High Prognostic Value of 18F-FDG PET for Metastatic Gastroenteropancreatic Neuro endocrine Tumors: A Long-Term Evaluation

被引:148
作者
Bahri, Haifa [1 ]
Laurence, Lenoir [1 ,2 ,3 ]
Edeine, Julien [2 ,3 ,4 ]
Leghzali, Houda [1 ]
Devillers, Anne [1 ]
Raoul, Jean-Luc [5 ]
Cuggia, Marc [6 ]
Mesbah, Habiba [7 ]
Clement, Bruno [2 ]
Boucher, Eveline [2 ,4 ]
Garin, Etienne [1 ,2 ,3 ]
机构
[1] Ctr Eugene Marquis, Dept Nucl Med, F-35042 Rennes, France
[2] INSERM, UMR991, Rennes, France
[3] Univ Rennes 1, Rennes, France
[4] Canc Inst Eugene Marquis, Dept Med Oncol, Rennes, France
[5] Inst J Paoli I Calmettes, Ctr Comprehens Canc, Dept Med Oncol, F-13009 Marseille, France
[6] CHU Pontchaillou, Dept Med Comp, Rennes, France
[7] Inst Eugene Marquis, Dept Med Informat, Rennes, France
关键词
prognosis; PET; FDG; neuroendocrine; POSITRON-EMISSION-TOMOGRAPHY; SOMATOSTATIN RECEPTOR SCINTIGRAPHY; NEUROENDOCRINE TUMORS; TNM CLASSIFICATION; GUIDELINES; SYSTEM;
D O I
10.2967/jnumed.114.144386
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
This study aimed to evaluate the long-term prognostic usefulness of F-18-FDG PET for patients with metastatic gastroenteropancreatic neuroendocrine tumors (GEPNETs). Methods: Thirty-eight patients with metastatic GEPNETs were prospectively enrolled. Initial check-up comprised CT scan, In-111-pentetreotide scintigraphy (SRS), and F-18-FDG PET. Only F-18-FDG PET-positive lesions with a maximum standardized uptake value (SUVmax) greater than 4.5 or an SUV ratio (SUVmax tumor to SUVmax nontumoral liver tissue, or T/NT ratio) of 2.5 or greater were considered positive for prognosis that is, indicating a poor prognosis. Progression-free survival (PFS) and overall survival (OS) were estimated using the Kaplan-Meier method. Factors associated with survival were assessed with univariate and multivariate analyses, using the Cox regression model. Results: Median PFS and OS were significantly higher for patients with a negative F-18-FDG PET finding, with an OS of 119.5 mo (95% confidence interval [CI], 72-infinity), than for patients with a positive F-18-FDG PET finding (only 15 mo [95% CI, 4-27]) (P < 10(-3)). Median PFS and OS were significantly higher for the patient group that had a positive SRS than the group with a negative SRS (P = 0.0002). For patients with a positive SRS, PFS and OS were significantly shorter when the F-18-FDG PET finding was positive: 19.5 mo (95% CI, 4-37) for PFS and 119.5 mo (95% CI, 81-infinity) for OS (P < 10(-8)). In the patient group with a low-grade GEPNET and a positive SRS, PFS and OS were also significantly lower for patients with a positive F-18-FDG PET. At 48-mo follow-up, 100% of patients who had a positive F-18-FDG PET for disease progression (of which 47% were also SRS-positive) were deceased, and 87% of patients with a negative F-18-FDG PET were alive (P < 0.0001). The T/NT ratio was the only parameter associated with OS on multivariate analysis. Conclusion: Overall, F-18-FOG PET appears to be of major importance in the prognostic evaluation of metastatic GEPNET. A positive F-18-FDG PET with an SUV ratio (TINT) of 2.5 or greater was a poor prognostic factor, with a 4-y survival rate of 0%. A positive SRS does not eliminate the need for performing F-18-FDG PET, which is of greater prognostic utility.
引用
收藏
页码:1786 / 1790
页数:5
相关论文
共 15 条
[1]   Indium-111-pentetreotide scintigraphy and somatostatin receptor subtype 2 expression: New prognostic factors for malignant well-differentiated endocrine tumors [J].
Asnacios, Amani ;
Courbon, Frederic ;
Rochaix, Philippe ;
Bauvin, Eric ;
Cances-Lauwers, Valerie ;
Susini, Christiane ;
Schulz, Stefan ;
Boneu, Andree ;
Guimbaud, Rosine ;
Buscail, Louis .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (06) :963-970
[2]   Fluorodeoxyglucose positron emission tomography and somatostatin receptor scintigraphy for diagnosing and staging carcinoid tumours: correlations with the pathological indexes p53 and Ki-67 [J].
Belhocine, T ;
Foidart, J ;
Rigo, P ;
Najjar, F ;
Thiry, A ;
Quatresooz, P ;
Hustinx, R .
NUCLEAR MEDICINE COMMUNICATIONS, 2002, 23 (08) :727-734
[3]   18F-Fluorodeoxyglucose Positron Emission Tomography Predicts Survival of Patients with Neuroendocrine Tumors [J].
Binderup, Tina ;
Knigge, Ulrich ;
Loft, Annika ;
Federspiel, Birgitte ;
Kjaer, Andreas .
CLINICAL CANCER RESEARCH, 2010, 16 (03) :978-985
[4]   Functional Imaging of Neuroendocrine Tumors: A Head-to-Head Comparison of Somatostatin Receptor Scintigraphy, 123I-MIBG Scintigraphy, and 18F-FDG PET [J].
Binderup, Tina ;
Knigge, Ulrich ;
Loft, Annika ;
Mortensen, Jann ;
Pfeifer, Andreas ;
Federspiel, Birgitte ;
Hansen, Carsten Palnaes ;
Hojgaard, Liselotte ;
Kjaer, Andreas .
JOURNAL OF NUCLEAR MEDICINE, 2010, 51 (05) :704-712
[5]  
Bombardieri E, 2001, Minerva Endocrinol, V26, P197
[6]  
Clark OH, 2009, J NATL COMPR CANC NE, V7, P712
[7]  
Ferretti S, 2010, EPIDEMIOL PREV, V34, P125
[8]   Predictive Value of 18F-FDG PET and Somatostatin Receptor Scintigraphy in Patients with Metastatic Endocrine Tumors [J].
Garin, Etienne ;
Le Jeune, Florence ;
Devillers, Anne ;
Cuggia, Marc ;
de Lajarte-Thirouard, Anne-Sophie ;
Bouriel, Catherine ;
Boucher, Eveline ;
Raoul, Jean-Luc .
JOURNAL OF NUCLEAR MEDICINE, 2009, 50 (06) :858-864
[9]   Functional Imaging of neuroendocrine tumors with combined PET/CT using 68Ga-DOTATATE (Dota-DPhe1,Tyr3-octreotate) and 18F-FDG [J].
Kayani, Irfan ;
Bomanji, Jamshed B. ;
Groves, Ashley ;
Conway, Gerard ;
Gacinovic, Sveto ;
Win, Thida ;
Dickson, John ;
Caplin, Martyn ;
Ell, Peter Joseph .
CANCER, 2008, 112 (11) :2447-2455
[10]   The gastroenteropancreatic neuroendocrine cell system and its tumors [J].
Klöppel, G ;
Perren, A ;
Heitz, PU .
GASTROENTEROPANCREATIC NEUROENDOCRINE TUMOR DISEASE: MOLECULAR AND CELL BIOLOGICAL ASPECTS, 2004, 1014 :13-27