Practical aspects of handling treatment switching in randomized clinical trials

Similar documents
2. Background This was the fourth submission for everolimus requesting listing for clear cell renal carcinoma.

Randomized trials versus observational studies

If several different trials are mentioned in one publication, the data of each should be extracted in a separate data extraction form.

Background. t 1/2 of days allows once-daily dosing (1.5 mg) with consistent serum concentration 2,3 No interaction with CYP3A4 inhibitors 4

Efficacy analysis and graphical representation in Oncology trials - A case study

TUTORIAL on ICH E9 and Other Statistical Regulatory Guidance. Session 1: ICH E9 and E10. PSI Conference, May 2011

Paper PO06. Randomization in Clinical Trial Studies

Clinical development of AZD9291 in non-small cell lung cancer

Vignette for survrm2 package: Comparing two survival curves using the restricted mean survival time

Stage IV Renal Cell Carcinoma. Changing Management in A Comprehensive Community Cancer Center. Susquehanna Health Cancer Center

The NCPE has issued a recommendation regarding the use of pertuzumab for this indication. The NCPE does not recommend reimbursement of pertuzumab.

With Big Data Comes Big Responsibility

Study Design and Statistical Analysis

Maintenance therapy in in Metastatic NSCLC. Dr Amit Joshi Associate Professor Dept. Of Medical Oncology Tata Memorial Centre Mumbai

Lapatinib for the treatment of advanced and metastatic breast cancer: a review of the response to the ACD provided by the manufacturer of Lapatinib

Introduction. Survival Analysis. Censoring. Plan of Talk

Clinical Trial Designs for Firstline Hormonal Treatment of Metastatic Breast Cancer

The Prevention and Treatment of Missing Data in Clinical Trials: An FDA Perspective on the Importance of Dealing With It

Supplementary appendix

The Harvard MPH in Epidemiology Online/On-Campus/In the Field. Two-Year, Part-Time Program. Sample Curriculum Guide

Guideline on missing data in confirmatory clinical trials

BIOM611 Biological Data Analysis

More details on the inputs, functionality, and output can be found below.

Clinical Trial Endpoints for Regulatory Approval First-Line Therapy for Advanced Ovarian Cancer

The Harvard MPH in Epidemiology Online/On-Campus/In the Field. Two-Year, Part-Time Program. Sample Curriculum Guide

What is the Optimal Front-Line Treatment for mrcc? Michael B. Atkins, MD Deputy Director, Georgetown-Lombardi Comprehensive Cancer Center

Guidance for Industry Diabetes Mellitus Evaluating Cardiovascular Risk in New Antidiabetic Therapies to Treat Type 2 Diabetes

Transferability of Economic Evaluations in Clinical Trials

Molecular markers and clinical trial design parallels between oncology and rare diseases?

Tips for surviving the analysis of survival data. Philip Twumasi-Ankrah, PhD

DECISION AND SUMMARY OF RATIONALE

Cancer Treatments Subcommittee of PTAC Meeting held 18 September (minutes for web publishing)

The Product Review Life Cycle A Brief Overview

Guide to Biostatistics

Understanding Clinical Trials

Regression Modeling Strategies

Avastin in breast cancer: Summary of clinical data

Personalized Predictive Medicine and Genomic Clinical Trials

The PCORI Methodology Report. Appendix A: Methodology Standards

Guidance for Industry

Endpoint Selection in Phase II Oncology trials

Statistical modelling with missing data using multiple imputation. Session 4: Sensitivity Analysis after Multiple Imputation

Methods for Meta-analysis in Medical Research

Intervention and clinical epidemiological studies

Title: Lending Club Interest Rates are closely linked with FICO scores and Loan Length

PROSPETTIVE FUTURE NEL TRATTAMENTO. Cinzia Ortega Dipartimento di Oncologia Medica Fondazione del Piemonte per l Oncologia I.R.C.C.S.

