Rogerio De Figueiredo profile picture
De Figueiredo
Docent, Institute of Biomedicine
InFLAMES Flagship
Academy Research Fellow, Institute of Biomedicine

Areas of expertise

Cancer Immunobiology and Immunotherapy
pharmacology and biochemistry with emphasis in drug discovery.


At the Institute of Translational Medicine, University of Liverpool, UK.

2018 - 2019  Lectures in the North West Cancer Research Seminar Series. Topic: Immunotherapy and Immune profile of Melanoma

At the Experimental Oncology Unit, Federal University of São Paulo.

2015 - 2017 Lectures on Cancer Immunology and Advanced Molecular and Cellular Immunology at the Department of Microbiology, Immunology, and Parasitology.  

At the Ibirapuera University, São Paulo

2015 - 2016  Lectures on Immunology, Microbiology, Epidemiology, Health promotion in the elderly, Molecular Biology


In Europe, the highest incidence rates of melanoma occur in Nordic countries and Switzerland, where the inhabitants are predominantly light-skinned. In Finland, melanoma is the 5th most prevalent form of cancer with 1.669 new cases per year (Globocan 2018, WHO).

Immunotherapies that target immune checkpoint regulatory (ICR) molecules, such as the cytotoxic T lymphocyte antigen 4 (CTLA-4) and the programmed cell death 1 (PD-1), also called immune checkpoint blockers (ICB) have become standard treatments for metastatic melanoma and other cancer types, achieving impressive clinical improvements.

However, only a subset of cancer patients shows clinical benefits with these treatments. In metastatic melanoma, 20% of patients with distant metastasis achieve 5-year survival following immunotherapies using ICB, and the vast majority are refractory or will relapse the initial treatments by developing resistance mechanisms.

Therefore, understanding the fundamental mechanisms that underlie ICB resistance in metastatic melanoma, and developing strategies that mitigate these mechanisms are critical steps to unleash the full power of ICBs. 

By applying state-of-the-art technologies, including Mass Cytometry and Digital Spatial Profiling (NanoString), we are uncovering novel pathways associated with ICB resistance, mostly involved in the mechanisms of T lymphocyte suppression, which will provide new directions towards combinatory therapies for metastatic cutaneous and uveal melanoma. 

These strategies are based on the combination of new drugs developed in my group, the Melanoma Immune Oncology Research Group (MIORG), or the validation of already approved molecules in clinical trials for the management of other diseases. These treatments are selected as potential candidates to modulate or reverse the immune profile of metastatic melanoma associated with innate and acquired resistance to immunotherapies. 

My research is aligned with sustainable development by engaging a participatory society for citizens. We are committed to promoting equal opportunities to enable all people to have access to the most recent updates related to the field of metastatic melanoma prognostication and therapy in Finland and worldwide.


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