Validation of Predictive Analyses for Interim Decisions in Clinical Trials

被引:2
作者
Avalos-Pacheco, Alejandra [1 ,2 ]
Ventz, Steffen [3 ]
Arfe, Andrea [4 ]
Alexander, Brian M. [5 ,6 ]
Rahman, Rifaquat [5 ,7 ]
Wen, Patrick Y. [8 ]
Trippa, Lorenzo [9 ,10 ,11 ]
机构
[1] TU Wien, Fac Math & Geoinformat, Appl Stat Res Unit, Vienna, Austria
[2] Harvard Med Sch, Harvard MIT Ctr Regulatory Sci, Boston, MA USA
[3] Univ Minnesota, Sch Publ Hlth, Div Biostat, Minneapolis, MN USA
[4] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY USA
[5] Dana Farber Canc Inst, Boston, MA USA
[6] Fdn Med, Cambridge, MA USA
[7] Harvard Med Sch, Boston, MA USA
[8] Dana Farber Canc Inst, Ctr Neurooncol, Boston, MA USA
[9] Dana Farber Canc Inst, Dept Data Sci, Boston, MA USA
[10] Harvard TH Chan Sch Publ Hlth, Boston, MA USA
[11] Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02115 USA
关键词
PHASE-II; TEMOZOLOMIDE; THERAPY; DESIGN; MODEL; RADIATION; SURVIVAL; CRITERIA;
D O I
10.1200/PO.22.00606
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSEAdaptive clinical trials use algorithms to predict, during the study, patient outcomes and final study results. These predictions trigger interim decisions, such as early discontinuation of the trial, and can change the course of the study. Poor selection of the Prediction Analyses and Interim Decisions (PAID) plan in an adaptive clinical trial can have negative consequences, including the risk of exposing patients to ineffective or toxic treatments.METHODSWe present an approach that leverages data sets from completed trials to evaluate and compare candidate PAIDs using interpretable validation metrics. The goal is to determine whether and how to incorporate predictions into major interim decisions in a clinical trial. Candidate PAIDs can differ in several aspects, such as the prediction models used, timing of interim analyses, and potential use of external data sets. To illustrate our approach, we considered a randomized clinical trial in glioblastoma. The study design includes interim futility analyses on the basis of the predictive probability that the final analysis, at the completion of the study, will provide significant evidence of treatment effects. We examined various PAIDs with different levels of complexity to investigate if the use of biomarkers, external data, or novel algorithms improved interim decisions in the glioblastoma clinical trial.RESULTSValidation analyses on the basis of completed trials and electronic health records support the selection of algorithms, predictive models, and other aspects of PAIDs for use in adaptive clinical trials. By contrast, PAID evaluations on the basis of arbitrarily defined ad hoc simulation scenarios, which are not tailored to previous clinical data and experience, tend to overvalue complex prediction procedures and produce poor estimates of trial operating characteristics such as power and the number of enrolled patients.CONCLUSIONValidation analyses on the basis of completed trials and real world data support the selection of predictive models, interim analysis rules, and other aspects of PAIDs in future clinical trials.
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页数:11
相关论文
共 72 条
  • [1] Validation and Utility Testing of Clinical Prediction Models Time to Change the Approach
    Adibi, Amin
    Sadatsafavi, Mohsen
    Ioannidis, John P. A.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2020, 324 (03): : 235 - 236
  • [2] Individualized Screening Trial of Innovative Glioblastoma Therapy (INSIGhT): A Bayesian Adaptive Platform Trial to Develop Precision Medicines for Patients With Glioblastoma
    Alexander, Brian M.
    Trippa, Lorenzo
    Gaffey, Sarah
    Arrillaga-Romany, Isabel C.
    Lee, Eudocia Q.
    Rinne, Mikael L.
    Ahluwalia, Manmeet S.
    Colman, Howard
    Fell, Geoffrey
    Galanis, Evanthia
    de Groot, John
    Drappatz, Jan
    Lassman, Andrew B.
    Meredith, David M.
    Nabors, L. Burt
    Santagata, Sandro
    Schiff, David
    Welch, Mary R.
    Ligon, Keith L.
    Wen, Patrick Y.
    [J]. JCO PRECISION ONCOLOGY, 2019, 3 : 1 - 13
  • [3] Berry SM, 2010, CH CRC BIOSTAT SER, P1, DOI 10.1201/EBK1439825488
  • [4] Alternative derivations of a rule for early stopping in favor of HO
    Betensky, RA
    [J]. AMERICAN STATISTICIAN, 2000, 54 (01) : 35 - 39
  • [5] Bishop C. M., 2006, Pattern Recognition and Machine Learning (Information Science and Statistics), DOI 10.1007/978-0-387-45528-0
  • [6] Brier G.W., 1950, MON WEATHER REV, V78, P1, DOI [10.1175/1520-0493(1950)078<0001:vofeit>2.0.co
  • [7] 2, DOI 10.1175/1520-0493(1950)078<0001:VOFEIT>2.0.CO
  • [8] 2]
  • [9] Impact of late treatment-related radiotherapy toxicity, depression, and anxiety on quality of life in long-term breast cancer survivors
    Brunault, Paul
    Toledano, Alain
    Aguerre, Colette
    Suzanne, Isabelle
    Garaud, Pascal
    Trzepidur-Edom, Magdalena
    Calais, Gilles
    Camus, Vincent
    [J]. BULLETIN DU CANCER, 2012, 99 (05) : 589 - 598
  • [10] Transforming the clinical trial process: The I-SPY 2 trial as a model for improving the efficiency of clinical trials and accelerating the drug-screening process
    Buxton, Meredith B.
    Natsuhara, Kelsey
    DeMichele, Angela
    Perimutter, Jane
    Hylton, Nola M.
    Yee, Douglas
    van't Veer, Laura
    Symmans, William Fraser
    Hogarth, Michael
    Lyandres, Julia
    Davis, Sarah E.
    Flynn, Susan
    Paoloni, Melissa
    Berry, Donald A.
    Esserman, Laura
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (15)