Supplementary Online Content

Appendix 1 to the guideline on the evaluation of anticancer medicinal products in man

Design and Analysis of Phase III Clinical Trials

Avastin in breast cancer: Summary of clinical data

Ovarian Cancer and Modern Immunotherapy: Regulatory Strategies for Drug Development

Avastin in Metastatic Breast Cancer

Big data size isn t enough! Irene Petersen, PhD Primary Care & Population Health

Randomization in Clinical Trials

Competing-risks regression

AVOIDING BIAS AND RANDOM ERROR IN DATA ANALYSIS

Pharmacogenomic markers in EGFR-targeted therapy of lung cancer

Adequacy of Biomath. Models. Empirical Modeling Tools. Bayesian Modeling. Model Uncertainty / Selection

The Kaplan-Meier Plot. Olaf M. Glück

Sorafenib. Bernard ESCUDIER Institut Gustave Roussy Villejuif, France

Department/Academic Unit: Public Health Sciences Degree Program: Biostatistics Collaborative Program

MOLOGEN AG. Q1 Results 2015 Conference Call Dr. Matthias Schroff Chief Executive Officer. Berlin, 12 May 2015

EMA EFPIA workshop Break-out session no. 4

Safety & Effectiveness of Drug Therapies for Type 2 Diabetes: Are pharmacoepi studies part of the problem, or part of the solution?

Clinical Spotlight in Breast Cancer

NOUVEAUTES THERAPEUTIQUES DANS LES TUMEURS NEUROENDOCRINES DIGESTIVES (Radiothérapie vectorisée et loco-régionale exclue) Philippe RUSZNIEWSKI

The Consequences of Missing Data in the ATLAS ACS 2-TIMI 51 Trial

OI PARP ΑΝΑΣΤΟΛΕΙΣ ΣΤΟΝ ΚΑΡΚΙΝΟ ΤΟΥ ΜΑΣΤΟΥ ΝΙΚΟΛΑΙΔΗ ΑΔΑΜΑΝΤΙΑ ΠΑΘΟΛΟΓΟΣ-ΟΓΚΟΛΟΓΟΣ Β ΟΓΚΟΛΟΓΙΚΗ ΚΛΙΝΙΚΗ ΝΟΣ. ΜΗΤΕΡΑ

Immunotherapy for Metastatic Renal Cell Carcinoma

Data Analysis, Research Study Design and the IRB

Kanıt: Klinik çalışmalarda ZYTIGA

Tumori rari del rene: trattamento per stadio ed istologia Dr. Camillo Porta

Study Design. Date: March 11, 2003 Reviewer: Jawahar Tiwari, Ph.D. Ellis Unger, M.D. Ghanshyam Gupta, Ph.D. Chief, Therapeutics Evaluation Branch

Decision to Continue the Development of Tecemotide (L-BLP25) in Non-Small Cell Lung Cancer to be Announced

R 2 -type Curves for Dynamic Predictions from Joint Longitudinal-Survival Models

Treatment of Metastatic Breast Cancer: Endocrine Therapies. Robert W. Carlson, M.D. Professor of Medicine Stanford University

Issues Concerning Development of Products for Treatment of Non-Metastatic Castration- Resistant Prostate Cancer (NM-CRPC)

A new score predicting the survival of patients with spinal cord compression from myeloma

Introduction to Event History Analysis DUSTIN BROWN POPULATION RESEARCH CENTER

Study Designs. Simon Day, PhD Johns Hopkins University

An Application of the G-formula to Asbestos and Lung Cancer. Stephen R. Cole. Epidemiology, UNC Chapel Hill. Slides:

PROMISE & PITFALLS OF OUTCOMES RESEARCH USING EMR DATABASES. Richard L. Tannen, M.D., Mark Weiner, Dawei Xie

Methodological Challenges in Analyzing Patient-reported Outcomes

Understanding, appraising and reporting meta-analyses that use individual participant data

Precision oncology: identifying predictive biomarkers for the treatment of metastatic renal cell carcinoma

A Guide to Imputing Missing Data with Stata Revision: 1.4

Lecture 2 ESTIMATING THE SURVIVAL FUNCTION. One-sample nonparametric methods

Critical appraisal. Gary Collins. EQUATOR Network, Centre for Statistics in Medicine NDORMS, University of Oxford

Is there a positive effect of participation on a clinical trial for patients with advanced nonsmall cell lung cancer?

