that some patients might be considered functionally cured if they have responded to treatment and remained treatment-free for at least 2 years without disease progression. Finally, we consider that, while there have been major advances in the treatment of melanoma in the past decade, there remains a need to improve outcomes for the patients with melanoma who do not experience durable survival.
引用
收藏
页数:13
相关论文
共 100 条
  • [1] Impact of the treatment-free interval on health-related quality of life in patients with multiple myeloma: a UK cross-sectional survey
    Acaster, S.
    Gaugris, S.
    Velikova, G.
    Yong, K.
    Lloyd, A. J.
    [J]. SUPPORTIVE CARE IN CANCER, 2013, 21 (02) : 599 - 607
  • [2] Neoadjuvant immune checkpoint blockade in high-risk resectable melanoma
    Amaria, Rodabe N.
    Reddy, Sangeetha M.
    Tawbi, Hussein A.
    Davies, Michael A.
    Ross, Merrick, I
    Glitza, Isabella C.
    Cormier, Janice N.
    Lewis, Carol
    Hwu, Wen-Jen
    Hanna, Ehab
    Diab, Adi
    Wong, Michael K.
    Royal, Richard
    Gross, Neil
    Weber, Randal
    Lai, Stephen Y.
    Ehlers, Richard
    Blando, Jorge
    Milton, Denai R.
    Woodman, Scott
    Kageyama, Robin
    Wells, Daniel K.
    Hwu, Patrick
    Patel, Sapna P.
    Lucci, Anthony
    Hessel, Amy
    Lee, Jeffrey E.
    Gershenwald, Jeffrey
    Simpson, Lauren
    Burton, Elizabeth M.
    Posada, Liberty
    Haydu, Lauren
    Wang, Linghua
    Zhang, Shaojun
    Lazar, Alexanderj
    Hudgens, Courtney W.
    Gopalakrishnan, Vancheswaran
    Reuben, Alexandre
    Andrews, Miles C.
    Spencer, Christine N.
    Prieto, Victor
    Sharma, Padmanee
    Allison, James
    Tetzlaff, Michael T.
    Wargo, Jennifer A.
    [J]. NATURE MEDICINE, 2018, 24 (11) : 1649 - +
  • [3] Final analyses of OPTiM: a randomized phase III trial of talimogene laherparepvec versus granulocyte-macrophage colony-stimulating factor in unresectable stage III- IV melanoma
    Andtbacka, Robert H., I
    Collichio, Frances
    Harrington, Kevin J.
    Middleton, Mark R.
    Downey, Gerald
    Ohrling, Katarina
    Kaufman, Howard L.
    [J]. JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2019, 7
  • [4] Talimogene Laherparepvec Improves Durable Response Rate in Patients With Advanced Melanoma
    Andtbacka, Robert H. I.
    Kaufman, Howard L.
    Collichio, Frances
    Amatruda, Thomas
    Senzer, Neil
    Chesney, Jason
    Delman, Keith A.
    Spitler, Lynn E.
    Puzanov, Igor
    Agarwala, Sanjiv S.
    Milhem, Mohammed
    Cranmer, Lee
    Curti, Brendan
    Lewis, Karl
    Ross, Merrick
    Guthrie, Troy
    Linette, Gerald P.
    Daniels, Gregory A.
    Harrington, Kevin
    Middleton, Mark R.
    Miller, Wilson H., Jr.
    Zager, Jonathan S.
    Ye, Yining
    Yao, Bin
    Li, Ai
    Doleman, Susan
    VanderWalde, Ari
    Gansert, Jennifer
    Coffin, Robert S.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (25) : 2780 - U98
  • [5] [Anonymous], 2019, J CLIN ONCOL S
  • [6] Arance AM, 2019, ANN ONCOL, V30, P906
  • [7] Ascierto PA, 2017, EUR SOC MED ONC ESMO
  • [8] Update on tolerability and overall survival in COLUMBUS: landmark analysis of a randomised phase 3 trial of encorafenib plus binimetinib vs vemurafenib or encorafenib in patients with BRAF V600-mutant melanoma
    Ascierto, Paolo A.
    Dummer, Reinhard
    Gogas, Helen J.
    Flaherty, Keith T.
    Arance, Ana
    Mandala, Mario
    Liszkay, Gabriella
    Garbe, Claus
    Schadendorf, Dirk
    Krajsova, Ivana
    Gutzmer, Ralf
    de Groot, Jan Willem B.
    Loquai, Carmen
    Gollerkeri, Ashwin
    Pickard, Michael D.
    Robert, Caroline
    [J]. EUROPEAN JOURNAL OF CANCER, 2020, 126 : 33 - 44
  • [9] Immunological effects of BRAF plus MEK inhibition
    Ascierto, Paolo A.
    Dummer, Reinhard
    [J]. ONCOIMMUNOLOGY, 2018, 7 (09):
  • [10] Ipilimumab 10 mg/kg versus ipilimumab 3 mg/kg in patients with unresectable or metastatic melanoma: a randomised, double-blind, multicentre, phase 3 trial
    Ascierto, Paolo A.
    Del Vecchio, Michele
    Robert, Caroline
    Mackiewicz, Andrzej
    Chiarion-Sileni, Vanna
    Arance, Ana
    Lebbe, Celeste
    Bastholt, Lars
    Hamid, Omid
    Rutkowski, Piotr
    McNeil, Catriona
    Garbe, Claus
    Loquai, Carmen
    Dreno, Brigitte
    Thomas, Luc
    Grob, Jean-Jacques
    Liszkay, Gabriella
    Nyakas, Marta
    Gutzmer, Ralf
    Pikiel, Joanna
    Grange, Florent
    Hoeller, Christoph
    Ferraresi, Virginia
    Smylie, Michael
    Schadendorf, Dirk
    Mortier, Laurent
    Svane, Inge Marie
    Hennicken, Delphine
    Qureshi, Anila
    Maio, Michele
    [J]. LANCET ONCOLOGY, 2017, 18 (05) : 611 - 622