Johnson A (2019). Textbooks and other publications on controlled clinical trials, 1948 to 1983.

© Tony Johnson, Medical Research Council Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, 90 High Holborn, London WC1V 6LJ. Email: tony.johnson11@ntlworld.com.


Cite as: Johnson A (2019). Textbooks and other publications on controlled clinical trials, 1948 to 1983. JLL Bulletin: Commentaries on the history of treatment evaluation (https://www.jameslindlibrary.org/articles/textbooks-and-other-publications-on-controlled-clinical-trials-1948-to-1983/)


This article is dedicated to the memory of Douglas G Altman (1948-2018), a dear friend and colleague, who was always good company, and who did so much to achieve better understanding of all aspects of clinical trials

Introduction

The evolution of controlled clinical trials to assess the effects of medical interventions began in the 1720s; progressed slowly through the 19th century; and gathered speed during the first half of the 20th century (Chalmers et al. 2011). Controlled clinical trials had increased particularly rapidly during the 1930s and 1940s, but it was a report of the Medical Research Council’s trial of streptomycin for pulmonary tuberculosis published in 1948 which attracted international attention, particularly for the clear description of what had been done and found. Contrary to widespread belief, the MRC streptomycin trial was not the earliest example of the use of random allocation to generate treatment comparison groups; but it does appear to be the earliest example of a randomized clinical trial in which steps had been taken to prevent foreknowledge of allocations, and so reduce the risk of biased tampering with the treatment allocation schedule (Chalmers 2010)

The streptomycin trial ushered in a golden age of MRC clinical trials during the 1950s and 1960s (Chalmers 2013), and this was reflected in articles and books referring to this research design, written by some of the scientists involved. One of the best known of these was Principles of Medical Statistics, a book based on a series of articles published in the Lancet in 1937 and which became a classic (Farewell and Johnson 2011). The author of the book was Austin Bradford Hill, a member of the team responsible for the streptomycin trial. Although controlled trials were mentioned briefly in the first edition of Hill’s book, it was not until the sixth edition, published in 1955, that a chapter specifically about clinical trials was introduced.

The earliest whole book focussing specifically on controlled trials I have been able to identify was also published in 1955. The author, Gustav Herdan (1897-1968), was an interesting polymath, with degrees from the German University in Prague for studies in law and sinology (East Asian languages) and English philology, and, after moving to England in 1938, a degree in mathematics and statistics. This mixture of talents led him to be a founder of quantitative linguistics. He became a lecturer in statistics at Bristol University in 1948, and it was while in that post that his book Statistics of Therapeutic Trials was published by Elsevier (Herdan 1955).

Between 1955 and 1960, seven further documents appeared – two published in 1958 were reports of symposia in London [Appendix Nos. 2 and 3); the third was an American book entitled The clinical evaluation of new drugs [Appendix No. 4]; and the 5th, 6th and 7th were books by British authors. The last of these was based on a meeting in Vienna organised by Bradford Hill under the aegis of UNESCO and was published in French as well as English (Bird 2014).

In the following years, further books arrived thick and fast. I have assembled all those I have found between Herdan’s 1955 book and that by Stuart Pocock published in 1983. The latter became both a major teaching text and an important source of reference for statisticians and doctors, to the extent that although it was never revised after the first edition it remains popular today.

What of the intervening years between 1960 and 1983? This was a period when the pharmaceutical industry was becoming interested in the new trial methodology, wanted to understand it, and to exploit it in their drug development programmes. At the same time, academic institutions, funding agencies and research organisations were also becoming interested and wanted to apply the methodology and extend it into programmes beyond drug evaluation, such as psychotherapy. There may be an impression that outside of scientific papers, comparatively little on clinical trials was published during this early period when in fact the converse is true. I have provided details of publications from 1948 to 1983, including their contents, with extracts from prefaces or forewords to convey their aims and scope. I have also added information about editors and authors, with their qualifications and locations, to provide some idea of their background in the field of clinical trials. In addition, I have made brief comments in a preamble to some of the texts. This detailed information can be consulted in the Appendix to this article on the James Lind Library.

How did I decide which books to include in the bibliography?

An initial list of texts was developed many years ago from a selection of booklets and texts belonging to Dr Ian Sutherland, Director of the Medical Research Council (MRC) Statistical Research and Services Unit in London (from 1969 to 1980), and of the MRC Biostatistics Unit in Cambridge (from 1980 to 1986). Ian Sutherland joined the MRC from the Institute of Social Science in Oxford in 1952, and he attended some of the meetings from which these early publications arose.

