Skin surface temperature rhythms as potential circadian biomarkers for personalized chronotherapeutics in cancer patients

被引:31
|
作者
Scully, Christopher G. [2 ,3 ]
Karaboue, Abdoulaye [1 ,4 ]
Liu, Wei-Min [2 ]
Meyer, Joseph [2 ]
Innominato, Pasquale F. [1 ,4 ,5 ]
Chon, Ki H. [3 ]
Gorbach, Alexander M. [2 ]
Levi, Francis [1 ,4 ,5 ]
机构
[1] INSERM, UMRS776, F-94807 Villejuif, France
[2] Natl Inst Biomed Imaging & Bioengn, NIH, Bethesda, MD USA
[3] Worcester Polytech Inst, Dept Biomed Engn, Worcester, MA 01609 USA
[4] Univ Paris 11, UMR S0776, F-91405 Orsay, France
[5] Hop Paul Brousse, Dept Cancerol, Unite Chronotherapie, AP HP, F-94807 Villejuif, France
基金
美国国家卫生研究院;
关键词
chronotherapeutics; circadian rhythm; biomarker; body temperature; cancer; personalized medicine; METASTATIC COLORECTAL-CANCER; QUALITY-OF-LIFE; WAVELET ANALYSIS; CLOCKS; SLEEP; OXALIPLATIN; SURVIVAL; DELIVERY; DISEASE; 5-FLUOROURACIL;
D O I
10.1098/rsfs.2010.0012
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chronotherapeutics involve the administration of treatments according to circadian rhythms. Circadian timing of anti-cancer medications has been shown to improve treatment tolerability up to fivefold and double efficacy in experimental and clinical studies. However, the physiological and the molecular components of the circadian timing system (CTS), as well as gender, critically affect the success of a standardized chronotherapeutic schedule. In addition, a wrongly timed therapy or an excessive drug dose disrupts the CTS. Therefore, a non-invasive approach to accurately detect and monitor circadian rhythms is needed for a dynamic assessment of the CTS in order to personalize chronomodulated drug delivery schedule in cancer patients. Since core body temperature is a robust circadian biomarker, we recorded temperature at multiple locations on the skin of the upper chest and back of controls and cancer patients continuously. Variability in the circadian phase existed among patch locations in individual subjects over the course of 2-6 days, demonstrating the need to monitor multiple skin temperature locations to determine the precise circadian phase. Additionally, we observed that locations identified by infrared imaging as relatively cool had the largest 24 h temperature variations. Disruptions in skin temperature rhythms during treatment were found, pointing to the need to continually assess circadian timing and personalize chronotherapeutic schedules.
引用
收藏
页码:48 / 60
页数:13
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