TY - JOUR
T1 - Strategic use of new generation antidepressants for depression
T2 - SUN(^_^) D protocol update and statistical analysis plan
AU - for the SUN(^_^)D Investigators
AU - Yonemoto, Naohiro
AU - Tanaka, Shiro
AU - Furukawa, Toshi A.
AU - Kato, Tadashi
AU - Mantani, Akio
AU - Ogawa, Yusuke
AU - Tajika, Aran
AU - Takeshima, Nozomi
AU - Hayasaka, Yu
AU - Shinohara, Kiyomi
AU - Miki, Kazuhira
AU - Inagaki, Masatoshi
AU - Shimodera, Shinji
AU - Akechi, Tatsuo
AU - Yamada, Mitsuhiko
AU - Watanabe, Norio
AU - Guyatt, Gordon H.
N1 - Funding Information:
This trial was funded by a Grant-in-Aid from the Ministry of Health, Labor and Welfare, Japan (H22-Seishin-Ippan-008) (from April 2010 to March 2012) and by a research project “Pragmatic Psychopharmacotherapy Research” of the Japan Foundation for Neuroscience and Mental Health (from April 2012 to present).
Funding Information:
NY has received grants or research support from the Japanese Ministry of Education, Science, and Technology; the Japanese Ministry of Health, Labor and Welfare; and the Japanese Society of Clinical Pharmacology and Therapeutics. ST has received lecture fees from Kobe City, Astra-Zeneca, Taiho and Ono. He has received consultation fees from the Pharmaceuticals and Medical Devices Agency, DeNA Life Science, and CanBus. He has received outsourcing fees from the Public Health Research Foundation, Japan Breast Cancer Research Group, Satt, and Asahi Kasei Pharma. He has received research funds from the Japanese Ministry of Education, Science, and Technology and the Japanese Ministry of Health, Labor and Welfare. His wife has been engaged in a research project of Bayer. TAF has received lecture fees from Eli Lilly, Meiji, Mochida, MSD, Otsuka, Pfizer and Tanabe-Mitsubishi, and consultancy fees from Sekisui Chemicals and Takeda Science Foundation. He has received royalties from Igaku-Shoin, Seiwa-Shoten and Nihon Bunka Kagaku-sha publishers. He has received grant or research support from the Japanese Ministry of Education, Science, and Technology, the Japanese Ministry of Health, Labor and Welfare, the Japan Society for the Promotion of Science, the Japan Foundation for Neuroscience and Mental Health, Mochida and Tanabe-Mitsubishi. TK has received lecture fees from Eli Lilly and Tanabe-Mitsubishi, and has contracted research with GlaxoSmithKline, MSD and Tanabe-Mitsubishi. He has received royalties from Kyowa Yakuhin and Medical Tribune. YO has received honoraria for speaking at meetings sponsored by Eli Lilly and research funds from the Japan Society for the Promotion of Science. AT has received honoraria for speaking at a meeting sponsored by Eli Lilly and Tanabe-Mitsubishi. KM has received speaking fees from Eisai, GlaxoSmithKline, Meiji, MSD, Otsuka, Pfizer, Lilly, Mochida, Yoshitomi, Dainippon-Sumitomo, Takeda and Shionogi. MI has received lecture fees from Pfizer, Mochida, Shionogi, and Daiichi-Sankyo outside the submitted work. He has received royalties from Nippon Hyoron Sha, Nanzando, Seiwa Shoten, Igaku-shoin, and Technomics outside the submitted work. He has received grant or research support from the Japanese Ministry of Health, Labor and Welfare and the Japanese Ministry of Education, Science, and Technology. The Institution of MI received grant or research support from Eisai, Mochida, Astellas, Otsuka, GlaxoSmithKline, Shionogi, Sumitomo Dainippon, Jansen, Pfizer, MSD, Yoshitomi, Daiichi Sankyo, Meiji Seika Pharma, Tsumura, AbbVie, Ono, and Eli Lilly outside the submitted work. SS has received lecture fees from Otsuka, MSD, Meiji, Eli Lilly, Mochida, Pfizer, Takeda Janssen and Tanabe-Mitsubishi. He has received royalties from Sentan Igaku-sha, Chuohoki, Medical Review publishers. He has received grant or research support from the Japanese Ministry of Education, Science, and Technology and the Japanese Ministry of Health, Labor and Welfare. TA has received speaking fees and/or research funds from Eisai, Astra-Zeneca, GlaxoSmithKline, Meiji, MSD, Otsuka, Pfizer, Lilly, Mochida, Tanabe, Yoshitomi, Dainippon-Sumitomo, Takeda, and Shionogi. He has received royalties from Igaku-Shoin, Nanzando, Chugai-igakusya, Kyorin medical supply and NHK enterprise. The Japanese Ministry of Education, Science, and Technology and the Japanese Ministry of Health, Labor and Welfare have funded his research projects. MY has received speaking fees from Meiji Seika Pharma and has contracted research with Nippon Chemiphar. NW has research funds from the Japanese Ministry of Health Labor and Welfare and the Japanese Ministry of Education, Science, and Technology. He has also received royalties from Sogensha and Paquet and speaking fees and research funds from Asahi Kasei, Sumitomo Dainippon, Eli Lilly, GlaxoSmithKline, Janssen, Meiji, MSD, Otsuka and Pfizer. All the other authors declare that they have no competing interests.
