An INTERVIEW with
Dr. Giorgio Parmiani
ESI Special Topics,
November 2005
Citing URL - http://www.esi-topics.com/melanoma/interviews/GiorgioParmiani.html
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the interview below, Special Topics talks with Dr. Giorgio
Parmiani of the Instituto Nazionale per lo Studio e la Cura
dei Tumori (INT) in Milan, Italy, about his highly cited
melanoma research. According to a recent analysis, Dr.
Parmiani’s work ranks at #8 among researchers publishing on
melanoma in the past decade, with 75 papers cited a total of
2,614 times. His most-cited paper ranks at #10 in our
analysis, with 411 cites, "Tumor regressions observed in
patients with metastatic melanoma treated with an antigenic
peptide encoded by gene MAGE-3 and presented by HLA-A1,"
(M Marchand et al., International Journal of Cancer
80:219-30, 1999). In the ISI
Essential
Science Indicators
Web product, Dr. Parmiani’s work appears in the fields of
Clinical Medicine and Immunology. At the INT, Dr. Parmiani is
deputy scientific director and the head of both the Unit of
Immunotherapy of Human Tumors and the Department of Diagnosis
and Innovative Therapies. He also holds a professorship of
oncology at the University of Milan.
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Why, in your view, is your work highly cited?
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“…the recent characterization of new molecular targets in melanoma cells will certainly generate new opportunity for more effective, non-immunological therapeutic interventions.”
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Because it is a typical translational research where findings are
obtained in the lab and attempts are made to assess their impact on
the disease by appropriate clinical trials. We thought that melanoma
was a good model to work with in this context.
What are the circumstances which led you to your work?
I wanted to spend a significant fraction of my time in research
to understand more on the biology of cancer as an essential step to
cure such a disease. As an M.D., I was particularly surprised by the
negative outcome of melanoma patients despite the alleged
immunogenicity of this tumor.
How would you describe the significance of this work for
your field?
We contributed to the molecular characterization of T-cell
recognized melanoma antigens and to the definition of the T-cell
response in patients, two crucial features for planning clinical
studies of immunotherapy of melanoma.
How much has this research advanced since you first started
publishing on it?
A lot. Nowadays we know the antigenic profile of melanoma cells,
the major features of the immune cell population involved in their
recognition (T, NK, NKT), and how are they regulated by other cells
and soluble factors (cytokines). This whole picture, while revealing
an unsuspected complexity in the activation and regulation of the
anti-tumor immune response and the interaction between tumor cells
with the microenvironment, allows the designing of new clinical
trials of immunotherapy.
Where do you see this research going 10 years from now?
Immunotherapy (vaccination or adoptive) is likely to become an
effective therapeutic option in melanoma, perhaps in combination
with other biological therapies. Moreover, the recent
characterization of new molecular targets in melanoma cells will
certainly generate new opportunity for more effective,
non-immunological therapeutic interventions. The many basic studies
in melanoma immunology have contributed significantly to understand
in more details the molecular pathogenesis of this disease.
Giorgio Parmiani, M.D.
Instituto Nazionale Tumori
Milan, Italy
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ESI Special Topics,
November 2005
Citing URL - http://www.esi-topics.com/melanoma/interviews/GiorgioParmiani.html
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