Real-time prognosis for metastatic thyroid carcinoma based on 2-[18F]fluoro-2-deoxy-D-glucose-positron emission tomography scanning

被引:414
作者
Robbins, RJ
Wan, Q
Grewal, RK
Reibke, R
Gonen, M
Strauss, HW
Tuttle, RM
Drucker, W
Larson, SM
机构
[1] Mem Hosp Canc & Allied Dis, Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY USA
[2] Mem Hosp Canc & Allied Dis, Mem Sloan Kettering Canc Ctr, Dept Radiol, New York, NY 10021 USA
[3] Mem Hosp Canc & Allied Dis, Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[4] Mem Hosp Canc & Allied Dis, Mem Sloan Kettering Canc Ctr, Dept Endocrine, New York, NY 10021 USA
[5] Mem Hosp Canc & Allied Dis, Mem Sloan Kettering Canc Ctr, Dept Nucl Med, New York, NY 10021 USA
[6] Mem Hosp Canc & Allied Dis, Mem Sloan Kettering Canc Ctr, Biostat Serv, New York, NY 10021 USA
关键词
D O I
10.1210/jc.2005-1534
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context/Objective: Approximately 15% of thyroid cancer patients develop subsequent metastases. The clinical course of patients with metastatic thyroid carcinoma is highly variable. We hypothesized that the metabolic activity of metastatic lesions, as defined by retention of 2-[F-18]fluoro-2-deoxyglucose (FDG), would correlate with prognosis. Design/Patients: The initial FDG-positron emission tomography (PET) scans from 400 thyroid cancer patients were retrospectively reviewed and compared with overall survival (median follow-up, 7.9 yr). We examined the prognostic value of clinical information such as gender, age, serum thyroglobulin, American Joint Committee on Cancer (AJCC) stage, histology, radioiodine avidity, FDG-PET positivity, number of FDG-avid lesions, and the glycolytic rate of the most active lesion. Results: Age, initial stage, histology, thyroglobulin, radioiodine uptake, and PET outcomes all correlated with survival by univariate analysis. However, only age and PET results continued to be strong predictors of survival under multivariate analysis. The initial American Joint Committee on Cancer stage was not a significant predictor of survival by multivariate analysis. There were significant inverse relationships between survival and both the glycolytic rate of the most active lesion and the number of FDG-avid lesions. Conclusions: FDG-PET scanning is a simple, expensive, but powerful means to restage thyroid cancer patients who develop subsequent metastases, assigning them to groups that are either at low (FDG negative) or high ( FDG positive) risk of cancer-associated mortality. We propose that the aggressiveness of therapy for metastases should match the FDG-PET status.
引用
收藏
页码:498 / 505
页数:8
相关论文
共 33 条
[1]   PAPILLARY THYROID-CARCINOMA ETIOLOGY, ASSESSMENT, AND THERAPY [J].
AIN, KB .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1995, 24 (04) :711-+
[2]  
[Anonymous], 2002, AJCC CANC STAG MAN
[3]  
[Anonymous], 1997, AJCC CANC STAG MAN
[4]  
CADY B, 1988, SURGERY, V104, P947
[5]   Recombinant human thyrotropin stimulation of fluoro-D-glucose positron emission tomography uptake in well-differentiated thyroid carcinoma [J].
Chin, BB ;
Patel, P ;
Cohade, C ;
Ewertz, M ;
Wahl, R ;
Ladenson, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (01) :91-95
[6]   DISTANT METASTASES IN PAPILLARY THYROID-CARCINOMA - 100 CASES OBSERVED AT ONE INSTITUTION DURING 5 DECADES [J].
DINNEEN, SF ;
VALIMAKI, MJ ;
BERGSTRALH, EJ ;
GOELLNER, JR ;
GORMAN, CA ;
HAY, ID .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (07) :2041-2045
[7]   Annual report to the Nation on the status of cancer, 1975-2002, featuring population-based trends in cancer treatment [J].
Edwards, BK ;
Brown, ML ;
Wingo, PA ;
Howe, HL ;
Ward, E ;
Ries, LAG ;
Schrag, D ;
Jamison, PM ;
Jemal, A ;
Wu, XC ;
Friedman, C ;
Harlan, L ;
Warren, J ;
Anderson, RN ;
Pickle, LW .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (19) :1407-1427
[8]  
FEINE U, 1995, NUKLEARMED, V34, P127
[9]  
Feine U, 1996, J NUCL MED, V37, P1468
[10]   Whole-body PET/CT:: Spectrum of physiological variants, artifacts and interpretative pitfalls in cancer patients [J].
Gorospe, L ;
Raman, S ;
Echeveste, J ;
Avril, N ;
Herrero, Y ;
Hernández, S .
NUCLEAR MEDICINE COMMUNICATIONS, 2005, 26 (08) :671-687