Treatment with Sunitinib for Patients with Progressive Metastatic Pheochromocytomas and Sympathetic Paragangliomas

被引:173
作者
Ayala-Ramirez, Montserrat
Chougnet, Cecile N. [4 ]
Habra, Mouhammed Amir
Palmer, J. Lynn [2 ]
Leboulleux, Sophie [4 ]
Cabanillas, Maria E.
Caramella, Caroline [4 ]
Anderson, Pete [3 ]
Al Ghuzlan, Abir [5 ]
Waguespack, Steven G.
Deandreis, Desiree [4 ]
Baudin, Eric [4 ]
Jimenez, Camilo [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Endocrine Neoplasia & Hormonal Disorders, Unit 1461, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Pediat, Houston, TX 77030 USA
[4] Inst Gustave Roussy, Dept Nucl Med & Endocrine Tumors, F-94805 Villejuif, France
[5] Inst Gustave Roussy, Dept Pathol, F-94805 Villejuif, France
关键词
MALIGNANT PHEOCHROMOCYTOMAS; INHIBITOR SUNITINIB; MAMMALIAN TARGET; EXPRESSION; MUTATIONS; ANGIOGENESIS; ANTITUMOR; THERAPY; GENES; MTOR;
D O I
10.1210/jc.2012-2356
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Patients with progressive metastatic pheochromocytomas (PHEOs) or sympathetic paragangliomas (SPGLs) face a dismal prognosis. Current systemic therapies are limited. Objectives: The primary end point was progression-free survival determined by RECIST 1.1 criteria or positron emission tomography with [F-18] fluorodeoxyglucose/computed tomography ([F-18] FDG-PET/CT), in the absence of measurable soft tissue targets. Secondary endpoints were tumor response according to RECIST criteria version 1.1 or FDG uptake, blood pressure control, and safety. Design: We conducted a retrospective review of medical records of patients with metastatic PHEO/SPGL treated with sunitinib from December 2007 through December 2011. An intention-to-treat analysis was performed. Patients and Setting: Seventeen patients with progressive metastatic PHEO/SPGLs treated at the Institut Gustave-Roussy and MD Anderson Cancer Center. Interventions: Patients treated with sunitinib. Results: According to RECIST 1.1, eight patients experienced clinical benefit; three experienced partial response, and five had stable disease, including four with predominant skeletal metastases that showed a 30% or greater reduction in glucose uptake on [F-18]FDG-PET/CT. Of 14 patients who had hypertension, six became normotensive and two discontinued antihypertensives. One patient treated with sunitinib and rapamycin experienced a durable benefit beyond 36 months. The median overall survival from the time sunitinib was initiated was 26.7 months with a progression-free survival of 4.1 months (95% confidence interval = 1.4-11.0). Most patients who experienced a clinical benefit were carriers of SDHB mutations. Conclusion: Sunitinib is associated with tumor size reduction, decreased [F-18]FDG-PET/CT uptake, disease stabilization, and hypertension improvement in some patients with progressive metastatic PHEO/PGL. Prospective multi-institutional clinical trials are needed to determine the true benefits of sunitinib. (J Clin Endocrinol Metab 97: 4040-4050, 2012)
引用
收藏
页码:4040 / 4050
页数:11
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