BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 36789566)

  • 1. Sample size calculation for the combination test under nonproportional hazards.
    Cheng H; He J
    Biom J; 2023 Apr; 65(4):e2100403. PubMed ID: 36789566
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comparison of survival distributions in clinical trials: A practical guidance.
    Chen X; Wang X; Chen K; Zheng Y; Chappell RJ; Dey J
    Clin Trials; 2020 Oct; 17(5):507-521. PubMed ID: 32594788
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A simulation study comparing the power of nine tests of the treatment effect in randomized controlled trials with a time-to-event outcome.
    Royston P; B Parmar MK
    Trials; 2020 Apr; 21(1):315. PubMed ID: 32252820
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A unified approach to power and sample size determination for log-rank tests under proportional and nonproportional hazards.
    Tang Y
    Stat Methods Med Res; 2021 May; 30(5):1211-1234. PubMed ID: 33819109
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sample size calculation for logrank test and prediction of number of events over time.
    Lu K
    Pharm Stat; 2021 Mar; 20(2):229-244. PubMed ID: 32909395
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sample size calculation for two-arm trials with time-to-event endpoint for nonproportional hazards using the concept of Relative Time when inference is built on comparing Weibull distributions.
    Phadnis MA; Mayo MS
    Biom J; 2021 Oct; 63(7):1406-1433. PubMed ID: 34272897
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A clinical trial design using the concept of proportional time using the generalized gamma ratio distribution.
    Phadnis MA; Wetmore JB; Mayo MS
    Stat Med; 2017 Nov; 36(26):4121-4140. PubMed ID: 28815655
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Using the geometric average hazard ratio in sample size calculation for time-to-event data with composite endpoints.
    Cortés Martínez J; Geskus RB; Kim K; Melis GG
    BMC Med Res Methodol; 2021 May; 21(1):99. PubMed ID: 33957892
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An approach to trial design and analysis in the era of non-proportional hazards of the treatment effect.
    Royston P; Parmar MK
    Trials; 2014 Aug; 15():314. PubMed ID: 25098243
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Average Hazard Ratio - A Good Effect Measure for Time-to-event Endpoints when the Proportional Hazard Assumption is Violated?
    Rauch G; Brannath W; Brückner M; Kieser M
    Methods Inf Med; 2018 May; 57(3):89-100. PubMed ID: 29719915
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Augmenting the logrank test in the design of clinical trials in which non-proportional hazards of the treatment effect may be anticipated.
    Royston P; Parmar MK
    BMC Med Res Methodol; 2016 Feb; 16():16. PubMed ID: 26869168
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sample size calculation for the augmented logrank test in randomized clinical trials.
    Hattori S; Komukai S; Friede T
    Stat Med; 2022 Jun; 41(14):2627-2644. PubMed ID: 35319100
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Critical review of oncology clinical trial design under non-proportional hazards.
    Ananthakrishnan R; Green S; Previtali A; Liu R; Li D; LaValley M
    Crit Rev Oncol Hematol; 2021 Jun; 162():103350. PubMed ID: 33989767
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sample size calculation for mixture model based on geometric average hazard ratio and its applications to nonproportional hazard.
    Wang Z; Zhang Q; Xue A; Whitmore J
    Pharm Stat; 2024; 23(3):325-338. PubMed ID: 38152873
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Delayed treatment effects, treatment switching and heterogeneous patient populations: How to design and analyze RCTs in oncology.
    Ristl R; Ballarini NM; Götte H; Schüler A; Posch M; König F
    Pharm Stat; 2021 Jan; 20(1):129-145. PubMed ID: 32830428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sample size and power for the weighted log-rank test and Kaplan-Meier based tests with allowance for nonproportional hazards.
    Yung G; Liu Y
    Biometrics; 2020 Sep; 76(3):939-950. PubMed ID: 31797363
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Log-Rank Test vs MaxCombo and Difference in Restricted Mean Survival Time Tests for Comparing Survival Under Nonproportional Hazards in Immuno-oncology Trials: A Systematic Review and Meta-analysis.
    Mukhopadhyay P; Ye J; Anderson KM; Roychoudhury S; Rubin EH; Halabi S; Chappell RJ
    JAMA Oncol; 2022 Sep; 8(9):1294-1300. PubMed ID: 35862037
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Versatile tests for window mean survival time.
    Paukner M; Chappell R
    Stat Med; 2022 Aug; 41(19):3720-3736. PubMed ID: 35611993
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Randomized two-stage optimal design for interval-censored data.
    Shan G
    J Biopharm Stat; 2022 Mar; 32(2):298-307. PubMed ID: 34890525
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Impact of a non-constant baseline hazard on detection of time-dependent treatment effects: a simulation study.
    Jachno K; Heritier S; Wolfe R
    BMC Med Res Methodol; 2021 Aug; 21(1):177. PubMed ID: 34454428
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.