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Marvin Zelen (biostatistician) : ウィキペディア英語版
Marvin Zelen

Marvin Zelen (June 21, 1927 – November 15, 2014) was Professor Emeritus of Biostatistics in the Department of Biostatistics at the Harvard T.H. Chan School of Public Health (HSPH), and Lemuel Shattuck Research Professor of Statistical Science (the first recipient).〔(Awarded newly-established Lemuel Shattuck Research Professorship in Statistical Science, established and named by Harvard President Derek Bok, effective September 1, 2007 )〕 During the 1980s, Zelen chaired HSPH’s Department of Biostatistics. Among colleagues in the field of statistics, he was widely known as a leader who shaped the discipline of biostatistics.〔(HSPH Biostatistics Department Zelen Award page )〕 He "transformed clinical trial research into a statistically sophisticated branch of medical research."〔(Lagakos Symposium profile for Marvin Zelen )〕
Zelen was noted for his developing some of the statistical methods and study designs still used in clinical cancer trials, in which experimental drugs are tested for toxicity, effectiveness, and proper dosage. He introduced measures to ensure that data gathered from human trials would be as free as possible of errors and biases - measures that are now standard practice. Zelen helped transform clinical trial research into a well-managed and statistically sophisticated branch of medical science. His work in this area led to significant medical advances, such as improved treatments for several different forms of cancer. His research also focused on improved early detection of cancer; on modeling the progression of cancer and its response to treatment; and on using statistical models to help determine optimal screening strategies for various common cancers, especially breast cancer. Ironically, he died after a prolonged battle with cancer.
One of those experimental design models for randomized clinical trials is known as Zelen's design or Zelen's randomized consent design,〔(Joy Adamson & Sarah Cockayne & David J. Torgerson, Zelen's randomized consent design, Encyclopedia of Research Design, Neil J. Salkind, Ed., 2010, DOI: http://dx.doi.org/10.4135/9781412961288, Print ISBN 9781412961271; Online ISBN 9781412961288 )〕 in which patients are randomized to either the treatment or to the control group before they give their informed consent. Because the group to which any given patient is assigned is known at the time of consenting, the study patient's consent can be sought conditionally.
==Education==

* Diploma - Evander Childs High School, New York City, 1944
* B.S. - City College of New York, New York City, mathematics, 1949
* M.S. - University of North Carolina at Chapel Hill, mathematical statistics, 1951
* Ph.D. - American University, Statistics, 1957

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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