يعرض 1 - 10 نتائج من 17 نتيجة بحث عن '"molecularly targeted agent"', وقت الاستعلام: 1.03s تنقيح النتائج
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    دورية أكاديمية

    المساهمون: Université Paris Descartes - Paris 5 (UPD5), Université Pierre et Marie Curie - Paris 6 (UPMC), Institut de Recherches Internationales Servier (IRIS-Servier), Centre National de la Recherche Scientifique (CNRS), Centre Médical MD Anderson, The University of Texas Health Science Center at Houston (UTHealth)

    المصدر: ISSN: 0959-5341 ; Journal of the Statistical Society of London ; https://hal.sorbonne-universite.fr/hal-01298649Test ; Journal of the Statistical Society of London, 2015, 64 (1), pp.215-229. ⟨10.1111/rssc.12072⟩.

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    دورية أكاديمية
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    دورية أكاديمية

    المؤلفون: Gadducci A., Cosio S.

    المساهمون: Gadducci, A., Cosio, S.

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32456205; volume:12; issue:5; firstpage:1336; journal:CANCERS; http://hdl.handle.net/11568/1070217Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085524339

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    دورية أكاديمية

    المساهمون: Kim, Nam Kyu, Hur, Hyuk, Kim, Jin Soo, Roh, Jae Kyung, Min, Byung Soh, Sohn, Seung Kook, Ahn, Joong Bae, Cho, Chang Hwan, Choi, Jin Sub

    المصدر: T200800524.pdf

    وصف الملف: 184~191

    العلاقة: Journal of the Korean Society of Coloproctology; J01864; OAK-2008-00594; https://ir.ymlib.yonsei.ac.kr/handle/22282913/106714Test; Colorectal cancer; Liver metastasis; Molecularly targeted agent; Curative resection; T200800524; Journal of the Korean Society of Coloproctology, Vol.24(3) : 184-191, 2008; 49320