Supplementary webappendix

NATIONAL CANCER DRUG FUND PRIORITISATION SCORES

Can I have FAITH in this Review?

Programme du parcours Clinical Epidemiology UMR 1. Methods in therapeutic evaluation A Dechartres/A Flahault

A Mixed Model Approach for Intent-to-Treat Analysis in Longitudinal Clinical Trials with Missing Values

Supplementary webappendix

DECISION AND SUMMARY OF RATIONALE

Advances In Chemotherapy For Hormone Refractory Prostate Cancer. TAX 327 study results & SWOG study results presented at ASCO 2004

Organizing Your Approach to a Data Analysis

Should we use Docetaxel in hormone- naïve prostate cancer? Karim Fizazi, MD, PhD Institut Gustave Roussy Villejuif, France

Drug/Drug Combination: Bevacizumab in combination with chemotherapy

Transcription:

Practical aspects of handling treatment switching in randomized clinical trials BBS Spring Seminar Viktoriya Stalbovskaya, Novartis Basel, 28 April 2016

NVS Oncology Treatment Switching Guideline Team Valentine Jehl Gaelle Saint-Hilary Santosh Sutradhar Zhongwen Tang Simon Wandel Nigel Yateman Viktoriya Stalbovskaya 2 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Outline Motivating example Time-dependent confounding Rank preserving structured failure time model Inverse probability weighting General recommendations Recent publications and existing software Acknowledgements References 3 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Motivating example Everolimus in mrcc (RECORD-1) Phase III study of everolimus in metastatic renal cell carcinoma Motzer et al (2008, 2010) Double-blind, multicenter study with patients randomized to receive either everolimus (n = 277) or placebo (n = 139) Primary endpoint PFS (HR=0.30, 95% CI 0.22-0.40, p<0.0001) Regulatory approval based on PFS Protocol allowed crossover from placebo to everolimus upon progression 4 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Motivating example Everolimus in mrcc (RECORD-1) ~80% of placebo randomized patients switched to everolimus ITT analysis of OS: HR=0.87, 95% CI: 0.65-1.15, p-value=0.162 ITT analysis provides a valid assessment of the treatment policy What about assessment of treatment effect of everolimus on OS if placebo patients never received everolimus? 5 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Time-dependent confounding Covariates Treatment Outcome (survival) 1 Effect of interest 2 Confounding effect on occurrence of the outcome 3 Confounding effect on future exposure to treatment 6 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Rank preserving structural failure time (RPSFT) model Estimate the survival time gained/lost by receiving active treatment (i.e. either randomized or cross-over active treatment) Main assumption: treatment is acting by multiplying survival time by a given factor once patient starts receiving active treatment (transparent but un-testable assumption) Multiplicative factor interpreted as relative increase/decrease in survival if one took active treatment compared to taking control It works by reconstructing the survival duration of patients, as if they had never received active treatment 7 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

RPSFT acceleration factor exp( Ψ) exp( Ψ) Treatment multiplies life by acceleration factor exp( Ψ) Ψ<0 time on experimental therapy extends life compared to control Ψ>0 time on control therapy extends life compared to experimental 8 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

RPSFT G-estimation for psi (RECORD-1) p-value Test statistic Ψ = 0.66, 95% CI ( 2.16,0.69) 9 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Programming implementation for RPSFT Data preparation Data transformation and Statistical analysis Time to event dataset Covariates: stratification, baseline, exposure on treatment / treatment group approach Combined dataset G-estimation procedure Specify range of psi values and grid size For each psi value calculate U, C and test statistic Select psi for test statistic 0 Dataset with original and recensored survival time, estimated psi value Cox regression to estimate HR and recalculate CI Output: - Crossover corrected HR - KM plot - Psi value with CI - Patient level listing 10 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

