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

被引:172
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
相关论文
共 35 条
  • [1] Genetic testing in pheochromocytoma or functional paraganglioma
    Amar, L
    Bertherat, J
    Baudin, E
    Ajzenberg, C
    Bressac-de Paillerets, B
    Chabre, O
    Chamontin, B
    Delemer, B
    Giraud, S
    Murat, A
    Niccoli-Sire, P
    Richard, SP
    Rohmer, V
    Sadoul, JL
    Strompf, L
    Schlumberger, M
    Bertagna, X
    Plouin, PF
    Jeunemaitre, X
    Gimenez-Roqueplo, AP
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (34) : 8812 - 8818
  • [2] Long-term Postoperative Follow-up in Patients with Apparently Benign Pheochromocytoma and Paraganglioma
    Amar, L.
    Fassnacht, M.
    Gimenez-Roqueplo, A. -P.
    Januszewicz, A.
    Prejbisz, A.
    Timmers, H.
    Plouin, P. -F.
    [J]. HORMONE AND METABOLIC RESEARCH, 2012, 44 (05) : 385 - 389
  • [3] Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas
    Amar, Laurence
    Baudin, Eric
    Burnichon, Nelly
    Peyrard, Severine
    Silvera, Stephane
    Bertherat, Jerome
    Bertagna, Xavier
    Schlumberger, Martin
    Jeunemaitre, Xavier
    Gimenez-Roqueplo, Anne-Paule
    Plouin, Pierre-Francois
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (10) : 3822 - 3828
  • [4] Clinical Risk Factors for Malignancy and Overall Survival in Patients with Pheochromocytomas and Sympathetic Paragangliomas: Primary Tumor Size and Primary Tumor Location as Prognostic Indicators
    Ayala-Ramirez, Montserrat
    Feng, Lei
    Johnson, Marcella M.
    Ejaz, Shamim
    Habra, Mouhammed Amir
    Rich, Thereasa
    Busaidy, Naifa
    Cote, Gilbert J.
    Perrier, Nancy
    Phan, Alexandria
    Patel, Shreyaskumar
    Waguespack, Steven
    Jimenez, Camilo
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2011, 96 (03) : 717 - 725
  • [5] BEARD CM, 1983, MAYO CLIN PROC, V58, P802
  • [6] Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma
    Burnichon, Nelly
    Vescovo, Laure
    Amar, Laurence
    Libe, Rossella
    de Reynies, Aurelien
    Venisse, Annabelle
    Jouanno, Elodie
    Laurendeau, Ingrid
    Parfait, Beatrice
    Bertherat, Jerome
    Plouin, Pierre-Francois
    Jeunemaitre, Xavier
    Favier, Judith
    Gimenez-Roqueplo, Anne-Paule
    [J]. HUMAN MOLECULAR GENETICS, 2011, 20 (20) : 3974 - 3985
  • [7] The role of mammalian target of rapamycin inhibitors in the treatment of advanced renal cancer
    Cho, Daniel
    Signoretti, Sabina
    Regan, Meredith
    Mier, James W.
    Atkins, Michael B.
    [J]. CLINICAL CANCER RESEARCH, 2007, 13 (02) : 758S - 763S
  • [8] Sunitinib: From rational design to clinical efficacy
    Chow, Laura Q. M.
    Eckhardt, S. Gail
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (07) : 884 - 896
  • [9] A HIF1α regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas
    Dahia, PLM
    Ross, KN
    Wright, ME
    Hayashida, CY
    Santagata, S
    Barontini, M
    Kung, AL
    Sanso, G
    Powers, JF
    Tischler, AS
    Hodin, R
    Heitritter, S
    Moore, F
    Dluhy, R
    Sosa, JA
    Ocal, IT
    Benn, DE
    Marsh, DJ
    Robinson, BG
    Schneider, K
    Garber, J
    Arum, SM
    Korbonits, M
    Grossman, A
    Pigny, P
    Toledo, SPA
    Nosé, V
    Li, C
    Stiles, CD
    [J]. PLOS GENETICS, 2005, 1 (01): : 72 - 80
  • [10] Therapeutic targets - MTOR and related pathways
    Dancey, Janet E.
    [J]. CANCER BIOLOGY & THERAPY, 2006, 5 (09) : 1065 - 1073