Paolo Baldo

Dr. Paolo Baldo

Centro di Riferimento Oncologico, Aviano, Italy
orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 June 2018 in International Journal of Clinical Pharmacy
Verified
Journal Article
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GFGiulia Fornasier
Giulia Fornasier
SFSara Francescon
Sara Francescon
RLRoberto Leone
Roberto Leone
Paolo BaldoPaolo Baldo
Paolo Baldo
Pharmacovigilance started about 170 years ago, although it was not yet named as such at that time. It is structured activity in the professional health field, with important social and commercial implications aimed at monitoring the risk/benefit ratio of drugs, improving patient’s safety and the quality of life. In this commentary we report the milestones of pharmacovigilance up to the present day, in order to understand all the steps that have characterized the historical evolution; from the first reports, which were essentially letters or warnings sent by clinicians to publishers of important and famous scientific journals, up to today’s modern and ultra-structured electronic registries. The historical phases also help us to understand why pharmacovigilance helped us to achieve such important results for man’s health and for pharmacology itself, and to identify the challenges that await Pharmacovigilance in future years.

1 December 2008 in Current Cancer Drug Targets
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Journal Article
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Paolo BaldoPaolo Baldo
Paolo Baldo
SCSara Cecco
Sara Cecco
EGElisa Giacomin
Elisa Giacomin
RLRenzo Lazzarini
Renzo Lazzarini
BRBarbara Ros
Barbara Ros
SMStefano Marastoni
Stefano Marastoni
Research into mTOR, mammalian Target Of Rapamycin as an important drug target continues to be extremely interesting, both in terms of the increased molecular knowledge being acquired at the basis of various human diseases, and also for possible applications in drug cancer therapy. The mTOR signaling system plays a key role in several transduction pathways that are necessary for cell cycle progression and cellular proliferation. Drugs known as mTOR inhibitors have been included in ongoing and in recently completed cancer trials. New insights into the mTOR signaling system are helping to clarify the functionality of key mTOR components, and especially their possible role in apoptosis, angiogenesis and tumor progression. Three other molecules, already approved for therapeutic use and being commercialized (Everolimius, Temsirolimus and Zotarolimus) are added to Rapamycin (also known as Sirolimus), the parent drug of the mTOR inhibitors. Of these, only Temsirolimus is currently approved in the treatment of renal cell carcinoma, while the others are approved for organ transplant rejection and coronary artery restenosis. There are at least 10 other molecules currently under development for clinical and preclinical studies. This review offers an updated synopsis of the mTOR signaling system, in particular as regards relevant aspects of cancer research, looks at the known mTOR inhibitors and gives a systematic vision of current trials for each individual molecule subject to clinical investigation.

14 September 2018 in Advances in Therapy
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Journal Article
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GFGiulia Fornasier
Giulia Fornasier
SFSara Francescon
Sara Francescon
Paolo BaldoPaolo Baldo
Paolo Baldo

12 September 2012 in Cochrane Database of Systematic Reviews
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Journal Article
Closed access
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Paolo BaldoPaolo Baldo
Paolo Baldo
CDCarolyn Doree
Carolyn Doree
PMPaola Molin
Paola Molin
DMDon McFerran
Don McFerran
SCSara Cecco
Sara Cecco

1 August 2018 in International Journal of Clinical Pharmacy
Verified
Journal Article
Open access
PDF file
Paolo BaldoPaolo Baldo
Paolo Baldo
GFGiulia Fornasier
Giulia Fornasier
LCLaura Ciolfi
Laura Ciolfi
ISIvana Sartor
Ivana Sartor
SFSara Francescon
Sara Francescon
Background Side effects of cancer therapy are one of the most important issues faced by cancer patients during their illness. Pharmacovigilance, namely the science and activities aimed at monitoring the safety of drugs, is particularly important in oncology, due to the intrinsic biologic toxicity of antineoplastic agents, their narrow therapeutic windows, and the high doses and rigid timing of treatment regimens. Aim of the review To identify the main issues in carrying out an effective pharmacovigilance activity in oncology. Method We searched PubMed for articles about pharmacovigilance in relation to chemotherapy, radiotherapy and targeted therapy for cancer, using MeSH terms and text words. We also searched Embase, CINAHL, Scopus, Micromedex, the Cochrane Library, two pharmacovigilance databases and the gray literature for articles published in 2012–2018. Overall, 137 articles were considered potentially relevant and were critically appraised independently by two authors, leading to the inclusion of 44 relevant studies, guidelines and reviews. Another 10 important research reports were included in the review. Results Eight critical issues of pharmacovigilance in oncology were identified. These issues pertain to: terminology; range of side effects; targeted therapy and immunotherapy; chemoradiotherapy; generic drugs and biosimilars; drug interactions, pharmacogenetics and polypharmacy; special patient categories; and under-reporting of ADRs. Conclusion The importance of pharmacovigilance in oncology must be highlighted with every effort, to improve safety and offer cancer patients every possible help to improve their quality of life during such a critical period of their lives.

18 October 2006
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Reference Entry
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Paolo BaldoPaolo Baldo
Paolo Baldo
CDCarolyn Doree
Carolyn Doree
RLRenzo Lazzarini
Renzo Lazzarini
PMPaola Molin
Paola Molin
DMDon McFerran
Don McFerran