期刊论文详细信息
BMC Medical Research Methodology
Enhanced secondary analysis of survival data: reconstructing the data from published Kaplan-Meier survival curves
Nicky J Welton1  Mario JNM Ouwens2  AE Ades1  Patricia Guyot2 
[1]School of Social and Community Medicine, University of Bristol, Canynge Hall, 39 Whatley Road, Bristol BS8 2PS UK
[2]Mapi Consultancy, De Molen 84, 3995 AX Houten, the Netherlands
关键词: Health Technology Assessment;    Cost-Effectiveness Analysis;    life-table;    algorithm;    Kaplan-Meier;    Individual Patient Data;    Survival analysis;   
Others  :  1136836
DOI  :  10.1186/1471-2288-12-9
 received in 2011-06-20, accepted in 2012-02-01,  发布年份 2012
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【 摘 要 】

Background

The results of Randomized Controlled Trials (RCTs) on time-to-event outcomes that are usually reported are median time to events and Cox Hazard Ratio. These do not constitute the sufficient statistics required for meta-analysis or cost-effectiveness analysis, and their use in secondary analyses requires strong assumptions that may not have been adequately tested. In order to enhance the quality of secondary data analyses, we propose a method which derives from the published Kaplan Meier survival curves a close approximation to the original individual patient time-to-event data from which they were generated.

Methods

We develop an algorithm that maps from digitised curves back to KM data by finding numerical solutions to the inverted KM equations, using where available information on number of events and numbers at risk. The reproducibility and accuracy of survival probabilities, median survival times and hazard ratios based on reconstructed KM data was assessed by comparing published statistics (survival probabilities, medians and hazard ratios) with statistics based on repeated reconstructions by multiple observers.

Results

The validation exercise established there was no material systematic error and that there was a high degree of reproducibility for all statistics. Accuracy was excellent for survival probabilities and medians, for hazard ratios reasonable accuracy can only be obtained if at least numbers at risk or total number of events are reported.

Conclusion

The algorithm is a reliable tool for meta-analysis and cost-effectiveness analyses of RCTs reporting time-to-event data. It is recommended that all RCTs should report information on numbers at risk and total number of events alongside KM curves.

