000144259 001__ 144259
000144259 005__ 20240229123018.0
000144259 0247_ $$2doi$$a10.1002/bimj.201800395
000144259 0247_ $$2pmid$$apmid:31265159
000144259 0247_ $$2ISSN$$a0006-3452
000144259 0247_ $$2ISSN$$a0323-3847
000144259 0247_ $$2ISSN$$a1521-4036
000144259 0247_ $$2altmetric$$aaltmetric:63057753
000144259 037__ $$aDKFZ-2019-01779
000144259 041__ $$aeng
000144259 082__ $$a570
000144259 1001_ $$0P:(DE-He78)bb6a7a70f976eb8df1769944bf913596$$aKopp-Schneider, Annette$$b0$$eFirst author$$udkfz
000144259 245__ $$aPower gains by using external information in clinical trials are typically not possible when requiring strict type I error control.
000144259 260__ $$aBerlin$$bWiley-VCH$$c2020
000144259 3367_ $$2DRIVER$$aarticle
000144259 3367_ $$2DataCite$$aOutput Types/Journal article
000144259 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1601381356_28271
000144259 3367_ $$2BibTeX$$aARTICLE
000144259 3367_ $$2ORCID$$aJOURNAL_ARTICLE
000144259 3367_ $$00$$2EndNote$$aJournal Article
000144259 500__ $$a2020 Mar;62(2):361-374#EA:C060#LA:C060#
000144259 520__ $$aIn the era of precision medicine, novel designs are developed to deal with flexible clinical trials that incorporate many treatment strategies for multiple diseases in one trial setting. This situation often leads to small sample sizes in disease-treatment combinations and has fostered the discussion about the benefits of borrowing of external or historical information for decision-making in these trials. Several methods have been proposed that dynamically discount the amount of information borrowed from historical data based on the conformity between historical and current data. Specifically, Bayesian methods have been recommended and numerous investigations have been performed to characterize the properties of the various borrowing mechanisms with respect to the gain to be expected in the trials. However, there is common understanding that the risk of type I error inflation exists when information is borrowed and many simulation studies are carried out to quantify this effect. To add transparency to the debate, we show that if prior information is conditioned upon and a uniformly most powerful test exists, strict control of type I error implies that no power gain is possible under any mechanism of incorporation of prior information, including dynamic borrowing. The basis of the argument is to consider the test decision function as a function of the current data even when external information is included. We exemplify this finding in the case of a pediatric arm appended to an adult trial and dichotomous outcome for various methods of dynamic borrowing from adult information to the pediatric arm. In conclusion, if use of relevant external data is desired, the requirement of strict type I error control has to be replaced by more appropriateĀ metrics.
000144259 536__ $$0G:(DE-HGF)POF3-313$$a313 - Cancer risk factors and prevention (POF3-313)$$cPOF3-313$$fPOF III$$x0
000144259 588__ $$aDataset connected to CrossRef, PubMed,
000144259 7001_ $$0P:(DE-HGF)0$$aCalderazzo, Silvia$$b1
000144259 7001_ $$0P:(DE-He78)1042737c83ba70ec508bdd99f0096864$$aWiesenfarth, Manuel$$b2$$eLast author$$udkfz
000144259 773__ $$0PERI:(DE-600)1479920-0$$a10.1002/bimj.201800395$$gp. bimj.201800395$$n2$$p361-374$$tBiometrical journal$$v62$$x1521-4036$$y2020
000144259 909CO $$ooai:inrepo02.dkfz.de:144259$$pVDB
000144259 9101_ $$0I:(DE-588b)2036810-0$$6P:(DE-He78)bb6a7a70f976eb8df1769944bf913596$$aDeutsches Krebsforschungszentrum$$b0$$kDKFZ
000144259 9101_ $$0I:(DE-588b)2036810-0$$6P:(DE-HGF)0$$aDeutsches Krebsforschungszentrum$$b1$$kDKFZ
000144259 9101_ $$0I:(DE-588b)2036810-0$$6P:(DE-He78)1042737c83ba70ec508bdd99f0096864$$aDeutsches Krebsforschungszentrum$$b2$$kDKFZ
000144259 9131_ $$0G:(DE-HGF)POF3-313$$1G:(DE-HGF)POF3-310$$2G:(DE-HGF)POF3-300$$3G:(DE-HGF)POF3$$4G:(DE-HGF)POF$$aDE-HGF$$bGesundheit$$lKrebsforschung$$vCancer risk factors and prevention$$x0
000144259 9141_ $$y2020
000144259 915__ $$0StatID:(DE-HGF)0420$$2StatID$$aNationallizenz
000144259 915__ $$0StatID:(DE-HGF)0100$$2StatID$$aJCR$$bBIOMETRICAL J : 2017
000144259 915__ $$0StatID:(DE-HGF)0200$$2StatID$$aDBCoverage$$bSCOPUS
000144259 915__ $$0StatID:(DE-HGF)0300$$2StatID$$aDBCoverage$$bMedline
000144259 915__ $$0StatID:(DE-HGF)0199$$2StatID$$aDBCoverage$$bClarivate Analytics Master Journal List
000144259 915__ $$0StatID:(DE-HGF)0111$$2StatID$$aWoS$$bScience Citation Index Expanded
000144259 915__ $$0StatID:(DE-HGF)0150$$2StatID$$aDBCoverage$$bWeb of Science Core Collection
000144259 915__ $$0StatID:(DE-HGF)1050$$2StatID$$aDBCoverage$$bBIOSIS Previews
000144259 915__ $$0StatID:(DE-HGF)9900$$2StatID$$aIF < 5
000144259 9202_ $$0I:(DE-He78)C060-20160331$$kC060$$lC060 Biostatistik$$x0
000144259 9200_ $$0I:(DE-He78)C060-20160331$$kC060$$lC060 Biostatistik$$x0
000144259 9201_ $$0I:(DE-He78)C060-20160331$$kC060$$lC060 Biostatistik$$x0
000144259 980__ $$ajournal
000144259 980__ $$aVDB
000144259 980__ $$aI:(DE-He78)C060-20160331
000144259 980__ $$aUNRESTRICTED