Update of the role of PET/CT and PET/MRI in the management of patients with cervical cancer

被引:3
作者
Khiewvan, Benjapa [1 ,2 ]
Torigian, Drew A. [1 ]
Emamzadehfard, Sahra [1 ]
Paydary, Koosha [1 ]
Salavati, Ali [1 ]
Houshmand, Sina [1 ]
Shamchi, Sara Pourhassan [1 ]
Werner, Thomas J. [1 ]
Aydin, Aysel [1 ]
Roy, Shambo Guha [3 ]
Alavi, Abass [1 ]
Kumar, Rakesh [3 ]
机构
[1] Hosp Univ Penn, Dept Radiol, 3400 Spruce St, Philadelphia, PA 19104 USA
[2] Mahidol Univ, Div Nucl Med, Dept Radiol, Siriraj Hosp,Fac Med, Bangkok 10700, Thailand
[3] All India Inst Med Sci, Dept Nucl Med, Div Diagnost Nucl Med, New Delhi 110029, India
关键词
CC-F-18-FDG PET/CT; CT-MRI-Accuracy; Predictive value-Prognosis; POSITRON-EMISSION-TOMOGRAPHY; SQUAMOUS-CELL CARCINOMA; STANDARDIZED UPTAKE VALUE; LYMPH-NODE METASTASIS; F-18 FLUORODEOXYGLUCOSE UPTAKE; SIGNIFICANT PROGNOSTIC-FACTOR; MODULATED RADIATION-THERAPY; ASSESSING TUMOR HYPOXIA; MAGNETIC-RESONANCE; FDG-PET;
D O I
暂无
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
In cervical cancer (CC), uorine18-uorodeoxyglucose (F-18-FDG) positron emission tomography/computed tomography (PET/CT) has been proven to be benecial for patient management. Positron emission tomography/CT is useful in pretreatment evaluation due to the ability to evaluate disease extent and to assess regional lymph nodes as well as distant sites for metastases. PET/CT has an impact on treatment planning as well as it is incorporated in radiation therapy planning, resulting in more appropriate and eective treatment with less cost and radiation dose to normal tissues. Positron emission tomography/CT is used to predict early treatment response and to assess treatment response after completion of concurrent chemoradiation therapy. PET/CT has been used for surveillance after treatment as well as for restaging in suspected recurrent or metastatic disease. Qualitative PET/CT imaging findings as well as quantitative parameters such as maximum stan-dardized uptake value (SUVmax), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) are useful to predict prognosis and clinical outcome. Moreover, PET imaging using other radiotracers to detect and quantify hypoxia may help to identify aggressive tumors and predict treatment outcome even though it is not widely clinical used. Positron emission tomography/magnetic resonance imaging (PET/MRI) ins-truments are now available, which may potentially improve evaluation of primary tumors and metastatic sites given the improved soft tissue contrast resolution of MRI relative to CT. This article reviews the role of F-18-FDG PET/CT, hypoxia agent PET/CT, and F-18-FDG PET/MRI in the management of patients with CC.
引用
收藏
页码:254 / 268
页数:15
相关论文
共 154 条
[41]   Assessing tumor hypoxia in cervical cancer by positron emission tomography with 60Cu-ATSM:: Relationship to therapeutic response -: A preliminary report [J].
Dehdashti, F ;
Grigsby, PW ;
Mintun, MA ;
Lewis, JS ;
Siegel, BA ;
Welch, MJ .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2003, 55 (05) :1233-1238
[42]   Assessing tumor hypoxia in cervical cancer by PET with 60Cu-labeled diacetyl-bis(N4-methylthiosemicarbazone) [J].
Dehdashti, Farrokh ;
Grigsby, Perry W. ;
Lewis, Jason S. ;
Laforest, Richard ;
Siegel, Barry A. ;
Welch, Michael J. .