Decisions about inclusion and exclusion of specific publications were not easy. Basically, I have endeavoured to include those whose content extends beyond clinical pharmacology and basic experimental design to clinical assessment of drugs and other treatment modalities, and where consideration of clinical trials extends to more than a single chapter or paper. I have excluded papers in journals unless they appear as an issue devoted to a working party report, symposium, or conference. However, it is worth noting that during the period of interest the first journals devoted specifically to clinical trials were published. The first, Clinical Trials Journal, appeared in November 1964 and was published by Stuart Phillips Publications based in Sutton, Surrey, England, with Editor-in-Chief, Dr Kenneth Maclean MA, MD, FRCP; its aim was to record and provide reference to correctly conducted, ethical clinical trials. It continued until 1990 (volume 27) and then re-emerged as Clinical Trials and Meta-analysis (published by Elsevier) from 1992 to 1994 (volumes 28 and 29). From 1995 it was integrated into the second journal, Controlled Clinical Trials: Design, Methods, and Analysis, which started in 1980 with Editor, Dr Curtis Meinert PhD. It was published by Elsevier and became the designated journal of the Society for Clinical Trials, which was founded in USA in 1978. Coincidentally, in the same year, the International Society for Clinical Biostatistics was founded in Europe.

Altogether I have listed sixty-nine publications that appeared over the thirty-six-year period from 1948 (the year the MRC streptomycin trial was published) to 1983 (the year Pocock’s book was published.  Dividing this period of 36 years into five sextennial intervals shows no publications (1948-1953), five (1954-59), seven (1960 to 1965), twelve (1966 to 1971), fifteen (1972 to 1977), and thirty (1978 to 1983), respectively – a curvilinear increase with mode eight, unsurprisingly, towards the end of the period in 1981. Although I have included some publications in French and German in the series, it is inevitable that I will have either missed or have not been able to trace some relevant publications, particularly those in languages other than English.  I wish to be informed of potentially eligible candidates.

Over the period from 1948 to 1983 the concept of the randomised clinical trial was fully developed and underpinned by essential understanding of design, conduct, data collection, analysis and reporting, and the overarching principles of ethics and management; some or all of these appear within the individual texts presented. However there are several fundamental topics that were not covered by individual texts specifically within the context of clinical trials until after 1983; these are cross-over trials (first covered by B Jones and MG Kenward (1989) Design and Analysis of Cross-Over-Trials); group (cluster) randomised trials (DM Murray (1998) Design and Analysis of Group Randomized Trials); meta-analysis (AJ Sutton, KR Abrams, DR Jones, T Sheldon, and F Song (2000) Methods for Meta-Analysis in Medical Research and D Stangl and DA Berry (2000) Meta-Analysis in Medicine and Health Policy),  and sample size determination (D Machin and MJ Campbell (1987) Statistical Tables for the Design of Clinical Trials).

Presentation

I have numbered the publications in chronological order (and by alphabetical order of authorship within each year). For each entry I have provided the following details in the Appendix published in the James Lind Library :

  1. Authorship and year of publication; with title and publisher;
  2. A preamble for some publications to provide cross-references to other relevant publications in the list below, as well as reference to other editions either within the list, or published after 1983. For some reports from specific organisations, such as the World Health Organisation (WHO), there are references to other reports from the same or other organisations that have some bearing on drug testing but are not included in the list. Finally, there are comments on specific texts that may be regarded as milestones in the evolution of clinical trials.
  3. Aims of each publication as stated in Forewords and Prefaces. These are intended to provide an overview of each publication, and are extracts, not necessarily contiguous text.
  4. Contents (and total number of pages) comprising part, chapter, section and sub-section headings, but not sub-subsection headings unless the volume of text is substantial. (Omission of headings is noted for each publication where relevant);
  5. Details of authors including titles and qualifications with place of work when available. For publications under the umbrella of an Editor or Committee the names of contributors appear with chapter titles. These details provide some idea of the expertise of those contributing to the publications, the balance between industry, academia and regulators, and enable tracking of individuals who made multiple contributions (I have not included lists of participants at meetings; these can sometimes be found, in the original publications).

