Tumour heterogeneity in the clinic

被引:920
作者
Bedard, Philippe L. [1 ,2 ]
Hansen, Aaron R. [1 ,2 ]
Ratain, Mark J. [3 ]
Siu, Lillian L. [1 ,2 ]
机构
[1] Univ Hlth Network, Div Med Oncol & Hematol, Princess Margaret Canc Ctr, Toronto, ON, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Univ Chicago, Dept Med, Chicago, IL 60637 USA
关键词
FACTOR RECEPTOR 2; METASTATIC BREAST-CANCER; HER2 GENE AMPLIFICATION; ANTI-EGFR THERAPY; CELL LUNG CANCERS; ACQUIRED-RESISTANCE; COLORECTAL-CANCER; INTRATUMOR HETEROGENEITY; IN-SITU; MUTATIONAL EVOLUTION;
D O I
10.1038/nature12627
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent therapeutic advances in oncology have been driven by the identification of tumour genotype variations between patients, called interpatient heterogeneity, that predict the response of patients to targeted treatments. Subpopulations of cancer cells with unique genomes in the same patient may exist across different geographical regions of a tumour or evolve over time, called intratumour heterogeneity. Sequencing technologies can be used to characterize intratumour heterogeneity at diagnosis, monitor clonal dynamics during treatment and identify the emergence of clinical resistance during disease progression. Genetic interpatient and intratumour heterogeneity can pose challenges for the design of clinical trials that use these data.
引用
收藏
页码:355 / 364
页数:10
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