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Direct parametric inference for the cumulative incidence function

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  • Jong‐Hyeon Jeong
  • Jason Fine

Abstract

Summary. In survival data that are collected from phase III clinical trials on breast cancer, a patient may experience more than one event, including recurrence of the original cancer, new primary cancer and death. Radiation oncologists are often interested in comparing patterns of local or regional recurrences alone as first events to identify a subgroup of patients who need to be treated by radiation therapy after surgery. The cumulative incidence function provides estimates of the cumulative probability of locoregional recurrences in the presence of other competing events. A simple version of the Gompertz distribution is proposed to parameterize the cumulative incidence function directly. The model interpretation for the cumulative incidence function is more natural than it is with the usual cause‐specific hazard parameterization. Maximum likelihood analysis is used to estimate simultaneously parametric models for cumulative incidence functions of all causes. The parametric cumulative incidence approach is applied to a data set from the National Surgical Adjuvant Breast and Bowel Project and compared with analyses that are based on parametric cause‐specific hazard models and nonparametric cumulative incidence estimation.

Suggested Citation

  • Jong‐Hyeon Jeong & Jason Fine, 2006. "Direct parametric inference for the cumulative incidence function," Journal of the Royal Statistical Society Series C, Royal Statistical Society, vol. 55(2), pages 187-200, April.
  • Handle: RePEc:bla:jorssc:v:55:y:2006:i:2:p:187-200
    DOI: 10.1111/j.1467-9876.2006.00532.x
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    Cited by:

    1. Michael G. Hudgens & Chenxi Li & Jason P. Fine, 2014. "Parametric likelihood inference for interval censored competing risks data," Biometrics, The International Biometric Society, vol. 70(1), pages 1-9, March.
    2. Judith J. Lok & Shu Yang & Brian Sharkey & Michael D. Hughes, 2018. "Estimation of the cumulative incidence function under multiple dependent and independent censoring mechanisms," Lifetime Data Analysis: An International Journal Devoted to Statistical Methods and Applications for Time-to-Event Data, Springer, vol. 24(2), pages 201-223, April.
    3. Lu Mao & D. Y. Lin, 2017. "Efficient estimation of semiparametric transformation models for the cumulative incidence of competing risks," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 79(2), pages 573-587, March.
    4. Yosra Yousif & Faiz Elfaki & Meftah Hrairi & Oyelola Adegboye, 2022. "Bayesian Analysis of Masked Competing Risks Data Based on Proportional Subdistribution Hazards Model," Mathematics, MDPI, vol. 10(17), pages 1-10, August.
    5. Lo, Simon M.S. & Mammen, Enno & Wilke, Ralf A., 2020. "A nested copula duration model for competing risks with multiple spells," Computational Statistics & Data Analysis, Elsevier, vol. 150(C).
    6. Serge M. A. Somda & Eve Leconte & Andrew Kramar & Nicolas Penel & Christine Chevreau & Martine Delannes & Maria Rios & Thomas Filleron, 2014. "Determining the Length of Posttherapeutic Follow-up for Cancer Patients Using Competing Risks Modeling," Medical Decision Making, , vol. 34(2), pages 168-179, February.
    7. Marvin N. Wright & Sasmita Kusumastuti & Laust H. Mortensen & Rudi G. J. Westendorp & Thomas A. Gerds, 2021. "Personalised need of care in an ageing society: The making of a prediction tool based on register data," Journal of the Royal Statistical Society Series A, Royal Statistical Society, vol. 184(4), pages 1199-1219, October.
    8. Li, Chenxi, 2016. "The Fine–Gray model under interval censored competing risks data," Journal of Multivariate Analysis, Elsevier, vol. 143(C), pages 327-344.
    9. S. R. Haile & J.-H. Jeong & X. Chen & Y. Cheng, 2016. "A 3-parameter Gompertz distribution for survival data with competing risks, with an application to breast cancer data," Journal of Applied Statistics, Taylor & Francis Journals, vol. 43(12), pages 2239-2253, September.

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