An initial analysis

I hope that the resource I have created will be used by others interested in the history of controlled clinical trials. As an example of the kind of analysis I have in mind I have indicated in the Table below notable publications that were milestones in the series drawing attention to methodological insights or developments. Other milestones could have been chosen. I believe that most of these milestones are the first examples of books which illustrate or include particular methodological features. However, earlier examples may exist and I would be happy to have these drawn to my attention.

Table:  Some notable milestones in texts of clinical trials (1948 to 1983)

Appendix Article No. YearMilestone
11955The first published textbook on clinical trials.
21958First medical text setting out the rationale for random allocation.
31959A text including a chapter on sequential analysis.
51959The first (multi-author) textbook to include ‘Clinical Trials’ in the title;
61960

 

First single-author comprehensive textbook on clinical trials written by a medical statistician; first text on sequential trials; and first book to include sample size Tables and confidence intervals.
71960First text on clinical trials published in a language other than English.
101962Austin Bradford Hill’s only comprehensive textbook on clinical trials.
111963First comprehensive text to cover legal, ethical and moral aspects of controlled clinical trials in humans.
131966First of many WHO monographs and technical reports on clinical trials.
141967First text devoted to trials in a sub-specialty of medicine; and first text to include a section on crossover trials.
17

 

1968

 

Possibly the first text with a section on protocols for clinical trials.

First text with appendices of Tables for sample size calculations; and

21

 

1970

 

The first co-authored by both a physician and a statistician.

First textbook to distinguish between explanatory and pragmatic trials.

231970An early attempt to teach clinical trials using computer simulation.
25

 

1972

 

First text devoted to multi-centre clinical trials.

First text devoted to applied statistics in the pharmaceutical industry.

431979First text on clinical trials to include a chapter on survival analysis.


Acknowledgements

It is my pleasure to acknowledge the help and advice of Iain Chalmers, with whom a chance conversation generated the idea for this odyssey and whose guidance was key to its presentation.

Examining books and reports for inclusion in (or exclusion from) the list in the Appendix, as well as compiling details of their contents, authors, and aims, would have been impossible without access to the originals. I thank Vern Farewell for retrieving material held in the Bradford Hill Library, Medical Research Council Biostatistics Unit, Cambridge, and librarians and staff in the British Library, London; the Library at the London School of Economics and Political Science, London; the University of Cambridge Library, the Betty and Gordon Moore Library, Cambridge, and the Wellcome Library, London. I thank Dr Curtis Meinert who looked at my original list of publications and who pointed out several important omissions that are now included.

 

References

Bird SM (2014). The 1959 meeting in Vienna on controlled clinical trials – a methodological landmark. JLL Bulletin: Commentaries on the history of treatment evaluation (https://www.jameslindlibrary.org/articles/the-1959-meeting-in-vienna-on-controlled-clinical-trials-a-methodological-landmark/)

Chalmers I (2010). Why the 1948 MRC trial of streptomycin used treatment allocation based on random numbers. JLL Bulletin: Commentaries on the history of treatment evaluation (https://www.jameslindlibrary.org/articles/why-the-1948-mrc-trial-of-streptomycin-used-treatment-allocation-based-on-random-numbers/)

Chalmers I (2013). UK Medical Research Council and multicentre clinical trials: from a damning report to international recognition. JLL Bulletin: Commentaries on the history of treatment evaluation (https://www.jameslindlibrary.org/articles/uk-medical-research-council-and-multicentre-clinical-trials-from-a-damning-report-to-international-recognition/)

Chalmers I, Dukan E, Podolsky SH, Davey Smith G (2011). The advent of fair treatment allocation schedules in clinical trials during the 19th and early 20th centuries. JLL Bulletin: Commentaries on the history of treatment evaluation (https://www.jameslindlibrary.org/articles/the-advent-of-fair-treatment-allocation-schedules-in-clinical-trials-during-the-19th-and-early-20th-centuries/)

Farewell V, Johnson A (2011). The origins of Austin Bradford Hill’s classic textbook of medical statistics. JLL Bulletin: Commentaries on the history of treatment evaluation (https://www.jameslindlibrary.org/articles/the-origins-of-austin-bradford-hills-classic-textbook-of-medical-statistics/)

Herdan G (1955). Statistics of Therapeutic Trials. Amsterdam: Elsevier

Jones B, Kenward MG (1989). Design and Analysis of Cross-Over-Trials. London: Chapman and Hall.

