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1.
J Eur Acad Dermatol Venereol ; 32(8): 1292-1296, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29341266

ABSTRACT

BACKGROUND: Merkel cell carcinoma (MCC) is a rare primary cutaneous neuroendocrine carcinoma. Owing to its low incidence, epidemiological data are scarce and have never been analysed in France to identify the main epidemiological trends. METHODS: Data from MCC patients diagnosed between 1998 and 2010 were obtained from 11 French cancer registries in the FRANCIM network. The main epidemiological characteristics of MCC were investigated between 2006 and 2010 because comprehensive data were only available for this period. The main focus was tumour incidence and mortality over time. RESULTS: Between 1998 and 2010, 562 cases of MCC were reported in the registries. From 2006 to 2010 (290 cases), European- and world-standardized incidence rates were 0.26 and 0.43 per 100,000 person-years in men and 0.24 and 0.38 per 100,000 person-years in women. MCC is more frequent in females in France (56.9%) with male/female ratio 1.1. Relative survival rates were 84%, 56% and 42% at one, three and 5 years, respectively. CONCLUSIONS: The incidence of MCC clearly increased over time in all areas under focus. The standardized incidence in France was comparable to the incidence observed in other countries for the same period, but French data are too recent to conclude on an increase in MCC incidence. Prognosis remains poor in all countries in which data are available.


Subject(s)
Carcinoma, Merkel Cell/epidemiology , Skin Neoplasms/epidemiology , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Carcinoma, Merkel Cell/mortality , Child , Child, Preschool , Epidemiologic Studies , Female , France/epidemiology , Humans , Incidence , Infant , Infant, Newborn , Male , Middle Aged , Registries , Retrospective Studies , Sex Factors , Skin Neoplasms/mortality , Survival Rate , Young Adult
2.
Rev Epidemiol Sante Publique ; 65(4): 301-308, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28579185

ABSTRACT

BACKGROUND: In retrospective case-control studies performed following nuclear tests or nuclear accidents, individual thyroid radiation dose reconstructions are based on fallout and meteorological data from the residential area, demographic characteristics, and lifestyle as well as dietary information. Collecting the latter is a controversial step, as dietary declarations may be affected by the subjects' beliefs about their risk behavior. This report analyses the potential for such bias in a case-control study performed in eastern France. METHODS: The study included 765 cases of differentiated thyroid carcinoma matched with 831 controls. Risk perceptions and beliefs of cases and controls were compared using Chi2 tests and differences in dietary reports were analyzed using a two-way ANOVA. RESULTS: In general, atmospheric pollution and living near a nuclear power plant were the two major risks that may influence thyroid cancer occurrence cited by cases and controls. When focusing in particular on the consequences of the Chernobyl accident, cases were more likely to think that the consequences were responsible for thyroid cancer occurrence than controls. Vegetable consumption during the two months after the Chernobyl accident was correlated with the status of subjects, but not to their beliefs. Conversely, consumption of fresh dairy products was not correlated with the status or beliefs of subjects. CONCLUSION: We found no evidence of systematic bias in dietary reports according to the status or beliefs held by subjects about the link between thyroid cancer occurrence and Chernobyl fallout. As such, these dietary reports may be used in further studies involving individual dosimetric reconstructions.


Subject(s)
Chernobyl Nuclear Accident , Diet Records , Feeding Behavior/psychology , Food Contamination, Radioactive , Perception , Radioactive Fallout , Thyroid Neoplasms/epidemiology , Adolescent , Adult , Bias , Case-Control Studies , Child , Disasters , Female , France/epidemiology , Humans , Male , Nuclear Power Plants , Nutrition Surveys , Radioactive Fallout/analysis , Radioactive Fallout/statistics & numerical data , Retrospective Studies , Risk Factors , Risk Reduction Behavior , Young Adult
3.
J Stomatol Oral Maxillofac Surg ; 118(2): 84-89, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28330788

ABSTRACT

Despite the frequency and lethality of oral cancers in France, there are no detailed general population data regarding the characteristics of these patients to fuel the public health authorities' reflections about early detection policies. Thus, the objective of this study was to determine, in the general population, the characteristics of both patients and tumours at the time of the diagnosis. A high-resolution, population-based study using 13 French registries was conducted on 1089 tumours diagnosed in 2010. Men accounted for 75% of cases. The most frequent sites were tonsil (28.4%) and oral tongue (21.1%). The median age varied from 56.7 years for floor of mouth to 66.4 years for gum. The lesions were mainly diagnosed on pain and those diagnosed after routine clinical examination were scarce (2.6%). There were 65.5% stage III and IV at diagnosis. Oral tongue, floor of mouth and palate presented tumours less than 2cm only in 34 to 40% of cases. Advanced stage was associated with the presence of comorbidities, and tonsil or base of tongue topography. Stage was not associated with Département, deprivation index or gender. This study provided a picture of the characteristics of oral cancer patients and their tumours and showed that diagnoses are often made late, even for those tumours most easily accessible to direct visual and tactile examination. Nevertheless, it remains to define the target population of an early detection and to evaluate the benefit of such detection on the mortality rate.


Subject(s)
Early Detection of Cancer/statistics & numerical data , Mouth Neoplasms/diagnosis , Mouth Neoplasms/epidemiology , Adult , Aged , Aged, 80 and over , Female , France/epidemiology , Humans , Incidence , Male , Mass Screening/methods , Mass Screening/statistics & numerical data , Middle Aged , Mouth Neoplasms/pathology , Neoplasm Staging , Registries
4.
NeuroRx ; 2(4): 683-95, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16489375

ABSTRACT

Drug development for CNS disorders faces the same formidable hurdles as other therapeutic areas: escalating development costs; novel drug targets with unproven therapeutic potential; and health care systems and regulatory agencies demanding more compelling demonstrations of the value of new drug products. Extensive clinical testing remains the core of registration of new compounds; however, traditional clinical trial methods are falling short in overcoming these development hurdles. The most common CNS disorders targeted for drug treatment are chronic, slowly vitiating processes manifested by highly subjective and context dependent signs and symptoms. With the exception of a few rare familial degenerative disorders, they have ill-defined or undefined pathophysiology. Samples selected for treatment trials using clinical criteria are inevitably heterogeneous, and dependence on traditional endpoints results in early proof-of-concept trials being long and large, with very poor signal to noise. It is no wonder that pharmaceutical and biotechnology companies are looking to biomarkers as an integral part of decision-making process supported by new technologies such as genetics, genomics, proteomics, and imaging as a mean of rationalizing CNS drug development. The present review represent an effort to illustrate the integration of such technologies in drug development supporting the path of individualized medicine.


Subject(s)
Biomarkers , Central Nervous System Agents/pharmacology , Central Nervous System Diseases/drug therapy , Drug Design , Technology, Pharmaceutical/methods , Animals , Central Nervous System Diseases/genetics , Drug Evaluation, Preclinical/methods , Gene Expression , Gene Expression Profiling , Humans , Pharmacogenetics/methods , Pharmacogenetics/trends
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