The effect of age in breast conserving therapy: A retrospective analysis on pathology and clinical outcome data

被引:5
作者
Chen, Wei [1 ]
Sonke, Jan-Jakob [1 ]
Stroom, Joep [3 ]
Bartelink, Harry [1 ]
Verheij, Marcel [1 ]
Gilhuijs, Kenneth [2 ]
机构
[1] Netherlands Canc Inst, Dept Radiat Oncol, Amsterdam, Netherlands
[2] Univ Med Ctr Utrecht, Dept Radiol, Utrecht, Netherlands
[3] Fundacao Champalimaud, Dept Radiat Oncol, Lisbon, Portugal
关键词
Age; Breast conserving therapy; Microscopic disease quantity; Monte-Carlo simulation; Radiosensitivity; Tumor control probability; LOCAL RECURRENCE; CONSERVATIVE SURGERY; STAGE-I; CANCER; IMPACT; PROGNOSIS; SURVIVAL; MARGINS; TUMOR; BOOST;
D O I
10.1016/j.radonc.2015.01.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and propose: Age is an important prognostic marker of patient outcome after breast conserving therapy; however, it is not clear how age affects the outcome. This study aimed to explore the relationship between age with the cell quantity and the radiosensitivity of microscopic disease (MSD) in relation to treatment outcome. Materials and methods: We employed a treatment simulation framework which contains mathematic models for describing the load and spread of MSD based on a retrospective cohort of breast pathology specimens, a surgery simulation model for estimating the remaining MSD quantity and a tumor control probability model for predicting the risk of local recurrence following radiotherapy. Results: The average MSD cell quantities around the primary tumor in younger (age <= 50 years) and older patients were estimated at 1.9 * 10(8) cells and 8.4 * 10(7) cells, respectively (P < 0.01). Following surgical simulation, these numbers decreased to 2.0* 10(7) cells and 1.3 *10(7) cells (P < 0.01). Younger patients had smaller average surgical resection volume (118.9 cm(3)) than older patients (162.9 cm(3), P < 0.01) but larger estimated radiosensitivity of MSD cells (0.111 Gy(-1) versus 0.071 Gy(-1), P < 0.01). Conclusion: The higher local recurrence rate in younger patients could be explained by larger clonogenic microscopic disease cell quantity, even though the microscopic disease cells were found to be more radiosensitive. (c) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:314 / 321
页数:8
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