Machin D, Campbell MJ (1987). Statistical Tables for the Design of Clinical Trials. Oxford: Blackwell scientific publications.

Murray DM (1998). Design and Analysis of Group Randomized Trials. New York: Oxford University Press Inc.

Stangl D, Berry DA (2000). Meta-Analysis in Medicine and Health Policy, New York: Marcel Dekker, Inc.

Sutton AJ, Abrams KR, Jones DR, Sheldon T, Song F (2000). Methods for Meta-Analysis in Medical Research. Chichester: Wiley.

 
Appendix

Contents
(1)Gustav Herdan (1955), Statistics of Therapeutic Trials
(2)Report of a Symposium on Clinical Trials held at the Royal Society of Medicine, London on Friday, April 25th, 1958 (1958)
(3)DR Laurence (ed) (1959), Quantitative Methods in Human Pharmacology and Therapeutics. Proceedings of a symposium held in London on 24th and 25th March 1958
(4)Fourteen Authors [SO Waife and AP Shapiro (eds)] (1959), The Clinical Evaluation of New Drugs
(5)LJ Witts (ed) (1959), Medical Surveys and Clinical Trials: some methods and applications of group research in medicine
(6)Peter Armitage (1960), Sequential Medical Trials
(7)Organised under the direction of Professor A Bradford Hill (1960), Controlled Clinical Trials, and, D Schwartz, R Flamant, J Lellouch, C Rouquette (1960), Les essais therapeutiques cliniques: methods scientifique d’appreciation d’un traitement
(8)Francis M Forster (ed) (1961), Evaluation of Drug Therapy
(9)Max Hamilton (1961), Lectures on the Methodology of Clinical Research
(10)Sir Austin Bradford Hill (1962), Statistical Methods in Clinical and Preventive Medicine
(11)Irving Ladimer and Roger W Newman (1963), Clinical investigation in medicine: legal, ethical and moral aspects: an anthology and bibliography
(12)LJ Witts (ed) (1964), Medical Surveys and Clinical Trials: some methods and applications of group research in medicine (Second Edition)
(13)TM Pollock (1966), Trials of prophylactic agents for the control of communicable diseases: a guide to their organization and evaluation
(14)JB Chassan (1967), Research Design in Clinical Psychology and Psychiatry
(15)Greenberg Report (1967), Organization, review, and administration of cooperative studies
(16)Kenneth R Cox (1968), Planning Clinical Experiments
(17)Cyril Maxwell (1968), Foundation Course in Clinical Trials
(18)World Health Organization Scientific Group (1968), Principles for the clinical evaluation of drugs
(19)Cyril Maxwell (1969), Clinical Trials Protocol: a Primer for Clinical Trials
(20)Ben-Zion Taber (1969), Proving New Drugs: a Guide to Clinical Trials
(21)Walter J Burdette and Edmund A Gehan (1970), Planning and Analysis of Clinical Studies
(22)EL Harris and JD Fitzgerald (eds) (1970), The Principles and Practice of Clinical Trials
(23)Daniel Schwartz, Robert Flamant, and Joseph Lellouch (1970), L’essai thérapeutique chez l’homme
(24)Jerome Levine, Burtrum C Schiele, and Lorraine Bouthilet (eds) (1971), Principles and Problems in Establishing the Efficacy of Psychotropic Agents
(25)Cyril Maxwell, FR Smith, and Leong Ket Shing (1972), Instant Experience in Clinical Trials: a computerised teaching aid
(26)AJ Jouhar and MF Grayson (1973),  International Aspects of Drug Evaluation and Usage
(27)Cyril Maxwell (1973), Clinical Research For All
(28)World Health Organization Regional Office for Europe (1973), Clinical pharmaceutical evaluation in drug control: report on a symposium convened by the Regional Office for Europe of the World Health Organization, Heidelberg, 27-30 November 1972 (EURO 7406)
(29)Max Hamilton (1974), Lectures on the Methodology of Clinical Research (second edition)
(30)Medico-Pharmaceutical Forum (1974), A Report by the Forum’s Working Party on Clinical Trials
(31)International Union Against Cancer (1974), Controlled Therapeutic Trials in Cancer
(32)Peter Armitage (1975), Sequential Medical Trials (Second edition)
(33)World Health Organization Scientific Group (1975), Guidelines for Evaluation of Drugs for Use in Man