Publisher Copyright:
© 2015 Yonemoto et al.
PY - 2015/10/14
Y1 - 2015/10/14
N2 - Background: SUN(^_^)D, the Strategic Use of New generation antidepressants for Depression, is an assessor-blinded, parallel-group, multicenter pragmatic mega-trial to examine the optimum treatment strategy for the first- and second-line treatments for unipolar major depressive episodes. The trial has three steps and two randomizations. Step I randomization compares the minimum and the maximum dosing strategy for the first-line antidepressant. Step II randomization compares the continuation, augmentation or switching strategy for the second-line antidepressant treatment. Step III is a naturalistic continuation phase. The original protocol was published in 2011, and we hereby report its updated protocol including the statistical analysis plan. Results: We implemented two important changes to the original protocol. One is about the required sample size, reflecting the smaller number of dropouts than had been expected. Another is in the organization of the primary and secondary outcomes in order to make the report of the main trial results as pertinent and interpretable as possible for clinical practices. Due to the complexity of the trial, we plan to report the main results in two separate reports, and this updated protocol and the statistical analysis plan have laid out respective primary and secondary outcomes and their analyses. We will convene the blind interpretation committee before the randomization code is broken. Conclusion: This paper presents the updated protocol and the detailed statistical analysis plan for the SUN(^_^)D trial in order to avoid reporting bias and data-driven results. Trial registration: ClinicalTrials.gov: NCT01109693(registered on 21 April 2010).
AB - Background: SUN(^_^)D, the Strategic Use of New generation antidepressants for Depression, is an assessor-blinded, parallel-group, multicenter pragmatic mega-trial to examine the optimum treatment strategy for the first- and second-line treatments for unipolar major depressive episodes. The trial has three steps and two randomizations. Step I randomization compares the minimum and the maximum dosing strategy for the first-line antidepressant. Step II randomization compares the continuation, augmentation or switching strategy for the second-line antidepressant treatment. Step III is a naturalistic continuation phase. The original protocol was published in 2011, and we hereby report its updated protocol including the statistical analysis plan. Results: We implemented two important changes to the original protocol. One is about the required sample size, reflecting the smaller number of dropouts than had been expected. Another is in the organization of the primary and secondary outcomes in order to make the report of the main trial results as pertinent and interpretable as possible for clinical practices. Due to the complexity of the trial, we plan to report the main results in two separate reports, and this updated protocol and the statistical analysis plan have laid out respective primary and secondary outcomes and their analyses. We will convene the blind interpretation committee before the randomization code is broken. Conclusion: This paper presents the updated protocol and the detailed statistical analysis plan for the SUN(^_^)D trial in order to avoid reporting bias and data-driven results. Trial registration: ClinicalTrials.gov: NCT01109693(registered on 21 April 2010).
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UR - http://www.scopus.com/inward/citedby.url?scp=84944411466&partnerID=8YFLogxK
U2 - 10.1186/s13063-015-0985-6
DO - 10.1186/s13063-015-0985-6
M3 - Article
C2 - 26466684
AN - SCOPUS:84944411466
SN - 1745-6215
VL - 16
JO - Trials
JF - Trials
IS - 1
M1 - 459
ER -