Integrated PET/CT as a first-line re-staging modality in patients with suspected recurrence of ovarian cancer

被引:77
作者
Mangili, G.
Picchio, M.
Sironi, S.
Vigano, R.
Rabaiotti, E.
Bornaghi, D.
Bettinardi, V.
Crivellaro, C.
Messa, C.
Fazio, F.
机构
[1] Ist Sci San Raffaele, Dept Nucl Med, I-20132 Milan, Italy
[2] Ist Sci San Raffaele, Dept Obstet & Gynaecol, I-20132 Milan, Italy
[3] Univ Milano Bicocca, Milan, Italy
[4] San Gerardo Hosp, Dept Diagnost Radiol, Monza, Italy
[5] San Gerardo Hosp, Dept Nucl Med, Monza, Italy
[6] CNR, IBFM, I-20133 Milan, Italy
关键词
PET/CT; FDG; single-session staging procedure; ovarian cancer; clinical management;
D O I
10.1007/s00259-006-0306-0
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
Purpose The aims of this study were to compare CT with PET/CT results in patients with suspected ovarian cancer recurrence and to assess the impact of the PET/CT findings on their clinical management. Methods Thirty-two consecutive patients with suspected ovarian cancer recurrence were retrospectively included in the study. Abdominal contrast-enhanced CT and PET/CT with [F-18]FDG, in addition to conventional follow-up, were performed in all 32 patients. After the comparison between CT and PET/CT results, based on clinical reports, changes in the clinical management of patients (intermodality changes) due to PET/CT information were analysed. Results Twenty of the 32 patients were positive at CT (62.5%) versus 29 (90.6%) at PET/CT. Intermodality changes in management, i.e. use of a different treatment modality, after PET/CT examination were indicated in 14/32 (44%) patients. In particular, before PET/CT study, the planned management was as follows: wait-and-see in 7/32 (22%), further instrumental examinations in 4/32 (12%), chemotherapy in 10/32 (31%), diagnostic surgical treatment in 6/32 (19%) and surgical treatment in the remaining 5/32 (16%). After PET/CT study, wait-and-see was indicated in 1/32 (3%), further instrumental examinations in 7/32 (22%), chemotherapy in 16/32 (50%), diagnostic surgical treatment in 2/32 (6%) and surgical treatment in the remaining 6/32 (19%). Conclusion Integrated PET/CT could detect tumour relapse in a higher percentage of patients than could CT. A change in the clinical management was observed in 44% of cases when PET/CT information was added to conventional follow-up findings.
引用
收藏
页码:658 / 666
页数:9
相关论文
共 34 条
[1]   Positron emission tomography with 2-[18F]fluoro-2-deoxy-D-glucose in oncology Part II.: The clinical value in detecting and staging primary tumours [J].
Ak, I ;
Stokkel, MPM ;
Pauwels, EKJ .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2000, 126 (10) :560-574
[2]   PET/CT with intravenous contrast can be used for PET attenuation correction in cancer patients [J].
Berthelsen, AK ;
Holm, S ;
Loft, A ;
Klausen, TL ;
Andersen, F ;
Hojgaard, L .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2005, 32 (10) :1167-1175
[3]  
Beyer T, 2000, J NUCL MED, V41, P1369
[4]  
CASEY J, 2006, NATURE CLIN PRACTICE, V3, P184
[5]   Positron emission tomography with FDG in the detection of peritoneal and retroperitoneal metastases of ovarian cancer [J].
Drieskens, O ;
Stroobants, S ;
Gysen, M ;
Vandenbosch, G ;
Mortelmans, L ;
Vergote, I .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 2003, 55 (03) :130-134
[6]  
Gambhir SS, 2001, J NUCL MED, V42, p1S
[7]   Accuracy of positron emission tomography for diagnosis of pulmonary nodules and mass lesions - A meta-analysis [J].
Gould, MK ;
Maclean, CC ;
Kuschner, WG ;
Rydzak, CE ;
Owens, DK .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (07) :914-924
[8]   Cancer statistics, 2001 [J].
Greenlee, RT ;
Hill-Harmon, MB ;
Murray, T ;
Thun, M .
CA-A CANCER JOURNAL FOR CLINICIANS, 2001, 51 (01) :15-36
[9]   PET diagnostic accuracy: Improvement with in-line PET-CT system: Initial results [J].
Hany, TF ;
Steinert, HC ;
Goerres, GW ;
Buck, A ;
von Schulthess, GK .
RADIOLOGY, 2002, 225 (02) :575-581
[10]   FDG-PET for management of cervical and ovarian cancer [J].
Havrilesky, LJ ;
Kulasingam, SL ;
Matchar, DB ;
Myers, ER .
GYNECOLOGIC ONCOLOGY, 2005, 97 (01) :183-191