(34)CS Good (ed) (1976), The Principles and Practice of Clinical Trials
(35)PE Lucchelli, N Bergamini, and V Bachini (eds) (1976), Rationality in Drug Development
(36)WHO Regional Office for Europe (1976), Randomized Trials in Preventive Medicine and Health Service Research: report on a study group, Copenhagen, 8-12 December 1975
(37)Association of the British Pharmaceutical Industry (1977), Guidelines for Preclinical and Clinical Testing of New Medicinal Products, Part 1: Laboratory investigations, Part 2: Investigations in Man
(38)F Neil Johnson and Susan Johnson (eds) (1977), Clinical Trials
(39)US Department of Health, Education, and Welfare (1977), General Considerations for the Clinical Evaluation of Drugs
(40)P Armitage, D Bardelli, DAG Galton, EA Gehan, GA Higgins, K Magnus, AB Miller, SJ Pocock, and R Saracci (eds) (1978), Methods and Impact of Controlled Therapeutic Trials in Cancer: part I
(41)Byrom W Brown Jr (1978), Statistical Controversies in the Design of Clinical Trials
(42)JL Lortat-Jacob, G Mathé, and J Servier (1978), International meeting on comparative therapeutic trials
(43)JP Boissel and CR Klimt (eds) (1979), Essais Controles Multicentres: Principes et Problemes / Multi-centre Controlled Trials: Principles and Problems
(44)JB Chassan (1979), Research Design in Clinical Psychology and Psychiatry
(45)National Conference on Clinical T rials Methodology (1979), Clinical Pharmacology and Therapeutics
(46)Jerome Levine (ed) (1979), Coordinating Clinical Trials in Psychopharmacology: Planning, Documentation and Analysis
(47)Henri J Tagnon and Maurice J Staquet (eds) (1979), Controversies in cancer: design of trials and treatment.
(48)World Health Organization Regional Office for Europe (1979), Clinical Pharmacological Evaluation in Drug Control
(49)National Institutes of Health Symposium (1980), Issues in Research with Human Subjects
(50)Daniel Schwartz, Robert Flamant, and Joseph Lellouch (1980), L’essai therapeutique chez l’homme (Second edition); Clinical Trials (Translated by MJR Healy)
(51)John M Weiner (1980), Issues in the Design and Evaluation of Medical Trials
(52)JF Bithell and R Coppi (eds) (1981), Perspectives in Medical Statistics
(53)K Breddin and CR Klimt (eds) (1981), Second International Symposium on Clinical Trials
(54)C Ralph Buncher and Jia-Yeong Tsay (eds) (1981), Statistics in the Pharmaceutical Industry
(55)Lawrence M Friedman, Curt D Furberg, and David L DeMets (1981), Fundamentals of Clinical Trials
(56)Marsha D Hopwood, John C Mabry, and William L Sibley (1981), The Role of General Clinical Research Centers in Clinical Trials: a characterization with recommendations
(57)N Sartorius and H Helmchen (eds) (1981), Multicentre Trials
(58)Stanley KE, Stjernsward J, and Isley M (1981), The Conduct of a Cooperative Clinical Trial
(59)N Victor, J Dudeck, and EP Broszio (eds) (1981), Therapiestudien
(60)Thomas C Chalmers and Peter Amacher (eds) (1982), Proceedings of a conference on Recent History of Randomized Clinical Trials
(61)Sheila M Gore (1982), Statistics in Question: Assessing Clinical Trials
(62)Valerie Miké and Kenneth E Stanley (eds) (1982), Statistics in Medical Research: Methods and Issues, with Applications in Cancer Research
(63)Niels Tygstrup, John M Lachin, and Erik Juhl (eds) (1982), The Randomized Clinical Trial and Therapeutic Decisions
(64)Sibylle Biefang, Wolfgang Köpcke, and Martin A Schreiber (1983), Manual for the planning and Implementation of Therapeutic Studies
(65)Christopher J Bulpitt (1983), Randomised Controlled Clinical Trials
(66)Paul L Canner (ed) (1983), The Coronary Drug Project
(67)Stanley H Shapiro and Thomas A Louis (eds) (1983), Clinical Trials: Issues and Approaches
(68)John Whitehead (1983), The Design and Analysis of Sequential Clinical Trials
(69)Stuart J Pocock (1983), Clinical Trials: A Practical Approach

Stuart Pocock’s 1983 book closes the period of this survey of books on controlled clinical trials.

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