【 授权许可】

   
2012 Guyot et al; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Moher D, Hopewell S, Schulz KF, Montori V, Gotzsche PC, Devereaux PJ, Elbourne D, Egger M, Altman DG: CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials. BMJ 2010, 340:c869.
  • [2]Whitehead A, Whitehead J: A general parametric approach to the meta-analysis of randomized clinical trials. Statistics in medicine 1991, 10:1665-1677.
  • [3]Michiels S, Piedbois P, Burdett S, Syz N, Stewart L, Pignon JP: Meta-analysis when only the median survival times are known: a comparison with individual patient data results. Int J Technol Assess Health Care 2005, 21(1):119-25.
  • [4]Dear KBG: Alternative generalized least squares for meta-analysis of survival data at multiple time. Biometrics 1994, 50:989-1002.
  • [5]Arends L, Hunink M, Stijnen T: Meta-analysis of summary survival curve. Statistics in medicine 2008, 27:4381-4396.
  • [6]Fiocco M, Putter H, van Houwelingen JC: Meta-analysis of pairs of survival curves under heterogeneity: a Poisson correlated gamma-frailty approach. Statistics in medicine 2009, 28:3782-3797.
  • [7]Parmar MKB, Torri V, Stewart L: Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints. Statistics in medicine 1998, 17:2815-2834.
  • [8]Ouwens MJNM, Philips Z, Jansen JP: Network meta-analysis of parametric survival curves. Research Synthesis Methods 2010, 1(3-4):258-271.
  • [9]Jansen JP: Network meta-analysis of survival data with fractional polynomials. BMC Medical Research Methodology 2011, 11:61. BioMed Central Full Text
  • [10]Earle C, Wells G: An Assessment of Methods to Combine Published Survival Curves. Medical Decision Making 2000, 20:104-111.
  • [11]Williamson PR, Tudur Smith C, Hutton JL, Marson AG: Aggregate data meta-analysis with time-to-event outcomes. Statistics in medicine 2002, 21:3337-3351.
  • [12]Bonner JA, Harari PM, Giralt J, Azarnia N, Shin DM, Cohen RB, Jones CU, Sur R, Raben D, Jassem J, Ove R, Kies MS, Baselga J, Youssoufian H, Amellal N, Rowinsky EK, Ang KK: Radiotherapy plus Cetuximab for Squamous-Cell Carcinoma of the Head and Neck. N Engl J Med 2006, 354:567-78.
  • [13]Guyot P, Welton NJ, Ouwens MJNM, Ades AE: Survival time outcomes in randomised controlled trials and meta-analyses: the parallel universes of efficacy and cost-effectiveness. Value In Health 2011, 14(5):640-6.
  • [14]Williamson PR, Marson AG, Tudur C, Hutton JL, Chadwick D: Individual patient data meta-analysis of randomized anti-epileptic drug monotherapy trials. Journal of evaluation in clinical practice 2000, 6(2):205-214.
  • [15]Stewart LA, Tierney JF: To IPD or not to IPD? : Advantages and disadvantages of systematic reviews using individual patient data. Evaluation and the Health Professions 2002, 25:76.
  • [16]Bellera CA, MacGrogan G, Debled M, Tunon de Lara C, Brouste V, Mathoulin-Pélissier S: Variables with time-varying effects and the Cox model: Some statistical concepts illustrated with a prognostic factor study in breast cancer. BMC Medical Research Methodology 2010, 10:20. BioMed Central Full Text
  • [17]Collett D: Modelling Survival Data in Medical Research. Second edition. Boca Raton: Chapman & Hall/CRC; 2003.
  • [18]Cox C: The generalized F distribution: an umbrella for parametric survival analysis. Stat Med 2008, 27:4301-12.
  • [19]McDonald JB, Xub YJ: A generalization of the beta distribution with applications. Journal of Econometrics 1995, 66:133-152.
  • [20]Royston P, Parmar MKB: Flexible parametric proportional-hazards and proportional-odds models for censored survival data, with application to prognostic modeling and estimation of treatment effects. Stat Med 2002, 21:2175-97.
  • [21]Morden J, Lambert P, Latimer N: Assessing methods for dealing with treatment switching in randomised clinical trials. [http:/ / www.nicedsu.org.uk/ Crossover%20and%20survival%20-%20fi nal%20DSU%20report.pdf] webcite 2010.
  • [22]van Houwelingen HC, van de Velde CJH, Stijnen T: Interim analysis on survival data: its potential bias and how to repair it. Statistics in medicine 2005, 24:2823-2835.
  • [23]Hunink MGM, Wong JB: Meta-analysis of failure-time data with adjustment for covariates. Medical decision Making 1994, 14:59-70.
  • [24]Shore T, Nelson N, Weinerman B: A meta-analysis of stages I and II Hodgkin's disease. Cancer 1990, 65:1155-60.
  • [25]Voest EE, Van Houwelingen JC, Neijt JP: A meta-analysis of prognostic factors in advanced ovarian cancer with median survival and overall survival (measured with the log(relative risk)) as main objectives. European Journal of Cancer and Clinical Oncology 1989, 25:711-20.
  • [26]Rothman K, Greenland S, Lash TL: Modern epidemiology. Third edition. Lippincott Williams & Wilkins; 2008.
  • [27]Van Oers MH, Klasa R, Marcus RE, Wolf M, Gascoyne RD, Jack A, Van'tVeer M, Vranovsky A, Holte H, van Glabbeke M, Teodorovic I, Rozewicz C, Hagenbeek A: Rituximab maintenance improves clinical outcome of relapsed/resistant follicular non-Hodgkin's lymphoma, both in patients with and without rituximab during induction: results of a prospective randomized phase III study. Blood 2006, 108:3295-3301.
  • [28]Goss PE, Ingle JN, Martino S, Robert NJ, Muss HB, Piccart MJ, Castiglione M, Tu D, Shepherd LE, Pritchard KI, Livingston RB, Davidson NE, Norton L, Perez EA, Abrams JS, Cameron DA, Palmer MJ, Pater JL: Randomized Trial of Letrozole Following Tamoxifen as Extended Adjuvant Therapy in Receptor-Positive Breast Cancer: Updated Findings from NCIC CTG MA.17. JNCI Cancer Spectrum 2005, 97:1262-1271.
  • [29]Seymour MT, Maughan TS, Ledermann JA, Topham C, James R, Gwyther SJ, Smith DB, Sheperd S, Maraveyas A, Ferry DR, Meade AM, Thompson L, Griffiths GO, Parmar MKB, Stephens RJ: FOCUS Trial Investigators. Different strategies of sequential and combination chemotherapy for patients with poor prognosis advanced colorectal cancer (MRC FOCUS): a randomised controlled trial. Lancet 2007, 370(9582):143-52. Erratum in: Lancet. 2007 Aug 18; 370(9587):566
  • [30]Pan J-N: Evaluating the Gauge repeatability and reproducibility for different industries. Quality & Quantity 2006, 40:499-518.
  • [31]Wang F-K, Li E: Confidence intervals in repeatability and reproducibility using the Bootstrap method. Total quality management 2003, 14(3):341-354.
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