JOURNAL OF NUCLEAR MEDICINE, 2008, 49 (02) :201-205
[43]   Prospective Evaluation of 18F-Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography for Response Evaluation in Recurrent Carcinoma Cervix Does Metabolic Response Predicts Survival? [J].
Dhull, Varun Singh ;
Sharma, Punit ;
Sharma, Daya Nand ;
Maharjan, Sagar ;
Suman, Sudhir K. C. ;
Patel, Chetan ;
Bal, Chandrasekhar ;
Kumar, Rakesh .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2014, 24 (02) :312-320
[44]   Tumor Hypoxia Detected by Positron Emission Tomography with 60Cu-ATSM as a Predictor of Response and Survival in Patients Undergoing Neoadjuvant Chemoradiotherapy for Rectal Carcinoma: A Pilot Study [J].
Dietz, David W. ;
Dehdashti, Farrokh ;
Grigsby, Perry W. ;
Malyapa, Robert S. ;
Myerson, Robert J. ;
Picus, Joel ;
Ritter, Jon ;
Lewis, Jason S. ;
Welch, Michael J. ;
Siegel, Barry A. .
DISEASES OF THE COLON & RECTUM, 2008, 51 (11) :1641-1648
[45]  
Eren MS, 2012, HELL J NUCL MED, V15, P56
[46]   PROSPECTIVE CLINICAL TRIAL OF POSITRON EMISSION TOMOGRAPHY/COMPUTED TOMOGRAPHY IMAGE-GUIDED INTENSITY-MODULATED RADIATION THERAPY FOR CERVICAL CARCINOMA WITH POSITIVE PARA-AORTIC LYMPH NODES [J].
Esthappan, Jacqueline ;
Chaudhari, Summer ;
Santanam, Lakshmi ;
Mutic, Sasa ;
Olsen, Jeffrey ;
MacDonald, Dusten M. ;
Low, Daniel A. ;
Singh, Anurag K. ;
Grigsby, Perry W. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2008, 72 (04) :1134-1139
[47]   Can radicality of surgery be safely modulated on the basis of MRI and PET/CT imaging in locally advanced cervical cancer patients administered preoperative treatment? [J].
Ferrandina, Gabriella ;
Petrillo, Marco ;
Restaino, Gennaro ;
Rufini, Vittoria ;
Macchia, Gabriella ;
Carbone, Arnaldo ;
Zannoni, Gian Franco ;
Lucidi, Alessandro ;
D'Angelo, Giorgia ;
Scambia, Giovanni .
CANCER, 2012, 118 (02) :392-403
[48]   Transrectal ultrasound and magnetic resonance imaging in staging of early cervical cancer [J].
Fischerova, D. ;
Cibula, D. ;
Stenhova, H. ;
Vondrichova, H. ;
Calda, P. ;
Zikan, M. ;
Freitag, P. ;
Slama, J. ;
Dundr, P. ;
Belacek, J. .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2008, 18 (04) :766-772
[49]   Squamous cell carcinoma antigen in follow-up of cervical cancer treated with radiotherapy: Evaluation of cost-effectiveness [J].
Forni, Franca ;
Ferrandina, Gabriella ;
Deodato, Francesco ;
Macchia, Gabriella ;
Morganti, Alessio G. ;
Smaniotto, Daniela ;
Luzi, Stefano ;
D'Agostino, Giuseppe ;
Valentini, Vincenzo ;
Cellini, Numa ;
Giardina, Bruno ;
Scambia, Giovanni .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2007, 69 (04) :1145-1149
[50]   DETERMINANTS OF INCREASED RISK FOR RECURRENCE IN PATIENTS UNDERGOING RADICAL HYSTERECTOMY FOR STAGE-IB AND STAGE-IIA CARCINOMA OF THE CERVIX [J].
FULLER, AF ;
ELLIOTT, N ;
KOSLOFF, C ;
HOSKINS, WJ ;
LEWIS, JL .
GYNECOLOGIC ONCOLOGY, 1989, 33 (01) :34-39