Modeling Personalized Adjuvant TreaTment in EaRly stage coloN cancer (PATTERN)

被引:6
|
作者
Jongeneel, Gabrielle [1 ]
Greuter, Marjolein J. E. [1 ]
van Erning, Felice N. [2 ]
Koopman, Miriam [3 ]
Medema, Jan P. [4 ]
Kandimalla, Raju [5 ,6 ]
Goel, Ajay [5 ,6 ]
Bujanda, Luis [7 ]
Meijer, Gerrit A. [8 ]
Fijneman, Remond J. A. [8 ]
van Oijen, Martijn G. H. [9 ]
Ijzermans, Jan [10 ]
Punt, Cornelis J. A. [9 ]
Vink, Geraldine R. [2 ,3 ]
Coupe, Veerle M. H. [1 ]
机构
[1] Vrije Univ Amsterdam, Dept Epidemiol & Biostat, Amsterdam UMC, MF F Wing,POB 7057, NL-1007 MB Amsterdam, Netherlands
[2] Netherlands Comprehens Canc Org IKNL, Dept Res, Utrecht, Netherlands
[3] Univ Utrecht, Univ Med Ctr Utrecht, Dept Med Oncol, Utrecht, Netherlands
[4] Univ Amsterdam, Dept Radiotherapy, Amsterdam UMC, Amsterdam, Netherlands
[5] Baylor Univ, Med Ctr, Baylor Scott & White Res Inst, Ctr Gastrointestinal Res,Ctr Translat Genom & Onc, Dallas, TX USA
[6] Baylor Univ, Med Ctr, Charles A Sammons Canc Ctr, Dallas, TX USA
[7] Univ Pais Vasco UPV EHU, Ctr Invest Biomed Red Enfermedades Hepat & Digest, Inst Biodonostia, Dept Gastroenterol, San Sebastian, Spain
[8] Netherlands Canc Inst, Dept Pathol, Amsterdam, Netherlands
[9] Univ Amsterdam, Dept Med Oncol, Amsterdam UMC, Amsterdam, Netherlands
[10] Erasmus MC Univ Med Ctr, Dept Gen Surg, Rotterdam, Netherlands
关键词
Colon cancer; Adjuvant chemotherapy; Markov cohort model; Survival analysis; MISMATCH REPAIR STATUS; COLORECTAL-CANCER; SURVIVAL ANALYSIS; CLINICAL-TRIALS; RISK-FACTORS; FLUOROURACIL; CHEMOTHERAPY; MORTALITY; THERAPY; BRAF;
D O I
10.1007/s10198-020-01199-4
中图分类号
F [经济];
学科分类号
02 ;
摘要
Aim To develop a decision model for the population-level evaluation of strategies to improve the selection of stage II colon cancer (CC) patients who benefit from adjuvant chemotherapy. Methods A Markov cohort model with a one-month cycle length and a lifelong time horizon was developed. Five health states were included; diagnosis, 90-day mortality, death other causes, recurrence and CC death. Data from the Netherlands Cancer Registry were used to parameterize the model. Transition probabilities were estimated using parametric survival models including relevant clinical and pathological covariates. Subsequently, biomarker status was implemented using external data. Treatment effect was incorporated using pooled trial data. Model development, data sources used, parameter estimation, and internal and external validation are described in detail. To illustrate the use of the model, three example strategies were evaluated in which allocation of treatment was based on (A) 100% adherence to the Dutch guidelines, (B) observed adherence to guideline recommendations and (C) a biomarker-driven strategy. Results Overall, the model showed good internal and external validity. Age, tumor growth, tumor sidedness, evaluated lymph nodes, and biomarker status were included as covariates. For the example strategies, the model predicted 83, 87 and 77 CC deaths after 5 years in a cohort of 1000 patients for strategies A, B and C, respectively. Conclusion This model can be used to evaluate strategies for the allocation of adjuvant chemotherapy in stage II CC patients. In future studies, the model will be used to estimate population-level long-term health gain and cost-effectiveness of biomarker-based selection strategies.
引用
收藏
页码:1059 / 1073
页数:15
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