Hypoxia imaging-directed radiation treatment planning

被引:92
作者
Rajendran, J. G.
Hendrickson, K. R. G.
Spence, A. M.
Muzi, M.
Krohn, K. A.
Mankoff, D. A.
机构
[1] Univ Washington, Div Nucl Med, Seattle, WA 98195 USA
[2] Univ Washington, Dept Radiol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Radiat Oncol, Seattle, WA 98195 USA
[4] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
关键词
tissue hypoxia; radiotherapy; PET; image-guided treatment;
D O I
10.1007/s00259-006-0135-1
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Increasing evidence supports the role of the tumor microenvironment in modulating cancer behavior. Tissue hypoxia, an important and common condition affecting the tumor microenvironment, is well established as a resistance factor in radiotherapy. Increasing evidence points to the ability of hypoxia to induce the expression of gene products, which confer aggressive tumor behavior and promote broad resistance to therapy. These factors suggest that determining the presence or absence of tumor hypoxia is important in planning cancer therapy. Recent advances in PET hypoxia imaging, conformal radiotherapy, and imaging-directed radiotherapy treatment planning now make it possible to perform hypoxia-directed radiotherapy. We review the biological aspects of tumor hypoxia and PET imaging approaches for measuring tumor hypoxia, along with methods for conformal radiotherapy and image-guided treatment, all of which provide the underpinnings for hypoxia-directed therapy. As a case example, we review emerging data on PET imaging of hypoxia to direct radiotherapy.
引用
收藏
页码:S44 / S53
页数:10
相关论文
共 98 条
[1]   IMRT dose escalation for positive para-aortic lymph nodes in patients with locally advanced cervical cancer while reducing dose to bone marrow and other organs at risk [J].
Ahmed, RS ;
Kim, RY ;
Duan, J ;
Meleth, S ;
De Los Santos, JF ;
Fiveash, JB .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 60 (02) :505-512
[2]   On biologically conformal boost dose optimization [J].
Alber, M ;
Paulsen, F ;
Eschmann, SM ;
Machulla, HJ .
PHYSICS IN MEDICINE AND BIOLOGY, 2003, 48 (02) :N31-N35
[3]  
ALLEN N, 1972, EXPT BIOL BRAIN TUMO, P243
[4]   Imaging hypoxia in tumors [J].
Ballinger, JR .
SEMINARS IN NUCLEAR MEDICINE, 2001, 31 (04) :321-329
[5]   LOCAL INTERRELATIONSHIPS OF CEREBRAL OXYGEN-CONSUMPTION AND GLUCOSE-UTILIZATION IN NORMAL SUBJECTS AND IN ISCHEMIC STROKE PATIENTS - A POSITRON TOMOGRAPHY STUDY [J].
BARON, JC ;
ROUGEMONT, D ;
SOUSSALINE, F ;
BUSTANY, P ;
CROUZEL, C ;
BOUSSER, MG ;
COMAR, D .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1984, 4 (02) :140-149
[6]   Feasibility of detecting hypoxia in experimental mouse tumours with 18F-fluorinated tracers and positron emission tomography -: A study evaluating [18F]fluoromisonidazole and [18F]fluoro-2-deoxy-D-glucose [J].
Bentzen, L ;
Keiding, S ;
Horsman, MR ;
Falborg, L ;
Hansen, SB ;
Overgaard, J .
ACTA ONCOLOGICA, 2000, 39 (05) :629-637
[7]   Intensity-modulated radiotherapy: Current status and issues of interest [J].
Boyer, AL ;
Butler, EB ;
DiPetrillo, TA ;
Engler, MJ ;
Fraass, B ;
Grant, W ;
Ling, CC ;
Low, DA ;
Mackie, TR ;
Mohan, R ;
Purdy, JA ;
Roach, M ;
Rosenman, JG ;
Verhey, LJ ;
Wong, JW ;
Cumberlin, RL ;
Stone, H ;
Palta, JR .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 51 (04) :880-914
[8]   Pseudopalisades in glioblastoma are hypoxic, express extracellular matrix proteases, and are formed by an actively migrating cell population [J].
Brat, DJ ;
Castellano-Sanchez, AA ;
Hunter, SB ;
Pecot, M ;
Cohen, C ;
Hammond, EH ;
Devi, SN ;
Kaur, B ;
Van Meir, EG .
CANCER RESEARCH, 2004, 64 (03) :920-927
[9]   Exploiting the hypoxic cancer cell: mechanisms and therapeutic strategies [J].
Brown, JM .
MOLECULAR MEDICINE TODAY, 2000, 6 (04) :157-162
[10]  
Bruehlmeier M, 2004, J NUCL MED, V45, P1851