The future of cancer imaging

被引:55
作者
Benaron, DA [1 ]
机构
[1] Stanford Univ, Sch Med, Palo Alto, CA 94304 USA
关键词
CT; MRI; optical imaging; contrast agents; MRSI; PET; monoclonal antibody; molecular imaging; functional imaging; review;
D O I
10.1023/A:1020131208786
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Conventional (anatomical, structural) imaging is insensitive to the presence of cancer, often failing to yield the very information needed for accurate diagnosis and staging, for proper treatment selection and monitoring or for effective follow-up after treatment. This, fortunately, is changing. Newer techniques, already in clinical testing, are rapidly pushing clinical imaging in the same direction as the rest of medicine: away from simple detection of the gross structural end-effects of disease, and toward a patient-specific approach based on physiologic, histologic, antigenic, molecular, and (ultimately) genetic markers of disease. By 2010, unimodal, nonspecific, and insensitive radiological images may look as primitive to us as the first Roentgen radiographs. In some cases, these new scans will be so seamlessly integrated into therapeutic treatment that they may not even be thought of as imaging per se. This chapter looks forward to see how imaging for oncology may look in the coming decade, focusing upon near-term trends and techniques by selecting those already demonstrated in vivo in at least animals or which are now under human study, and thus which have moved far enough that they have already begun to impact patient care, or are likely to begin do so in the near future.
引用
收藏
页码:45 / 78
页数:34
相关论文
共 244 条
[31]  
BENARON DA, 2000, 7 ANN CAP CURE SCI R
[32]  
Berger F, 2001, BREAST CANCER RES, V3, P28
[33]   The spatial variation of the refractive index in biological cells [J].
Beuthan, J ;
Minet, O ;
Helfmann, J ;
Herrig, M ;
Muller, G .
PHYSICS IN MEDICINE AND BIOLOGY, 1996, 41 (03) :369-382
[34]   Optical imaging of Renilla luciferase reporter gene expression in living mice [J].
Bhaumik, S ;
Gambhir, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :377-382
[35]  
BIGIO IJ, 1999, J GRAVIT PHYSL, V6, P173
[36]  
Blankenberg FG, 2001, J NUCL MED, V42, P309
[37]   In vivo detection and imaging of phosphatidylserine expression during programmed cell death [J].
Blankenberg, FG ;
Katsikis, PD ;
Tait, JF ;
Davis, RE ;
Naumovski, L ;
Ohtsuki, K ;
Kopiwoda, S ;
Abrams, MJ ;
Darkes, M ;
Robbins, RC ;
Maecker, HT ;
Strauss, HW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6349-6354
[38]   Early prediction of treatment response to high-dose salvage chemotherapy in patients with relapsed germ cell cancer using [18F]FDG PET [J].
Bokemeyer, C ;
Kollmannsberger, C ;
Oechsle, K ;
Dohmen, BM ;
Pfannenberg, A ;
Claussen, CD ;
Bares, R ;
Kanz, L .
BRITISH JOURNAL OF CANCER, 2002, 86 (04) :506-511
[39]  
Bombardieri E, 1998, Q J NUCL MED, V42, P54
[40]   Fluorescent tissue site-selective lanthanide chelate, Tb-PCTMB for enhanced imaging of cancer [J].
Bornhop, DJ ;
Hubbard, DS ;
Houlne, MP ;
Adair, C ;
Kiefer, GE ;
Pence, BC ;
Morgan, DL .
ANALYTICAL CHEMISTRY, 1999, 71 (14) :2607-2615