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    دورية أكاديمية

    وصف الملف: application/pdf

    العلاقة: Muenz, Daniel G.; Taylor, Jeremy M. G.; Braun, Thomas M. (2019). "Phase I–II trial design for biologic agents using conditional auto‐regressive models for toxicity and efficacy." Journal of the Royal Statistical Society: Series C (Applied Statistics) 68(2): 331-345.; https://hdl.handle.net/2027.42/147824Test; Journal of the Royal Statistical Society: Series C (Applied Statistics); Rizvi, N. A., Mazières, J., Planchard, D., Stinchcombe, T. E., Dy, G. K., Antonia, S. J., Horn, L., Lena, H., Minenza, E., Mennecier, B., Otterson, G. A., Campos, L. T., Gandara, D. R., Levy, B. P., Nair, S. G., Zalcman, G., Wolf, J., Souquet, P. J., Baldini, E., Cappuzzo, F., Chouaid, C., Dowlati, A., Sanborn, R., Lopez‐Chavez, A., Grohe, C., Huber, R. M., Harbison, C. T., Baudert, C., Lestini, B. J. and Ramalingam, S. S. ( 2015 ) Activity and safety of nivolumab, an anti‐PD‐1 immune checkpoint inhibitor, for patients with advanced, refractory squamous non‐small‐cell lung cancer (CheckMate 063): a Phase 2, single‐arm trial. Lancet Oncol., 16, 257 – 265.; Hamid, O., Robert, C., Daud, A., Hodi, F. S., Hwu, W. J., Kefford, R., Wolchok, J. D., Hersey, P., Joseph, R. W., Weber, J. S., Dronca, R., Gangadhar, T. C., Patnaik, A., Zarour, H., Joshua, A. M., Gergich, K., Elassaiss‐Schaap, J., Algazi, A., Mateus, C., Boasberg, P., Tumeh, P. C., Chmielowski, B., Ebbinghaus, S. W., Li, X. N., Kang, S. P. and Ribas, A. ( 2013 ) Safety and tumor responses with lambrolizumab (anti‐PD‐1) in melanoma. New Engl. J. Med., 369, 134 – 144.; Jain, R. K., Lee, J. J., Hong, D., Markman, M., Gong, J., Naing, A., Wheler, J. and Kurzrock, R. ( 2010 ) Phase I oncology studies: evidence that in the era of targeted therapies patients on lower doses do not fare worse. Clin. Cancer Res., 16, 1289 – 1297.; Jin, I., Liu, S., Thall, P. and Yuan, Y. ( 2014 ) Using data augmentation to facilitate conduct of Phase I/II clinical trials with delayed outcomes. J. Am. Statist. Ass., 109, 525 – 536.; Lipson, E. J. and Drake, C. G. ( 2011 ) Ipilimumab: an anti‐ctla‐4 antibody for metastatic melanoma. Clin. Cancer Res., 17, 6958 – 6962.; Liu, S. and Johnson, V. E. ( 2016 ) A robust Bayesian dose‐finding design for phase I/II clinical trials. Biostatistics, 17, 249 – 263.; Luce, D. ( 1959 ) Individual Choice Behavior. New York: Wiley.; Minh, D. D. L. and Minh, D. L. P. ( 2015 ) Understanding the Hastings algorithm. Communs Statist. Simuln Computn, 44, 332 – 349.; O’Quigley, J., Pepe, M. and Fisher, L. ( 1990 ) Continual reassessment method: a practical design for Phase 1 clinical trials in cancer. Biometrics, 46, 33 – 48.; Plummer, M. ( 2003 ) JAGS: a program for analysis of Bayesian graphical models using Gibbs sampling. In Proc. 3rd Int. Wrkshp Distributed Statistical Computing (eds K. Hornik, F. Leisch and A. Zeileis).; Postel‐Vinay, S., Arkenau, H.‐T., Olmos, D., Ang, J., Barriuso, J., Ashley, S., Banerji, U., De‐Bono, J., Judson, I. and Kaye, S. ( 2009 ) Clinical benefit in Phase‐I trials of novel molecularly targeted agents: does dose matter? Br. J. Cancer, 100, 1373 – 1378.; Riviere, M.‐K., Yuan, Y., Dubois, F. and Zohar, S. ( 2015 ) A Bayesian dose finding design for clinical trials combining a cytotoxic agent with a molecularly targeted agent. Appl. Statist., 64, 215 – 229.; Riviere, M.‐K., Yuan, Y., Jourdan, J.‐H., Dubois, F. and Zohar, S. ( 2016 ) Phase I/II dose‐finding design for molecularly targeted agent: plateau determination using adaptive randomization. Statist. Meth. Med. Res., 27, 466 – 479.; Storer, B. E. ( 1989 ) Design and analysis of Phase I clinical trials. Biometrics, 45, 925 – 937.; Thall, P. F. and Cook, J. D. ( 2004 ) Dose‐finding based on efficacy‐toxicity trade‐offs. Biometrics, 60, 684 – 693.; Thall, P. F. and Nguyen, H. Q. ( 2012 ) Adaptive randomization to improve utility‐based dose‐finding with bivariate ordinal outcomes. J. Biopharm. Statist., 22, 785 – 801.; Thall, P. F. and Russell, K. E. ( 1998 ) A strategy for dose‐finding and safety monitoring based on efficacy and adverse outcomes in Phase I/II clinical trials. Biometrics, 54, 251 – 264.; Wages, N. A. and Tait, C. ( 2015 ) Seamless Phase I/II adaptive design for oncology trials of molecularly targeted agents. J. Biopharm. Statist., 25, 903 – 920.; Wall, M. M. ( 2004 ) A close look at the spatial structure implied by the CAR and SAR models. J. Statist. Planng Inf., 121, 311 – 324.; Yuan, Y., Nguyen, H. Q. and Thall, P. F. ( 2016 ) Bayesian Designs for Phase I‐II Clinical Trials. Boca Raton: Chapman and Hall–CRC.; Zang, Y., Lee, J. J. and Yuan, Y. ( 2014 ) Adaptive designs for identifying optimal biological dose for molecularly targeted agents. Clin. Trials, 11, 319 – 327.; Besag, J. ( 1974 ) Spatial interaction and the statistical analysis of lattice systems (with discussion). J. R. Statist. Soc. B, 36, 192 – 236.; Braun, T. M. ( 2002 ) The bivariate continual reassessment method: extending the CRM to Phase I trials of two competing outcomes. Contr. Clin. Trials, 23, 240 – 256.; Cai, C., Yuan, Y. and Ji, Y. ( 2014 ) A Bayesian dose finding design for oncology clinical trials of combinational biological agents. Appl. Statist., 63, 159 – 173.; Cheung, Y. K. and Chappell, R. ( 2000 ) Sequential designs for Phase I clinical trials with late‐onset toxicities. Biometrics, 56, 1177 – 1182.; Cressie, N. A. C. ( 2015 ) Statistics for Spatial Data, vol. II, Lattice Data, ch. 6. Hoboken: Wiley.; Cunanan, K. and Koopmeiners, J. S. ( 2014 ) Evaluating the performance of copula models in Phase I‐II clinical trials under model misspecification. BMC Med. Res. Methodol., 14, no. 51, 1 – 11.; Faries, D. ( 1994 ) Practical modifications of the continual reassessment method for Phase I cancer clinical trials. J. Biopharm. Statist., 4, 147 – 164.; Goodman, S. N., Zahurak, M. L. and Piantadosi, S. ( 1995 ) Some practical improvements in the continual reassessment method for Phase I studies. Statist. Med., 14, 1149 – 1161.; Gooley, T. A., Martin, P. J., Fisher, L. D. and Pettinger, M. ( 1994 ) Simulation as a design tool for Phase I/II clinical trials: an example from bone marrow transplantation. Contr. Clin. Trials, 15, 450 – 462.; Guo, B. and Li, Y. ( 2015 ) Bayesian dose‐finding designs for combination of molecularly targeted agents assuming partial stochastic ordering. Statist. Med., 34, 859 – 875.

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    دورية أكاديمية

    المصدر: 日本インターベンショナルラジオロジー学会雑誌 / The Official Journal of the Japanese Society of Interventional Radiology. 2013, 28(4):403

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    دورية أكاديمية

    المساهمون: Porta, C., Toscani, I., Czarnecka, A. M., Szczylik, C. A.

    وصف الملف: STAMPA

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27960591; info:eu-repo/semantics/altIdentifier/wos/WOS:000394439900002; volume:17; issue:2; firstpage:151; lastpage:162; numberofpages:12; journal:EXPERT OPINION ON BIOLOGICAL THERAPY; http://hdl.handle.net/11571/1301866Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85009990529

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