Metastatic Medullary Thyroid Cancer: The Role of 68Gallium-DOTA-Somatostatin Analogue PET/CT and Peptide Receptor Radionuclide Therapy

被引:26
作者
Hayes, Aimee R. [1 ]
Crawford, Alexander [2 ]
Al Riyami, Khulood [3 ,4 ]
Tang, Christine [3 ,4 ]
Bomanji, Jamshed [3 ]
Baldeweg, Stephanie E. [5 ,6 ]
Wild, Damian [7 ]
Morganstein, Daniel [8 ]
Harry, Alice [8 ]
Grozinsky-Glasberg, Simona [9 ,10 ]
Oleinikov, Kira [9 ,10 ]
Khoo, Bernard [1 ]
Caplin, Martyn E. [1 ]
Nicolas, Guillaume P. [7 ]
Grossman, Ashley B. [1 ]
机构
[1] Royal Free Hosp, ENETS Ctr Excellence, Neuroendocrine Tumour Unit, London NW3 2QG, England
[2] UCL, Med Sch, London, England
[3] Univ Coll London Hosp, Dept Nucl Med, London, England
[4] Univ Coll London Hosp, Dept Radiol, London, England
[5] Univ Coll London Hosp, Dept Endocrinol, London, England
[6] UCL, Div Med, London, England
[7] Univ Hosp Basel, ENETS Ctr Excellence, Div Nucl Med, Basel, Switzerland
[8] Royal Marsden Hosp, Thyroid Unit, London, England
[9] Hebrew Univ Jerusalem, Hadassah Med Org, ENETS Ctr Excellence, Dept Endocrinol & Metab,Neuroendocrine Tumour Uni, Jerusalem, Israel
[10] Hebrew Univ Jerusalem, Fac Med, Jerusalem, Israel
关键词
medullary thyroid cancer; somatostatin receptors; (68)Gallium-DOTATATE PET; F-18-FDG PET; peptide receptor radionuclide therapy; PRRT; ASSOCIATION GUIDELINES; PROGNOSTIC-FACTORS; CARCINOMA; SURVIVAL; PRRT; TUMORS; LU-177-DOTATATE; MANAGEMENT; F-18-FDG; EFFICACY;
D O I
10.1210/clinem/dgab588
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Metastatic medullary thyroid cancer (MTC) is a rare malignancy with minimal treatment options. Many, but not all, MTCs express somatostatin receptors. Objective: Our aim was to explore the role of Ga-68-DOTA-somatostatin analogue (SSA) positron emission tomography (PET)/computed tomography (CT) in patients with metastatic MTC and to determine their eligibility for peptide receptor radionuclide therapy (PRRT). Methods: We retrospectively identified patients with metastatic MTC who had Ga-68-DOTA-SSA PET/CT at 5 centers. We collected characteristics on contrast-enhanced CT, Ga-68-DOTA-SSA and F-18-FDG PET/CT. The efficacy of PRRT was explored in a subgroup of patients. Kaplan-Meier analysis was used to estimate time to treatment failure (TTF) and overall survival (OS). Results: Seventy-one patients were included (10 local recurrence, 61 distant disease). Of the patients with distant disease, 16 (26%) had >= 50% of disease sites with tracer avidity greater than background liver, including 10 (10/61, 16%) with >90%. In 19 patients with contemporaneous contrast-enhanced CT, no disease regions were independently identified on Ga-68-DOTA-SSA PET/CT. Thirty-five patients had an F-18-FDG PET/CT, with 18F-FDG positive/Ga-68-DOTA-SSA negative metastases identified in 15 (43%). Twenty-one patients had PRRT with a median TTF of 14 months (95% CI 8-25) and a median OS of 63 months (95% CI 21-not reached). Of the entire cohort, the median OS was 323 months (95% CI 152-not reached). Predictors of poorer OS included a short calcitonin doubling-time (<= 24 months), strong F-18-FDG avidity, and age >= 60 years. Conclusions: The prevalence of high tumor avidity on Ga-68-DOTA-SSA PET/CT is low in the setting of metastatic MTC; nevertheless, PRRT may still be a viable treatment option in select patients.
引用
收藏
页码:E4903 / E4916
页数:14
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