Guidelines for time-to-event end point definitions in sarcomas and gastrointestinal stromal tumors (GIST) trials: results of the DATECAN initiative (Definition for the Assessment of Time-to-event Endpoints in CANcer trials)

被引:41
作者
Bellera, C. A. [1 ,2 ]
Penel, N. [3 ]
Ouali, M. [4 ,5 ]
Bonvalot, S. [6 ]
Casali, P. G. [7 ]
Nielsen, O. S. [8 ]
Delannes, M. [9 ]
Litiere, S. [4 ]
Bonnetain, F. [10 ]
Dabakuyo, T. S. [11 ]
Benjamin, R. S. [12 ,13 ]
Blay, J. -Y. [14 ,15 ,16 ]
Bui, B. N. [17 ]
Collin, F. [18 ]
Delaney, T. F. [19 ,20 ]
Duffaud, F. [21 ]
Filleron, T. [5 ]
Fiore, M. [22 ,23 ]
Gelderblom, H. [24 ]
George, S. [25 ]
Grimer, R. [26 ]
Grosclaude, P. [27 ]
Gronchi, A. [23 ]
Haas, R. [28 ]
Hohenberger, P. [29 ]
Issels, R. [30 ,31 ]
Italiano, A. [17 ]
Jooste, V. [32 ]
Krarup-Hansen, A. [33 ]
Le Pechoux, C. [34 ]
Mussi, C. [35 ]
Oberlin, O. [36 ,37 ]
Patel, S. [12 ,13 ]
Piperno-Neumann, S. [38 ]
Raut, C. [39 ]
Ray-Coquard, I. [14 ]
Rutkowski, P. [40 ,41 ]
Schuetze, S. [42 ]
Sleijfer, S. [43 ]
Stoeckle, E. [44 ]
Van Glabbeke, M. [4 ]
Woll, P. [45 ]
Gourgou-Bourgade, S. [46 ]
Mathoulin-Pelissier, S. [1 ,2 ]
机构
[1] Ctr Comprehens Canc, Inst Bergonie, Clin & Epidemiol Res Unit, Bordeaux, France
[2] INSERM CIC 14 01 Clin Epidemiol, Clin Epidemiol Unit, F-33000 Bordeaux, France
[3] Ctr Comprehens Canc, Ctr Oscar Lambret, Dept Med Oncol, Lille, France
[4] European Org Res Treatment Canc, Dept Biostat, Brussels, Belgium
[5] Ctr Comprehens Canc, Inst Claudius Regaud, Biostat Unit, Toulouse, France
[6] Ctr Comprehens Canc, Inst Gustave Roussy, Dept Surg, Villejuif, France
[7] Fdn IRCCS Ist Nazl Tumori, Med Oncol, Milan, Italy
[8] Aarhus Univ, Fac Hlth Sci, Aarhus, Denmark
[9] Ctr Comprehens Canc, Inst Claudius Regaud, Dept Radiotherapy, Toulouse, France
[10] CHU Besancon, Methodol & Qual Life Unit Oncol EA3181, F-25030 Besancon, France
[11] Ctr Comprehens Canc, Ctr Georges Francois Leclerc, Biostat & Qual Life Unit EA4184, Dijon, France
[12] Univ Texas MD Anderson Canc Ctr, Div Canc Med, Houston, TX 77030 USA
[13] Univ Texas MD Anderson Canc Ctr, Sarcoma Ctr, Houston, TX 77030 USA
[14] Ctr Comprehens Canc, Ctr Leon Berard, Dept Med Oncol, Lyon, France
[15] Univ Lyon 1, F-69365 Lyon, France
[16] Hop Edouard Herriot, Med Oncol Unit, Lyon, France
[17] Ctr Comprehens Canc, Inst Bergonie, Dept Med Oncol, Bordeaux, France
[18] Ctr Comprehens Canc, Ctr Georges Francois Leclerc, Dept Biol & Pathol, Dijon, France
[19] Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02114 USA
[20] Massachusetts Gen Hosp, Ctr Sarcoma & Connect Tissue Oncol, Boston, MA 02114 USA
[21] La Timone Hosp Univ, Dept Med Oncol, Marseille, France
[22] Fdn IRCCS Ist Nazl Tumori, Dept Surg, Milan, Italy
[23] Fdn IRCCS Ist Nazl Tumori, Dept Surg, Sarcoma Unit, Sarcoma Serv, Milan, Italy
[24] Leiden Univ, Med Ctr, Dept Clin Oncol, Leiden, Netherlands
[25] Harvard Univ, Brigham & Womens Hosp, Dana Farber Canc Inst, Dept Med Oncol,Med Sch, Boston, MA 02115 USA
[26] Royal Orthopaed Hosp NHS Trust, Birmingham, W Midlands, England
[27] Ctr Comprehens Canc, Inst Claudius Regaud, Canc Registry Tarn, Toulouse, France
[28] Antoni van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Radiat Oncol, Amsterdam, Netherlands
[29] Univ Mannheim, Med Ctr, Div Surg Oncol & Thorac Surg, D-68131 Mannheim, Germany
[30] Univ Munich, Sarcoma Ctr, Munich, Germany
