Beginning in mid-February 2008, the 1997-2007 online version of the Science Watch® newsletter, ESI-Topics.com, and in-cites.com, will all be featured together on the redesigned ScienceWatch.com. All previous content from the three sites will be permanently archived, and remain accessible from any existing bookmarks to the archived pages. No new content will be added to this site. Updates and new content (updated biweekly) are available at ScienceWatch.com now.
Thomson
Essential Science Indicators - Special Topics  RSS feeds for the editorial Web sites of Essential Science Indicators.
All Topics Menu
Help || About || Contact

  
|  Previous Page  |
  |  Special Topics Menu  |  |  Next Page  |
  

ESI Special Topic of:
"Melanoma," Published September 2005

•> Search Special Topics
Melanoma Menu

Melanoma

An INTERVIEW with Dr. Giorgio Parmiani

ESI Special Topics, November 2005
Citing URL - http://www.esi-topics.com/melanoma/interviews/GiorgioParmiani.html

In 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.

ST:  Why, in your view, is your work highly cited?


“…the recent characterization of new molecular targets in melanoma cells will certainly generate new opportunity for more effective, non-immunological therapeutic interventions.”

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.

ST:  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.

ST:  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.

ST:  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.

ST:  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.End

Giorgio Parmiani, M.D.
Instituto Nazionale Tumori
Milan, Italy

ESI Special Topics, November 2005
Citing URL - http://www.esi-topics.com/melanoma/interviews/GiorgioParmiani.html

ESI Special Topic of:
"Melanoma," Published September 2005

•> Search Special Topics
Melanoma Menu || All Topics Menu ||
Interview Index
Help || About || Contact

ScienceWatch.com - Tracking Trends and Perfomance in Basic Research
Go to the new ScienceWatch.com

Write to the Webmaster with questions/comments. Terms of Usage.
The Research Services Group of Thomson Scientific |
(c) 2008 The Thomson Corporation.