BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 38331394)

  • 21. Performance of Cox regression models for composite time-to-event endpoints with component-wise censoring in randomized trials.
    Speiser JL; Ambrosius WT; Pajewski NM
    Clin Trials; 2023 Oct; 20(5):507-516. PubMed ID: 37243355
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Restricted Net Treatment Benefit in oncology.
    Piffoux M; Ozenne B; De Backer M; Buyse M; Chiem JC; Péron J
    J Clin Epidemiol; 2024 Jun; 170():111340. PubMed ID: 38570079
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evaluation of three definitions of progression-free survival in preoperative cancer therapy (JCOG0801-A).
    Nakamura K; Shibata T; Takashima A; Yamamoto S; Fukuda H
    Jpn J Clin Oncol; 2012 Oct; 42(10):896-902. PubMed ID: 22844128
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Analyzing overall survival in randomized controlled trials with crossover and implications for economic evaluation.
    Jönsson L; Sandin R; Ekman M; Ramsberg J; Charbonneau C; Huang X; Jönsson B; Weinstein MC; Drummond M
    Value Health; 2014 Sep; 17(6):707-13. PubMed ID: 25236994
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Composite event-free-survival as an endpoint in oncology drug evaluation: Review and guidance perspectives from the Haute Autorité de Santé (HAS).
    Lengliné E; Baba J; de Boissieu P; Beaufils A; Desbiolles A; Diatta T; Cochat P; Chevret S
    Eur J Cancer; 2024 Jun; 204():114047. PubMed ID: 38653034
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Two-stage estimation to adjust for treatment switching in randomised trials: a simulation study investigating the use of inverse probability weighting instead of re-censoring.
    Latimer NR; Abrams KR; Siebert U
    BMC Med Res Methodol; 2019 Mar; 19(1):69. PubMed ID: 30935369
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Statistical considerations of designs for single-arm proof-of-concept oncology trial with time-to-event endpoint.
    Zhou H; Sun L; Wang M
    Contemp Clin Trials; 2023 Jun; 129():107200. PubMed ID: 37068588
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Differential Treatment Effects of Subgroup Analyses in Phase 3 Oncology Trials From 2004 to 2020.
    Sherry AD; Hahn AW; McCaw ZR; Abi Jaoude J; Kouzy R; Lin TA; Minsky B; Fuller CD; Meirson T; Msaouel P; Ludmir EB
    JAMA Netw Open; 2024 Mar; 7(3):e243379. PubMed ID: 38546648
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Deficiencies in health-related quality-of-life assessment and reporting: a systematic review of oncology randomized phase III trials published between 2012 and 2016.
    Marandino L; La Salvia A; Sonetto C; De Luca E; Pignataro D; Zichi C; Di Stefano RF; Ghisoni E; Lombardi P; Mariniello A; Reale ML; Trevisi E; Leone G; Muratori L; Marcato M; Bironzo P; Novello S; Aglietta M; Scagliotti GV; Perrone F; Di Maio M
    Ann Oncol; 2018 Dec; 29(12):2288-2295. PubMed ID: 30304498
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Adjusting overall survival for treatment switches: commonly used methods and practical application.
    Watkins C; Huang X; Latimer N; Tang Y; Wright EJ
    Pharm Stat; 2013; 12(6):348-57. PubMed ID: 24136868
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Empirical power comparison of statistical tests in contemporary phase III randomized controlled trials with time-to-event outcomes in oncology.
    Horiguchi M; Hassett MJ; Uno H
    Clin Trials; 2020 Dec; 17(6):597-606. PubMed ID: 32933339
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Impact of COVID-19 pandemic on oncology clinical trial design, data collection and analysis.
    Tang RS; Zhu J; Chen TT; Liu F; Jiang X; Huang B; Lee JJ; Beckman RA
    Contemp Clin Trials; 2022 May; 116():106736. PubMed ID: 35331946
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Potential surrogate endpoints for prostate cancer survival: analysis of a phase III randomized trial.
    Ray ME; Bae K; Hussain MH; Hanks GE; Shipley WU; Sandler HM
    J Natl Cancer Inst; 2009 Feb; 101(4):228-36. PubMed ID: 19211454
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Use of suboptimal control arms in randomized clinical trials of investigational cancer drugs in China, 2016-2021: An observational study.
    Zhang Y; Chen D; Cheng S; Liang Z; Yang L; Li Q; Bai L; Li H; Liu W; Shi L; Guan X
    PLoS Med; 2023 Dec; 20(12):e1004319. PubMed ID: 38085706
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Evaluation of Treatment Effect with Paired Failure Times in a Single-Arm Phase II Trial in Oncology.
    Texier M; Rotolo F; Ducreux M; Bouché O; Pignon JP; Michiels S
    Comput Math Methods Med; 2018; 2018():1672176. PubMed ID: 29568321
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Missing data and censoring in the analysis of progression-free survival in oncology clinical trials.
    Denne JS; Stone AM; Bailey-Iacona R; Chen TT
    J Biopharm Stat; 2013; 23(5):951-70. PubMed ID: 23957509
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Are experimental treatments for cancer in children superior to established treatments? Observational study of randomised controlled trials by the Children's Oncology Group.
    Kumar A; Soares H; Wells R; Clarke M; Hozo I; Bleyer A; Reaman G; Chalmers I; Djulbegovic B;
    BMJ; 2005 Dec; 331(7528):1295. PubMed ID: 16299015
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Optimal decision-making in oncology development programs based on probability of success for phase III utilizing phase II/III data on response and overall survival.
    Götte H; Xiong J; Kirchner M; Demirtas H; Kieser M
    Pharm Stat; 2020 Nov; 19(6):861-881. PubMed ID: 32662598
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Consistency of phase III clinical trial abstracts presented at an annual meeting of the American Society of Clinical Oncology compared with their subsequent full-text publications.
    Tam VC; Hotte SJ
    J Clin Oncol; 2008 May; 26(13):2205-11. PubMed ID: 18445846
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Analysis of composite endpoints with component-wise censoring in the presence of differential visit schedules.
    Eaton AA; Zabor EC
    Stat Med; 2022 Apr; 41(9):1599-1612. PubMed ID: 35043427
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.