RPSFT model results for RECORD-1 The corrected results used reconstructed survival time for all control arm patients 11 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Inverse probability weighting (IPW) approach Model-based method that reweights control arm patients using propensity score methods. Treatment effect is expressed on the hazard ratio scale and estimated using weighted Cox model. Main assumption: no unmeasured confounders (all factors influencing crossover and survival are included in the model), non-testable 12 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Inverse probability weighted analysis (IPW) Patient in the control arm with crossover w 1 w 2 w n w e Control IPCW (weighted censoring at crossover) IPTW (weighted time-varying) Experimental weight treatment weighted analysis Patient in the control arm without crossover w 1 w 2 w n Control IPCW (weighted censoring at crossover) weight treatment weighted analysis IPTW (weighted time-varying) Patient in the experimental arm 1 Experimental IPCW (weighted censoring at crossover) weight treatment weighted analysis IPTW (weighted time-varying) 13 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Programming implementation for IPW Data preparation Data transformation Statistical analysis Time to event dataset Split time into time intervals Subset Control arm patients Set weight for experimental arm patients to 1 Dataset with covariates (baseline, timevarying) Impute missing values for time-var covariates Calculate probabilities of remaining untreated Datasets with weights per time interval per patient Format variables for the analysis macros Combined time to event dataset with covariates Datasets with probabilities per time interval Calculate weights for various models Datasets with weights Weighted Cox regression Output: - Crossover corrected HR, p-value - Weighted KM plot - Statistics for weights - Patient level listing 14 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

IPCW application to RECORD-1 Model 4: best model fit (AIC) 15 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

General recommendations Points to consider Describe the treatment switching mechanism When was switching permitted? Patient-level or study-level Why did switching occur? Post-progression switch, switch based on study milestone Quantify the extent of switching and characterize the population of switchers Number and percentage of patients who switched, proportion of total exposure and/or follow up time that was affected by switch Timing of treatment switching in a form of Kaplan-Meier plot estimated median, range Baseline characteristics for switchers Select method to account for treatment switching, implementation and description of results Consider feasibility of the underlying assumptions for each method Identify potential sources of bias and describe them for the method selected Ideally, provide a document with the details of the model(s) 16 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Recent publications and software Harvard School of Public Health Software for MSM, SNM, etc (SAS) http://www.hsph.harvard.edu/causal/software/ Causal inference book by Robins and Hernan Parts of the book and the code available (in draft) http://www.hsph.harvard.edu/miguel-hernan/causal-inference-book/ Medical Research Council Software for RPSFT (STATA) http://www.mrc-bsu.cam.ac.uk/software/stata-software/ 17 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Acknowledgments Mike Branson Bee Chen Beat Neuenschwander All the reviewers 18 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

References Korhonen P, Malangone E, Sherman S et al. Overall survival (OS) of metastatic renal cell carcinoma (mrcc) patients corrected for crossover using inverse probability of censoring weights (IPCW) and rank preserving structural failure time (RPSFT) models: Two analyses from the RECORD-1 trial. J Clin Oncol 28:15s, 2010 (suppl; abstr 4595) Korhonen P, Zuber E, Branson M et al. Correcting overall survival for the impact of crossover via a rank-preserving structural failure time (RPSFT) model in the RECORD- 1 trial of everolimus in metastatic renal-cell carcinoma. J Biopharm Stat 2012 Latimer NR, Abrams KR, Lambert PC et al. Adjusting survival time estimates to account for treatment switching in randomized controlled trials--an economic evaluation context: methods, limitations, and recommendations. Med Decis Making 2014 Motzer RJ, Escudier B, Oudard S et al. Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial. Lancet 2008 Motzer, R., Escudier, B., Oudard, S., et al. (2010). Phase 3 trial of everolimus for metastatic renal cell carcinoma: Final results and analysis of prognostic factors. Cancer 116:4256 4265. 19 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

Back up 20 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only

RPSFT Artificial censoring algorithm An additional algorithm ( artificial-censoring ) allows to maintain the assumption of independent random censoring required for unbiased estimation The artificial censoring algorithm works by shrinking the total follow-up time (time between randomization to analysis cut-off date) for all patients regardless of randomization group or treatment received Therefore every patient censored in the ITT analysis remains censored with duration equal or shorter to the original one; in addition, patients with an event in the original analysis may become censored via the artificial-censoring algorithm 21 BBS Spring Seminar V Stalbovskaya 28 April 2016 Practical aspects of treatment switching Business Use Only