[31] Univ Munich, Klinikum Grosshadern Med Ctr, Dept Internal Med, Munich, Germany
[32] Univ Burgundy, INSERM, U866, Burgundy Digest Canc Registry, Dijon, France
[33] Univ Copenhagen, Herlev Hosp, Dept Oncol, DK-2730 Herlev, Denmark
[34] Ctr Comprehens Canc, Inst Gustave Roussy, Dept Radiotherapy, Villejuif, France
[35] Humanitas Clin & Res Ctr, Dept Surg, Milan, Italy
[36] Ctr Comprehens Canc, Inst Gustave Roussy, Dept Surg, Villejuif, France
[37] Ctr Comprehens Canc, Inst Gustave Roussy, Dept Pediat & Adolescent Oncol, Villejuif, France
[38] Ctr Comprehens Canc, Inst Curie, Dept Med Oncol, Paris, France
[39] Harvard Univ, Brigham & Womens Hosp, Dana Farber Canc Inst, Dept Surg,Med Sch, Boston, MA 02115 USA
[40] Maria Sklodowska Curie Mem Canc Ctr, Dept Soft Tissue Bone Sarcoma & Melanoma, Warsaw, Poland
[41] Inst Oncol, Warsaw, Poland
[42] Univ Michigan, Dept Med Oncol, Ann Arbor, MI 48109 USA
[43] Erasmus Univ, Med Ctr, Daniel den Hoed Canc Ctr, Dept Med Oncol, Rotterdam, Netherlands
[44] Ctr Comprehens Canc, Inst Bergonie, Dept Surg Oncol, Bordeaux, France
[45] Weston Pk Hosp, Sheffield Canc Res Ctr, Dept Oncol, Sheffield, S Yorkshire, England
[46] Ctr Comprehens Canc, Montpellier Canc Inst, Montpellier, France
关键词
guidelines; randomized controlled trial; time-to-event end point; efficacy measure; sarcoma; gastrointestinal stromal tumors; CLINICAL-TRIALS; MURAMYL TRIPEPTIDE; PEDIATRIC-ONCOLOGY; RESPONSE CRITERIA; PLUS DOXORUBICIN; EWINGS-SARCOMA; BREAST-CANCER; IFOSFAMIDE; OSTEOSARCOMA; ETOPOSIDE;
D O I
10.1093/annonc/mdu360
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The use of potential surrogate end points for overall survival, such as disease-free survival (DFS) or timeto-treatment failure (TTF) is increasingly common in randomized controlled trials (RCTs) in cancer. However, the definition of time-to-event (TTE) end points is rarely precise and lacks uniformity across trials. End point definition can impact trial results by affecting estimation of treatment effect and statistical power. The DATECAN initiative (Definition for the Assessment of Time-to-event End points in CANcer trials) aims to provide recommendations for definitions of TTE end points. We report guidelines for RCT in sarcomas and gastrointestinal stromal tumors (GIST). Methods: We first carried out a literature review to identify TTE end points (primary or secondary) reported in publications of RCT. An international multidisciplinary panel of experts proposed recommendations for the definitions of these end points. Recommendations were developed through a validated consensus method formalizing the degree of agreement among experts. Results: Recommended guidelines for the definition of TTE end points commonly used in RCT for sarcomas and GIST are provided for adjuvant and metastatic settings, including DFS, TTF, time to progression and others. Conclusion: Use of standardized definitions should facilitate comparison of trials' results, and improve the quality of trial design and reporting. These guidelines could be of particular interest to research scientists involved in the design, conduct, reporting or assessment of RCT such as investigators, statisticians, reviewers, editors or regulatory authorities.
引用
收藏
页码:865 / 872
页数:8
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