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DOI 10.1210/jc.2012-2356

Медицинская библиотека · The Journal of clinical endocrinology and metabolism · 2012

Treatment with sunitinib for patients with progressive metastatic pheochromocytomas and sympathetic paragangliomas.

Ayala-Ramirez Montserrat, Chougnet Cecile N, Habra Mouhammed Amir, Palmer J Lynn, Leboulleux Sophie, Cabanillas Maria E, Caramella Caroline, Anderson Pete, Al Ghuzlan Abir, Waguespack Steven G, Deandreis Desirée, Baudin Eric, Jimenez Camilo

СтатьяПоддержка NIH: внешняя программаПеревод пока не подготовлен

Аннотация

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 [(18)F]fluorodeoxyglucose/computed tomography ([(18)F]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 [(18)F]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 [(18)F]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.

Для цитирования: Ayala-Ramirez Montserrat, Chougnet Cecile N, Habra Mouhammed Amir, Palmer J Lynn, Leboulleux Sophie, Cabanillas Maria E, Caramella Caroline, Anderson Pete, Al Ghuzlan Abir, Waguespack Steven G, Deandreis Desirée, Baudin Eric, Jimenez Camilo. Treatment with sunitinib for patients with progressive metastatic pheochromocytomas and sympathetic paragangliomas.. The Journal of clinical endocrinology and metabolism. 2012. DOI: 10.1210/jc.2012-2356.

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