Targeted Therapies and Immuno-Oncology in Melanoma

A special issue of Journal of Clinical Medicine (ISSN 2077-0383). This special issue belongs to the section "Oncology".

Deadline for manuscript submissions: closed (30 November 2019) | Viewed by 11015

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Guest Editor
Centre for Cancer Biology, SA Pathology and University of South Australia, North Tce, Adelaide, SA 5001, Australia
Interests: cancer immunotherapy; T cell biology; checkpoint inhibitors; CAR-T cell therapy; melanoma; glioblastoma
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Special Issue Information

Dear Colleagues,

We are in the midst of a revolution in the treatment of melanoma. Less than a decade ago, patients with metastatic melanoma had no effective treatment options and prognosis was extremely poor, with melanoma being largely resistant to chemotherapy and radiotherapy. Now, newly developed immunotherapies and targeted therapies are changing this treatment landscape in dramatic ways.

Small molecule inhibitors targeting components of the MAPK signaling pathway (including inhibitors of BRAF and MEK) can induce rapid and dramatic tumor shrinkage. However, these benefits are usually not sustained long term. Identifying mechanisms of resistance and discovering approaches to overcome them has therefore become a key research question. Also of great value would be the identification of treatment strategies that prevent the development of resistance in the first place.

In contrast to targeted therapies, checkpoint blockade immunotherapy (for example, anti-PD1 and anti-CTLA-4) can induce long-lasting tumor regression. However, these deep responses are relatively rare, and the same treatment produces little or no benefit for other patients. The great challenge therefore remains to increase response rates so that all melanoma patients can benefit from this potentially curative treatment. This goal would be significantly advanced by a better understanding of the biology underpinning effective anti-cancer immune responses, and the identification of new therapeutic targets and combination strategies. And until these therapies become effective for all patients, the development of accurate methods to predict who is going to respond will support precision medicine approaches that avoid unnecessary toxicities and  target these expensive therapies to patients who will actually benefit.

This Special Issue welcomes submissions of original clinical research articles, case reports and high-quality reviews that address these and related questions, as well as articles on other novel approaches to melanoma therapy.

Dr. Lisa M. Ebert
Guest Editor

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Keywords

  • melanoma
  • targeted therapy
  • immunotherapy
  • checkpoint blockade
  • precision medicine
  • tumor immunology

Published Papers (2 papers)

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Review

17 pages, 806 KiB  
Review
Nanosystems for Improved Targeted Therapies in Melanoma
by Cristina Beiu, Calin Giurcaneanu, Alexandru Mihai Grumezescu, Alina Maria Holban, Liliana Gabriela Popa and Mara Mădălina Mihai
J. Clin. Med. 2020, 9(2), 318; https://doi.org/10.3390/jcm9020318 - 23 Jan 2020
Cited by 35 | Viewed by 3777
Abstract
Melanoma is one of the most aggressive forms of skin cancer, with limited therapeutic options. Since its incidence has been rapidly rising in recent years, the study of new targeted therapeutic strategies has increased. The implication of nanoscience in the development of alternative [...] Read more.
Melanoma is one of the most aggressive forms of skin cancer, with limited therapeutic options. Since its incidence has been rapidly rising in recent years, the study of new targeted therapeutic strategies has increased. The implication of nanoscience in the development of alternative targeted therapies for melanoma has multiple benefits and could significantly improve the outcome of melanoma patients. In this paper, we review the most recent progress in the field of targeted therapies, emphasizing the impact of nanoscale materials on the targeting and controlled release of anti-tumor drugs. The applications of nanomedicine in the management of melanoma are extensive and refer to sentinel lymph node mapping, chemotherapy, and RNA interference; each of these applications harboring the potential to develop efficient and personalized diagnostic techniques and therapies. Further research, especially in clinical trials, is needed to establish whether fighting melanoma on the nanoscale level represents the key to reaching a critical inflection point in mankind’s battle with metastatic melanoma. Full article
(This article belongs to the Special Issue Targeted Therapies and Immuno-Oncology in Melanoma)
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14 pages, 2109 KiB  
Review
The Clinical Trial Landscape for Melanoma Therapies
by Sonia Wróbel, Małgorzata Przybyło and Ewa Stępień
J. Clin. Med. 2019, 8(3), 368; https://doi.org/10.3390/jcm8030368 - 15 Mar 2019
Cited by 45 | Viewed by 6648
Abstract
(1) Despite many years of research, melanoma still remains a big challenge for modern medicine. The purpose of this article is to review publicly available clinical trials to find trends regarding the number of trials, their location, and interventions including the most frequently [...] Read more.
(1) Despite many years of research, melanoma still remains a big challenge for modern medicine. The purpose of this article is to review publicly available clinical trials to find trends regarding the number of trials, their location, and interventions including the most frequently studied drugs and their combinations. (2) We surveyed clinical trials registered in the International Clinical Trials Registry Platform (ICTRP), one of the largest databases on clinical trials. The search was performed on 30 November 2018 using the term “melanoma”. Data have been supplemented with the information obtained from publicly available data repositories including PubMed, World Health Organization, National Cancer Institute, Centers for Disease Control and Prevention, European Cancer Information System, and many others to bring the historical context of this study. (3) Among the total of 2563 clinical trials included in the analysis, most have been registered in the USA (1487), which is 58% of the total. The most commonly studied drug in clinical trials was ipilimumab, described as applied intervention in 251 trials. (4) An increase in the number of melanoma clinical trials using immunomodulating monoclonal antibody therapies, small molecule-targeted therapies (inhibitors of BRAF, MEK, CDK4/6), and combination therapies is recognized. This illustrates the tendency towards precision medicine. Full article
(This article belongs to the Special Issue Targeted Therapies and Immuno-Oncology in Melanoma)
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